Topical DHEA Against Vaginal Atrophy

PHASE3CompletedINTERVENTIONAL
Enrollment

218

Participants

Timeline

Start Date

June 30, 2007

Primary Completion Date

May 31, 2008

Study Completion Date

October 31, 2008

Conditions
Vaginal Atrophy
Interventions
DRUG

Placebo

Placebo vaginal suppository containing 0.0% (0 mg) DHEA; daily dosing with one suppository for 12 weeks.

DRUG

DHEA (0.25%)

Vaginal suppository containing 0.25% (3.25 mg) DHEA; daily dosing with one suppository for 12 weeks.

DRUG

DHEA (0.5%)

Vaginal suppository containing 0.5% (6.5 mg) DHEA; daily dosing with one suppository for 12 weeks.

DRUG

DHEA (1.0%)

Vaginal suppository containing 1.0% (13 mg) DHEA; daily dosing with one suppository for 12 weeks.

Trial Locations (8)

23507

EndoCeutics site # 03, Norfolk

44122

EndoCeutics site # 05, Cleveland

H1T 1P6

EndoCeutics site # 10, Montreal

H3A 1A1

EndoCeutics site # 09, Montreal

G9N 2H6

EndoCeutics site # 08, Shawinigan

J1H 1Z1

EndoCeutics site # 11, Sherbrooke

G1S 2L6

EndoCeutics site # 02, Québec

G1V 4G2

EndoCeutics site # 01, Québec

Sponsors

Lead Sponsor

All Listed Sponsors
lead

EndoCeutics Inc.

INDUSTRY