A Phase 1 Dose Escalation Study of AV-380 in Combination with Standard of Care Chemotherapy in Metastatic Cancer Patients with Cachexia and Elevated GDF-15 Levels
- Sponsor:
- AVEO Pharmaceuticals, Inc.
- Sponsor Study ID:
- AV-380-22-102
- CTO #:
- 103743
- NCT Number:
- NCT05865535
- Phase:
- I
- Protocol Type:
- Treatment
- Age Group:
- Adults
- Disease Sites:
- Colon; Pancreas
- Study Objectives:
- To refine the dose and schedule of AV-380 and establish its adverse event (AE), pharmacokinetic (PK), and pharmacodynamic (PD) profile in metastatic cancer patients with cachexia and elevated GDF-15, receiving SoC chemotherapy for metastatic cancer
- 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, Dincman, Toros, at dincmant@musc.edu .
- Study Coordinator, Summers, Andrew, at summeran@musc.edu .
Trial opened at the following institutions:
Medical University of South Carolina