Ozmosi | HMPL-A830 Drug Profile
Drug Profile
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HMPL-A830

Alternative Names: HMPL-A830, HMPLA830, HMPL A830
Clinical Status: Active
Latest Update: 2026-07-22
Latest Update Note: Clinical Trial Update

Product Description

Progressed ATTC drug candidate with plans for global IND filings and clinical trial initiations in 2026. (Sourced from: https://www.benzinga.com/pressreleases/26/03/g51060341/hutchmed-reports-2025-full-year-results-and-business-updates)

Mechanisms of Action: Unknown

Novel Mechanism: No

Modality: Antibody Drug Conjugate

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: GSK
Company Location: Europe
Company Founding Year: 2000
Additional Commercial Interests: Hutchmed

Clinical Description

Map of Global Clinical Trials for HMPL-A830

Countries in Clinic: China

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Oncology Solid Tumor Unspecified

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT07718581

2026-830-GLOB1

P2

Not yet recruiting

Oncology Solid Tumor Unspecified

2028-06-26

61%

2026-07-23

Primary Endpoints|Treatments

Recent News Events

Date

Type

Title