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Biohaven Therapeutics clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA, UK, India and EU (CTIS) registers with Biohaven Therapeutics as lead sponsor. Synced 26 Sep 2026
13Current trials
7Recruiting now
4Drugs in these trials
4Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Biohaven Therapeutics is the lead sponsor of 13 current clinical trials in our USA, UK, India and EU (CTIS) registers. 7 are recruiting patients now. The most common phase is Phase 1. The drugs named most often in its trials are BHV-7000, BHV-1300 and Cemiplimab. The most-studied condition is Focal Epilepsy.

ClinicalTrials.gov trials by status

  • Recruiting758%
  • Active, closed325%
  • By invitation217%

Trials by phase

  • Phase 1433%
  • Phase 2/3325%
  • Phase 2217%
  • Phase 318%
  • Phase 1/218%
  • Observational18%
01

Clinical trials sponsored by Biohaven Therapeutics

12 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Study to Determine if BHV-1300 is Effective and Safe in Adults With Graves' Disease
NCT07661056 · ClinicalTrials.gov ↗ · Graves Disease
Drug: BHV-1300
Phase 3 Recruiting 2026-06 USA
Study of BHV-1400 in IgA Nephropathy
NCT07054684 · ClinicalTrials.gov ↗ · IgA Nephropathy
Phase 1 Recruiting 2025-07 UK, USA
A Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy
NCT06132893 · ClinicalTrials.gov ↗ · Focal Epilepsy
Drug: BHV-7000
Phase 2/3 Recruiting 2024-03 USA
A Phase 1/2 Study of BHV-1510 (Previously PBI-410) in Advanced Solid Tumors
NCT06384807 · ClinicalTrials.gov ↗ · Solid Tumor
Phase 1/2 Recruiting 2024-04 USA
Study of BHV-1300 in Graves' Disease
NCT06980649 · ClinicalTrials.gov ↗ · Graves Disease
Drug: BHV-1300
Phase 1 Recruiting 2025-08 USA
A Study to Determine if BHV-8000 is Effective, Safe and Tolerable as a Treatment for Adults Living With Early Parkinson's Disease
NCT06976268 · ClinicalTrials.gov ↗ · Parkinson Disease
Phase 2/3 Recruiting 2025-05 USA
A Phase 1 Study of BHV-1530 in Advanced Solid Tumors
NCT06874335 · ClinicalTrials.gov ↗ · Solid Tumor
Phase 1 Recruiting 2025-03 USA
Long-term Safety and Tolerability of BHV-7000
NCT06443463 · ClinicalTrials.gov ↗ · Focal Epilepsy
Drug: BHV-7000
Phase 2 By invitation 2024-07 UK, USA, India
A Phase 1b Study of BHV-7000 in Participants With Inherited Erythromelalgia
NCT07262268 · ClinicalTrials.gov ↗ · Familial Erythromelalgia
Drug: BHV-7000
Phase 1 By invitation 2026-01 USA
Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy
NCT06309966 · ClinicalTrials.gov ↗ · Focal Epilepsy
Drug: BHV-7000
Phase 2/3 Active, closed 2024-05 UK, USA, India
Taldefgrobep Alfa in Adults With Overweight and Obesity
NCT07281495 · ClinicalTrials.gov ↗ · Obesity, Overweight
Phase 2 Active, closed 2025-11 USA
Real-World Data Study of Troriluzole-Treated Patients With Spinocerebellar Ataxia (SCA) Compared to a Matched Natural History Control
NCT06529146 · ClinicalTrials.gov ↗ · Spinocerebellar Ataxias
Observational Active, closed 2019-03 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Biohaven Therapeutics in the EU trials register (CTIS)

1 trial

Authorised or ongoing trials in the EU Clinical Trials Information System with Biohaven Therapeutics as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Phase 2/3, Double-Blind, Placebo-Controlled Study of BHV-8000 in Participants with Early Parkinson’s Disease
2025-521113-13-00 · CTIS ↗ · Nervous System Diseases
Phase 3 Authorised Germany, France, Italy + 7 more
03

Drugs in Biohaven Therapeutics trials

4 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Biohaven Therapeutics trials

9 conditions
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA127
Clinical trials in UK31
Clinical trials in India20
EU register (CTIS)1—

A trial with sites in more than one country appears in each of those registers.

06

Other sponsors in Focal Epilepsy

SponsorTrials
Rapport Therapeutics3
Xenon Pharmaceuticals2

Sponsors with the most current trials registered for this condition.

07

Questions about Biohaven Therapeutics trials

How many clinical trials does Biohaven Therapeutics sponsor?

Biohaven Therapeutics is the lead sponsor of 12 current trials on ClinicalTrials.gov in our USA, UK and India registers, and 1 authorised or ongoing trial in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Biohaven Therapeutics trials recruiting?

Yes. 7 of its 12 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Biohaven Therapeutics testing?

Its current trials name 4 drugs and biologicals as interventions. The most frequent are BHV-7000 (4), BHV-1300 (2), Cemiplimab (2) and Taldefgrobep alfa (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.