EFTA01734942

Low Sexual Interest, Desire, and/or Arousal in Women: Developing Drugs for Treatment Guidance for Industry DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Comments and suggestions regarding this draft document should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance. Submit electronic comments to http://www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. All comments should be identified with the docket number listed in the notice of availability that publishes in the Federal Register. For questions regarding this draft document, contact Jennifer Mercier at 301-796-0957. U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) October 2016 Clinical/Medical 477695dft.doc 09/16/16 EFTA_R1_00015156 EFTA01734942 Low Sexual Interest, Desire, and/or Arousal in Women: Developing Drugs for Treatment Guidance for Industry Additional copies are available from: Office of Communications, Division of Drug Information Center for Drug Evaluation and Research Food and Drug Administration 10001 New Hampshire Ave., Hillandale Bldg., 4th Floor Silver Spring. MD 20993-0002 Phone: 855-543-3784 or 301-796-3400; Fax: 301-431-6353; Email: [email protected] hap:/Avww.fda.gov/Drugs/GuidanceComplianceRegulatotylnfortnation/Guidanceildefault.htm U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) October 2016 Clinical/Medical EFTA_R1_00015157 EFTA01734943 TABLE OF CONTENTS I. INTRODUCTION II. BACKGROUND 2 III. DEVELOPMENT PROGRAM 3 A. General Considerations 3 B. Specific Efficacy Trial Considerations 4 C. Trial Populations 4 I. Appropriate Target Population 4 2. Eligibility 5 3. Menopausal Status 5 D. Clinical Outcome Assessment Instruments 6 1. Recall Period 6 2. Format of Data Capture 7 3. Instruments for Measuring Patient-Reported Outcomes 7 a. Female Sexual Function Index 8 b. Female Sexual Distress Scale-Revised, Item I3 9 c. Other scoring proposals 9 E. Trial Endpoints 9 1. Primary and Key Secondary Endpoints 10 2. Other Secondary Endpoints 11 F. Other Considerations 11 1. Safety Considerations 11 2. Pharmacokinetic/Pharmacodynamic Considerations 12 EFTA_R1_00015158 EFTA01734944 Contains Nonbinding Recommendations Draft — Not for Implementation Low Sexual Interest, Desire, and/or Arousal in Women: Developing Drugs for Treatment 3 Guidance for Industry' 4 5 6 7 8 9 10 11 12 13 This draft guidance, when finalized, will represent the current thinking of the Food and Drug Administration (FDA or Agency) on this topic. It does not establish any rights for any person and is not binding on FDA or the public. You can use an alternative approach if it satisfies the requirements of the applicable statutes and regulations. To discuss an alternative approach, contact the FDA staff responsible for this guidance as listed on the title page. 14 15 16 17 I. INTRODUCTION 18 19 The purpose of this guidance is to assist sponsors in developing drugs for the treatment of low 20 sexual interest, desire, and/or arousal in women.2 Specifically, this guidance addresses the Food 21 and Drug Administration's (FDA's) current thinking regarding the overall clinical development 22 program, with a focus on phase 3 trial designs, to support an indication for the treatment of these 23 conditions. This draft guidance is intended to serve as a focus for continued discussions among 24 the Division of Bone, Reproductive, and Urologic Products, pharmaceutical companies, the 25 academic community, and the public .3 26 27 This guidance focuses on conditions of low sexual interest, desire, and/or arousal that cause 28 marked distress or interpersonal difficulty in women, including female sexual interest/arousal 29 disorder (FSIAD), hypoactive sexual desire disorder (HSDD), and female sexual arousal disorder 30 (FSAD). The symptoms of these conditions are NOT considered to be caused by: 31 32 • A coexisting medical or psychiatric condition 33 • Problems within the relationship 34 • The effects of a medication or other drug substance I This guidance has been prepared by the Division of Bone, Reproductive, and Urologic Products in the Center for Drug Evaluation and Rcscarch at the Food and Drug Administration. 2 For the purposes of this guidance, all references to drugs include both human drugs and therapeutic biological products unless otherwise specified. In addition to consulting guidances, sponsors are encouraged to contact the division to discuss specific issues that arise during drug development. FSIAD is a clinical entity described in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM) that was published in 2013, whereas HSDD and FSAD are conditions described in the fourth edition of the DSM. FFTA_R1_00015159 EFTA01734945 Contains Nonbinding Recommendations Draft — Not for Implementation 35 36 The diagnostic criteria for disorders of low sexual interest, desire, and/or arousal in women were 37 recently revised in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders 38 (DSM). These revisions have not been universally accepted by the scientific community. The 39 recommendations proposed in this guidance can be applied to the diagnostic framework outlined 40 in both the fourth and fifth editions of the DSM. 41 42 This guidance does not address the development of drugs to treat other forms of female sexual 43 dysfunction such as orgasmic disorder, genito-pelvic pain/penetration disorder, or 44 substance/medication-induced sexual dysfunction in women. In addition, this guidance does not 45 address the treatment of dyspareunia, which is often, but not always, related to vulvovaginal 46 atrophy (VVA) associated with menopause. VVA symptoms are addressed in a separate 47 guidance? 48 49 Although this guidance discusses the selection of endpoints for clinical trials, it does not address 50 detailed design considerations for patient-reported outcome (PRO) instruments. Those issues are 51 addressed in the guidance for industry Patient-Reported Outcome Measures: Use in Medical 52 Product Development to Support Labeling Claims (PRO guidance).6 In addition, this guidance 53 does not contain discussion of the general issues of statistical analysis or clinical trial design. 54 Those topics are addressed in the ICH guidances for industry E9 Statistical Principles for 55 Clinical Trials and E 10 Choice of Control Group and Related Issues in Clinical Trials, 56 respectively. 57 58 In general, FDA's guidance documents do not establish legally enforceable responsibilities. 59 Instead, guidances describe the Agency's current thinking on a topic and should be viewed only 60 as recommendations, unless specific regulatory or statutory requirements are cited. The use of 61 the word should in Agency guidances means that something is suggested or recommended, but 62 not required. 63 64 65 II. BACKGROUND 66 67 The term female sexual dysfunction encompasses a heterogeneous group of sexual disorders, 68 such as dyspareunia and problems related to sexual arousal, desire, interest, or orgasm. The 69 sexual response has a physiological basis but can be affected by interpersonal context, such as 70 emotional and relationship dynamics. Significant changes in any of these components can affect 71 a woman's sexual desire, response, and satisfaction. A variety of factors can cause or contribute 72 to sexual dysfunction, including medical conditions (such as symptoms of VVA related to 5 See the draft guidance for industry Estrogen and Estrogen/Progestin Drug Products to Treat Vasomotor Symptoms and Vu/var and Vaginal Atrophy Symptoms — Recommendations for Clinical Evaluation. When final, this guidance will represent the FDA's current thinking on this topic. For the most recent version of a guidance, check the FDA Drugs guidance Web page at http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInfonnation/Guidanceridefault.htm. 6 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/GuidanceComplianceRegulatoryInfonnation/Guidancesidefault.htm. 2 EFTA_R1_00015160 EFTA01734946 Contains Nonbinding Recommendations Draft — Not for Implementation 73 menopause), psychiatric conditions (such as depression and anxiety), use of medications (such as 74 selective serotonin-reuptake inhibitors), and stressors (such as fatigue or relationship 75 difficulties). Sexual dysfunction can adversely affect various aspects of life for a woman, 76 including her relationship with her partner. There is a medical need for development of drugs 77 with a favorable benefit-risk profile to treat women with sexual dysfunction. 78 79 80 III. DEVELOPMENT PROGRAM 81 82 A. General Considerations 83 84 As with any drug development program, early clinical development should include appropriate 85 dose-finding in the target population to ensure that the most appropriate dosing regimen(s) are 86 selected for further study. The FDA recommends evaluating more than one dose in phase 3 87 trials. See the following for additional information regarding dose response: 88 89 • The Fit-for-Purpose Initiative dose-finding tool MCP-MOD (Multiple Comparison 90 Procedure-modeling), a statistical methodology for dose response7 91 92 • The guidance for industry Exposure-Response Relationships — Study Design, Data 93 Analysis, and Regulatory Applications 94 95 • The guidance for industry Providing Clinical Evidence of Effectiveness for Human Drug 96 and Biological Products 97 98 • The ICH guidance for industry E4 Dose-Response Information to Support Drug 99 Registration 100 101 If the investigational drug contains two or more drug components, the sponsor should address the 102 combination drug rule by demonstrating that: (I) each component makes a contribution to the 103 claimed effects; and (2) the dosage of each component (amount, frequency, duration) is such that 104 the combination is safe and effective for the intended patient population." 105 106 Exploration of new PRO instruments or novel diagnostic measures in early development may 107 allow correlation of results obtained from these modalities with dose-response findings. We 108 encourage early and regular discussions with the FDA regarding trial design to help ensure the 109 use of adequate and interpretable assessments of treatment benefit. 110 7 See the Drug Development Tools: Fit-for-Purpose Initiative Web page at http://www.fda.gov/Drugs/DevelopmentApprovalProcess/ucm505485.htm. See also Bretz F, Pinheiro SC, and Branson M. 2005. Combining Multiple Comparisons and Modeling Techniques in Dose-Response Studies. Biometrics, 61(3), 738-748. 8 21 CFR 300.50(a) 3 E FTA_R 1_00015161 EFTA01734947 Contains Nonbinding Recommendations Draft — Not for Implementation 111 B. Specific Efficacy Trial Considerations 1 12 1 13 In general, support from two adequate and well-controlled trials is required to establish efficacy.9 114 These trials should be randomized and placebo-controlled, but do not need to be identical in 1 15 design. Each trial should include at least 24 weeks of blinded treatment to allow demonstration 116 of effect onset and persistence while on treatment. A placebo run-in period is recommended for 1 17 assessing whether subjects will likely adhere to the proposed dosing regimen through the trial 1 18 and for obtaining baseline data for the key efficacy measures. 119 120 For a drug intended for use as needed, we recommend that the sponsor determine the time period 121 following each dose of the investigational drug when the drug is likely to exert its effect, taking 122 into account pharmacokinetic/pharmacodynamic relationships. This information should inform 123 key aspects of the phase 3 trial design, such as the time interval following drug administration 124 for assessing efficacy and the appropriate recall periods for PRO instruments. 125 126 If, in addition to the investigational drug, the proposed treatment involves a novel companion 127 diagnostic procedure or device, contemporaneous development of the drug and the diagnostic is 128 preferable such that the clinical performance and the clinical significance of the diagnostic can 129 be established using data from the drug development program.' The FDA encourages sponsors 130 to seek advice on the diagnostic as early in development as possible. The FDA's review of the 131 investigational drug and the diagnostic procedure or device will be carried out collaboratively 132 among relevant review staff. 133 134 C. Trial Populations 135 136 1. Appropriate Target Population 137 138 The FDA encourages sponsors to conduct trials in a well-defined patient population. This is 139 particularly relevant for sponsors who propose to study women with FSIAD, because patients 140 could meet the DSM-5 criteria for this condition if they predominantly have symptoms of low 141 sexual desire, if they predominantly have symptoms of low sexual arousal, or if they have 142 symptoms of both low sexual desire and low sexual arousal. Including women with these 143 various combinations of symptoms in clinical trials is only recommended if the investigational 144 drug is expected to have beneficial effects on both sexual desire and sexual arousal (e.g., based 145 on the drug's mechanism of action). For those investigational drugs that are expected to have 146 beneficial effects on either sexual desire or sexual arousal — but not both — the FDA 147 recommends that the enrolled population include patients with the symptoms most likely to 148 respond to the investigational drug. Otherwise, the sponsor risks a failed study. 149 150 The phase 3 trials should be conducted in North America (i.e., United States and Canada) 151 because of differences in the diagnosis, practice of medicine, and expectation of treatment effects 9 21 U.S.C. 355(d) 10 See the guidance for industry and Food and Mug Administration staff In Vitro Companion Diagnostic Devices available on the Guidance Documents (Medical Devices and Radiation-Emitting Products) Web page at http://www.fda.goviMedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/default.htm. 4 EFTA_R1_00015162 EFTA01734948 Contains Nonbinding Recommendations Draft — Not for Implementation 152 in different geographical regions. These differences may affect the general izability of efficacy 153 data from patients outside the United States to the U.S. population. If the development program 154 includes trials conducted in other geographical regions, these data can be used to support safety. 155 156 To support efficacy, the trial population should be representative of U.S. women in whom the 157 drug will be intended for use and should reflect the demographic characteristics of the target 158 population with the disorder. Trial subjects should be North American patients who are sexually 159 active and are at least 18 years of age. They should have a documented history of personal 160 distress related to low sexual interest, desire, and/or arousal. Although women who are not in a 161 stable relationship may also experience sexual dysfunction, the FDA recommends that the 162 clinical trials limit enrollment to women who are in a stable relationship. This approach reduces 163 the likelihood of having changes in relationship status during the trials, which could confound 164 the results. Patients should be excluded if the symptoms and associated distress are related to a 165 comorbidity, problems within the relationship, or the effects of a drug or other drug substance. 166 167 Female sexual dysfunction occurs in adult women. Sponsors can request a full waiver for 168 pediatric studies on the grounds that necessary studies would be impossible because the 169 condition does not exist in the pediatric age group. 170 171 2. Eligibility 172 173 The exclusion criteria (e.g., coexisting medical conditions, concomitant medications, restrictions 174 based on body mass index, history of substance use) should be limited to ensure that the trial 175 population is representative of North American women anticipated to use the drug, if approved. 176 We also encourage sponsors to include patients with a broad range of severity of sexual 177 dysfunction at baseline, provided that the dysfunction causes marked distress (see section 178 III.D.3., Instruments for Measuring Patient-Reported Outcomes, for an assessment of distress). 179 Furthermore, because the eligibility criteria do not need to be identical in all phase 3 trials 180 comprising the clinical program, subsequent trial(s) can have less restrictive entry criteria than 181 the first trial. 182 183 3. Menopausal Status 184 185 Because conditions of low sexual interest, desire, and/or arousal occur in both pre- and 186 postmenopausal women, both groups represent appropriate target populations. Development 187 programs targeting only one of these subgroups should be justified by safety concerns or other 188 clinical grounds. 189 190 Sponsors can choose to study pre- and postmenopausal women in separate trials or study these 191 populations within the same trial. If studied in the same trial, randomization of subjects should 192 be stratified by menopausal status. Regardless of the approach chosen, dose-finding, safety, and 193 efficacy should be established independently for each of these populations, because the benefit- 194 risk profile may differ and there may be differences in etiologies and treatment responses. 195 Therefore, if both pre- and postmenopausal women are included in the same clinical trial, the 196 trial should be powered adequately to demonstrate statistical and clinical significance for each of 197 these subgroups. 5 EFTA_R1_00015163 EFTA01734949 Contains Nonbinding Recommendations Draft — Not for Implementation 198 199 The FDA recommends subgroup analyses based on the cause of menopause (natural versus 200 surgical) if both naturally and surgically menopausal women are enrolled in the same trial. The 201 FDA also recommends subgroup analyses according to baseline hormonal contraceptive use (for 202 premenopausal women) and according to baseline hormone therapy use (for postmenopausal 203 women, if these drugs are allowed during the trials). 204 205 The FDA also requires additional subgroup analyses based on age and race." 206 207 D. Clinical Outcome Assessment Instruments 208 209 Because decreased sexual interest, desire, and/or arousal are symptomatic conditions, a PRO is 210 the most appropriate clinical outcome assessment for evaluating symptoms. It is essential that 211 sponsors use well-defined and reliable PRO instruments.12 For any PRO instrument proposed as 212 a key study endpoint to support labeling claims, the sponsor should provide supportive 213 information for FDA review (e.g., a copy of the assessment, the instrument's conceptual 214 framework and scoring, evidence of the instrument's content validity" and other measurement 215 properties including reliability, construct validity, and ability to detect change). See the PRO 216 guidance for additional information. 217 218 I. Recall Period 219 220 Key signs and symptoms should be recorded frequently by subjects to minimize inaccurate 221 responses resulting from problems with subject recall. We recognize that shorter recall periods 222 may be more burdensome to subjects over the course of a lengthy trial and could lead to diaty 223 fatigue, which could adversely affect compliance with diary entry over time. However, longer 224 recall periods (e.g., monthly) may adversely affect the ability to accurately reflect on symptoms. 225 For example, the longer recall period may increase noise in the assessment making it more 226 difficult to detect or interpret change during a trial. With a longer recall, it is also possible that 227 subject recollection could be more heavily influenced by other experiences or by more recent 228 experiences. 229 230 Because of the problems with long-term recall, we recommend using a short recall period 231 (sponsors using a short recall period who are concerned about subject burden can propose 232 approaches to minimizing burden). Sponsors who wish to use a longer recall period should 233 evaluate the accuracy of the longer recall period compared to shorter recall. 234 " 21 CFR 314.50(dX5Xv) I2 21 CFR 3I4.126(aX6) 13 Content validity is defined as the "Evidence from qualitative research demonstrating that the instrument measures the concept of interest including evidence that the items and domains of an instrument are appropriate and comprehensive relative to its intended measurement concept, population, and use. Testing other measurement properties will not replace or rectify problems with content validity." See section 111.D., Content Validity, of the PRO guidance. 6 EFTA_R1_00015164 EFTA01734950 Contains Nonbinding Recommendations Draft — Not for Implementation 235 For drugs intended to be administered on an as-needed basis, the FDA recommends that 236 symptoms be assessed following each dose of the placebo and investigational drug. The length 237 of time after each dose when symptoms should be assessed should be based on the 238 investigational drug's expected duration of action, taking into account 239 pharmacokinetic/pharmacodynamic relationships. Including efficacy data from days when the 240 investigational drug is not used may increase the difficulty in detecting and attributing a 241 treatment difference to the drug, and is not recommended. For similar reasons, the FDA does not 242 recommend recall periods longer than 24 hours for an as-needed drug. A longer recall period 243 may make it more difficult for subjects to accurately reflect on symptoms because their recall 244 may be affected by symptoms that occurred on the days when the placebo and investigational 245 drug were not used. 246 247 For drugs that are administered continuously, we also recommend shorter (e.g., daily or weekly) 248 recall periods with a 1-day lockout period for evaluation of primary endpoints such as desire or 249 arousal. 250 251 2. Format of Data Capture 252 253 Sponsors should specify the format used by subjects to record daily signs and symptoms, such as 254 an interactive voice response system (IVRS), electronic tablet, smartphone, personal digital 255 assistant, or paper diary. We prefer use of an electronic format with reminders or alarms, when 256 appropriate and feasible, to ensure real-time data capture and limit missing data, as well as to 257 accurately capture the timing of the assessment. Sponsors should address lockout of delayed 258 entry (see section III.D.I., Recall Period) and frequency of downloads. In addition, sponsors 259 should be able to generate, upon request, accurate and completed copies of electronic records in a 260 form suitable for FDA review and inspection. 261 262 Such a diary should capture, at a minimum, whether a sexual encounter occurred, whether the 263 investigational drug was taken, and any other information pertinent to the key efficacy endpoints. 264 Sponsors should account for the occurrence of multiple sexual encounters on the same day or 265 within a 24-hour period. Dosing times for drugs administered on an as-needed basis also should 266 be captured. The FDA recommends that the diary be submitted for review (e.g., screenshots, 267 script for IVRS) in advance of its use. 268 269 3. Instruments for Measuring Patient-Reported Outcomes 270 271 Phase 2 studies represent an important opportunity to evaluate measurement properties of PRO 272 instruments. Therefore, piloting the instrument and obtaining results from such exploratory 273 studies can inform instrument design and the adequacy for use in the phase 3 trials. Before use 274 in phase 2 studies, it is important to establish that the questionnaire instructions and items are 275 interpreted by subjects as intended and that the items adequately cover the relevant symptoms 276 and are worded such that they do not overlap in their measurement concept. 277 278 We strongly recommend that sponsors discuss the selection and implementation of proposed 279 PRO instruments with the FDA as early as possible during drug development. Two instruments 280 are discussed below. The FDA is open to considering other instruments to measure sexual desire 7 EFTA_R1_00015165 EFTA01734951 Contains Nonbinding Recommendations Draft — Not for Implementation 281 and distress. We encourage the research and drug development community to collaborate with 282 the FDA in development of a publicly available fit-for-purpose PRO instrument that can be used 283 across multiple drug development programs over time. A framework for such collaboration is 284 available within the FDA Development Tool Qualification program. See the guidance for 285 industry and FDA Staff Qualification Process for Drug Development Tools. 286 287 a. Female Sexual Function Index14 288 289 The Female Sexual Function Index (FSFI) is a 19-item instrument that has been used in clinical 290 trials to measure overall sexual function, although the FDA is unaware of data that adequately 291 establish the validity of the instrument as a whole for regulatory purposes. Individual domain 292 questions from the FSFI have been used to measure specific components of sexual function such 293 as sexual desire (questions 1 and 2) and sexual arousal (questions 3 through 6). Below we focus 294 on the FSFI sexual desire domain. To date, the FDA's experience with the FSFI sexual arousal 295 domain is limited. Sponsors who wish to use that domain or other portions of the FSFI to 296 establish efficacy for other aspects of sexual function should provide supporting data consistent 297 with the recommendations in the PRO guidance. 298 299 The assessment of desire in the FSFI includes introductory instructions that define desire as 300 being "a feeling that includes wanting to have a sexual experience, feeling receptive to a 301 partner's sexual initiation, and thinking or fantasizing about having sex." Question I asks "How 302 often did you feel sexual desire or interest?" with response options ranging from 5 (Almost 303 always or always) to 1 (Almost never or never). Question 2 asks "How would you rate your 304 level (degree) of sexual desire or interest?" with response options ranging from 5 (Very high) to 305 1 (Very low or none at all). These two questions ask the subject to reflect on her symptoms over 306 the preceding 4 weeks. The two response scores are summed, and raw scores are multiplied by a 307 factor of 0.6, providing a sexual desire domain score that ranges from 1.2 to 6.0. 308 309 The FDA has the following concerns with the content validity and response scale of the FSFI 310 desire domain, in addition to the long recall period (28 days) as discussed in section 111.D.1., 311 Recall Period. 312 313 • The FDA's content validity concerns for the sexual desire domain arise from the 314 multibarreled instructions that make it unclear what is driving any change identified on 315 the assessment (e.g., receptivity, sexual fantasies, or initiating sexual activity). For 316 example, if only one component (e.g., sexual fantasies) is increased with the drug, but 317 other components (e.g., wanting, initiating, or feeling receptive to sexual activity) have 318 not improved, a score change suggesting improvement could be shown; however, it is 319 unclear whether this represents a meaningful benefit to patients. 320 321 • The FDA's concerns with the response scale relate to the response option of "Almost 322 always or always" feeling sexual desire or interest (question 1) and a response indicating 323 a "Very high" level of sexual desire or interest (question 2). For example, it is unclear 14 Rosen R. Brown C, et al., 2000, The Female Sexual Function Index (FSFI): A Multidimensional Self-Report Instrument for the Assessment of Female Sexual Function, Sex Marital Ther, 26(2):191-208. 8 EFTA_R1_00015166 EFTA01734952 Contains Nonbinding Recommendations Draft— Not for Implementation 324 whether women experiencing sexual desire all or most of the time would identify this as a 325 benefit, or whether this could represent a different concern to women. 326 327 If a sponsor elects to use the FSFI, or a modified FSFI, some potential approaches for doing so 328 are delineated below: 329 330 (1) A sponsor could develop a new modified FSFI desire domain that includes individual 331 assessment of the components of desire captured on a daily basis with subsequent 332 validation (evaluation of measurement properties). This approach is preferred because it 333 addresses each of the concerns delineated above. 334 335 (2) A sponsor could use the FSFI desire domain and 28-day recall as currently designed and 336 show that this recall period does not affect conclusions by comparing these results with a 337 subset of subjects who use a shorter recall period (e.g., daily assessment) for the 338 individual desire items. 339 340 (3) A sponsor could use the FSFI desire domain but remove the multibarreled instructions in 341 the current instrument, and consider including secondary endpoints assessing other 342 components of desire. 343 344 (4) A sponsor could use the FSFI desire domain and 28-day recall as currently designed 345 without any modifications. This approach carries more risk because the aforementioned 346 issues could make it more difficult to detect or interpret changes in a trial. 347 348 b. Female Sexual Distress Scale-Revised, Item 1315 349 350 Question 13 of the Female Sexual Distress Scale-Revised (FSDS-R) instrument is considered 351 acceptable for measuring bother (a component of distress) related to decreased sexual desire. 352 This question asks "How often did you feel: Bothered by low sexual desire?" Subjects assess 353 their sexual distress over a 7-day recall period and respond on a scale of 0 (never) to 4 (always). 354 355 c. Other scoring proposals 356 357 Total scores of the FSFI and FSDS-R are not specific to the outcome measures of interest for the 358 conditions addressed in this guidance. Therefore, the total scores will not be considered 359 acceptable for any labeling claim. 360 361 E. Trial Endpoints 362 363 Primary efficacy assessments for adequate and well-controlled trials should be well-defined and 364 reliable to provide a basis for determining whether there is "substantial evidence" to support the 365 claims of effectiveness for a new drug." Endpoint decisions should reflect the primary IS DeRogatis L, Clayton A, et al.. 2008. Validation of the Female Sexual Distress Scale-Revised for Assessing Distress in Women With Hypoactive Sexual Desire Disorder, J Sex Mai, 5:357-364. 16 21 CFR 314.126 9 EFTA_R1_00015167 EFTA01734953 Contains Nonbinding Recommendations Draft — Not for Implementation 366 symptoms targeted by the drug (e.g., low sexual interest, desire, and/or arousal) and should be 367 supported by the proposed mechanism(s) of action of the drug, if known. Sponsors are 368 encouraged to discuss endpoint selection with the FDA early in drug development. 369 370 The following outcome measures can be used as primary endpoints: 371 372 • The change from baseline in the number of satisfying sexual events (SSEs) 373 • The change from baseline in the level of sexual interest or desire 374 • The change from baseline in the level of sexual arousal 375 • The change from baseline in the level of distress 376 377 If a trial will use an endpoint of SSEs, the protocol and PRO instruments should define the term 378 satisfying and what activities will be classified as a sexual encounter. 379 380 Baseline has been defined as a 4-week no-treatment phase or a 4-week placebo run-in period. 381 Changes from baseline typically refer to the treatment responses obtained during the last 4 weeks 382 of the double-blinded treatment period relative to the baseline. With this approach, the time 383 period used for assessing baseline status (e.g., 4 weeks) should be the same as the time period 384 used for assessing treatment responses (e.g., 4 weeks at the end of the treatment period). 385 However, one limitation is that this approach uses only a small portion of the efficacy data 386 collected during the treatment period. The FDA recommends alternative approaches that use a 387 greater portion of the efficacy data obtained during the course of the treatment period. 388 389 I. Primary and Key Secondary Endpoints 390 391 The primary efficacy analysis should demonstrate a clinically meaningful treatment benefit that 392 is statistically significant. Sponsors should describe in detail what constitutes a clinically 393 meaningful change for each of the scales used in the trials and provide justification of the 394 selected clinically meaningful threshold to define treatment success. In clinical programs for 395 drugs intended to treat decreased sexual interest or desire, one approach is to assess the change 396 from baseline in SSEs and the change from baseline in sexual interest or desire scores as 397 coprimary endpoints," and associated distress as a key secondary endpoint. Similarly, in clinical 398 programs for drugs intended to treat decreased sexual arousal, one approach is to assess the 399 change from baseline in SSEs and the change from baseline in sexual arousal as coprimary 400 endpoints, and associated distress as a key secondary endpoint. 401 402 However, it is important to note that the definitions for disorders of low sexual interest or desire 403 and low sexual arousal include associated distress and do not include a reduction in SSEs. For 404 this reason, comments received from two October 2014 public meetings have stated that 405 associated distress should replace SSEs as a coprimary efficacy endpoint for trials of drugs 17 Multiple primary endpoints become coprimary endpoints when it is necessary to demonstrate an effect on each of the endpoints to conclude that a drug is effective. 10 EFTA_R1_00015168 EFTA01734954 Contains Nonbinding Recommendations Draft — Not for Implementation 406 intended to treat low sexual interest, desire, and/or arousal disorders, with SSEs relegated to a 407 secondary endpoint:8 The FDA also considers this approach acceptable. 408 409 2. Other Secondary Endpoints 410 411 Definitions of a responder demonstrating improvement in SSEs, interest, desire, arousal, or 412 distress also can be assessed as secondary endpoints. Responder definitions should be 413 prospectively described before starting the trial and should be based on actual data that establish 414 that the change is clinically important. 415 416 Responder definitions should be derived using anchor-based methods. At a minimum, a static 417 current-state patient global impression of severity (PGI-S) should be used as the anchor to 418 evaluate the responder definition. The PGI-S is not subject to recall error like the patient global 419 impression of change (POI-C) anchor. A PGI-C can be used in addition to the PGI-S to provide 420 additional evidence in interpreting a clinically meaningful change. See the PRO guidance for 421 additional information. The FDA is open to considering other anchor-based methods as well. 422 423 If the investigational drug is expected to have an effect on both sexual desire and sexual arousal, 424 the sponsor should designate, a priori, whether all these components will be evaluated as 425 coprimary endpoints or whether some of these components will be tested as secondary endpoints. 426 The sponsor should include justification for the proposed approach in the protocol, including the 427 plan for controlling type I error for endpoints the sponsor hopes will lead to labeling claims. 428 429 F. Other Considerations 430 431 I. Safety Considerations 432 433 Drugs treating conditions of low sexual interest, desire, and/or arousal are likely to be taken 434 long-term (defined as continuous or intermittent use for at least 6 months during the course of a 435 lifetime). Therefore, the safety database should meet the patient exposures outlined in the ICH 436 guidance for industry El The Extent of Population Exposure to Assess Clinical Safety: For 437 Drugs Intended for Long-Term Treatment of Non-Life-Threatening Conditions. Note that these 438 are minimum patient exposures and that larger exposures may be needed for specific drugs 439 depending on safety concerns identified during drug development. 440 441 Drugs intended for as-needed use may also cumulatively lead to use of at least 6 months during 442 the course of a lifetime, and, in this case, should meet the patient exposures outlined in ICH El, 443 unless the sponsor provides adequate justification for why cumulative use would not exceed 6 444 months. 445 18 See the Patient-Focused Drug Development Public Meeting and Scientific Workshop on Female Sexual Dysfunction Web page at http://www.fda.gov/Drugs/NewsEventsittem401I67.htm. See also the public meeting minutes The Voice of the Patient, A series of reports from the U.S. Food and Drug Administration's (FDA's) Patient-Focused Drug Development Initiative: Female Sexual Dysfunction, accessed at http://www.fda.govidownloads/Drugs/NewsEvents/UCM4537I8.pdf. I EFTA_R1_00015169 EFTA01734955 Contains Nonbinding Recommendations Draft — Not for Implementation 446 The FDA may request additional studies based on specific characteristics of the drug, such as its 447 pharmacology, signals that emerge during drug development, or the intended route of 448 administration. Sponsors should discuss these specifics with the FDA during drug development. 449 450 Development programs for all new molecular entities, including treatments for low sexual 451 interest, desire, and/or arousal, should include an assessment of cardiac repolarization potential.19 452 Development programs for drugs with a potential psychotropic mechanism of action should also 453 include prospective assessment of treatment-emergent suicidal ideation and behavior.20 454 455 2. Pharmaeokinetie/Pharmacodynamie Considerations 456 457 We recommend conducting an adequately designed dose-finding study with measurements of 458 systemic exposure to assess the dose and exposure-response relationship. If feasible, blood 459 samples collected during the phase 3 trials would also be helpful in correlating efficacy or safety 460 findings with systemic exposure. 461 l° See the guidance for industry E I 4 Clinical Evaluation of QT/QTc Interval Prolongation and Proarrhythmic Potential for Non-Antiarrhythmic Drugs. 2° See the revised draft guidance for industry Suicidal Ideation and Behavior Prospective Assessment of Occurrence in Clinical Trials. When final, this guidance will represent the FDA's current thinking on this topic. 12 EFTA_R1_00015170 EFTA01734956