Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 5/100

Failure Rate

5.3%

1 terminated/withdrawn out of 19 trials

Late-Stage Pipeline

68%

13 trials in Phase 3/4

Results Transparency

100%

2 of 2 completed trials have results

Key Signals

11 recruiting2 with results

Enrollment reporting

Analytics

Phase 3
13(68.4%)
Phase 1
4(21.1%)
Phase 2
2(10.5%)
19Total
Phase 3(13)
Phase 1(4)
Phase 2(2)

Activity Timeline

Global Presence

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Clinical Trials (19)

Showing 19 of 19 trials
NCT07196501Phase 3Recruiting

A Study to Evaluate the Maintenance Effect of Osavampator as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

Role: lead

NCT07105098Phase 3Recruiting

NBI-1117568-SCZ3030: Evaluation of NBI-1117568 in Inpatient Adults With Schizophrenia

Role: lead

NCT07114874Phase 3Recruiting

NBI-1117568-SCZ3032: Long-Term Evaluation of NBI-1117568 in Adults With Schizophrenia

Role: lead

NCT06911112Phase 3Recruiting

NBI-1065845-MDD3025: Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

Role: lead

NCT06963021Phase 3Recruiting

NBI-1065845-MDD3026: Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

Role: lead

NCT06966401Phase 3Recruiting

Long-Term Study to Assess the Safety and Tolerability of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

Role: lead

NCT07288333Phase 2Recruiting

Evaluation of NBI-1117570 in Inpatient Adults With Schizophrenia

Role: lead

NCT07365462Phase 2Recruiting

Efficacy, Safety, and Tolerability of NBI-1065890 Versus Placebo in Adults With Tardive Dyskinesia

Role: lead

NCT04490915Phase 3Active Not Recruiting

Global Safety and Efficacy Registration Study of Crinecerfont for Congenital Adrenal Hyperplasia

Role: lead

NCT05206513Phase 3Completed

Study to Assess the Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Dyskinesia Due to Cerebral Palsy

Role: lead

NCT05110157Phase 3Completed

Journey Study: Evaluate the Efficacy, Safety, and Tolerability of Valbenazine as Adjunctive Treatment for Schizophrenia

Role: lead

NCT06786624Phase 3Recruiting

Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

Role: lead

NCT04806451Phase 3Active Not Recruiting

Global Safety and Efficacy Registration Study of Crinecerfont in Pediatric Participants With Classic Congenital Adrenal Hyperplasia (CAHtalyst Pediatric Study)

Role: lead

NCT05654870Phase 3Terminated

Study to Evaluate the Efficacy, Safety, and Tolerability of Valbenazine as an Adjunctive Treatment for Schizophrenia

Role: lead

SYF157db8723c824fd798158fc36041d93aPhase 1Recruiting

Effect of NBI-921355 on corticospinal excitability in healthy participants

Role: lead

SYF3812f592cd4c4d49bafada868a7e11aaPhase 1Unknown

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NBI-1117570 in Healthy Adults

Role: lead

SYF89632d08d467436cba762870277f7886Phase 1Recruiting

A First-in-Human, Open-label, Phase 1 Study to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of NBIM-1008 in Patients with Rheumatoid Arthritis

Role: lead

SYF9c7e4b94591a4707acb2f7b3f4698684Phase 1Active Not Recruiting

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NBI-1076986 in Healthy Adults.

Role: lead

SYFaf8e579c6b054c5bb566bb0fa45694d5Phase 3Not Yet Recruiting

An open-label study to evaluate the effect of crinecerfont on androgen reduction and related outcomes in adults with classic CAH

Role: lead

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