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FDA approves erdafitinib for locally advanced or metastatic urothelial carcinoma (JNJ)

FDA approves erdafitinib for locally advanced or metastatic urothelial carcinoma (JNJ)
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Drug administrationJanssen biotechAssessment aidExpedited programsSerious conditions drugsWatch reporting system

FDA OKs Crizotinib for Myofibroblastic Tumors

The tyrosine kinase inhibitor has already been approved for certain patients with non-small cell lung cancer and anaplastic large cell lymphoma.

Drug administrationMedscapemedical newsWatch reporting systemLung cancerUng carcinomaAncer lungNon small cell lung cancerDrug developmentBiologic therapyUs food and drug administrationNited states food and drug administrationTyrosine kinase inhibitorAnaplastic lymphoma kinase alkLk tyrosine kinase receptorD246 cluster of differentiation 246

FDA Approves Innovative Treatment for Pediatric Patients with Congenital Athymia

FDA Approves Innovative Treatment for Pediatric Patients with Congenital Athymia
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Peter marksUs department of healthHuman servicesDrug administrationRethymic to enzyvant therapeutics incBiologics evaluationRare pediatric disease priority review vouchersEnzyvant therapeuticsWatch reporting system

FDA Approves Innovative Treatment for Pediatric Patients with Congenital Athymia

/PRNewswire/ Today, the U.S. Food and Drug Administration approved Rethymic for the treatment of pediatric patients with congenital athymia, a rare immune.

Peter marksVeronika pfaeffleDrug administrationRethymic to enzyvant therapeutics incBiologics evaluationRare pediatric disease priority reviewEnzyvant therapeuticsWatch reporting systemUs food and drug administration

FDA Approves Innovative Treatment for Pediatric Patients with Congenital Athymia

/PRNewswire/ Today, the U.S. Food and Drug Administration approved Rethymic for the treatment of pediatric patients with congenital athymia, a rare immune.

Peter marksVeronika pfaeffleDrug administrationRethymic to enzyvant therapeutics incBiologics evaluationRare pediatric disease priority reviewEnzyvant therapeuticsWatch reporting systemUs food and drug administration

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