
The FDA issued final guidances on performance status, washout periods, and laboratory values aimed at expanding oncology trial participation.
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The FDA granted accelerated approval to vusolimogene oderparepvec-wtpg (Tudriqev; RP1) plus nivolumab (Opdivo) for adults with unresectable advanced cutaneous melanoma that progressed on anti–PD-1 therapy, based on the phase 1/2 IGNYTE trial (NCT03767348). What type of agent is RP1?






