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Development of a conditional in vivo model to evaluate the efficacy of small molecule inhibitors for the treatment of Raf-transformed hematopoietic cells

The Food and Drug Administration is weighing whether to allow compounding pharmacies to produce seven peptides that were previously banned over safety concerns

The limited human data available indicate that both peptides appear to be generally well-tolerated, yet comprehensive safety and efficacy assessments from large, well-designed clinical trials are absent

Chandalia HB et al