81 FR 85573 - Report on the Performance of Drug and Biologics Firms in Conducting Postmarketing Requirements and Commitments; Availability
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration Federal Register Volume 81, Issue 228 (November 28, 2016)
Food and Drug Administration
Federal Register Volume 81, Issue 228 (November 28, 2016)
| Page Range | 85573-85579 | |
| FR Document | 2016-28442 |
[Federal Register Volume 81, Number 228 (Monday, November 28, 2016)] [Notices] [Pages 85573-85579] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-28442] [[Page 85573]] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2016-N-3083] Report on the Performance of Drug and Biologics Firms in Conducting Postmarketing Requirements and Commitments; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice of availability. ----------------------------------------------------------------------- SUMMARY: Under the Federal Food, Drug, and Cosmetic Act (the FD&C Act), the Food and Drug Administration (FDA or Agency) is required to report annually in the Federal Register on the status of postmarketing requirements (PMRs) and postmarketing commitments (PMCs) required of, or agreed upon by, holders of approved drug and biological products. This notice is the Agency's report on the status of the studies and clinical trials that applicants have agreed to, or are required to, conduct. A supplemental report containing additional information and analyses on the status of PMRs and PMCs is available on FDA's Web site.\1\ --------------------------------------------------------------------------- \1\ http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Post-marketingPhaseIVCommitments/ucm064436.htm. FOR FURTHER INFORMATION CONTACT: Cathryn C. Lee, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 6484, Silver Spring, MD 20993-0002, 301- 796-0700; or Stephen Ripley, Center for Biologics Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. --------------------------------------------------------------------------- 71, Rm. 7301, Silver Spring, MD 20993-0002, 240-402-7911. SUPPLEMENTARY INFORMATION: I. Background A. Postmarketing Requirements and Commitments A PMR is a study or clinical trial that an applicant is required by statute or regulation to conduct postapproval. A PMC is a study or clinical trial that an applicant agrees in writing to conduct postapproval, but that is not required by statute or regulation. PMRs and PMCs can be issued upon approval of a drug\2\ or postapproval, if warranted. --------------------------------------------------------------------------- \2\ For the purposes of this notice, references to ``drugs'' or ``drug products'' include drugs approved under the FD&C Act and biological products licensed under the Public Health Service Act, other than biological products that also meet the definition of a device in section 201(h) of the FD&C Act (21 U.S.C. 321(h)). --------------------------------------------------------------------------- FDA can require application holders to conduct postmarketing studies and clinical trials:To assess a known serious risk, assess signals of serious risk, or identify an unexpected serious risk related to the use of a drug product (section 505(o)(3) of the FD&C Act (21 U.S.C. 355(o)(3)), as added by the Food and Drug Administration Amendments Act of 2007 (FDAAA)). Under the Pediatric Research Equity Act (PREA), to study certain new drugs for pediatric populations, when these drugs are not adequately labeled for children. Under section 505B(a)(3) of the FD&C Act (21 U.S.C. 355c), the initiation of these studies may be deferred until required safety information from other studies in adults has first been submitted and reviewed. To verify and describe the predicted effect or other clinical benefit for drugs approved in accordance with the accelerated approval provisions in section 506(c)(2)(A) of the FD&C Act (21 U.S.C. 356(c)(2)(A)) (Sec. Sec. 314.510 and 601.41 (21 CFR 314.510 and 601.41)). For a drug that was approved on the basis of animal efficacy data because human efficacy trials are not ethical or feasible (Sec. Sec. 314.610(b)(1) and 601.91(b)(1)). PMRs for drug products approved under the animal efficacy rule\3\ can be conducted only when the drug product is used for its indication and when an exigency (or event or need) arises. In the absence of a public health emergency, these studies or clinical trials will remain pending indefinitely. --------------------------------------------------------------------------- \3\ 21 CFR 314.600 for drugs; 21 CFR 601.90 for biological products. --------------------------------------------------------------------------- B. Reporting Requirements Under the regulations (Sec. Sec. 314.81(b)(2)(vii) and 601.70), applicants of approved drugs are required to submit annually a report on the status of each clinical safety, clinical efficacy, clinical pharmacology, and nonclinical toxicology study or clinical trial either required by FDA or that they have committed to conduct, either at the time of approval or after approval of their new drug application (NDA), abbreviated new drug application (ANDA), or biologics license application (BLA). Applicants are required to report to FDA on these requirements and commitments made for NDAs and ANDAs under Sec. 314.81(b)(2)(viii). The status of PMCs concerning chemistry, manufacturing, and production controls and the status of other studies or clinical trials conducted on an applicant's own initiative are not required to be reported under Sec. Sec. 314.81(b)(2)(vii) and 601.70 and are not addressed in this report. Furthermore, section 505(o)(3)(E) of the FD&C Act requires that applicants report periodically on the status of each required study or clinical trial and each study or clinical trial ``otherwise undertaken * * * to investigate a safety issue * * * .'' An applicant must report on the progress of the PMR/PMC on the anniversary of the drug product's approval\4\ until the PMR/PMC is completed or terminated and FDA determines that the PMR/PMC has been fulfilled or that the PMR/PMC is either no longer feasible or would no longer provide useful information. The annual status report (ASR) must include a description of the PMR/PMC, a schedule for completing the PMR/PMC, and a characterization of the current status of the PMR/PMC. The report must also provide an explanation of the PMR/PMC status by describing briefly the progress of the PMR/PMC. A PMR/PMC schedule is expected to include the actual or projected dates for the following: (1) Submission of the final protocol to FDA; (2) completion of the study or clinical trial; and (3) submission of the final report to FDA. --------------------------------------------------------------------------- \4\ An applicant must submit an annual status report on the progress of each open PMR/PMC within 60 days of the anniversary date of U.S. approval of the original application or on an alternate reporting date that was granted by FDA in writing. Some applicants have requested and been granted by FDA alternate annual reporting dates to facilitate harmonized reporting across multiple applications. --------------------------------------------------------------------------- C. PMR/PMC Status Categories The status of the PMR/PMC must be described in the ASR according to the terms and definitions provided in Sec. Sec. 314.81 and 601.70. For its own reporting purposes, FDA has also established terms to describe when the conditions of the PMR/PMC have been met, and when it has been determined that a PMR/PMC is no longer necessary.\5\ The PMR/PMC status categories are summarized in the following list. As reflected in the definitions, the status of a PMR/PMC is generally determined based on the original schedule.\6\ --------------------------------------------------------------------------- \5\ See the guidance for industry entitled ``Reports on the Status of Postmarketing Study Commitments--Implementation of Section 130 of the Food and Drug Administration Modernization Act of 1997.'' We update guidances periodically. To make sure you have the most recent version of a guidance, check the FDA Drugs guidance Web page at http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm. \6\ The definitions for the terms ``pending,'' ``ongoing,'' ``delayed,'' ``terminated,'' and ``submitted'' are adapted from Sec. Sec. 314.81 and 601.70; the definitions for the terms ``fulfilled'' and ``released'' are described in the guidance for industry entitled ``Reports on the Status of Postmarketing Study Commitments--Implementation of Section 130 of the Food and Drug Administration Modernization Act of 1997.'' --------------------------------------------------------------------------- [[Page 85574]] Pending: The study or clinical trial has not been initiated (i.e., no subjects have been enrolled or animals dosed), but does not meet the criteria for delayed (i.e., the original projected date for initiation of subject accrual or initiation of animal dosing has not passed).\7\ --------------------------------------------------------------------------- \7\ It is important to note that PMRs/PMCs that are in pending status are not yet delayed; that is, per the milestones, the studies or clinical trials are indeed on schedule and are not expected to be underway yet. --------------------------------------------------------------------------- Ongoing: The study or clinical trial is proceeding according to or ahead of the original schedule. Delayed: The study or clinical trial is behind the original schedule.\8\ --------------------------------------------------------------------------- \8\ In some instances, an applicant may have justifiable reasons for delay of its PMR/PMC (see section I.D). --------------------------------------------------------------------------- Terminated: The study or clinical trial was ended before completion, but a final report has not been submitted to FDA. Submitted: The study or clinical trial has been completed or terminated, and a final report has been submitted to FDA. Fulfilled: The final report for the study or clinical trial was submitted to FDA and FDA notified the applicant that the requirement or commitment was fulfilled through written correspondence. Released: FDA has informed the applicant in writing that it is released from its obligation to conduct the study or clinical trial because the study or clinical trial is no longer feasible, would no longer provide useful information, or the underlying application has been formally withdrawn. In addition to the above statuses, PMRs/PMCs may also be characterized as closed or open. Open PMRs/PMCs comprise those that are pending, ongoing, delayed, submitted, or terminated; whereas closed \9\ PMRs/PMCs are either fulfilled or released. Open PMRs are also described by whether they are on- or off-schedule. On-schedule PMRs/ PMCs are those that are pending, ongoing, or submitted. Off-schedule PMRs/PMCs are those that have missed one of the milestone dates in the original schedule and are categorized as either delayed or terminated. --------------------------------------------------------------------------- \9\ Previous FDA reports on the status of PMRs/PMCs used the term ``completed'' to refer to PMRs/PMCs that are closed. --------------------------------------------------------------------------- D. Additional Requirements If an applicant fails to comply with the original schedule for completion of postmarketing studies or clinical trials required under section 505(o)(3) of the FD&C Act (i.e., under the FDAAA authorities), or fails to submit periodic reports on the status of the studies or clinical trials, the applicant is considered to be in violation of section 505(o)(3), unless it has demonstrated good cause for its noncompliance or other violation. Failure to meet an original milestone and, as a result, falling behind the original schedule is one type of noncompliance with a PMR issued under FDAAA. In these circumstances, the FDAAA PMR is considered delayed, with or without good cause. Section 505B(a)(3)(B) of the FD&C Act, as amended by the Food and Drug Administration Safety and Innovation Act, authorizes FDA to grant an extension of the deferred pediatric assessments that are required under PREA.\10\ On its own initiative or upon request, FDA may grant an extension of a pediatric assessment deferral, provided that certain applicable PREA criteria for deferral are still met and the applicant submits certain materials in support of the extension.\11\ Applicants must submit requests for deferral extensions to FDA not less than 90 days before the date the deferral would otherwise expire. If FDA grants the extension of a pediatric study deferral, this new deferral date is considered the original due date of the PMR. Consequently, the status of PREA PMRs would be determined based on the new deferral date (and not the original PREA PMR schedule). --------------------------------------------------------------------------- \10\ This provision does not apply to PMRs required under other provisions, or to PMCs. \11\ See section 505B(a)(3)(B) of the FD&C Act. --------------------------------------------------------------------------- FDA may take enforcement action against applicants who are noncompliant with or otherwise fail to conduct studies and clinical trials required under FDA statutes and regulations (see, for example, sections 505(o)(1), 502(z), and 303(f)(4) of the FD&C Act (21 U.S.C. 355(o)(1), 352(z), and 333(f)(4))). II. Understanding FDA's Data on Postmarketing Studies and Clinical Trials A. FDA's Internal PMR/PMC Databases Databases containing information on PMRs/PMCs are maintained at the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER). The information in these databases is periodically updated as new PMRs/PMCs are issued, upon FDA review of PMR/PMC ASRs or other PMR/PMC correspondence, upon receipt of final reports from completed studies and clinical trials, and after the final reports are reviewed and FDA determines that the PMR/PMC has been fulfilled, or when FDA determines that the PMR/PMC is either no longer feasible or would no longer provide useful information. Because applicants typically report on the status of their PMRs/PMCs annually, and because updating the status of PMRs/PMCs in FDA's databases involves FDA review of received information, there is an inherent lag in updating the data (that is, the data are not real time). FDA strives to maintain as accurate information as possible on the status of PMRs/ PMCs. Both CDER and CBER have established policies and procedures to help ensure that FDA's data on PMRs/PMCs are current and accurate. When identified, data discrepancies are addressed as expeditiously as possible and/or are corrected in later reports. B. Publicly Available PMR/PMC Data FDA also maintains an online searchable and downloadable database that contains information about PMRs/PMCs that is publicly reportable (i.e., for which applicants must report on the status of the study or clinical trial, as required under section 506B of the FD&C Act (21 U.S.C. 356b)). The data are a subset of all PMRs/PMCs and reflect only those postmarketing studies and clinical trials that, at the time of data retrieval, either had an open status or were closed within the past year. Information on PMRs/PMCs closed more than a year before the date the data are extracted (i.e., September 30, 2015) are not included on the public Web site. The FDA Web site is updated quarterly.\12\ The FDA Web site does not include information about PMCs concerning chemistry, manufacturing, and controls. It is FDA policy not to post information on the Web site until it has been verified and reviewed for suitability for public disclosure. --------------------------------------------------------------------------- \12\ http://www.accessdata.fda.gov/scripts/cder/pmc/index.cfm. --------------------------------------------------------------------------- III. About This Report This report is published to fulfill the annual reporting requirement under section 506B(c) of the FD&C Act. Information in this report covers any PMR/PMC that was made, in writing, at the time of approval or after approval of an application or a supplement to an application (see section I.A), and summarizes the status of PMRs/PMCs in fiscal year (FY) 2015 (FY2015) (i.e., as of September 30, 2015). Specifically, the report summarizes the status of all open [[Page 85575]] PMRs/PMCs through the end of the fiscal year, and the status of only those PMRs/PMCs that were closed in the fiscal year. If a requirement or commitment did not have a schedule, or an ASR was not received in the previous 12 months, the PMR/PMC is categorized according to the most recent information available to the Agency.\13\ --------------------------------------------------------------------------- \13\ Although the data included in this report do not include a summary of reports that applicants have failed to file by their due date, the Agency notes that it may take appropriate regulatory action in the event reports are not filed on a timely basis. --------------------------------------------------------------------------- This report reflects combined data from CDER and CBER. Information summarized in the report includes the following: (1) The number of applicants with open PMRs/PMCs; \14\ (2) the number of open PMRs/PMCs; (3) the number of applications for which an ASR was expected but was not submitted within 60 days of the anniversary date of U.S. approval or an alternate reporting date that was granted by FDA; (4) FDA- verified status of open PMRs/PMCs reported in Sec. Sec. 314.81(b)(2)(vii) or 601.70 ASRs; (5) the status of closed PMRs/PMCs; and (6) the distribution of the status by fiscal year of establishment \15\ (FY2009 to FY2015) for PMRs and PMCs open at the end of FY2015, or those closed within FY2015. The tables in this report distinguish between PMRs and PMCs, PMRs/PMCs for NDAs and BLAs, and on-schedule and off-schedule PMRs/PMCs, according to the original schedule milestones. A more detailed summary of this information and additional information about PMRs/PMCs is provided on FDA's Web site at http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Post-marketingPhaseIVCommitments/default.htm. In the supplemental report on FDA's Web site, information is presented separately for CDER and CBER. --------------------------------------------------------------------------- \14\ At the end of FY2015, there were no PMRs/PMCs for ANDAs that met the reporting requirements under the Food and Drug Administration Modernization Act of 1997. Therefore, this report reflects information for NDAs and BLAs only. \15\ The establishment date is the date of the formal FDA communication to the applicant that included the final FDA required (PMR) or requested (PMC) postmarketing study or clinical trial. --------------------------------------------------------------------------- Numbers published in this report and in the supplemental report on FDA's Web site cannot be compared with the numbers resulting from searches of the publicly accessible and downloadable database. This is because this report incorporates data for all PMRs/PMCs in FDA databases as of the end of the fiscal year, including PMRs/PMCs undergoing review for accuracy. The publicly accessible and downloadable database includes a subset of PMRs/PMCs, specifically those that, at the time of data retrieval, either had an open status or were closed within the past 12 months. In addition, the status information in this report is updated annually while the downloadable database is updated quarterly (i.e., in January, April, July, and October). IV. Summary of Information on PMR/PMC Status This report provides information on PMRs/PMCs as of September 30, 2015 (i.e., for FY2015). It is important to note that a comparison of the number of open and on-schedule or off-schedule PMRs/PMCs over time can be misleading because it does not take into account that the cohort of open PMRs/PMCs is not static from year to year. New PMRs/PMCs are continually being established for studies and clinical trials with varying start dates and durations; and other PMRs/PMCs are closed because they are either fulfilled or released. Also, ongoing PMRs/PMCs are carried forward into the subsequent fiscal year. Therefore, the number of on- and off-schedule PMRs/PMCs can vary from year to year, and a year-to-year comparison of on- or off-schedule PMRs (e.g., to assess for a potential trend) is not appropriate. Finally, due to rounding, the percentages in the tables may not add up to 100 percent. A. Applicants With Open PMRs/PMCs An applicant may have multiple approved drug products, and an approved drug product may have multiple PMRs and/or PMCs. Table 1 shows that as of September 30, 2015, there were 269 unique applicants with open PMRs/PMCs under 856 unique NDAs and BLAs. There were 194 unique NDA applicants (and 716 associated applications) and 75 unique BLA applicants (and 140 associated applications) with open PMRs/PMCs. B. Annual Status Reports Received As previously mentioned, applicants must submit an ASR on the progress of each open PMR/PMC within 60 days of the anniversary date of U.S. approval of the original application or an alternate reporting date that was granted by FDA (Sec. Sec. 314.81 and 21 CFR 601.70).\16\ Table 2 shows that there were 575 NDAs and BLAs with an ASR due in FY2015 (451 NDAs and 124 BLAs).\17\ Of the 451 NDA ASRs due in that fiscal year, 67 percent (304/451) were received on time, 14 percent (62/451) were not received on time, and 19 percent (85/451) were not received during FY2015. Of the 124 BLA ASRs due, 78 percent (97/124) were received on time, 13 percent (16/124) were not received on time, and 9 percent (11/124) were not received during FY2015. --------------------------------------------------------------------------- \16\ An applicant must submit an ASR on the progress of each open PMR/PMC within 60 days of the anniversary date of U.S. approval of the original application or on an alternate reporting date that was granted by FDA in writing. Some applicants have requested and been granted by FDA alternate annual reporting dates to facilitate harmonized reporting across multiple applications. \17\ The number of ASRs that were expected is different from the total number of unique applications with open PMRs/PMCs because not all applications had an ASR due during FY2015. Applicants with PMRs/ PMCs associated with multiple applications may have submitted the ASR to only one of the applications. In addition, if all of the PMRs/PMCs for an application were established in the preceding fiscal year, or if all PMRs/PMCs for an application were closed before the ASR due date, submission of an ASR would not have been expected. --------------------------------------------------------------------------- C. Overview of On- and Off-Schedule Open PMRs/PMCs Table 3 shows that as of September 30, 2015, most open PMRs (88 percent for NDAs and 91 percent for BLAs) and most open PMCs (69 percent for NDAs and 78 percent for BLAs) were progressing on schedule. D. Open and On-Schedule PMRs Table 4 shows that as of September 30, 2015, the majority of PMRs were pending (53 percent (535/1,010) of open NDA PMRs and 45 percent (100/223) of open BLA PMRs). PREA PMRs and FDAAA PMRs comprised 53 percent (336/635) and 43 percent (270/635) of pending PMRs, respectively. The next largest category of open and on-schedule PMRs comprised those that were ongoing (29 percent (288/1,010) of NDA PMRs and 36 percent (80/223) of BLA PMRs). E. Open and Off-Schedule PMRs Table 5 provides additional information on the status of open and off-schedule (i.e., delayed and terminated) PMRs. At the end of September 30, 2015, 12 percent (123/1,010) of the open NDA PMRs and 9 percent (20/223) of the open BLA PMRs were off-schedule. Of the off- schedule NDA PMRs, 97 percent (119/123) were off-schedule because they were delayed and the remaining 3 percent (4/123) were terminated. Similarly, 90 percent of the off-schedule BLA PMRs were delayed (18/ 20). In certain situations, the original PMR schedules were adjusted for unanticipated delays in the progress of the study or clinical trial (e.g., difficulties with subject enrollment in a clinical trial for a marketed drug or need for additional time to analyze results). [[Page 85576]] In this report, study or clinical trial status reflects the status in relation to the original\18\ study or clinical trial schedule regardless of whether FDA has acknowledged that additional time was required to complete the study or clinical trial. --------------------------------------------------------------------------- \18\ With the exception of PREA PMRs for which a deferral extension of the final report submission date has been granted. --------------------------------------------------------------------------- F. Open On-Schedule and Off-Schedule PMCs Table 6 provides the status of open on-schedule and off-schedule PMCs and shows that as of September 30, 2015, the largest category of all open NDA PMCs were those that were pending (36 percent; 71/197). Most of the open BLA PMCs were ongoing at the end of FY2015 (39 percent; 80/204). Off-schedule PMCs accounted for 31 percent (62/197) of open NDA PMCs and 22 percent (45/204) of open BLA PMCs. The majority of off-schedule NDA and BLA PMCs were delayed according to the original schedule milestones. G. Closed PMRs and PMCs Table 7 provides details about PMRs and PMCs that were closed (released or fulfilled) within FY2015. The majority of closed PMRs were fulfilled (69 percent of NDA PMRs and 90 percent of BLA PMRs at the end of FY2015). Similarly, the majority of closed PMCs within FY2015 were fulfilled. H. Distribution of the Status of PMRs and PMCs Tables 8 and 9 show the distribution of the statuses of PMRs/PMCs as of September 30, 2015, presented by the year that the PMR/PMC was established\19\ (FY2009 to FY2015).20 21 Note that the data shown for closed (fulfilled or released) PMRs/PMCs are for all PMRs/ PMCs that were closed as of FY2015. Therefore, data for PMRs/PMCs that were closed in prior fiscal years are included. Based on the data shown in table 8, an average of 254 PMRs were established each year since FY2009.\22\ Most PMRs that were established in the earlier years were either fulfilled or released. For example, as of September 30, 2015, 44 percent (109/248) of the PMRs that were established in FY2009 were fulfilled, and 22 percent (55/248) were released. The majority of PMRs that were established in more recent years were either pending (i.e., not yet underway) or ongoing (i.e., still in progress and on schedule). For example, as of September 30, 2015, 89 percent (250/280) of the PMRs established in FY2015 were pending, and 6 percent (16/280) were ongoing. Overall, of the PMRs that were pending as of September 30, 2015, 86 percent (527/616) were created within the past 3 years (FY2013, FY2014, and FY2015). Finally, table 8 shows that, on average, 6 percent of the PMRs established since FY2009 were delayed as of September 30, 2015. Table 9 provides an overview of PMCs in a similar manner as table 8 does for PMRs and shows similar results for PMCs as those for PMRs as described above and in table 8. --------------------------------------------------------------------------- \19\ The establishment date is the date of the formal FDA communication to the applicant that included the final FDA required (PMR) or requested (PMC) postmarketing study or clinical trial. \20\ Tables 8 and 9 include data for only the past 7 fiscal years. Data on the distribution of statuses for PMRs/PMCs established in FY2008 and as of FY2014 are presented in the FY2014 status of postmarketing requirements and commitments report (81 FR 75411) (https://www.thefederalregister.org/fdsys/pkg/FR-2016-10-31/html/2016-26247.htm). \21\ The total number of PMRs/PMCs established in FY2009 through FY2014 reflects the data in FDA's databases as of September 30, 2015. As a result of data corrections, as well as improvements in ascertainment of the PMR/PMC establishment date, some of the total numbers of PMRs/PMCs established in each fiscal year are different from those reported in the prior fiscal year's (FY 2014) Federal Register report. \22\ The number of PMRs issued at any particular period is determined by a variety of factors including but not necessarily limited to: (1) The number of NDAs approved in that period; (2) whether additional efficacy or clinical benefit issues were evaluated; (3) if any drug-associated serious risk(s) have been identified; and (4) whether or not FDA determines that a postmarketing study or clinical trial is necessary to further assess risk(s) or efficacy issues. Table 1--Applicants and Applications (NDA/BLA) With Open Postmarketing Requirements and Commitments [Numbers as of September 30, 2015] ---------------------------------------------------------------------------------------------------------------- Total (NDA NDA \1\ BLA \2\ and BLA) ---------------------------------------------------------------------------------------------------------------- Number of unique applicants with open PMRs/PMCs................. 194 75 269 Number of applications with open PMRs/PMCs...................... 716 140 856 ---------------------------------------------------------------------------------------------------------------- \1\ Includes two NDAs with associated PMRs/PMCs managed by CBER. \2\ Includes BLAs managed by both CDER and CBER. Table 2--Annual Status Reports Received [Numbers as of September 30, 2015] \1\ ---------------------------------------------------------------------------------------------------------------- Received, not Expected but Received, on on time \4\ not received Expected \2\ time \3\ (% (% of (% of of expected) expected) expected) ---------------------------------------------------------------------------------------------------------------- NDA............................................. 451 304 (67%) 62 (14%) 85 (19%) BLA............................................. 124 97 (78%) 16 (13%) 11 (9%) --------------------------------------------------------------- Total....................................... 575 401 (70%) 78 (14%) 96 (17%) ---------------------------------------------------------------------------------------------------------------- \1\ Percentages may not total 100 due to rounding. \2\ ASR expected during fiscal year (within 60 days (before or after) of the anniversary of original approval date or alternate agreed-upon date). \3\ ASR was received within 60 days (before or after) of the anniversary of the original approval date or alternate agreed-upon date. \4\ ASR was received, but not within 60 days (before or after) of the anniversary of the original approval date or alternate agreed-upon date. [[Page 85577]] Table 3--Summary of On- and Off-Schedule Postmarketing Requirements and Commitments [Numbers as of September 30, 2015] \1\ ---------------------------------------------------------------------------------------------------------------- Open PMRs N = 1,233 Open PMCs N = 401 --------------------------------------------------------------- NDA (% of BLA (% of NDA (% of BLA (% of Open NDA PMRs) Open BLA PMRs) Open NDA PMCs) Open BLA PMCs) ---------------------------------------------------------------------------------------------------------------- On-schedule..................................... 887 (88%) 203 (91%) 135 (69%) 159 (78%) Off-schedule.................................... 123 (12%) 20 (9%) 62 (31%) 45 (22%) --------------------------------------------------------------- Total....................................... 1,010 223 197 204 ---------------------------------------------------------------------------------------------------------------- \1\ Percentages may not total 100 due to rounding. Table 4--Summary of Open and On-Schedule Postmarketing Requirements [Numbers as of September 30, 2015] \1\ -------------------------------------------------------------------------------------------------------------------------------------------------------- NDA N = 1,010 (% of Open NDA PMRs) BLA N = 223 (% of Open BLA PMRs) Reporting authority/PMR status ----------------------------------------------------------------------------------------------- Pending Ongoing Submitted Pending Ongoing Submitted -------------------------------------------------------------------------------------------------------------------------------------------------------- Accelerated approval.................................... 12 (1%) 25 (3%) 3 (<1%) 7 (3%) 7 (2%) 1 (<1%) PREA \2\................................................ 290 (29%) 121 (12%) 18 (2%) 46 (20%) 18 (8%) 9 (4%) Animal efficacy \3\..................................... 4 (<1%) 0 1 (<1%) 6 (3%) 0 0 FDAAA safety \4\........................................ 229 \3\ (23%) 142 (14%) 42 (4%) 41 (18%) 55 (25%) 13 (6%) (since March 25, 2008).................................. ----------------------------------------------------------------------------------------------- Total............................................... 535 (53%) 288 (29%) 64 (6%) 100 (45%) 80 (36%) 23 (10%) -------------------------------------------------------------------------------------------------------------------------------------------------------- \1\ Percentages may not total 100 due to rounding. \2\ Many PREA studies have a pending status. PREA studies are usually deferred because the drug product is ready for approval in adults. Initiation of these studies may be deferred until additional safety information from other studies has first been submitted and reviewed before beginning the studies in pediatric populations. \3\ PMRs for drug products approved under the animal efficacy rule (Sec. 314.600 for drugs; Sec. 601.90 for biological products) can be conducted only when the drug product is used for its indication and when an exigency (or event or need) arises. In the absence of a public health emergency, these studies or clinical trials will remain pending indefinitely. \4\ Includes one NDA PMR FDAAA safety study from CBER in pending status. Table 5--Summary of Open and Off-Schedule Postmarketing Requirements [Numbers as of September 30, 2015] \1\ ---------------------------------------------------------------------------------------------------------------- NDA N = 1,010 (% of Open NDA BLA N = 223 (% of Open BLA PMRs) PMRs) Reporting authority/PMR status --------------------------------------------------------------- Delayed Terminated Delayed Terminated ---------------------------------------------------------------------------------------------------------------- Accelerated approval............................ 3 (<1%) 2 (<1%) 1 (<1%) 0 PREA............................................ 64 (6%) 2 (<1%) 5 (2%) 2 (<1%) Animal efficacy................................. 0 0 0 0 FDAAA safety.................................... 52 (5%) 0 12 (5%) 0 (since March 25, 2008).......................... --------------------------------------------------------------- Total....................................... 119 (12%) 4 (<1%) 18 (8%) 2 (<1%) ---------------------------------------------------------------------------------------------------------------- \1\ Percentages may not total 100 due to rounding. Table 6--Summary of Open Postmarketing Commitments [Numbers as of September 30, 2015] \1\ ------------------------------------------------------------------------ NDA N = 197 (% BLA N = 204 (% Open PMCs) Open PMCs) ------------------------------------------------------------------------ On-Schedule............................. .............. .............. Pending................................. 71 (36%) 54 (26%) Ongoing................................. 40 (20%) 80 (39%) Submitted............................... 24 (12%) 25 (12%) Total................................... 135 (68%) 159 (77%) Off-Schedule............................ .............. .............. Delayed................................. 59 (30%) 43 (21%) [[Page 85578]] Terminated.............................. 3 (2%) 2 (1%) ------------------------------- Total............................... 62 (31%) 45 (22%) ------------------------------------------------------------------------ \1\ Percentages may not total 100 due to rounding. Table 7--Summary of Closed \1\ Postmarketing Requirements and Commitments [Numbers as of September 30, 2015] \2\ ------------------------------------------------------------------------ Postmarketing requirements NDA N = 195 BLA N = 40 ------------------------------------------------------------------------ Closed PMRs (% of Total Closed PMRs) .............. .............. Requirement met (fulfilled)............. 134 (69%) 36 (90%) Requirement not met (released and new 31 (16%) 1 (2%) revised requirement issued)............ Requirement no longer feasible or drug 30 (15%) 3 (8%) product withdrawn (released)........... ------------------------------------------------------------------------ Postmarketing Commitments NDA BLA N = 56 N = 32 ------------------------------------------------------------------------ Closed PMCs (% of Total Closed PMCs).... .............. .............. Requirement met (fulfilled)............. 46 (82%) 27 (84%) Requirement not met (released and new 1 (2%) 2 (6%) revised requirement issued)............ Requirement no longer feasible or drug 9 (16%) 3 (9%) product withdrawn (released)........... ------------------------------------------------------------------------ \1\ The table shows data for those PMRs/PMCs that were closed (fulfilled or released) within FY2015. Therefore, data for PMRs/PMCs that were closed in prior fiscal years are not included. \2\ Percentages may not total 100 due to rounding. Table 8--Summary of Status of Postmarketing Requirements Established \1\ Between FY2009 and FY2015 \2\ [Numbers as of September 30, 2015] \3\ -------------------------------------------------------------------------------------------------------------------------------------------------------- Fiscal year of PMR establishment PMR Status as of FY2015 (% of total PMRs --------------------------------------------------------------------------------------------------------------- in each establishment year) 2009 2010 2011 2012 2013 2014 2015 -------------------------------------------------------------------------------------------------------------------------------------------------------- Pending................................. 14 (6%) 11 (5%) 27 (10%) 37 (17%) 91 (33%) 186 (68%) 250 (89%) Ongoing................................. 38 (15%) 40 (18%) 54 (21%) 59 (27%) 79 (28%) 46 (17%) 16 (6%) Submitted............................... 10 (4%) 16 (7%) 11 (4%) 14 (7%) 11 (4%) 9 (3%) 10 (4%) Delayed................................. 21 (8%) 18 (8%) 16 (6%) 19 (9%) 22 (8%) 7 (3%) 0 Terminated.............................. 1 (<1%) 0 0 0 0 0 0 Released................................ 55 (22%) 27 (12%) 56 (22%) 28 (13%) 16 (6%) 7 (3%) 2 (1%) Fulfilled............................... 109 (44%) 112 (50%) 95 (37%) 58 (27%) 59 (21%) 19 (7%) 2 (1%) --------------------------------------------------------------------------------------------------------------- Total \4\........................... 248 224 259 215 278 274 280 -------------------------------------------------------------------------------------------------------------------------------------------------------- \1\ The establishment date is the date of the formal FDA communication to the applicant that included the final FDA required (PMR) or requested (PMC) postmarketing study or clinical trial. \2\ The table shows data for PMRs that were closed (fulfilled or released) as of FY2015. Therefore, data for PMRs that were closed in prior fiscal years are included. \3\ Percentages may not total 100 due to rounding. \4\ The total number of PMRs/PMCs established in FY2009 through FY2014 reflects the data in FDA's databases as of September 30, 2015. As a result of data corrections, as well as improvements in ascertainment of the PMR/PMC establishment date, some of the total numbers of PMRs/PMCs established in each fiscal year are different from those reported in the prior fiscal year's (FY2014) Federal Register report. Table 9--Summary of Status of Postmarketing Commitments Established \1\ Between FY2009 and FY2015 \2\ [Numbers as of September 30, 2015] \3\ -------------------------------------------------------------------------------------------------------------------------------------------------------- Fiscal year of PMC establishment PMC Status as of FY2015 (% of total PMCs --------------------------------------------------------------------------------------------------------------- in each establishment year) 2009 2010 2011 2012 2013 2014 2015 -------------------------------------------------------------------------------------------------------------------------------------------------------- Pending................................. 3 (6%) 2 (2%) 3 (4%) 1 (2%) 8 (17%) 35 (57%) 49 (90%) Ongoing................................. 3 (6%) 18 (19%) 23 (28%) 14 (30%) 15 (33%) 14 (23%) 1 (2%) Submitted............................... 1 (2%) 11 (12%) 3 (4%) 2 (4%) 4(9%) 2 (3%) 2 (4%) [[Page 85579]] Delayed................................. 6 (13%) 12 (13%) 8 (10%) 6 (13%) 4 (9%) 0 0 Terminated.............................. 1 (2%) 0 0 0 0 0 0 Released................................ 4 (8%) 7 (7%) 10 (12%) 1 (2%) 1 (2%) 0 1 (2%) Fulfilled............................... 30 (63%) 44 (47%) 35 (43%) 22 (48%) 14 (30%) 10 (16%) 1 (2%) --------------------------------------------------------------------------------------------------------------- Total \4\........................... 48 94 82 46 46 61 54 -------------------------------------------------------------------------------------------------------------------------------------------------------- \1\ The establishment date is the date of the formal FDA communication to the applicant that included the final FDA required (PMR) or requested (PMC) postmarketing study or clinical trial. \2\ The table shows data for PMCs that were closed (fulfilled or released) as of FY2015. Therefore, data for PMCs that were closed in prior fiscal years are included. \3\ Percentages may not total 100 due to rounding. \4\ The total number of PMRs/PMCs established in FY2009 through FY2014 reflects the data in FDA's databases as of September 30, 2015. As a result of data corrections, as well as improvements in ascertainment of the PMR/PMC establishment date, some of the total numbers of PMRs/PMCs established in each fiscal year are different from those reported in the prior fiscal year's (FY2014) Federal Register report. Dated: November 21, 2016. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2016-28442 Filed 11-25-16; 8:45 am] BILLING CODE 4164-01-P
![Federal Register / Vol. 81, No. 228 / Monday, November 28, 2016 / Notices 85573
DEPARTMENT OF HEALTH AND FDA can require application holders not addressed in this report.
HUMAN SERVICES to conduct postmarketing studies and Furthermore, section 505(o)(3)(E) of the
clinical trials: FD&C Act requires that applicants
Food and Drug Administration • To assess a known serious risk, report periodically on the status of each
assess signals of serious risk, or identify required study or clinical trial and each
[Docket No. FDA–2016–N–3083] an unexpected serious risk related to the study or clinical trial ‘‘otherwise
use of a drug product (section 505(o)(3) undertaken * * * to investigate a safety
Report on the Performance of Drug of the FD&C Act (21 U.S.C. 355(o)(3)), as issue * * * .’’
and Biologics Firms in Conducting added by the Food and Drug An applicant must report on the
Postmarketing Requirements and Administration Amendments Act of progress of the PMR/PMC on the
Commitments; Availability 2007 (FDAAA)). anniversary of the drug product’s
AGENCY: Food and Drug Administration, • Under the Pediatric Research Equity approval4 until the PMR/PMC is
HHS. Act (PREA), to study certain new drugs completed or terminated and FDA
for pediatric populations, when these determines that the PMR/PMC has been
ACTION: Notice of availability.
drugs are not adequately labeled for fulfilled or that the PMR/PMC is either
SUMMARY: Under the Federal Food, children. Under section 505B(a)(3) of no longer feasible or would no longer
Drug, and Cosmetic Act (the FD&C Act), the FD&C Act (21 U.S.C. 355c), the provide useful information. The annual
the Food and Drug Administration (FDA initiation of these studies may be status report (ASR) must include a
or Agency) is required to report deferred until required safety description of the PMR/PMC, a schedule
annually in the Federal Register on the information from other studies in adults for completing the PMR/PMC, and a
status of postmarketing requirements has first been submitted and reviewed. characterization of the current status of
(PMRs) and postmarketing • To verify and describe the predicted the PMR/PMC. The report must also
commitments (PMCs) required of, or effect or other clinical benefit for drugs provide an explanation of the PMR/PMC
agreed upon by, holders of approved approved in accordance with the status by describing briefly the progress
drug and biological products. This accelerated approval provisions in of the PMR/PMC. A PMR/PMC schedule
notice is the Agency’s report on the section 506(c)(2)(A) of the FD&C Act (21 is expected to include the actual or
status of the studies and clinical trials U.S.C. 356(c)(2)(A)) (§§ 314.510 and projected dates for the following: (1)
that applicants have agreed to, or are 601.41 (21 CFR 314.510 and 601.41)). Submission of the final protocol to FDA;
required to, conduct. A supplemental • For a drug that was approved on the (2) completion of the study or clinical
report containing additional information basis of animal efficacy data because trial; and (3) submission of the final
and analyses on the status of PMRs and human efficacy trials are not ethical or report to FDA.
PMCs is available on FDA’s Web site.1 feasible (§§ 314.610(b)(1) and
601.91(b)(1)). PMRs for drug products C. PMR/PMC Status Categories
FOR FURTHER INFORMATION CONTACT:
approved under the animal efficacy The status of the PMR/PMC must be
Cathryn C. Lee, Center for Drug rule3 can be conducted only when the described in the ASR according to the
Evaluation and Research, Food and
drug product is used for its indication terms and definitions provided in
Drug Administration, 10903 New
and when an exigency (or event or need) §§ 314.81 and 601.70. For its own
Hampshire Ave., Bldg. 22, Rm. 6484,
arises. In the absence of a public health reporting purposes, FDA has also
Silver Spring, MD 20993–0002, 301–
emergency, these studies or clinical established terms to describe when the
796–0700; or Stephen Ripley, Center for
trials will remain pending indefinitely. conditions of the PMR/PMC have been
Biologics Evaluation and Research,
B. Reporting Requirements met, and when it has been determined
Food and Drug Administration, 10903
that a PMR/PMC is no longer
New Hampshire Ave., Bldg. 71, Rm. Under the regulations necessary.5 The PMR/PMC status
7301, Silver Spring, MD 20993–0002, (§§ 314.81(b)(2)(vii) and 601.70), categories are summarized in the
240–402–7911. applicants of approved drugs are following list. As reflected in the
SUPPLEMENTARY INFORMATION: required to submit annually a report on definitions, the status of a PMR/PMC is
the status of each clinical safety, clinical generally determined based on the
I. Background
efficacy, clinical pharmacology, and original schedule.6
A. Postmarketing Requirements and nonclinical toxicology study or clinical
Commitments trial either required by FDA or that they 4 An applicant must submit an annual status
A PMR is a study or clinical trial that have committed to conduct, either at the report on the progress of each open PMR/PMC
time of approval or after approval of within 60 days of the anniversary date of U.S.
an applicant is required by statute or approval of the original application or on an
regulation to conduct postapproval. A their new drug application (NDA), alternate reporting date that was granted by FDA in
PMC is a study or clinical trial that an abbreviated new drug application writing. Some applicants have requested and been
applicant agrees in writing to conduct (ANDA), or biologics license application granted by FDA alternate annual reporting dates to
(BLA). Applicants are required to report facilitate harmonized reporting across multiple
postapproval, but that is not required by applications.
statute or regulation. PMRs and PMCs to FDA on these requirements and 5 See the guidance for industry entitled ‘‘Reports
can be issued upon approval of a drug2 commitments made for NDAs and on the Status of Postmarketing Study
or postapproval, if warranted. ANDAs under § 314.81(b)(2)(viii). The Commitments—Implementation of Section 130 of
status of PMCs concerning chemistry, the Food and Drug Administration Modernization
Act of 1997.’’ We update guidances periodically. To
1 http://www.fda.gov/Drugs/
manufacturing, and production controls make sure you have the most recent version of a
mstockstill on DSK3G9T082PROD with NOTICES
GuidanceComplianceRegulatoryInformation/Post- and the status of other studies or guidance, check the FDA Drugs guidance Web page
marketingPhaseIVCommitments/ucm064436.htm. clinical trials conducted on an at http://www.fda.gov/Drugs/
2 For the purposes of this notice, references to
applicant’s own initiative are not GuidanceComplianceRegulatoryInformation/
‘‘drugs’’ or ‘‘drug products’’ include drugs approved Guidances/default.htm.
required to be reported under
under the FD&C Act and biological products 6 The definitions for the terms ‘‘pending,’’
licensed under the Public Health Service Act, other §§ 314.81(b)(2)(vii) and 601.70 and are ‘‘ongoing,’’ ‘‘delayed,’’ ‘‘terminated,’’ and
than biological products that also meet the ‘‘submitted’’ are adapted from §§ 314.81 and 601.70;
definition of a device in section 201(h) of the FD&C 3 21 CFR 314.600 for drugs; 21 CFR 601.90 for the definitions for the terms ‘‘fulfilled’’ and
Act (21 U.S.C. 321(h)). biological products. Continued
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![85576 Federal Register / Vol. 81, No. 228 / Monday, November 28, 2016 / Notices
In this report, study or clinical trial G. Closed PMRs and PMCs either fulfilled or released. For example,
status reflects the status in relation to Table 7 provides details about PMRs as of September 30, 2015, 44 percent
the original18 study or clinical trial and PMCs that were closed (released or (109/248) of the PMRs that were
schedule regardless of whether FDA has fulfilled) within FY2015. The majority established in FY2009 were fulfilled,
acknowledged that additional time was of closed PMRs were fulfilled (69 and 22 percent (55/248) were released.
required to complete the study or percent of NDA PMRs and 90 percent of The majority of PMRs that were
clinical trial. BLA PMRs at the end of FY2015). established in more recent years were
Similarly, the majority of closed PMCs either pending (i.e., not yet underway)
F. Open On-Schedule and Off-Schedule within FY2015 were fulfilled. or ongoing (i.e., still in progress and on
PMCs
H. Distribution of the Status of PMRs schedule). For example, as of September
Table 6 provides the status of open and PMCs 30, 2015, 89 percent (250/280) of the
on-schedule and off-schedule PMCs and PMRs established in FY2015 were
Tables 8 and 9 show the distribution
shows that as of September 30, 2015, the pending, and 6 percent (16/280) were
of the statuses of PMRs/PMCs as of
largest category of all open NDA PMCs ongoing. Overall, of the PMRs that were
September 30, 2015, presented by the
were those that were pending (36 year that the PMR/PMC was pending as of September 30, 2015, 86
percent; 71/197). Most of the open BLA established19 (FY2009 to FY2015).20 21 percent (527/616) were created within
PMCs were ongoing at the end of Note that the data shown for closed the past 3 years (FY2013, FY2014, and
FY2015 (39 percent; 80/204). Off- (fulfilled or released) PMRs/PMCs are FY2015). Finally, table 8 shows that, on
schedule PMCs accounted for 31 for all PMRs/PMCs that were closed as average, 6 percent of the PMRs
percent (62/197) of open NDA PMCs of FY2015. Therefore, data for PMRs/ established since FY2009 were delayed
and 22 percent (45/204) of open BLA PMCs that were closed in prior fiscal as of September 30, 2015. Table 9
PMCs. The majority of off-schedule years are included. Based on the data provides an overview of PMCs in a
NDA and BLA PMCs were delayed shown in table 8, an average of 254 similar manner as table 8 does for PMRs
according to the original schedule PMRs were established each year since and shows similar results for PMCs as
milestones. FY2009.22 Most PMRs that were those for PMRs as described above and
established in the earlier years were in table 8.
TABLE 1—APPLICANTS AND APPLICATIONS (NDA/BLA) WITH OPEN POSTMARKETING REQUIREMENTS AND COMMITMENTS
[Numbers as of September 30, 2015]
Total (NDA
NDA 1 BLA 2 and BLA)
Number of unique applicants with open PMRs/PMCs ................................................................ 194 75 269
Number of applications with open PMRs/PMCs ......................................................................... 716 140 856
1 Includes two NDAs with associated PMRs/PMCs managed by CBER.
2 Includes BLAs managed by both CDER and CBER.
TABLE 2—ANNUAL STATUS REPORTS RECEIVED
[Numbers as of September 30, 2015] 1
Expected
Received, Received, but not
on time 3 not on time 4
Expected 2 (% of (% of received
(% of
expected) expected) expected)
NDA ................................................................................................................. 451 304 (67%) 62 (14%) 85 (19%)
BLA .................................................................................................................. 124 97 (78%) 16 (13%) 11 (9%)
Total .......................................................................................................... 575 401 (70%) 78 (14%) 96 (17%)
1 Percentagesmay not total 100 due to rounding.
2 ASR expected during fiscal year (within 60 days (before or after) of the anniversary of original approval date or alternate agreed-upon date).
3 ASR was received within 60 days (before or after) of the anniversary of the original approval date or alternate agreed-upon date.
4 ASR was received, but not within 60 days (before or after) of the anniversary of the original approval date or alternate agreed-upon date.
18 With the exception of PREA PMRs for which postmarketing requirements and commitments 22 The number of PMRs issued at any particular
a deferral extension of the final report submission report (81 FR 75411) (https://www.gpo.gov/fdsys/ period is determined by a variety of factors
pkg/FR-2016-10-31/html/2016-26247.htm).
mstockstill on DSK3G9T082PROD with NOTICES
date has been granted. including but not necessarily limited to: (1) The
21 The total number of PMRs/PMCs established in
19 The establishment date is the date of the formal number of NDAs approved in that period; (2)
FDA communication to the applicant that included FY2009 through FY2014 reflects the data in FDA’s whether additional efficacy or clinical benefit
databases as of September 30, 2015. As a result of
the final FDA required (PMR) or requested (PMC) issues were evaluated; (3) if any drug-associated
data corrections, as well as improvements in
postmarketing study or clinical trial. serious risk(s) have been identified; and (4) whether
ascertainment of the PMR/PMC establishment date,
20 Tables 8 and 9 include data for only the past or not FDA determines that a postmarketing study
some of the total numbers of PMRs/PMCs
7 fiscal years. Data on the distribution of statuses established in each fiscal year are different from or clinical trial is necessary to further assess risk(s)
for PMRs/PMCs established in FY2008 and as of those reported in the prior fiscal year’s (FY 2014) or efficacy issues.
FY2014 are presented in the FY2014 status of Federal Register report.
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![Federal Register / Vol. 81, No. 228 / Monday, November 28, 2016 / Notices 85577
TABLE 3—SUMMARY OF ON- AND OFF-SCHEDULE POSTMARKETING REQUIREMENTS AND COMMITMENTS
[Numbers as of September 30, 2015] 1
Open PMRs Open PMCs
N = 1,233 N = 401
NDA BLA NDA BLA
(% of Open (% of Open (% of Open (% of Open
NDA PMRs) BLA PMRs) NDA PMCs) BLA PMCs)
On-schedule ..................................................................................................... 887 (88%) 203 (91%) 135 (69%) 159 (78%)
Off-schedule ..................................................................................................... 123 (12%) 20 (9%) 62 (31%) 45 (22%)
Total .......................................................................................................... 1,010 223 197 204
1 Percentages may not total 100 due to rounding.
TABLE 4—SUMMARY OF OPEN AND ON-SCHEDULE POSTMARKETING REQUIREMENTS
[Numbers as of September 30, 2015] 1
NDA BLA
N = 1,010 N = 223
Reporting authority/PMR status (% of Open NDA PMRs) (% of Open BLA PMRs)
Pending Ongoing Submitted Pending Ongoing Submitted
Accelerated approval ............................... 12 (1%) 25 (3%) 3 (<1%) 7 (3%) 7 (2%) 1 (<1%)
PREA 2 ..................................................... 290 (29%) 121 (12%) 18 (2%) 46 (20%) 18 (8%) 9 (4%)
Animal efficacy 3 ....................................... 4 (<1%) 0 1 (<1%) 6 (3%) 0 0
FDAAA safety 4 ........................................
(since March 25, 2008) ............................ 229 3 (23%) 142 (14%) 42 (4%) 41 (18%) 55 (25%) 13 (6%)
Total .................................................. 535 (53%) 288 (29%) 64 (6%) 100 (45%) 80 (36%) 23 (10%)
1 Percentages may not total 100 due to rounding.
2 Many PREA studies have a pending status. PREA studies are usually deferred because the drug product is ready for approval in adults. Initi-
ation of these studies may be deferred until additional safety information from other studies has first been submitted and reviewed before begin-
ning the studies in pediatric populations.
3 PMRs for drug products approved under the animal efficacy rule (§ 314.600 for drugs; § 601.90 for biological products) can be conducted only
when the drug product is used for its indication and when an exigency (or event or need) arises. In the absence of a public health emergency,
these studies or clinical trials will remain pending indefinitely.
4 Includes one NDA PMR FDAAA safety study from CBER in pending status.
TABLE 5—SUMMARY OF OPEN AND OFF-SCHEDULE POSTMARKETING REQUIREMENTS
[Numbers as of September 30, 2015] 1
NDA BLA
N = 1,010 N = 223
Reporting authority/PMR status (% of Open NDA PMRs) (% of Open BLA PMRs)
Delayed Terminated Delayed Terminated
Accelerated approval ....................................................................................... 3 (<1%) 2 (<1%) 1 (<1%) 0
PREA ............................................................................................................... 64 (6%) 2 (<1%) 5 (2%) 2 (<1%)
Animal efficacy ................................................................................................. 0 0 0 0
FDAAA safety ..................................................................................................
(since March 25, 2008) .................................................................................... 52 (5%) 0 12 (5%) 0
Total .......................................................................................................... 119 (12%) 4 (<1%) 18 (8%) 2 (<1%)
1 Percentages may not total 100 due to rounding.
TABLE 6—SUMMARY OF OPEN POSTMARKETING COMMITMENTS
[Numbers as of September 30, 2015] 1
NDA BLA
N = 197 N = 204
(% Open (% Open
PMCs) PMCs)
mstockstill on DSK3G9T082PROD with NOTICES
On-Schedule ............................................................................................................................................................ ........................ ........................
Pending .................................................................................................................................................................... 71 (36%) 54 (26%)
Ongoing ................................................................................................................................................................... 40 (20%) 80 (39%)
Submitted ................................................................................................................................................................. 24 (12%) 25 (12%)
Total ......................................................................................................................................................................... 135 (68%) 159 (77%)
Off-Schedule ............................................................................................................................................................ ........................ ........................
Delayed .................................................................................................................................................................... 59 (30%) 43 (21%)
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![85578 Federal Register / Vol. 81, No. 228 / Monday, November 28, 2016 / Notices
TABLE 6—SUMMARY OF OPEN POSTMARKETING COMMITMENTS—Continued
[Numbers as of September 30, 2015] 1
NDA BLA
N = 197 N = 204
(% Open (% Open
PMCs) PMCs)
Terminated ............................................................................................................................................................... 3 (2%) 2 (1%)
Total .................................................................................................................................................................. 62 (31%) 45 (22%)
1 Percentages may not total 100 due to rounding.
TABLE 7—SUMMARY OF CLOSED 1 POSTMARKETING REQUIREMENTS AND COMMITMENTS
[Numbers as of September 30, 2015] 2
NDA BLA
Postmarketing requirements N = 195 N = 40
Closed PMRs (% of Total Closed PMRs) ........................ ........................
Requirement met (fulfilled) ...................................................................................................................................... 134 (69%) 36 (90%)
Requirement not met (released and new revised requirement issued) .................................................................. 31 (16%) 1 (2%)
Requirement no longer feasible or drug product withdrawn (released) .................................................................. 30 (15%) 3 (8%)
Postmarketing Commitments NDA BLA
N = 56 N = 32
Closed PMCs (% of Total Closed PMCs) ............................................................................................................... ........................ ........................
Requirement met (fulfilled) ...................................................................................................................................... 46 (82%) 27 (84%)
Requirement not met (released and new revised requirement issued) .................................................................. 1 (2%) 2 (6%)
Requirement no longer feasible or drug product withdrawn (released) .................................................................. 9 (16%) 3 (9%)
1 The table shows data for those PMRs/PMCs that were closed (fulfilled or released) within FY2015. Therefore, data for PMRs/PMCs that were
closed in prior fiscal years are not included.
2 Percentages may not total 100 due to rounding.
TABLE 8—SUMMARY OF STATUS OF POSTMARKETING REQUIREMENTS ESTABLISHED 1 BETWEEN FY2009 AND FY2015 2
[Numbers as of September 30, 2015] 3
PMR Status as of Fiscal year of PMR establishment
FY2015
(% of total PMRs in
each establishment 2009 2010 2011 2012 2013 2014 2015
year)
Pending ........................ 14 (6%) 11 (5%) 27 (10%) 37 (17%) 91 (33%) 186 (68%) 250 (89%)
Ongoing ........................ 38 (15%) 40 (18%) 54 (21%) 59 (27%) 79 (28%) 46 (17%) 16 (6%)
Submitted ..................... 10 (4%) 16 (7%) 11 (4%) 14 (7%) 11 (4%) 9 (3%) 10 (4%)
Delayed ........................ 21 (8%) 18 (8%) 16 (6%) 19 (9%) 22 (8%) 7 (3%) 0
Terminated ................... 1 (<1%) 0 0 0 0 0 0
Released ...................... 55 (22%) 27 (12%) 56 (22%) 28 (13%) 16 (6%) 7 (3%) 2 (1%)
Fulfilled ......................... 109 (44%) 112 (50%) 95 (37%) 58 (27%) 59 (21%) 19 (7%) 2 (1%)
Total 4 .................... 248 224 259 215 278 274 280
1 The establishment date is the date of the formal FDA communication to the applicant that included the final FDA required (PMR) or requested
(PMC) postmarketing study or clinical trial.
2 The table shows data for PMRs that were closed (fulfilled or released) as of FY2015. Therefore, data for PMRs that were closed in prior fiscal
years are included.
3 Percentages may not total 100 due to rounding.
4 The total number of PMRs/PMCs established in FY2009 through FY2014 reflects the data in FDA’s databases as of September 30, 2015. As
a result of data corrections, as well as improvements in ascertainment of the PMR/PMC establishment date, some of the total numbers of PMRs/
PMCs established in each fiscal year are different from those reported in the prior fiscal year’s (FY2014) FEDERAL REGISTER report.
TABLE 9—SUMMARY OF STATUS OF POSTMARKETING COMMITMENTS ESTABLISHED 1 BETWEEN FY2009 AND FY2015 2
[Numbers as of September 30, 2015] 3
mstockstill on DSK3G9T082PROD with NOTICES
PMC Status as of Fiscal year of PMC establishment
FY2015
(% of total PMCs in
each establishment 2009 2010 2011 2012 2013 2014 2015
year)
Pending ........................ 3 (6%) 2 (2%) 3 (4%) 1 (2%) 8 (17%) 35 (57%) 49 (90%)
Ongoing ........................ 3 (6%) 18 (19%) 23 (28%) 14 (30%) 15 (33%) 14 (23%) 1 (2%)
Submitted ..................... 1 (2%) 11 (12%) 3 (4%) 2 (4%) 4(9%) 2 (3%) 2 (4%)
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![Federal Register / Vol. 81, No. 228 / Monday, November 28, 2016 / Notices 85579
TABLE 9—SUMMARY OF STATUS OF POSTMARKETING COMMITMENTS ESTABLISHED 1 BETWEEN FY2009 AND FY2015 2—
Continued
[Numbers as of September 30, 2015] 3
PMC Status as of Fiscal year of PMC establishment
FY2015
(% of total PMCs in
each establishment 2009 2010 2011 2012 2013 2014 2015
year)
Delayed ........................ 6 (13%) 12 (13%) 8 (10%) 6 (13%) 4 (9%) 0 0
Terminated ................... 1 (2%) 0 0 0 0 0 0
Released ...................... 4 (8%) 7 (7%) 10 (12%) 1 (2%) 1 (2%) 0 1 (2%)
Fulfilled ......................... 30 (63%) 44 (47%) 35 (43%) 22 (48%) 14 (30%) 10 (16%) 1 (2%)
Total 4 .................... 48 94 82 46 46 61 54
1 The establishment date is the date of the formal FDA communication to the applicant that included the final FDA required (PMR) or requested
(PMC) postmarketing study or clinical trial.
2 The table shows data for PMCs that were closed (fulfilled or released) as of FY2015. Therefore, data for PMCs that were closed in prior fiscal
years are included.
3 Percentages may not total 100 due to rounding.
4 The total number of PMRs/PMCs established in FY2009 through FY2014 reflects the data in FDA’s databases as of September 30, 2015. As
a result of data corrections, as well as improvements in ascertainment of the PMR/PMC establishment date, some of the total numbers of PMRs/
PMCs established in each fiscal year are different from those reported in the prior fiscal year’s (FY2014) Federal Register report.
Dated: November 21, 2016. ADDRESSES: To ensure that comments on Federal jobs. Collecting applications for
Leslie Kux, the information collection are received, the Medical Device Fellowship Program
Associate Commissioner for Policy. OMB recommends that written will allow FDA’s Center for Devices and
[FR Doc. 2016–28442 Filed 11–25–16; 8:45 am] comments be faxed to the Office of Radiological Health (CDRH) to easily
BILLING CODE 4164–01–P Information and Regulatory Affairs, and efficiently elicit and review
OMB, Attn: FDA Desk Officer, FAX: information from students and health
202–395–7285, or emailed to oira_ care professionals who are interested in
DEPARTMENT OF HEALTH AND submission@omb.eop.gov. All becoming involved in CDRH activities.
HUMAN SERVICES comments should be identified with the The process will reduce the time and
OMB control number 0910–0551. Also cost of submitting written
Food and Drug Administration include the FDA docket number found documentation to the Agency and lessen
[Docket No. FDA–2013–N–1064] in brackets in the heading of this the likelihood of applications being
document.
misrouted within the Agency mail
Agency Information Collection FOR FURTHER INFORMATION CONTACT: FDA system. It will assist the Agency in
Activities; Submission for Office of PRA Staff, Office of Operations, Food promoting and protecting the public
Management and Budget Review; and Drug Administration, Three White
Comment Request; Application for health by encouraging outside persons
Flint North 10A63, 11601 Landsdown to share their expertise with CDRH.
Participation in the Medical Device St., North Bethesda, MD 20852,
Fellowship Program PRAStaff@fda.hhs.gov. In the Federal Register of September
6, 2016 (81 FR 61221), FDA published
AGENCY: Food and Drug Administration, SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA a 60-day notice requesting public
HHS.
has submitted the following proposed comment on the proposed collection of
ACTION: Notice.
collection of information to OMB for information. No comments were
SUMMARY: The Food and Drug review and clearance. received.
Administration (FDA) is announcing FDA estimates the burden of this
that a proposed collection of Application for Participation in the
collection of information as follows:
information has been submitted to the Medical Device Fellowship Program—
Office of Management and Budget OMB Control Number 0910–0551—
(OMB) for review and clearance under Extension
the Paperwork Reduction Act of 1995. Sections 1104, 1302, 3301, 3304,
DATES: Fax written comments on the 3320, 3361, 3393, and 3394 of Title 5 of
collection of information by December the United States Code authorize
28, 2016. Federal Agencies to rate applicants for
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN1
Number of Average
Number of Total annual
mstockstill on DSK3G9T082PROD with NOTICES
FDA Form responses per burden per Total hours
respondents responses
respondent response
Application Form (FDA 3608) .............................................. 250 1 250 1 250
1 There are no capital costs or operating and maintenance costs associated with this collection of information.
VerDate Sep<11>2014 21:15 Nov 25, 2016 Jkt 241001 PO 00000 Frm 00072 Fmt 4703 Sfmt 4703 E:\FR\FM\28NON1.SGM 28NON1](https://thefederalregister.org/doc/81_FR_85801/page/7.svg)
Document Created: 2018-02-14 08:35:35
Document Modified: 2018-02-14 08:35:35
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice of availability. | |
| Contact | Cathryn C. Lee, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 6484, Silver Spring, MD 20993-0002, 301- 796-0700; or Stephen Ripley, Center for Biologics Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. | |
| FR Citation | 81 FR 85573 |
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