Industry Nervous That User Fee Reauthorization Legislation Will Get Bogged Down With Extraneous Asks

The industry is speaking out about worries that must-pass legislation that reauthorizes FDA’s user fee programs might get bogged down with lawmakers’ projects and other effluvium that could alter the…

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FDA Yanks Accelerated Approval for Bristol-Myers Squibb’s/Celgene’s 10-year-old Istodax for Lymphoma

Almost 11 years after it granted Accelerated Approval, the FDA is withdrawing approval for Celgene’s (now Bristol Myers Squibb’s) peripheral T-cell lymphoma (PTCL) indication for Istodax (romidepsin) after the cancer…

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AstraZeneca’s Ultomiris Delivers in Phase 3 for Rare Autoimmune Disorder

AstraZeneca’s complement-5 inhibitor Ultomiris (ravulizumab-cwvz) has shown benefit in people living with a rare degenerative neuromuscular disorder called anti-aquaporin-4 (AQP4) antibody-positive (Ab+) neuromyelitis optica spectrum disorder (NMOSD). Source: Drug Industry…

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