drugset / Trial / NCT04485013

TTX-080 HLA-G Antagonist in Subjects With Advanced Cancers

NCT04485013 ↗

Phase 1 Recruiting 240 enrolled Tizona Therapeutics, Inc
RandomizedParallel-groupOpen-labelTreatment

Summary

TTX-080-001 is a Phase 1, open label, dose escalation and dose expansion clinical study to determine the safety, tolerability, and recommended Phase 2 dose of TTX-080 monotherapy (HLA-G inhibitor) and in combination with either pembrolizumab (PD-1 inhibitor), cetuximab (EGFR inhibitor) or FOLFIRI plus cetuximab (EGFR inhibitor) in patients with advanced refractory / resistant solid malignancies including metastatic colorectal cancer (mCRC) patients.

Timeline

Start
2020-07-14
Primary completion
2027-06-01
Completion
2027-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody — —
Subject Pembrolizumab Monoclonal antibody — —
Subject TTX-080 Monoclonal antibody — —

Indications