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Acknowledgments
Editorial assistance for this Letter was provided by Wendy Morris, Fleishman-Hillard Group Ltd. (contracted by Boehringer Ingelheim). Dr. DeRogatis is a Consultant to Boehringer Ingelheim, Biosante, Inc., Faber-Kramer Pharmaceuticals, and Endoceutics, Inc. Dr. Clayton led the development and validation of the Changes in Sexual Functioning Questionnaire (CSFQ), Sexual Interest and Desire Inventory (SIDI-F), and the Decreased Sexual Desire Screener (DSDS). She was Chair of the Third International Consultation on Sexual Medicine Committee for Standards for Clinical Trials in Sexual Dysfunction in Women: Research Designs and Outcomes Assessment (2009). She has been the Principal Investigator for many studies of Hypoactive Sexual Desire Disorder (HSDD): GlaxoSmithKline Phase IV trial of bupropion, Boehringer Ingelheim Phase III trials of flibanserin in premenopausal women, and BioSante Phase III trials of libigel in postmenopausal women. She is a Consultant to Boehringer Ingelheim, TransTech Pharma, and New England Research Institutes regarding Female Sexual Dysfunction (FSD), and to AstraZeneca, Bristol-Myers Squibb, Eli Lilly, Labopharm, Pfizer, PGxHealth, sanofi-aventis, and Takeda about sexual effects of psychotropic medications. Dr. Clayton has been a speaker for CME programs on HSDD supported by Boehringer Ingelheim. She receives royalties from: “Satisfaction: Women, Sex, and the Quest for Intimacy” published by Ballantine Books/Random House, “Women’s Mental Health: A Comprehensive Textbook” published by Guilford Publications, and the CSFQ. Dr. Rosen is a Consultant to Boehringer Ingelheim, Endo Pharmaceuticals, Eli Lilly, and Johnson and Johnson. Dr. Sand is the Global Strategic Leader for the flibanserin clinical development program at Boehringer Ingelheim. Dr. Pyke has been the Team Member (for) Medicine for the flibanserin premenopausal HSDD clinical development project at Boehringer Ingelheim since 2003. He was involved in the management of protocol content, field conduct, and interpretation of results for two Phase 2 trials (over 400 patients evaluated), seven Phase 3 trials (over 6,000 patients evaluated), two trials of SSRI users (over 100 patients evaluated so far), and six non-treatment studies on validation of measures of FSD (over 1000 patients evaluated). In this role, he helped lead development and testing of an integrated set of diagnostic evaluations for FSD, including a 60-question structured clinical interview appropriate for DSM-IV-TR, checklists on DSM-IV-TR and AUAF consensus diagnostic criteria, an AUAF consensus contributory factors checklist, and a brief form for non-expert clinicians to diagnose HSDD; one or more of these forms have been used in diagnostic interviews conducted with over 10,000 women in North America and Europe.
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DeRogatis, L.R., Clayton, A.H., Rosen, R.C. et al. Should Sexual Desire and Arousal Disorders in Women Be Merged?. Arch Sex Behav 40, 217–219 (2011). https://doi.org/10.1007/s10508-010-9677-1
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DOI: https://doi.org/10.1007/s10508-010-9677-1