drugset / Trial / NCT02890368

Trial of Intratumoral Injections of TTI-621 in Subjects With Relapsed and Refractory Solid Tumors and Mycosis Fungoides

NCT02890368

Phase 1 Terminated 56 enrolled Pfizer
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, phase 1 study conducted to test intratumoral injections of TTI-621 in subjects that have relapsed and refractory percutaneously accessible solid tumors or mycosis fungoides. The study will be performed in two different parts. Part 1 is the Dose Escalation phase and Part 2 is the Dose Expansion phase. The purpose of this study is to characterize the safety profile of TTI-621 and to determine the optimal dose and delivery schedule of TTI-621. In addition, the safety and antitumor activity of TTI-621 will be evaluated in combination with other anti-cancer agents or radiation.

Timeline

Start
2016-09
Primary completion
2020-03-31
Completion
2020-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Ontorpacept Protein / enzyme biologic 1 mg Other
Subject Ontorpacept Protein / enzyme biologic 3 mg Other
Subject Ontorpacept Protein / enzyme biologic 10 mg Other
Background Atezolizumab Monoclonal antibody
Background Avelumab Monoclonal antibody
Background Durvalumab Monoclonal antibody
Background Nivolumab Monoclonal antibody
Background Pembrolizumab Monoclonal antibody 200 mg
Background pegylated interferon-α2a Unknown 90 ug Subcutaneous