Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

0.0%

0 terminated/withdrawn out of 17 trials

Success Rate

100.0%

+13.5% vs industry average

Late-Stage Pipeline

29%

5 trials in Phase 3/4

Results Transparency

27%

4 of 15 completed trials have results

Key Signals

2 recruiting4 with results

Enrollment Performance

Analytics

Phase 1
7(46.7%)
Phase 3
5(33.3%)
Phase 2
3(20.0%)
15Total
Phase 1(7)
Phase 3(5)
Phase 2(3)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT04090957Phase 3Completed

Estetrol for the Treatment of Moderate to Severe Vasomotor Symptoms in Postmenopausal Women (E4Comfort II)

Role: lead

NCT06308614Phase 2Completed

Estetrol for the Treatment of Female Sexual Arousal Disorder in Postmenopausal Women

Role: lead

NCT06186271Recruiting

International Active Surveillance Study: Safety of Estrogen Estetrol (E4) Contraceptive Study (INAS-SEECS)

Role: collaborator

NCT06028555Recruiting

International Active Surveillance Study: Native Estrogen Estetrol (E4) Safety Study

Role: collaborator

NCT04209543Phase 3Completed

Estetrol for the Treatment of Moderate to Severe Vasomotor Symptoms in Postmenopausal Women (E4Comfort Study I)

Role: lead

NCT04792385Phase 3Completed

Safety, Compliance and Pharmacokinetics of Estetrol Monohydrate/Drospirenone 15/3 mg in Post-menarchal Female Adolescents

Role: lead

NCT04819906Phase 1Completed

Effect of Estetrol Monohydrate (E4) on QTc Interval

Role: lead

NCT03091595Phase 2Completed

E4/DRSP Ovarian Function Inhibition Study

Role: lead

NCT02817841Phase 3Completed

E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - United States/Canada Study

Role: lead

NCT02817828Phase 3Completed

E4 FREEDOM (Female Response Concerning Efficacy and Safety of Estetrol/Drospirenone as Oral Contraceptive in a Multicentric Study) - EU/Russia Study

Role: lead

NCT02720224Phase 1Completed

Study Conducted to Further Understand the Elimination Pathways, Metabolite Profile and PK Profile of 14C-estetrol

Role: lead

NCT03512860Phase 1Completed

Estetrol (E4)/Drospirenone (DRSP) Drug-drug Interaction (DDI) Study

Role: lead

NCT02957630Phase 1Completed

"E4/DRSP Endocrine Function, Metabolic Control and Hemostasis Study"

Role: lead

NCT03075956Phase 1Completed

Safety, Tolerability and Pharmacokinetics of Estetrol (E4) After Single and Multiple Oral Doses in Healthy Female Volunteers

Role: lead

NCT02874248Phase 1Completed

E4/DRSP Single and Multiple Dose PK and Early QT Study

Role: lead

NCT02852681Phase 1Completed

Effect of Food on the Bioavailability of 15 mg Estetrol/3 mg Drospirenone Tablets in Healthy Female Volunteers

Role: lead

NCT01221831Phase 2Completed

Cycle Control Assessment of a Combined Oral Contraceptive Containing Estetrol and a Progestin P1 or P2

Role: lead

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