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Last update: Dec 5, 2024
Designation was based on early efficacy data demonstrating an 83.3% (10/12) overall response rate and a 50% (6/12) complete response rate, with a well-managed safety profile in Relapsed/Refractory Hodgkin Lymphoma patients
Read more at globenewswire.comNASDAQ:AFMD (3/7/2025, 8:03:52 PM)
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