drugset / Trial / NCT05878691

A Study of GRC 54276 in Participants With Advanced Solid Tumors and Lymphomas.

NCT05878691 ↗

Phase 1 Active not recruiting 320 enrolled Glenmark Specialty S.A.
Non-randomizedSequentialOpen-labelTreatment

Summary

This is first in human (FIH) study to a) evaluate the safety and tolerability profile of GRC54276, b) determine the maximum tolerated dose (MTD) and recommended Phase 2 doses (RP2D), and c) pharmacokinetic profile of GRC54276 alone and in combination with pembrolizumab or atezolizumab in participants with advanced solid tumors and lymphomas.

Timeline

Start
2022-06-28
Primary completion
2027-07-30
Completion
2027-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Atezolizumab Monoclonal antibody — Intravenous
Subject GRC 54276 Unknown — Oral
Subject Pembrolizumab Monoclonal antibody — Intravenous

Indications