Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

14.2%

47 terminated/withdrawn out of 331 trials

Success Rate

84.4%

-2.1% vs industry average

Late-Stage Pipeline

37%

123 trials in Phase 3/4

Results Transparency

49%

125 of 255 completed trials have results

Key Signals

10 recruiting125 with results37 terminated10 withdrawn

Enrollment Performance

Analytics

Phase 3
93(38.0%)
Phase 2
71(29.0%)
Phase 4
30(12.2%)
N/A
28(11.4%)
Phase 1
22(9.0%)
Early Phase 1
1(0.4%)
245Total
Phase 3(93)
Phase 2(71)
Phase 4(30)
N/A(28)
+2 more

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (331)

Showing 20 of 331 trials
NCT06510374Phase 3Recruiting

Trial of Nadofaragene Firadenovec vs. Observation in Participants With Intermediate Risk Non-Muscle Invasive Bladder Cancer

Role: lead

NCT07154888Not ApplicableCompleted

Fast Track to Fertility

Role: collaborator

NCT01630967Phase 2Withdrawn

Efficacy Study of Switching to a Lutenizing Hormone-releasing Hormone (LHRH) Antagonist From a LHRH Agonist to Treat Progressive Castrate Resistant Prostate Cancer (CRPC)

Role: collaborator

NCT06561958Active Not Recruiting

Prospective, Multi-centre, Non-Interventional Study to Investigate the Effectiveness of REKOVELLE® for Ovarian Stimulation for Asian Women in Real World Settings

Role: lead

NCT07029451Active Not Recruiting

To Investigate REKOVELLE in Chinese Women Undergoing Assisted Reproductive Technologies: Effectiveness, Safety, and Patterns of Use in Real-world Practice

Role: lead

NCT06545955Phase 3Recruiting

A Trial to Evaluate Intravesical Nadofaragene Firadenovec Alone or in Combination With Chemotherapy or Immunotherapy in Participants With High-grade BCG Unresponsive Non-muscle Invasive Bladder Cancer

Role: lead

NCT07332351Phase 2Not Yet Recruiting

Neoadjuvant Intravesical Nadofaragene Firadenovec With Gemcitabine, Cisplatin and Durvalumab for the Treatment of Muscle Invasive Bladder Cancer, TRIFECTA Trial

Role: collaborator

NCT06668493Phase 1Recruiting

Low-grade UTUC Treated With Nadofaragene Firadenovec Administered to Renal Pelvis

Role: lead

NCT07816562Phase 3Recruiting

Ovulation Trigger Strategies in Low Ovarian Reserve (TRIGGERBEST)

Role: collaborator

NCT04113382Phase 1Recruiting

Study Assessing CLENPIQ as Bowel Preparation for Pediatric Colonoscopy

Role: lead

NCT06545877Completed

REKOVELLE PEN for S.C. Injection General Drug Use Survey (Controlled Ovarian Stimulation in Assisted Reproductive Technologies)

Role: lead

NCT05704244Phase 3Active Not Recruiting

Safety and Efficacy of FE 999326 Administered Intravesically to Japanese Subjects With High-grade, BCG Unresponsive, Non-muscle Invasive Bladder Cancer (NMIBC)

Role: lead

NCT05403476Phase 2Terminated

A Trial to Compare Efficacy and Safety of Follitropin Delta Versus Placebo (Inactive Treatment) in the Treatment of Men With Idiopathic Infertility (Unexplained Reduction of Semen Quality) (ADAM)

Role: lead

NCT01542021Not ApplicableCompleted

Androgen Deprivation Therapy Prior to Prostatectomy for Patients With Intermediate and High Risk Prostate Cancer

Role: collaborator

NCT07691073Phase 4Not Yet Recruiting

Embryo QUAlity in Ovarian Stimulation With hMG.

Role: collaborator

NCT02020070Phase 2Completed

Combining Ipilimumab, Degarelix, and Radical Prostatectomy in Men With Newly Diagnosed Metastatic Castration Sensitive Prostate Cancer or Ipilimumab and Degarelix in Men With Biochemically Recurrent Castration Sensitive Prostate Cancer After Radical Prostatectomy

Role: collaborator

NCT05831189Phase 3Completed

A Multi-center, Single-arm Trial Exploring the Safety and Clinical Effectiveness of RBX2660 Administered by Colonoscopy to Adults With Recurrent Clostridioides Difficile Infection

Role: lead

NCT07263490Recruiting

PRIOR Study (Pre-eclampsia Risk In Oocyte Recipients)

Role: collaborator

NCT07153367Phase 2Recruiting

Using a Fixed Dosage of Follitropin Delta for Ovarian Stimulation for Intrauterine Insemination: Rekovelle for Intrauterine Successful Experience (RISE)

Role: collaborator

NCT06511791Phase 1Terminated

An Exploratory Study to Investigate the Effect of FE 999302 When Given Together With Follitropin Delta at Different Time Intervals During Controlled Ovarian Stimulation.

Role: lead