drugset / Trial / NCT04044859

ADP-A2M4CD8 as Monotherapy or in Combination With Either Nivolumab or Pembrolizumab in HLA-A2+ Subjects With MAGE-A4 Positive Tumors (SURPASS)

NCT04044859 ↗

Phase 1 Active not recruiting 120 enrolled USWM CT, LLC
NaSingle-groupOpen-labelTreatment

Summary

This study will investigate the safety and tolerability of ADP-A2M4CD8 T-cell therapy in subjects who have the appropriate human leukocyte antigen (HLA) and MAGE-A4 tumor antigen. Tumor indications include endometrial, esophageal, esophagogastric junction (EGJ), gastric, head and neck, melanoma, non-small cell lung (NSCLC), ovarian or urothelial cancer.

Timeline

Start
2019-08-20
Primary completion
2026-12-23
Completion
2037-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 480 mg Intravenous
Subject Pembrolizumab Monoclonal antibody 400 mg Intravenous
Subject UZATRESGENE AUTOLEUCEL Cell therapy — Other