Citius Pharmaceuticals plans to refile its experimental drug for a rare blood cancer in early 2024 following an FDA rejection in July.
The drug, Lymphir, is a reformulated version of Eisai’s cutaneous T-cell lymphoma (CTCL) treatment Ontak, which was voluntarily pulled from the US market in 2014 over manufacturing issues. Citius CEO Leonard Mazur told Endpoints News on Friday that “there’s no relationship” between those issues and the FDA’s recent complete response letter.
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