A Phase I, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of DN1508052-01 as a Single Agent When Administered Subcutaneously to Adult Patients With Advanced Solid Tumors
Latest Information Update: 22 Nov 2022
At a glance
- Drugs DN 1508052 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Shanghai De Novo Pharmatech
- 17 Nov 2022 Status changed from recruiting to completed.
- 13 Nov 2019 Status changed from not yet recruiting to recruiting.
- 18 Sep 2019 According to a De Novo Pharmaceuticals media release, the company has completed dosing in the first patient of this study.