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Sept 8: At the end of July, Citius Pharmaceuticals received a Complete Response Letter from the FDA pertaining to its Biologics License Application for Lymphir, an engineered IL-2-diphtheria toxin fusion protein intended to treat relapsed or refractory cutaneous T-cell lymphoma

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Brand-name semaglutide reflects patent protection, large-scale advertising, FDA approval infrastructure, and manufacturer profit margins

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