Trial intelligence / Profile preview

Continuous levonorgestrel + ethinyl estradiol for premenstrual dysphoric disorder

2004-005173-27Phase 3Completed

Sponsor
Wyeth
Start
Jun 2005
Modality
Small Molecules
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in Premenstrual Dysphoric Disorder (PMDD) comparing Levonorgestrel + ethinyl estradiol continuous daily regimen with Placebo (2 arms). Primary endpoints: Mean change in DRSP 21-item total daily score from baseline to cycle 1 efficacy period and Mean change in DRSP 21-item total daily score from baseline to last on-therapy efficacy period. Started Jun 2005; status: completed.

02

Drugs

avatrombopagethinyl estradiol
03

Conditions

Premenstrual Dysphoric Disorder (PMDD)

Beyond the preview

Go deeper on 2004-005173-27.

Study design, results and competitive context are available in the Gosset platform where reported.

Study design & results

Available in the Gosset platform where reported.

Competitive context

Available in the Gosset platform where reported.

Bring the full picture into focus.

See how Gosset can support your research on 2004-005173-27.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call