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Prothena Corporation plc: Prothena Announces FDA Clearance of IND for PRX012, a Subcutaneous Anti-Amyloid Beta Antibody Under Investigation for the Treatment of Alzheimer's Disease

Prothena has initiated Phase 1 SAD study of PRX012, under investigation for the treatment of Alzheimer's disease DUBLIN, Ireland, March 28, 2022 (GLOBE NEWSWIRE) Prothena Corporation plc (NASDAQ:PRTA) ....

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Roche to present data across broad and impactful neuroscience portfolio at 2022 AAN Annual Meeting

Maximally sustaining IL-6 suppression in a chronic disease like NMOSD and enabling subcutaneous dosing every four weeks. Positive Phase III results for ENSPRYNG, as both monotherapy and in. | March 25, 2022 ....

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argenx SE: argenx Announces Positive Topline Phase 3 Data From ADAPT-SC Study Evaluating Subcutaneous Efgartigimod for Generalized Myasthenia Gravis

Study met primary endpoint, demonstrating noninferior total IgG reduction at day 29 with subcutaneously administered efgartigimod compared to intravenous (IV) administration Secondary endpoints show ....

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Sanofi: Blackstone Life To Provide Investment To Advance Subcutaneous Dosage Form For Sarclisa

PARIS (dpa-AFX) - Sanofi (SNYNF, SNY) and Blackstone (BX) announced a risk-sharing collaboration under which funds managed by Blackstone Life Sciences will contribute up to 300 million euros to ....

France General , Blackstone Life Sciences ,

Junshi Biosciences Announces Acceptance by NMPA of Investigational New Drug Application for the Subcutaneous Injection of Anti-BLyS Monoclonal Antibody

SHANGHAI, China, Aug. 27, 2021 (GLOBE NEWSWIRE) Junshi Biosciences (HKEX: 1877; SSE: 688180), a leading innovation-driven biopharmaceutical company dedicated to the discovery, development, and commercialization ....

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