Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD) - Second Study

PHASE3WithdrawnINTERVENTIONAL
0
Timeline

Start Date

November 13, 2018

Primary Completion Date

August 15, 2019

Study Completion Date

December 6, 2019

Conditions
Hypoactive Sexual Desire Disorder (HSDD)
Interventions
DRUG

Placebo Vaginal Insert

Daily administration of a placebo vaginal insert.

DRUG

Prasterone 6.5 mg (0.50%) Vaginal Insert

Daily administration of a 6.5 mg (0.50%) prasterone vaginal insert.

Trial Locations (10)

10016

Endoceutics site # 20, New York

29910

Endoceutics site # 127, Bluffton

30075

Endoceutics site # 119, Roswell

31406

Endoceutics site # 91, Savannah

33709

Endoceutics site # 114, St. Petersburg

35801

Endoceutics site # 106, Huntsville

58103

Endoceutics site # 115, Fargo

78229

Endoceutics site # 102, San Antonio

92120

Endoceutics site # 17, San Diego

06320

Endoceutics site # 125, New London

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

AMAG Pharmaceuticals, Inc.

INDUSTRY

lead

EndoCeutics Inc.

INDUSTRY