A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics and Preliminary Efficacy of HLX53 (an Anti-TIGIT Fc Fusion Protein) in Patients With Advanced/Metastatic Solid Tumors
Latest Information Update: 04 Apr 2024
At a glance
- Drugs HLX 53 (Primary)
- Indications Lymphoma; Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Shanghai Henlius Biotech
Most Recent Events
- 28 Mar 2024 Planned End Date changed from 4 Feb 2025 to 4 Mar 2025.
- 28 Mar 2024 Planned primary completion date changed from 4 Aug 2024 to 4 Dec 2024.
- 28 Mar 2024 Status changed from recruiting to active, no longer recruiting.