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BLA resubmitted to FDA for denileukin diftitox in relapsed/refractory cutaneous T-cell lymphoma – Citius Pharmaceuticals

Written by | 22 Feb 2024

The biologics license application (BLA) for the interleukin (IL)-2–based immunotherapy denileukin diftitox (Lymphir) in patients with relapsed or refractory cutaneous T-cell lymphoma (CTCL) following at least 1 prior… read more.

BMS statement on Istodax for relapsed/refractory peripheral T-cell lymphoma FDA Indication

Written by | 12 Aug 2021

In 2011, Celgene Corporation, now a wholly owned subsidiary of Bristol Myers Squibb, received accelerated approval by the FDA for Istoda (romidepsin), a histone deacetylase (HDAC) inhibitor, as… read more.

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