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Cytovation raises $8 million in Series A extension financing round for clinical advancement of CyPep-1, a first-in-class targeted tumor membrane immunotherapy

Cytovation ASA, a clinical stage immune-oncology company focused on the development of its first-in-class targeted tumor membrane immunotherapy CyPep-1, announces the successful closing of its $8 million Series A extension financing round.

Cytovation raises $8 million in Series A extension financing round for clinical advancement of CyPep-1, a first-in-class targeted tumor membrane immunotherapy Read More »

NMPA accepted Akeso’s ebronucimab (PCSK9) marketing application in two cardiovascular indications

Akeso Inc. announced that China’s National Medical Products Administration has accepted its New Drug Application for its fully human anti-PCSK9 monoclonal antibody ebronucimab for 2 indications 1) primary hypercholesterolemia and mixed hyperlipidemia, and 2) heterozygous familial hypercholesterolemia.

NMPA accepted Akeso’s ebronucimab (PCSK9) marketing application in two cardiovascular indications Read More »

CANbridge Announces Marketing Approval of CAN108 (迈芮倍®/LIVMARLI®) in China for the Treatment of Cholestatic Pruritus in Patients with Alagille Syndrome

CANbridge Pharmaceuticals, Inc. announced that the Chinese National Medical Products Administration has approved CAN108 to be marketed for the treatment of cholestatic pruritus in patients with Alagille syndrome 1 year of age and older.

CANbridge Announces Marketing Approval of CAN108 (迈芮倍®/LIVMARLI®) in China for the Treatment of Cholestatic Pruritus in Patients with Alagille Syndrome Read More »

Medivir has completed the dose escalation part (phase 1b) of the 1b/2a study in HCC and focuses on the combination of fostrox and Lenvima

Medivir AB announces that a safe dose has been established for treatment with the drug candidate fostroxacitabine bralpamide in combination with Keytruda® in the initial dose escalation part of the company’s 1b/2a study in hepatocellular carcinoma.

Medivir has completed the dose escalation part (phase 1b) of the 1b/2a study in HCC and focuses on the combination of fostrox and Lenvima Read More »

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