Neurocrine Biosciences

65 total trials 12 currently recruiting 42 completed

Neurocrine Biosciences sponsors 65 registered US clinical trials on ClinicalTrials.gov, 12 of them currently recruiting, and 42 completed. 23 of these trials are in Phase 3-4 (later-stage) and 40 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Schizophrenia, with 6 trials.

Trial Pipeline

65 total, page 2 of 2

COMPLETED Phase 3

Rollover Study for Continuing Valbenazine (NBI-98854) Administration for the Treatment of Tardive Dyskinesia

NCT02736955

COMPLETED Phase 1

Phase 1 TAK-041 First-in-Human Safety, Tolerability, and Pharmacokinetics Study

NCT02748694

COMPLETED Phase 2

Safety and Efficacy Study of NBI-98854 in Children and Adolescents With Tourette Syndrome

NCT02679079

COMPLETED Phase 2

Safety and Efficacy Study of NBI-98854 in Adults With Tourette Syndrome

NCT02581865

COMPLETED Phase 3

Safety and Tolerability Study of NBI-98854 for the Treatment of Tardive Dyskinesia

NCT02405091

COMPLETED Phase 3

A Phase 3 Study of NBI-98854 for the Treatment of Tardive Dyskinesia

NCT02274558

COMPLETED Phase 1

Safety, Pharmacokinetics, and Pharmacodynamics of NBI-98854 in Children and Adolescents With Tourette Syndrome

NCT02256475

COMPLETED Phase 1

Safety Study of AADC Gene Therapy (VY-AADC01) for Parkinson's Disease

NCT01973543

COMPLETED Phase 1

Safety, Tolerability, and Pharmacokinetics of a Single Dose of NBI-98854 in Subjects With Mild,Moderate, or Severe Hepatic Insufficiency

NCT01916993

COMPLETED Phase 1

Study to Assess the Effect of Ketoconazole on the Pharmacokinetics of NBI-98854 in Healthy Subjects

NCT01910480

COMPLETED Phase 2

NBI-98854 Dose Titration Study for the Treatment of Tardive Dyskinesia

NCT01733121

COMPLETED Phase 2

NBI-98854 for the Treatment of Tardive Dyskinesia in Subjects With Schizophrenia or Schizoaffective Disorder (KINECT Study)

NCT01688037

COMPLETED Phase 2

NBI-98854 for the Treatment of Tardive Dyskinesia in Subjects With Schizophrenia or Schizoaffective Disorder

NCT01393600

COMPLETED Phase 1

Intravenous Interleukin-4 PE38KDEL Cytotoxin in Treating Patients With Recurrent or Metastatic Kidney Cancer, Non-Small Cell Lung Cancer, or Breast Cancer

NCT00039052

COMPLETED Phase 2

NBI-3001 Followed by Surgery in Treating Patients With Recurrent Glioblastoma Multiforme

NCT00014677

← Previous Page 2 of 2

What the Pipeline for Neurocrine Biosciences Shows

According to the ClinicalTrials.gov registry, Neurocrine Biosciences is linked to 65 US clinical trials across every stage of research activity. Of those, 12 studies are currently recruiting, about 18% of the sponsor's indexed portfolio, and 42 are already marked complete, representing roughly 65% of the total.

The phase mix for Neurocrine Biosciences reports 23 late-stage studies (Phase 3 and Phase 4 combined) and 40 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Neurocrine Biosciences is Schizophrenia with 6 linked trials, and 9 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.