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One month after FDA temporarily suspended its approvals of all blood immunotherapy cancer treatments for children, the agency is proposing further action against the industry in pediatric oncology drugs. Written to the Pediatric and Neonatal (P&N) Clinical Pharmacology Advisory Committee (CPAC), the FDA has provided further guidance from its office of medical and scientific affairs (OMSSA) regarding product label exclusions and modifications for blood and immune-based treatments. The agency is requesting comment from industry and the 50e0806aeb yordjann
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