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CTLA-4 Inhibitors Pipeline Analysis 2024: EMA, PDMA, FDA Approvals, Clinical Trials, Therapies, Mechanism Of Action, Route Of Administration, And Comp...

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United-states , Innovent-biologics , Bristol-myers-squibb , Akeso-biopharma , Drugs-under-different-phases-of-clinical-development , Pharmaceuticals-inc , Drug-administration , University-collaborations-licensing-partnering-analysis , Alpine-immune-sciences , Akeso-biopharma-co-ltd , Route-of-administration , Astrazeneca

Alligator Bioscience To Present Positive Phase 2 Mitazalimab Data in Pancreatic Cancer at 2024 ASCO

OPTIMIZE-1 study results showed confirmed ORR of 40.4%, unconfirmed ORR of 50.9% and DCR of 79% in 57 evaluable patients with chemotherapy-naïve mPDACThe encouraging duration of response (median 12.5 months) and overall survival (median 14.3 months) support continued development of mitazalimab in a randomized confir. ....

Chicago , Illinois , United-states , Sweden , Hall-on , Orebro , American , Peter-ellmark , Jean-luc-van-laethem , Frank-hoerning-andersen , Sumeet-ambarkhane , Aptevo-therapeutics-inc

European Medicines Agency (EMA) Validates Henlius and Organon Filings for Prolia® and Xgeva® (denosumab) Biosimilar Candidate HLX14

European Medicines Agency (EMA) Validates Henlius and Organon Filings for Prolia® and Xgeva® (denosumab) Biosimilar Candidate HLX14
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Shanghai , China , United-states , Jersey-city , New-jersey , Canada , Instagram , European-medicines-agency , Shanghai-henlius-biotech-inc , Twitter , Exchange-commission

Organon & Co.: European Medicines Agency (EMA) Validates Henlius and Organon Filings for Prolia and Xgeva (denosumab) Biosimilar Candidate HLX14

Organon & Co.: European Medicines Agency (EMA) Validates Henlius and Organon Filings for Prolia and Xgeva (denosumab) Biosimilar Candidate HLX14
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China , Shanghai , Canada , New-jersey , United-states , Jersey-city , Jennifer-halchak , Renee-mcknight , Felicia-bisaro , Janice-han , Bella-zhou , European-medicines-agency

Shanghai Henlius Biotech, Inc. and Organon Announces That the European Medicines Agency Has Validated the Marketing Authorization Applications for Hlx14

Shanghai Henlius Biotech, Inc. and Organon Announces That the European Medicines Agency Has Validated the Marketing Authorization Applications for Hlx14
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