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Active, not recruiting Phase 2 Interventional

Taldefgrobep Alfa in Adults With Overweight and Obesity

ClinicalTrials.gov ID: NCT07281495

Public ClinicalTrials.gov record NCT07281495. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 11:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Multiple Dose Study With Open-Label Extension to Assess the Efficacy, Safety, and Pharmacokinetics of Subcutaneously Administered Taldefgrobep Alfa in Adults Living With Overweight and Obesity

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter, randomized, double-blind, placebo-controlled, multiple dose study to evaluate the efficacy, safety, and tolerability of taldefgrobep alfa in adults with overweight and obesity, with an open-label extension.

Study identification

NCT ID
NCT07281495
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Biohaven Therapeutics Ltd.
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 24, 2025 (Actual)
Primary completion
Sep 2026 (Estimated)
Completion
Sep 2026 (Estimated)
Last update posted
Mar 20, 2026

2025 – 2026

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
Site-001 Chula Vista California 91911 —
Site-014 Montclair California 97163 —
Site-011 Sacramento California 95821 —
Site-018 Tustin California 92780 —
Site-020 Orlando Florida 32804 —
Site-008 Palm Springs Florida 33461 —
Site-015 St. Petersburg Florida 33704 —
Site-007 Chicago Illinois 60625 —
Site-016 Indianapolis Indiana 46254 —
Site-010 Baton Rouge Louisiana 70808 —
Site-009 Metairie Louisiana 70006 —
Site-006 City of Saint Peters Missouri 63303 —
Site-003 Springfield Missouri 65807 —
Site-019 Monroe North Carolina 28112 —
Site-002 Fargo North Dakota 58104 —
Site-017 North Charleston South Carolina 29405 —
Site-005 Austin Texas 78745 —
Site-012 McKinney Texas 75069 —
Site-013 San Antonio Texas 78229 —
Site-004 Arlington Virginia 22205 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07281495, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 20, 2026 · Synced Oct 29, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07281495 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →