Drugs / HLX60
last change Aug 2025 re-read 9 days ago

HLX60

Monoclonal antibody

Developed for
lymphoma
Investigated by
Shanghai Henlius Biotech

Trials 2

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT05483530 Dec 2022 → Dec 2024 — Shanghai Henlius Biotech Unknown No outcome recorded
Phase 1 NCT05606380 Dec 2022 → Aug 2024 lymphoma Shanghai Henlius Biotech Unknown No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2022-10-17 Shanghai Henlius Biotech Regulatory The IND Application of Henlius’ Novel Anti-GARP mAb HLX60 Approved by NMPA henlius.com ↗
Shanghai, China, Oct 17th, 2022 - Shanghai Henlius Biotech, Inc. (2696.HK) announced that the investigational new drug (IND) application for clinical trial of HLX60 (recombinant anti-GARP humanised monoclonal antibody injection), independently developed by the company, was approved by the National Medical Products Administration (NMPA) for the treatment of solid tumours and lymphomas.
2022-08-26 Shanghai Henlius Biotech Regulatory Henlius Novel Anti-GARP and Anti-PD-1 Dual mAb Therapy Received Clinical Trial Approval in Australia henlius.com ↗
Clinical Trial Notification (CTN) has been acknowledged by the Therapeutic Goods Administration (TGA), Australia.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as HLX60 ClinicalTrials.gov intervention name — accepted as the source's own label NCT05483530 ↗
1

NCT05606380 ↗

Modality Monoclonal antibody “HLX60 (Anti-GARP Monoclonal Antibody)” NCT05483530 ↗
Route Intravenous “intravenous infusion” NCT05606380 ↗