A Phase I, First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of AT03-65 in Adults with Advanced Solid Tumors
- Sponsor:
- Axcynsis Therapeutics Pte, Ltd
- Sponsor Study ID:
- AT0365-P1-01
- CTO #:
- 104199
- NCT Number:
- NCT06809114
- Phase:
- Early Phase I
- Protocol Type:
- Treatment
- Age Group:
- Adults
- Disease Sites:
- Lung; Ovary
- Study Objectives:
- To evaluate the safety and tolerability of AT03-65 in subjects with advanced/ metastatic solid tumors. To explore the MTD by observing dose limiting toxicity of AT03-65 and/or to provide support for the determination of the RP2D.
- eConsent:
- Not available
- Study Documents:
-
Open Study Documents
(MUSC NetID required for document access)
For more information about this trial please contact the study team:
-
Medical University of South Carolina
- Principal Investigator, Alexander, Mariam, at alexanma@musc.edu
- Study Coordinator, Gillam, Erin, at gillame@musc.edu
Trial opened at the following institutions:
Medical University of South Carolina