HMPL-A83
/ Hutchmed
- LARVOL DELTA
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October 04, 2025
A first-in-human (FIH), dose escalation study of HMPL-A83 (A83), an anti-CD47 monoclonal antibody (mAb) in patients (pts) with advanced solid tumors
(ESMO Asia 2025)
- P1 | "A83 was well-tolerated up to 30 mpk Q2W and 45 mpk Q3W with no hemolytic anemia observed. A83 did not require a lower 'priming' dose to prevent anemia. Combination with immunotherapy may warrant further evaluation."
Clinical • First-in-human • Metastases • P1 data • Oncology • Pancreatic Cancer • Solid Tumor • SIRPA
November 26, 2025
Results from a first-in-human study of the anti-CD47 monoclonal antibody HMPL-A83 in advanced solid tumors…will be presented at the ESMO Asia Congress 2025
(GlobeNewswire)
First-in-human • P1 data • Solid Tumor
June 18, 2025
A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant Neoplasm
(clinicaltrials.gov)
- P1 | N=40 | Completed | Sponsor: Hutchmed | Recruiting ➔ Completed | N=99 ➔ 40 | Trial completion date: Sep 2025 ➔ Apr 2025
Enrollment change • Trial completion • Trial completion date • Acute Myelogenous Leukemia • Lymphoma • Myelodysplastic Syndrome • Oncology
March 06, 2024
A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant Neoplasm
(clinicaltrials.gov)
- P1 | N=99 | Recruiting | Sponsor: Hutchmed | Trial primary completion date: Feb 2024 ➔ Jun 2025
Metastases • Trial primary completion date • Acute Myelogenous Leukemia • Lymphoma • Myelodysplastic Syndrome • Oncology
December 21, 2022
A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant Neoplasm
(clinicaltrials.gov)
- P1 | N=99 | Recruiting | Sponsor: Hutchmed | Not yet recruiting ➔ Recruiting
Enrollment open • Oncology • Solid Tumor
July 15, 2022
HUTCHMED Initiates Phase I Trial of Anti-CD47 Monoclonal Antibody HMPL-A83 in Patients with Advanced Malignant Neoplasms in China
(GlobeNewswire)
- "HUTCHMED...announces that it has initiated a Phase I trial in China of HMPL-A83, an investigational novel IgG4-type humanized anti-CD47 monoclonal antibody. The first patient received their first dose on July 15, 2022. The Phase I trial is a multicenter, open-label study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of HMPL-A83 in patients with advanced malignant neoplasms."
Trial status • Oncology
June 23, 2022
A Phase I Clinical Study of HMPL-A83 in Patients With Advanced Malignant Neoplasm
(clinicaltrials.gov)
- P1 | N=99 | Not yet recruiting | Sponsor: Hutchison Medipharma Limited
New P1 trial • Oncology • Solid Tumor
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