OmniAb Investor Conference Presentation Deck slide image

OmniAb Investor Conference Presentation Deck

Sugemalimab THE SECOND APPROVED OMNIRAT-DERIVED ANTIBODY ● ● ● ● 1351 基石药业 CSTONE PHARMACEUTICALS Fully human, full-length anti-PD-L1 immunoglobulin G4 (IgG4) mAb, which may reduce risk of immunogenicity and toxicity, a unique advantage over similar drugs - Pfizer EQR Sugemalimab (Cejemly®) was approved in China in June of 2022 for unresectable stage III non-small cell lung cancer (NSCLC) following concurrent or sequential chemoradiotherapy Previously approved in China in December 2021, and launched in January 2022, for first-line treatment of metastatic non-squamous NSCLC in combination with chemotherapy Becomes first anti-PD-1/PD-L1 mAb approved for stage III NSCLC, and is also the only one approved for both stage III and stage IV NSCLC Pfizer responsible for commercializing in China via 2020 strategic collaboration with CStone EQRx licensed exclusive rights to sugemalimab for development / commercialization outside of China, targeting first regulatory filings ex-US in 2H 2022 42 OmniAb
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