Abstract

Atezo (anti–PD-L1) IV is approved in NSCLC, SCLC, triple-negative breast cancer, hepatocellular carcinoma, urothelial carcinoma and unresectable/metastatic melanoma. To reduce treatment burden and improve convenience and efficiencies in healthcare, a novel fixed-dose atezo SC co-formulated with recombinant human hyaluronidase is being developed. We report Part 2 (Phase III) of the open-label, randomized, multicentre IMscin001 study (NCT03735121) to investigate non-inferiority of drug exposure at Cycle 1 after atezo SC vs IV administration in NSCLC.

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