Notices. Notice

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BILLING CODE 4164-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2014-N-1721] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Investigational New Drug Applications AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration

(FDA)is announcing that a proposed collection of information has been submitted to the Office of Management and Budget

(OMB)for review and clearance under the Paperwork Reduction Act of 1995. DATES: Fax written comments on the collection of information by April 2, 2015. ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202-395-7285, or emailed to *oira_submission@omb.eop.gov.* All comments should be identified with the OMB control number 0910-0014. Also include the FDA docket number found in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver Spring, MD 20993-0002, *PRAStaff@fda.hhs.gov.* SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. Investigational New Drug

(IND)Regulations—21 CFR Part 312 (OMB Control Number 0910-0014)—Extension FDA is requesting OMB approval for the reporting and recordkeeping requirements contained in FDA regulations entitled “Investigational New Drug Application” in part 312 (21 CFR part 312). Part 312 implements provisions of section 505(i) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 355(i)) to issue regulations under which the clinical investigation of the safety and effectiveness of unapproved new drugs and biological products can be conducted. FDA is charged with implementing statutory requirements that drug products marketed in the United States be shown to be safe and effective, properly manufactured, and properly labeled for their intended uses. Section 505(a) of the FD&C Act provides that a new drug may not be introduced or delivered for introduction into interstate commerce in the United States unless FDA has previously approved a new drug application (NDA). FDA approves an NDA only if the sponsor of the application first demonstrates that the drug is safe and effective for the conditions prescribed, recommended, or suggested in the product's labeling. Proof must consist, in part, of adequate and well-controlled studies, including studies in humans, that are conducted by qualified experts. The IND regulations establish reporting requirements that include an initial application as well as amendments to that application, reports on significant revisions of clinical investigation plans, and information on a drug's safety or effectiveness. In addition, the sponsor is required to give FDA an annual summary of the previous year's clinical experience. Submissions are reviewed by medical officers and other Agency scientific reviewers assigned responsibility for overseeing the specific study. The IND regulations also contain recordkeeping requirements that pertain to the responsibilities of sponsors and investigators. The detail and complexity of these requirements are dictated by the scientific procedures and human subject safeguards that must be followed in the clinical tests of investigational new drugs. The IND information collection requirements provide the means by which FDA can monitor the clinical investigation of the safety and effectiveness of unapproved new drugs and biological products, including the following:

(1)Monitor the safety of ongoing clinical investigations;

(2)determine whether the clinical testing of a drug should be authorized;

(3)ensure production of reliable data on the metabolism and pharmacological action of the drug in humans;

(4)obtain timely information on adverse reactions to the drug;

(5)obtain information on side effects associated with increasing doses;

(6)obtain information on the drug's effectiveness;

(7)ensure the design of well-controlled, scientifically valid studies; and

(8)obtain other information pertinent to determining whether clinical testing should be continued, and information related to the protection of human subjects. Without the information provided by industry as required under the IND regulations, FDA cannot authorize or monitor the clinical investigations which must be conducted prior to authorizing the sale and general use of new drugs. These reports enable FDA to monitor a study's progress, to assure subject safety, to assure that a study will be conducted ethically, and to increase the likelihood that the sponsor will conduct studies that will be useful in determining whether the drug should be marketed and available for use in medical practice. There are two forms that are required under part 312: Form FDA-1571—“Investigational New Drug Application.” A person who intends to conduct a clinical investigation submits this form to FDA. It includes the following information:

(1)A cover sheet containing background information on the sponsor and investigator;

(2)A table of contents;

(3)An introductory statement and general investigational plan;

(4)An investigator's brochure describing the drug substance;

(5)A protocol for each planned study;

(6)Chemistry, manufacturing, and control information for each investigation;

(7)Pharmacology and toxicology information for each investigation; and

(8)Previous human experience with the investigational drug. Form FDA-1572—“Investigator Statement.” Before permitting an investigator to begin participation in an investigation, the sponsor must obtain and record this form. It includes background information on the investigator and the investigation, and a general outline of the planned investigation and the study protocol. FDA is requesting OMB approval for the following reporting and recordkeeping requirements in part 312. I. Reporting Requirements Section 312.2(e)—Requests for FDA advice on the applicability of part 312 to a planned clinical investigation. Section 312.6—Labeling of an investigational new drug. Estimates for the information collection in this requirement are included under § 312.23(a)(7)(iv)(d). Section 312.8—Charging for investigational drugs under an IND. Section 312.10—Applications for waiver of requirements under part 312. As indicated in § 312.10(a), estimates for the information collection in this requirement are included under §§ 312.23 and 312.31. In addition, other waiver requests under § 312.10 are estimated in table 1. Section 312.20(c)—Applications for investigations involving an exception from informed consent under § 50.24 (21 CFR 50.24). Estimates for the information collection in this requirement are included under § 312.23. Section 312.23—IND (content and format). Section 312.23(a)(1)—Cover sheet FDA-1571. Section 312.23(a)(2)—Table of Contents. Section 312.23(a)(3)—Investigational plan for each planned study. Section 312.23(a)(5)—Investigator's brochure. Section 312.23(a)(6)—Protocols—Phase 1, 2, and 3. Section 312.23(a)(7)—Chemistry, manufacturing, and control information. Section 312.23(a)(7)(iv)(a),(b),(c)—A description of the drug substance, a list of all components, and any placebo used. Section 312.23(a)(7)(iv)( *d* )—Labeling: Copies of labels and labeling to be provided each investigator. Section 312.23(a)(7)(iv)( *e* )—Environmental impact analysis regarding drug manufacturing and use. Section 312.23(a)(8)—Pharmacological and toxicology information. Section 312.23(a)(9)—Previous human experience with the investigational drug. Section 312.23(a)(10)—Additional information. Section 312.23(a)(11)—Relevant information. Section 312.23(f)—Identification of exception from informed consent. Section 312.30—Protocol amendments. § 312.30(a)—New protocol § 312.30(b)—Changes in protocol § 312.30(c)—New investigator. § 312.30(d)—Content and format. § 312.30(e)—Frequency. Section 312.31—Information amendments. § 312.31(b)—Content and format. — Chemistry, toxicology, or technical information. Section 312.32—Safety reports. § 312.32(c)(1)—Written reports to FDA and to investigators. § 312.32(c)(2)—Telephone reports to FDA for fatal or life-threatening experience. § 312.32(c)(3)—Format or frequency. § 312.32(d)—Followup submissions. Section 312.33—Annual reports. § 312.33(a)—Individual study information. § 312.33(b)—Summary information. § 312.33(b)(1)—Adverse experiences. § 312.33(b)(2)—Safety report summary. § 312.33(b)(3)—List of fatalities and causes of death. § 312.33(b)(4)—List of discontinuing subjects. § 312.33 (b)(5)—Drug action. § 312.33 (b)(6)—Preclinical studies and findings. § 312.33 (b)(7)—Significant changes. § 312.33(c)—Next year general investigational plan. § 312.33(d)—Brochure revision. § 312.33(e)—Phase I protocol modifications. § 312.33(f)—Foreign marketing developments. Section 312.38(b) and (c)—Notification of withdrawal of an IND. Section 312.41—Comment and advice on an IND. Estimates for the information collection in this requirement are included under § 312.23. Section 312.42—Sponsor requests that a clinical hold be removed, and submits a complete response to the issues identified in the clinical hold order. Section 312.44(c) and (d)—Opportunity for sponsor response to FDA when IND is terminated. Section 312.45(a) and (b)—Sponsor request for, or response to, an inactive status determination of an IND. Section 312.47—Meetings, including “End-of-Phase 2” meetings and “Pre-NDA” meetings. Section 312.48—Dispute resolution. Estimates for the information collection in this requirement are included under § 312.47. Section 312.53(c)—Investigator information. Investigator report (Form FDA-1572) and narrative; Investigator's background information; Phase 1 outline of planned investigation and Phase 2 outline of study protocol. Section 312.54(a) and (b)—Sponsor submissions concerning investigations involving an exception from informed consent under § 50.24. § 312.55(b)—Sponsor reports to investigators on new observations, especially adverse reactions and safe use. Only “new observations” are estimated under this section; investigator brochures are included under § 312.23. Section 312.56(b), (c), and (d)—Sponsor monitoring of all clinical investigations, investigators, and drug safety; notification to FDA and others. Section 312.58(a)—Sponsor's submission of records to FDA on request. Section 312.64—Investigator reports to the sponsor. § 312.64(a)—Progress reports. § 312.64(b)—Safety reports § 312.64(c)—Final reports. § 312.64(d)—Financial disclosure reports. Section 312.66—Investigator reports to institutional review board (IRB). Estimates for the information collection in this requirement are included under § 312.53. Section 312.70—Investigator disqualification; opportunity to respond to FDA. Section 312.83—Sponsor submission of treatment protocol. Estimates for this requirement are included under § 312.320. Section 312.85—Sponsors conducting phase 4 studies. Estimates for the information collection in this requirement are included under § 312.23, and under §§ 314.50, 314.70, and 314.81 in OMB control number 0910-0001. Section 312.110(b)—Requests to export an investigational drug. Section 312.120—Submissions related to foreign clinical studies not conducted under an IND. Section 312.130—Requests for disclosable information in an IND and from investigations involving an exception from informed consent under § 50.24. Sections 312.310(b); 312.305(b)—Submissions related to expanded access and treatment of an individual patient. Section 312.310(d)—Submissions related to emergency use of an investigational new drug. Sections 312.315(c); 312.305(b)—Submissions related to expanded access and treatment of an intermediate-size patient population. Section 312.320—Submissions related to a treatment IND or treatment protocol. II. Recordkeeping Requirements Section 312.52(a)—Transfer of obligations to a contract research organization. Section 312.57—Sponsor recordkeeping on the investigational drug. Section 312.59—Sponsor recordkeeping of disposition of unused supply of drugs. Estimates for the information collection in this requirement are included under § 312.57. Section 312.62(a)—Investigator recordkeeping of disposition of drugs. Section 312.62(b)—Investigator recordkeeping of case histories of individuals. Section 312.120(d)—Recordkeeping requirements for submissions related to foreign clinical studies not conducted under an IND. Estimates for the information collection in this requirement are included under § 312.57. Section 312.160(a)(3)—Records pertaining to the shipment of drugs for investigational use in laboratory research animals or in vitro tests. Section 312.160(c)—Shipper records of alternative disposition of unused drugs. In the **Federal Register** of November 5, 2014 (79 FR 65663), FDA published a 60-day notice requesting public comment on the proposed collection of information. FDA received 24 comments, however, these comments did not address the information collection. FDA estimates the burden of this collection of information as follows: Table 1—Estimated Annual Reporting Burden for Human Drugs 1 21 CFR section Number of respondents Number of responses per respondent Total annual responses Average burden per response Total hours 312.2(e), Requests for FDA advice on the applicability of part 312 to a planned clinical investigation 800 1 800 24 19,200 312.8, Requests to charge for an investigational drug 56 1.25 70 48 3,360 312.10, Requests to waive a requirement in part 312 50 1.76 88 24 2,112 312.23(a) through (f), IND content and format (including Form FDA 1571) 1,689 1.57 2,648 1,600 4,236,800 312.30(a) through (e), Protocol amendments 3,739 5.77 21,588 284 6,130,992 312.31 (b), Information amendments 4,537 3.39 15,377 100 1,537,700 312.32(c) and (d), IND Safety reports 755 24.28 18,332 32 586,624 312.33(a) through (f), IND Annual reports 2,877 2.76 7,953 360 2,863,080 312.38(b) and (c), Notifications of withdrawal of an IND 862 1.54 1,328 28 37,184 312.42, Sponsor requests that a clinical hold be removed, including sponsor submission of a complete response to the issues identified in the clinical hold order 158 1.30 205 284 58,220 312.44(c) and (d), Sponsor responses to FDA when IND is terminated 12 1 12 16 192 312.45(a) and (b), Sponsor requests for or responses to an inactive status determination of an IND by FDA 260 1.73 451 12 5,412 312.47, Meetings, including “End-of-Phase 2” meetings and “Pre-NDA” meetings 225 1.86 419 160 67,040 312.53(c), Investigator reports submitted to the sponsor, including Form FDA 1572, curriculum vitae, clinical protocol, and financial disclosure. (Third party disclosure) 1,444 8.38 12,087 80 966,960 312.54(a), Sponsor submissions to FDA concerning investigations involving an exception from informed consent under 21 CFR 50.24 7 5 35 48 1,680 312.54(b), Sponsor notifications to FDA and others concerning an IRB determination that it cannot approve research because it does not meet the criteria in the exception from informed consent in § 50.24(a). (Includes third party disclosure) 7 1 7 48 336 312.55(a), Investigator brochures submitted by the sponsor to each investigator. (Third party disclosure) 590 3.50 2,067 48 99,216 312.55(b), Sponsor reports to investigators on new observations, especially adverse reactions and safe use. (Third party disclosure) 590 3.50 2,067 48 99,216 312.56(b),(c), and (d), Sponsor notifications to FDA and others resulting from:

(1)The sponsor's monitoring of all clinical investigations and determining that an investigator is not in compliance with the investigation agreements;

(2)the sponsor's review and evaluation of the evidence relating to the safety and effectiveness of the investigational drug; and

(3)the sponsor's determination that the investigational drug presents an unreasonable and significant risk to subjects. (Includes third party disclosure) 3,584 6.52 23,355 80 1,868,400 312.58(a), Sponsor's submissions of clinical investigation records to FDA on request during FDA inspections 60 1 60 8 480 312.64, Investigator reports to the sponsor, including progress reports, safety reports, final reports, and financial disclosure reports. (Third party disclosure) 1,444 1 1,444 24 34,656 312.70, During the disqualification process of a clinical investigator by FDA, the number of investigator responses or requests to FDA following FDA's notification to an investigator of its failure to comply with investigation requirements 4 1 4 40 160 312.110(b)(4) and (b)(5), Written certifications and written statements submitted to FDA relating to the export of an investigational drug 11 26.28 289 75 21,675 312.120(b), Submissions to FDA of “supporting information” related to the use of foreign clinical studies not conducted under an IND 1,414 8.63 12,198 32 390,336 312.120(c), Waiver requests submitted to FDA related to the use of foreign clinical studies not conducted under an IND 35 2.34 82 24 1,968 312.130, Requests for disclosable information in an IND and for investigations involving an exception from informed consent under § 50.24 3 1 3 8 24 312.310(b) and 312.305(b), Submissions related to expanded access and treatment of an individual patient 228 1.76 401 8 3,208 312.310(d), Submissions related to emergency use of an investigational new drug 410 2.19 899 16 14,384 312.315(c) and 312.305(b), Submissions related to expanded access and treatment of an intermediate-size patient population 44 7.07 311 120 37,320 312.320(b), Submissions related to a treatment IND or treatment protocol 12 12.67 152 300 45,600 Total 19,134,039 1 There are no capital costs or operating and maintenance costs associated with this collection of information. Table 2—Estimated Annual Recordkeeping Burden for Human Drugs 1 21 CFR section Number of recordkeepers Number of records per recordkeeper Total annual records Average burden per recordkeeping Total hours 312.52(a), Sponsor records for the transfer of obligations to a contract research organization 335 1.50 503 2 1,006 312.57, Sponsor recordkeeping showing the receipt, shipment, or other disposition of the investigational drug, and any financial interests 1,689 1 1,689 100 168,900 312.62(a), Investigator recordkeeping of the disposition of drugs 1,444 1 1,444 40 57,760 312.62(b), Investigator recordkeeping of case histories of individuals 1,444 1 1,444 40 57,760 312.160(a)(3), Records pertaining to the shipment of drugs for investigational use in laboratory research animals or in vitro tests 547 1.40 782 * 0.50 391 312.160(c), Shipper records of alternative disposition of unused drugs 547 1.40 782 * 0.50 391 Total 286,190 1 There are no capital costs or operating and maintenance costs associated with this collection of information. * Thirty

(30)minutes. Table 3—Estimated Annual Reporting Burden for Biologics 1 21 CFR section Number of respondents Number of responses per respondent Total annual responses Average burden per response Total hours 312.2(e), Requests for FDA advice on the applicability of part 312 to a planned clinical investigation 217 1.18 255 24 6,120 312.8, Requests to charge for an investigational drug 20 1.50 30 48 1,440 312.10, Requests to waive a requirement in part 312 2 1 2 24 48 312.23(a) through (f), IND content and format 335 1.35 452 1,600 723,200 312.30(a) through (e), Protocol amendments 694 5.84 4,050 284 1,150,200 312.31(b), Information amendments 77 2.43 187 100 18,700 312.32(c) and (d), IND Safety reports 161 8.83 1,421 32 45,472 312.33(a) through (f), IND Annual reports 745 2.14 1,595 360 574,200 312.38(b) and (c), Notifications of withdrawal of an IND 134 1.69 227 28 6,356 312.42, Sponsor requests that a clinical hold be removed, including sponsor submission of a complete response to the issues identified in the clinical hold order 67 1.30 87 284 24,708 312.44(c) and (d), Sponsor responses to FDA when IND is terminated 34 1.15 39 16 624 312.45(a) and (b), Sponsor requests for or responses to an inactive status determination of an IND by FDA 55 1.38 76 12 912 312.47, Meetings, including “End-of-Phase 2” meetings and “Pre-NDA” meetings 88 1.75 154 160 24,640 312.53(c), Investigator reports submitted to the sponsor, including Form FDA-1572, curriculum vitae, clinical protocol, and financial disclosure 453 6.33 2,869 80 229,520 312.54(a), Sponsor submissions to FDA concerning investigations involving an exception from informed consent under § 50.24 1 1 1 48 48 312.54(b), Sponsor notifications to FDA and others concerning an IRB determination that it cannot approve research because it does not meet the criteria in the exception from informed consent in § 50.24(a) 1 1 1 48 48 312.55(a), Number of investigator brochures submitted by the sponsor to each investigator 239 1.91 457 48 21,936 312.55(b), Number of sponsor reports to investigators on new observations, especially adverse reactions and safe use 243 4.95 1,203 48 57,744 312.56(b), (c), and (d), Sponsor notifications to FDA and others resulting from:

(1)The sponsor's monitoring of all clinical investigations and determining that an investigator is not in compliance with the investigation agreements;

(2)the sponsor's review and evaluation of the evidence relating to the safety and effectiveness of the investigational drug; and

(3)the sponsor's determination that the investigational drug presents an unreasonable and significant risk to subjects 108 2.21 239 80 19,120 312.58(a), Number of sponsor's submissions of clinical investigation records to FDA on request during FDA inspections 7 1 7 8 56 312.64, Number of investigator reports to the sponsor, including progress reports, safety reports, final reports, and financial disclosure reports 2,728 3.82 10,411 24 249,864 312.70, During the disqualification process of a clinical investigator by FDA, the number of investigator responses or requests to FDA following FDA's notification to an investigator of its failure to comply with investigation requirements 5 1 5 40 200 312.110(b)(4) and (b)(5), Number of written certifications and written statements submitted to FDA relating to the export of an investigational drug 18 1 18 75 1,350 312.120(b), Number of submissions to FDA of “supporting information” related to the use of foreign clinical studies not conducted under an IND 280 9.82 2,750 32 88,000 312.120(c), Number of waiver requests submitted to FDA related to the use of foreign clinical studies not conducted under an IND 7 2.29 16 24 384 312.130, Number of requests for disclosable information in an IND and for investigations involving an exception from informed consent under § 50.24 350 1.34 470 8 3,760 312.310(b) and 312.305(b), Number of submissions related to expanded access and treatment of an individual patient 78 1.08 84 8 672 312.310(d), Number of submissions related to emergency use of an investigational new drug 76 2.76 210 16 3,360 312.315(c) and 312.305(b), Number of submissions related to expanded access and treatment of an intermediate-size patient population 9 1 9 120 1,080 312.320(b), Number of submissions related to a treatment IND or treatment protocol 1 1 1 300 300 Total 3,254,062 1 There are no capital costs or operating and maintenance costs associated with this collection of information. Table 4—Estimated Annual Recordkeeping Burden for Biologics 1 21 CFR section Number of recordkeepers Number of records per recordkeeper Total annual records Average burden per recordkeeping Total hours 312.52(a), Sponsor records for the transfer of obligations to a contract research organization 75 1.40 105 2 210 312.57, Sponsor recordkeeping showing the receipt, shipment, or other disposition of the investigational drug, and any financial interests 335 2.70 904 100 90,400 312.62(a), Investigator recordkeeping of the disposition of drugs 453 1 453 40 18,120 312.62(b), Investigator recordkeeping of case histories of individuals 453 1 453 40 18,120 312.160(a)(3), Records pertaining to the shipment of drugs for investigational use in laboratory research animals or in vitro tests 111 1.40 155 * 0.50 78 312.160(c), Shipper records of alternative disposition of unused drugs 111 1.40 155 * 0.50 78 Total 127,006 1 There are no capital costs or operating and maintenance costs associated with this collection of information. * Thirty

(30)minutes. Dated: February 24, 2015. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2015-04379 Filed 3-2-15; 8:45 am]

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