A Phase I/II, Open-label, Multi-centre Study Evaluating the Safety,Tolerability,Pharmacokinetic (PK), Pharmacodynamics, and Preliminary Efficacy of HRS-6719 in Patients With Advanced/Metastatic Solid Tumors With MTAP Deficiency
Latest Information Update: 22 May 2025
At a glance
- Drugs HRS 6719 (Primary)
- Indications Solid tumours
- Focus Adverse reactions
- Sponsors Shandong Suncadia Medicine
Most Recent Events
- 14 May 2025 Status changed from not yet recruiting to recruiting.
- 17 Apr 2025 New trial record
- 03 Apr 2025 According to Jiangsu Hengrui Medicine media release, The Drug Clinical Trial Approval Notice for HRS-6719 Tablets was approved and issued by the State Food and Drug Administration (SFDA) in the near future.