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FDA Confirms Decision to Withdraw Melphalan Flufenamide Approval in Multiple Myeloma

The FDA has determined that sufficient criteria have been met to withdraw the approval for melphalan flufenamide in patients with multiple myeloma. ....

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European Commission approves Oncopeptides' Pepaxti for the treatment of patients with relapsed refractory multiple myeloma

/PRNewswire/ Oncopeptides AB (publ) (Nasdaq Stockholm: ONCO), a biotech company focused on research and development of therapies for difficult-to-treat. ....

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Oncopeptides AB: European Commission approves Oncopeptides' Pepaxti for the treatment of patients with relapsed refractory multiple myeloma

STOCKHOLM, Aug. 18, 2022 /PRNewswire/ Oncopeptides AB (publ) (Nasdaq Stockholm: ONCO), a biotech company focused on research and development of therapies for difficult-to-treat hematological ....

United Kingdom , Oncopeptides Pepaxti , Rolf Gulliksen , Jakob Lindberg , Oncopeptide Pepaxti , European Commission , Global Head Of Corporate Communications , Nasdaq Stockholm , European Economic Area , Global Head , Corporate Communications , Mid Cap ,

European Commission approves Oncopeptides' Pepaxti for the treatment of patients with relapsed refractory multiple myeloma | Small Molecules

European Commission approves Oncopeptides Pepaxti for the treatment of patients with relapsed refractory multiple myeloma ....

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CHMP Recommends EU Approval of Oncopeptides' Pepaxti for Patients with Refractory Multiple Myeloma

CHMP Recommends EU Approval of Oncopeptides' Pepaxti for Patients with Refractory Multiple Myeloma
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