Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

8.0%

2 terminated/withdrawn out of 25 trials

Success Rate

92.0%

+5.5% vs industry average

Late-Stage Pipeline

60%

15 trials in Phase 3/4

Results Transparency

39%

9 of 23 completed trials have results

Key Signals

9 with results

Enrollment Performance

Analytics

Phase 3
14(58.3%)
Phase 2
9(37.5%)
Phase 4
1(4.2%)
24Total
Phase 3(14)
Phase 2(9)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (25)

Showing 20 of 25 trials
NCT00782769Phase 3Completed

A Safety Extension Study of DR-OXY-301

Role: lead

NCT00382408Phase 3Completed

A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001

Role: lead

NCT00781456Phase 2Completed

A Multicenter Study to Evaluate the Efficacy of a 91-Day Extended Cycle Oral Contraceptive for Menstrually-Related Migraine Headaches

Role: lead

NCT00986089Withdrawn

Intrauterine Device (IUD) Placement at the Time of Cesarean Section

Role: collaborator

NCT00196326Phase 3Completed

Open-label Study to Evaluate the Efficacy and Safety of an Extended-cycle, Low Dose Combination Oral Contraceptive

Role: lead

NCT00196313Phase 2Completed

A Study to Evaluate the Efficacy of Seasonique for the Treatment of Cyclic Pelvic Pain

Role: lead

NCT00196339Phase 2Completed

A Clinical Trial to Study DR-2031 for the Treatment of Hot Flashes in Prostate Cancer Patients

Role: lead

NCT00685113Phase 3Completed

A Clinical Trial to Evaluate the Efficacy and Safety of DR-3001 in Women With Overactive Bladder

Role: lead

NCT00361569Phase 3Completed

A Clinical Trial to Evaluate the Safety and Efficacy of DR-2041(Synthetic Conjugated Estrogens, A) for Treatment of Vulvovaginal Atrophy

Role: lead

NCT00924560Phase 2Completed

A Multicenter Study to Evaluate the Effects of a 91-day Oral Contraceptive on Bone Mineral Density in Adolescent Females

Role: lead

NCT00196391Phase 2Completed

A Trial to Evaluate DR-2021 in Women With Secondary Amenorrhea

Role: lead

NCT00117468Phase 2Completed

Comparison of DR-2011 to a Progesterone Vaginal Gel for Luteal Phase Replacement

Role: lead

NCT00196365Phase 3Completed

A Study to Evaluate the Efficacy of Seasonique for the Treatment of Cyclic Pelvic Pain

Role: lead

NCT00117481Phase 2Completed

Evaluation of DR-2001 for the Management of Endometriosis-Related Pelvic Pain

Role: lead

NCT00117273Phase 3Completed

A Study to Evaluate Suppression of the Pituitary-Ovarian Axis With Three Different Oral Contraceptive Regimens

Role: lead

NCT00196352Phase 3Completed

A Multicenter Study to Evaluate the Safety of Seasonique, an Oral Contraceptive.

Role: lead

NCT00615251Phase 3Completed

A Clinical Trial to Evaluate the Efficacy and Safety of DR-2011 for In Vitro Fertilization

Role: lead

NCT00196378Phase 3Completed

A Clinical Trial to Evaluate the Safety and Efficacy of Enjuvia 0.3 mg for the Treatment of Vulvovaginal Atrophy

Role: lead

NCT00362479Phase 3Completed

Open-Label Study to Evaluate the Safety and Efficacy of a Low-Dose 28-Day Oral Contraceptive

Role: lead

NCT00117260Phase 3Withdrawn

Study to Evaluate the Safety and Efficacy of Seasonale for Treatment of Low Bone Mineral Density

Role: lead