Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

5.3%

1 terminated/withdrawn out of 19 trials

Success Rate

92.9%

+6.4% vs industry average

Late-Stage Pipeline

26%

5 trials in Phase 3/4

Results Transparency

31%

4 of 13 completed trials have results

Key Signals

4 with results

Enrollment Performance

Analytics

Phase 1
8(42.1%)
Phase 2
6(31.6%)
Phase 3
5(26.3%)
19Total
Phase 1(8)
Phase 2(6)
Phase 3(5)

Activity Timeline

Global Presence

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Clinical Trials (19)

Showing 19 of 19 trials
NCT05600777Phase 3Active Not Recruiting

A 24-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough

Role: lead

NCT06222892Phase 1Completed

A Study of Camlipixant in Male and Female Healthy Participants and Participants With Hepatic Impairment Aged 18-75 Years of Age

Role: lead

NCT05599191Phase 3Active Not Recruiting

A 52-Week Study of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough

Role: lead

NCT05570539Phase 1Completed

Assessment of the Pharmacokinetics of BLU-5937 Extended Release Prototypes and a BLU-5937 Immediate Release Reference Formulation

Role: lead

NCT05959447Phase 1Completed

Evaluation of the Potential Drug-drug Interactions Between Gemfibrozil or Dabigatran Etexilate and Camlipixant

Role: lead

NCT06497517Phase 1Completed

A Study to Investigate the Effect of Food on Camlipixant Concentrations in Healthy Participants

Role: lead

NCT05899829Phase 1Completed

Evaluation of the Effect of Rifampin and Rabeprazole on the Pharmacokinetics of Camlipixant

Role: lead

NCT06179537Phase 1Completed

Evaluation of the Pharmacokinetics and Safety of BLU-5937 in Healthy Adult Japanese and Caucasian Subjects

Role: lead

NCT04693195Phase 2Completed

A Multiple-Dose Study of BLU-5937 in Chronic Pruritus Associated With Atopic Dermatitis

Role: lead

NCT05244759Phase 1Completed

Mass Balance Recovery, Absorption, Metabolism and Excretion of [14C]-BLU-5937

Role: lead

NCT04678206Phase 2Completed

Evaluation of the Efficacy and Safety of BLU-5937 in Adults With Refractory Chronic Cough

Role: lead

NCT03979638Phase 2Terminated

A Dose Escalation Study of BLU-5937 in Unexplained or Refractory Chronic Cough

Role: lead

NCT03638180Phase 1Completed

BLU-5937: First-in-Human, Single and Multiple Doses Escalation, Safety, Tolerability, Pharmacokinetics and Food Effect

Role: lead

NCT00675857Phase 2Completed

A Phase IIa Proof-of-concept Study of NC-503 in Patients With Type II Diabetes

Role: lead

NCT00217763Phase 3Unknown

European Study of 3APS in Mild to Moderate Alzheimer's Disease Patients

Role: lead

NCT00314912Phase 3Unknown

Open-Label Extension of the Phase III Study With Tramiprosate (3APS) in Patients With Mild to Moderate Alzheimer's Disease

Role: lead

NCT00088673Phase 3Unknown

Evaluation of 3APS in Patients With Mild to Moderate Alzheimer's Disease

Role: lead

NCT00035334Phase 2Completed

Study of the Safety and Efficacy of NC-503 in Secondary (AA) Amyloidosis

Role: lead

NCT00056238Phase 2Completed

Cerebril™ in Patients With Lobar Hemorrhage Related to Cerebral Amyloid Angiopathy

Role: lead

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