Overview

Phase I/II Assessment of Immuno-Oncology Drugs Elotuzumab, Anti-LAG-3 and Anti-TIGIT

Status:
Not yet recruiting
Trial end date:
2023-10-01
Target enrollment:
Participant gender:
Summary
This a Phase I/II randomized trial for patients with relapsed refractory Multiple Myeloma who have relapsed after treatment with prior therapies. The protocol is designed to evaluate two agents, Anti-LAG-3 and Anti-TIGIT, in order to understand their immunologic effects and safety both as single agents and in combination with pomalidomide and dexamethasone. In these arms, patients will be treated with either Anti-LAG-3 or Anti-TIGIT respectively for one cycle as single agent followed by the addition of pomalidomide and dexamethasone in combination for subsequent cycles. A third arm allows patients to be treated with the FDA approved combination of elotuzumab plus pomalidomide and dexamethsone as a control. This arm will thus allow a concurrent standard of care comparator for the experimental arms.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Multiple Myeloma Research Consortium
Collaborator:
Bristol-Myers Squibb
Treatments:
Antibodies
Antibodies, Monoclonal
Antineoplastic Agents, Immunological
BB 1101
Dexamethasone
Dexamethasone acetate
Elotuzumab
Immunoglobulins
Pomalidomide
Thalidomide