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Innate Pharma Secures FDA Granted BTD for Lacutamab
The BTD is granted based on Phase 1 study results as well as results from the Phase 2 TELLOMAK study, where lacutamab demonstrated encouraging efficacy and a favorable safety profile in heavily pretreated, post-mogamulizumab patients with advanced Sézary syndrome.
Innate Pharma | 18/02/2025 | By Aishwarya
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