CancerLinQ LLC, an initiative of the American Society of Clinical Oncology, announced a long-term partnership with FDA that will rely on cancer patient information and big data analytics to examine the real-world use of emerging and newly approved cancer therapies.
Last week, FDA granted accelerated approval to Replimune Group Inc. for it’s biologic, RP1 (vusolimogene oderparepvec), following the FDA Cellular, Tissue, and Gene Therapies Advisory Committee’s 10:3 vote in support of the biologic in combination with nivolumab for the treatment of advanced melanoma in patients who have progressed on prior anti-PD-1 therapy.
