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OSE Immunotherapeutics Announces H1 2021 Results and Provides a Corporate Update

OSE Immunotherapeutics Announces H1 2021 Results and Provides a Corporate Update
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European Commission approves second indication of Sarclisa® (isatuximab) for relapsed multiple myeloma

European Commission approves second indication of Sarclisa® (isatuximab) for relapsed multiple myeloma
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European Commission approves second indication of Sarclisa® (isatuximab) for relapsed multiple

Press release content from Globe Newswire. The AP news staff was not involved in its creation. European Commission approves second indication of Sarclisa® (isatuximab) for relapsed multiple . SanofiApril 19, 2021 GMT European Commission approves second indication of Sarclisa® (isatuximab) for relapsed multiple myeloma Approval based on Phase 3 IKEMA study demonstrating Sarclisa added to standard of care carfilzomib and dexamethasone reduced risk of disease progression or death by 47% in patients who had relapsed after one to three prior therapies Sarclisa combination therapy was associated with undetectable levels of multiple myeloma (MM) in nearly 30% of patients with relapsed MM Second EU approval in less than 12 months for Sarclisa in combination with a standard of care regimen for the treatment of relapsed or refractory MM

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