Cullinan Oncology announces U.S. FDA clearance of IND for CLN-619

Cullinan Oncology announced the U.S. Food and Drug Administration, FDA, has cleared its Investigational New Drug, IND, application for CLN-619 in relapsed/refractory multiple myeloma. The company will commence a Phase 1 dose-escalation and dose-expansion trial of CLN-619. “Multiple myeloma remains incurable, and most patients experience sequential relapses. The response to treatment is typically shorter with each relapse, so novel treatments are still needed,” said Jeffrey Jones, MD, MPH, MBA, Chief Medical Officer, Cullinan Oncology. “Multiple myeloma is another example of a malignancy where MICA/B shedding from tumor cells allows for immune evasion. As we shared at SITC 2023, CLN-619 restores MICA/B expression on tumor cells, enabling immune recognition. This Phase 1 trial will assess CLN-619 in patients with multiple myeloma, and, given the safety profile shown to date for CLN-619, we believe there is an opportunity to combine the monoclonal antibody with multiple standard therapies. With clinical studies in both solid tumors and hematologic malignancies, we look forward to assessing the full potential of CLN-619 to address multiple areas of unmet clinical need.”