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The second NPC approval in a week highlights the FDAs commitment to supporting the development of innovative therapies for rare diseases, Janet Maynard, director of the FDAs Office of Rare Diseases, Pediatrics, Urologic and Reproductive Medicine, said in a statement
Medical Consultation Requirement: ReadyRx requires thorough medication and health history review before approving injectable glutathione protocols
Safety is good for most adults at typical doses, but some people should avoid it or use it only with clinician oversight
Patients in the treatment arm survived a median 13.3 months without disease progression, while those in the control group lived only 4.4 months without their disease advancing
Xuan W, Li X, Gao H, Zhang L, Hu J, Sun L, et al
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