Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 60/100

Failure Rate

35.6%

16 terminated/withdrawn out of 45 trials

Success Rate

60.0%

-26.5% vs industry average

Late-Stage Pipeline

58%

26 trials in Phase 3/4

Results Transparency

88%

21 of 24 completed trials have results

Key Signals

3 recruiting21 with results10 terminated6 withdrawn

Enrollment Performance

Analytics

Phase 3
22(52.4%)
Phase 2
7(16.7%)
Phase 1
6(14.3%)
Phase 4
4(9.5%)
N/A
3(7.1%)
42Total
Phase 3(22)
Phase 2(7)
Phase 1(6)
Phase 4(4)
+1 more

Activity Timeline

Global Presence

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Clinical Trials (45)

Showing 20 of 45 trials
NCT04593784Phase 2Terminated

Study of Ciraparantag for Reversal of Anticoagulation Induced by Edoxaban, Apixaban or Rivaroxaban in Healthy Adults

Role: lead

NCT03893045Phase 3Recruiting

A Study to Evaluate Ferumoxytol for the Treatment of Iron Deficiency Anemia (IDA) in Pediatric Subjects

Role: lead

NCT03619850Phase 3Recruiting

A Study to Evaluate the Safety (Compared to Iron Sucrose), Efficacy and Pharmacokinetics of Ferumoxytol for the Treatment of Iron Deficiency Anemia (IDA) in Pediatric Subjects With Chronic Kidney Disease (CKD)

Role: lead

NCT00707876Phase 2Completed

Magnetic Resonance Angiography for Peripheral Arterial Disease (PAD)

Role: lead

NCT01374919Not ApplicableCompleted

Total Dose Infusion of Ferumoxytol(1020mg) in 15 Minutes for Iron Deficiency Anemia

Role: collaborator

NCT04268849Phase 3Recruiting

Trial of IV vs Oral Iron Treatment of Iron Deficiency Anemia in the Post-Operative Bariatric Surgical Patient

Role: collaborator

NCT04493333Phase 2Terminated

Vaginal Dehydroepiandrosterone (DHEA) in Postmenopausal Breast Cancer Survivors on Aromatase Inhibitors

Role: collaborator

NCT04179734Phase 4Completed

Role of the Melanocortin-4 Receptor in Hypoactive Sexual Desire Disorder

Role: collaborator

NCT02499354Phase 2Completed

Pilot Study: Randomized, Placebo-controlled Comparator Trial of IV vs Oral Iron Treatment of RLS With IDA. (IVOR-IDA)

Role: collaborator

NCT04205266Phase 4Unknown

IV Iron vs Oral Iron for Treatment of Anemia in Women With Abnormal Uterine Bleeding

Role: collaborator

NCT04183452Terminated

17-OHPC in Pregnancy: IM vs SC Routes

Role: collaborator

NCT01052779Phase 2Completed

A Trial Comparing Ferumoxytol to Iron Sucrose for the Treatment of Iron Deficiency Anemia in Adult Subjects With Chronic Kidney Disease

Role: lead

NCT02694978Phase 3Completed

A Phase III Safety Study of Ferumoxytol Compared to Ferric Carboxymaltose for the Treatment of Iron Deficiency Anemia (IDA)

Role: lead

NCT03657433Phase 3Completed

Intravenous Infusions of Ferumoxytol Compared to Oral Ferrous Sulfate for the Treatment of Anemia in Pregnancy

Role: collaborator

NCT01004029Phase 3Completed

Confirmatory Study of 17P vs Vehicle for Prevention of Preterm Birth in Women w/ Previous Spontaneous Preterm Delivery

Role: lead

NCT01146990Completed

A Prospective, Noninterventional Follow-Up Study of Children Aged 23 to 25 Months, Born to Mothers Who Received Hydroxyprogesterone Caproate Injection, 250 mg/mL, or Vehicle for Prevention of Preterm Birth

Role: lead

NCT02940522Phase 1Completed

Comparing Bioavailability When Preservative-free Makena® (Hydroxyprogesterone Caproate Injection, 250 mg/mL) is Administered as an Intramuscular Manual Injection or as a Subcutaneous Injection Using an Auto-injector in Healthy Post-menopausal Women

Role: lead

NCT01155388Phase 3Terminated

A Trial of Ferumoxytol for the Treatment of Iron Deficiency Anemia in Pediatric Participants With Nondialysis-Dependent Chronic Kidney Disease

Role: lead

NCT01264679Phase 3Terminated

A Trial of Ferumoxytol for the Episodic Treatment of Iron Deficiency Anemia in Pediatric Participants With Chronic Kidney Disease

Role: lead

NCT01114217Phase 3Completed

A Trial of Ferumoxytol for the Episodic Treatment of Iron Deficiency Anemia

Role: lead