Ozmosi | Bempikibart Drug Profile
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Bempikibart

Pronounced as: bem-pih-kee-bart

Alternative Names: Bempikibart, adx-914, adx914, adx 914, BMS-986265, BMS986265, BMS 986265
Clinical Status: Active
Latest Update: 2026-04-08
Latest Update Note: News Article

Product Description

ADX-914 is a fully human anti-IL-7Ra antibody that re-regulates adaptive immune function by blocking signaling mediated by both IL-7 and TSLP. (Sourced from: https://ir.horizontherapeutics.com/news-releases/news-release-details/q32-bio-and-horizon-therapeutics-plc-announce-dosing-first)

Mechanisms of Action: IL7 Inhibitor

Novel Mechanism: Yes

Modality: Antibody

Route of Administration: Subcutaneous

FDA Designation: Fast Track - Alopecia Areata *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Q32 Bio
Company Location: Eastern America
Company Founding Year: 2017
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Bempikibart

Countries in Clinic: Canada, Poland, United States

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

  • Clinical Outcomes Reported - Q32 Bio presented P2 Alopecia Areata results on 2026-07-13 for Bempikibart
  • Clinical Outcomes Expected - Q32 Bio announced they will present P2 Alopecia Areata results in 3Q26 for Bempikibart

Highest Development Phases

Phase 2: Alopecia Areata|Dermatitis|Dermatitis, Atopic

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06018428

SIGNAL-AA

P2

Active, not recruiting

Dermatitis|Alopecia Areata

2026-06-01

12%

2025-11-01

Primary Endpoints

NCT05509023

SIGNAL-AD

P2

Active, not recruiting

Dermatitis, Atopic

2024-12-01

2024-10-04

Primary Endpoints

2023-510238-10-00

ADX-914-202

P2

Completed

Dermatitis, Atopic

2024-12-10

2025-05-02

Treatments