Phase 1b/2a Unblinded Study of Responses in Premenopausal Women With HSDD to Lorexys Evaluating Efficacy and Safety
Summary
The lay summary the sponsor registered on ClinicalTrials.gov.
Investigators
The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.
- Molly Katz, MD
Katz and Kade, Inc.
Principal Investigator - Robert E Pyke, MD, PhD
Chief Medical Officer, S1 Biopharma, Inc.
Study Director - Robert T Segraves, MD, PhD
Levine, Risen & Associates, Inc.
Principal Investigator
A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.
Sites
2 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.
- Robert Taylor Segraves, Md, Phd
Beachwood, Ohio, United States
- Molly Katz, Md
Cincinnati, Ohio, United States
Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.
Drugs studied
The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.
Registration & key dates
Registry attributes as recorded on the ClinicalTrials.gov study record.
- Start
- 30 Apr 2013
- Primary completion
- 31 Oct 2014
- Completion
- 31 Oct 2014
- Last update posted
- 28 Oct 2014
- Registered enrollment
- 30
- Registry id
- NCT01857596
Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.