BioCryst Pharmaceuticals

29 total trials 2 currently recruiting 24 completed

BioCryst Pharmaceuticals sponsors 29 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 24 completed. 6 of these trials are in Phase 3-4 (later-stage) and 23 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Gout, with 2 trials.

Trial Pipeline

29 total, page 1 of 1

RECRUITING Phase 1

A Study of Avoralstat In Participants With Diabetic Macular Edema

NCT07228559

RECRUITING Phase 1

A Study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of BCX17725

NCT06539507

COMPLETED Phase 1

A Study to Evaluate the Single Dose Safety, Tolerability and Pharmacokinetics of IV BCX4430

NCT03800173

COMPLETED Phase 2

A Long Term Safety Study of BCX7353 in Hereditary Angioedema

NCT03472040

COMPLETED Phase 3

Efficacy and Safety Study of BCX7353 as an Oral Treatment for the Prevention of Attacks in HAE

NCT03485911

COMPLETED Phase 3

Safety, PK and Effectiveness of IV Peramivir in Elderly and Higher Risk Subjects With Uncomplicated Influenza

NCT02635724

COMPLETED Phase 3

Safety, PK and Effectiveness of IV Peramivir Versus Oseltamivir in Pediatric Subjects With Uncomplicated Influenza

NCT02369159

COMPLETED Phase 2

12-Week Safety and Efficacy Study of BCX4161 as an Oral Prophylaxis Against HAE Attacks

NCT02303626

COMPLETED Phase 2

A Randomized, Double-Blind, Dose-Response Study of the Safety and Uric Acid Effects of Oral Ulodesine Added to Allopurinol in Subjects With Gout and Concomitant Moderate Renal Insufficiency

NCT01407874

COMPLETED Phase 2

Study to Evaluate sUA Lowering Activity, Safety and Efficacy of Oral Ulodesine Added to Allopurinol

NCT01265264

COMPLETED Phase 2

Study to Evaluate sUA-Lowering Activity, Safety & PK Interaction of Oral BCX4208 & Allopurinol Admin. in Subjects w/Gout

NCT01129648

TERMINATED Phase 3

A Study to Evaluate the Efficacy and Safety of IV Peramivir in Addition to Standard of Care Compared to Standard of Care Alone in Adults and Adolescents Who Are Hospitalized Due to Influenza

NCT00958776

COMPLETED Phase 3

Safety Study of IV Peramivir in Hospitalized Subjects With Confirmed or Suspected Influenza

NCT00957996

COMPLETED Phase 2

Study to Evaluate the Urate-Lowering Activity and Safety of Oral BCX4208 Administered in Subjects With Gout

NCT00985127

COMPLETED Phase 2

A Phase II, Multicenter, Randomized, Placebo -Controlled, Study To Evaluate The Efficacy and Safety Of Intramuscular Peramivir 600 mg In Subjects With Uncomplicated Acute Influenza

NCT00705406

COMPLETED Phase 2

Phase II Study of Forodesine in Subjects With Chronic Lymphocytic Leukemia (CLL)

NCT00640523

TERMINATED Phase 3

Intramuscular Peramivir in Subjects With Uncomplicated Acute Influenza

NCT00610935

COMPLETED Phase 2

Evaluation of Efficacy and Safety of Peramivir in Adults With Acute Serious or Potentially Life-threatening Influenza

NCT00453999

COMPLETED Phase 2

Forodesine in the Treatment of Cutaneous T-Cell Lymphoma

NCT00501735

COMPLETED Phase 2

Evaluation of the Efficacy and Safety of Peramivir in Subjects With Uncomplicated Acute Influenza.

NCT00419263

TERMINATED Phase 2

Study of Forodesine Hydrochloride in Patients With Relapsed/Refractory Precursor T-Lymphoblastic Leukemia/Lymphoma Who Have Failed Two or More Prior Treatment Regimens

NCT00419081

COMPLETED Phase 2

Study of Forodesine Hydrochloride in Patients With Advanced, Fludarabine-refractory Chronic Lymphocytic Leukemia (CLL)

NCT00289549

COMPLETED Phase 1

Forodesine (BCX-1777) in Treating Patients With Refractory Stage IIA, Stage IIB, Stage III, Stage IVA, or Stage IVB Cutaneous T-Cell Lymphoma

NCT00098332

COMPLETED Phase 1

Forodesine Hydrochloride (BCX-1777) for B-Cell Acute Lymphoblastic Leukemia

NCT00289562

COMPLETED Phase 2

Repeat-Dose of Forodesine Hydrochloride (BCX-1777) Infusion in Patients With Advanced T-Cell Leukemia

NCT00095381

COMPLETED Phase 1

BCX-1777 in Treating Patients With Refractory Cancer

NCT00073944

COMPLETED Phase 1

BCX-1777 in Treating Patients With Refractory Cutaneous T-Cell Lymphoma

NCT00061880

COMPLETED Phase 1

Study of Intravenous BCX-1777 in Relapsed or Refractory Aggressive T-Cell Leukemias or Lymphomas

NCT00035022

COMPLETED Phase 1

A Study of Peldesine (BCX-34) in HIV-Infected Patients

NCT00002237

Phase Distribution

PhaseTrial count
Phase 1 9
Phase 2 14
Phase 3 6

What the Pipeline for BioCryst Pharmaceuticals Shows

According to the ClinicalTrials.gov registry, BioCryst Pharmaceuticals is linked to 29 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 7% of the sponsor's indexed portfolio, and 24 are already marked complete, representing roughly 83% of the total.

The phase mix for BioCryst Pharmaceuticals reports 6 late-stage studies (Phase 3 and Phase 4 combined) and 23 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for BioCryst Pharmaceuticals is Gout with 2 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.