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Cullinan Therapeutics Receives Approval from European Medicines Agency to Initiate Phase 1 Trial of CLN-978, a Bispecific CD19 T Cell Engager Administered Subcutaneously, in Patients with Rheumatoid Arthritis

Company-sponsored clinical trial will be initiated at FAU Erlangen-Nuremberg in Germany and Università Cattolica del Sacro Cuore, Rome in Q2 2025 CLN-978 is also being studied in the U.S., Europe, and Australia for systemic lupus erythematosus CAMBRIDGE, Mass., April 16, 2025 (GLOBE NEWSWIRE) -- Cullinan Therapeutics, Inc. (Nasdaq: CGEM), a biopharmaceutical company focused on developing modality-agnostic targeted therapies, today announced that the European Medicines Agency (EMA) approved the C

articleCullinan Therapeutics, Inc.April 16, 20258/company/cullinan-oncology-llc/news/cullinan-therapeutics-receives-approval-european-110000424
Cullinan Therapeutics Receives Approval from European Medicines Agency to Initiate Phase 1 Trial of CLN-978, a Bispecific CD19 T Cell Engager Administered Subcutaneously, in Patients with Rheumatoid Arthritis

About this update from Cullinan Therapeutics, Inc.

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More updates from Cullinan Therapeutics, Inc.

rheumatoid arthritisautoimmune diseasesbiopharmaceutical companyPhase 1 clinical trialClinical TrialEuropean Medicines AgencyCullinanpatientssystemic lupus erythematosus