MicroVention Celebrates One-Year Anniversary of FRED™ X Flow Diverter with Over 1,000 Patients Treated Across the U.S.

MicroVention, Inc., a global neurovascular company and wholly owned subsidiary of Terumo Corporation, is celebrating the one-year anniversary of the company’s FRED™ X Flow Diverter. In close collaboration with physician partners across the United States, over 1,000 patients have been…

Read MoreMicroVention Celebrates One-Year Anniversary of FRED™ X Flow Diverter with Over 1,000 Patients Treated Across the U.S.

Global Medical Tubing Market Analysis Report 2023-2030: Manufacturers Seeking Collaborations to Help Spur Innovative Solutions – ResearchAndMarkets.com

The global medical tubing market size is anticipated to reach USD 19,498.5 million by 2030. The market is expected to expand at a CAGR of 6.0% from 2023 to 2030 The prevalence of respiratory diseases such as asthma, lung cancer,…

Read MoreGlobal Medical Tubing Market Analysis Report 2023-2030: Manufacturers Seeking Collaborations to Help Spur Innovative Solutions – ResearchAndMarkets.com

KLAS Report Highlights MedSitter as a Leader in Virtual Patient Observation Solutions

MedSitter, a leading virtual patient observation solution received top marks from a KLAS Emerging Solutions Spotlight report released today, which revealed positive customer experiences with MedSitter’s innovative solution. The virtual patient observation market is experiencing significant growth as healthcare organizations look…

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Replimune and Incyte Enter into Clinical Trial Collaboration and Supply Agreement to Evaluate RP1 and INCB99280 in Patients with Cutaneous Squamous Cell Carcinoma

Replimune Group, Inc. (NASDAQ:REPL), a clinical stage biotechnology company pioneering the development of a novel portfolio of tumor-directed oncolytic immunotherapies, and Incyte (NASDAQ:INCY), a global biopharmaceutical company, today announced a clinical trial collaboration and supply agreement to study RP1, Replimune’s…

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Jemperli (dostarlimab-gxly) plus chemotherapy approved in the US as the first new frontline treatment option in decades for dMMR/MSI-H primary advanced or recurrent endometrial cancer

GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has approved Jemperli (dostarlimab-gxly) in combination with carboplatin and paclitaxel, followed by Jemperli as a single agent for the treatment of adult patients with primary advanced or recurrent endometrial cancer…

Read MoreJemperli (dostarlimab-gxly) plus chemotherapy approved in the US as the first new frontline treatment option in decades for dMMR/MSI-H primary advanced or recurrent endometrial cancer