Study identifier:NT-112-301
ClinicalTrials.gov identifier:NCT06218914
EudraCT identifier:N/A
CTIS identifier:N/A
An Open-label, Phase 1, Multicenter Study to Evaluate the Safety and Preliminary Anti-tumor activity of NT‑112 in Human Leukocyte Antigen-C*08:02‑Positive Adult Subjects with Unresectable, Advanced, and/or Metastatic Solid Tumors That Are Positive for the KRAS G12D Mutation
Non-small Cell Lung Cancer
Phase 1
No
-
All
24
Interventional
n/a - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: Sequential Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Dec 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: NT-112 Dose Escalation of NT-112. | - |