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Intrance Medical Systems Establishes U S Operations and Names Patrick Shea Chief Executive Officer
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New STRENGTH Analysis Reignites Debate on Omega-3 CV Benefits
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Pharmaceutical industry leader to build organization from ground up with commitment to bringing innovation to the advanced Parkinson s disease community
Company plans to initiate U.S. clinical development of its fixed-dose combination treatment for enteral infusion in advanced Parkinson s disease patients
Intrance Medical Systems, Inc., a subsidiary of Sweden-based Intrance Holdings AB, today announced the company has officially established its U.S. operations with the appointment of Patrick M. Shea as Chief Executive Officer and member of the Board of Directors. Mr. Shea will be responsible for building the company s operational and business structure and initiating the U.S. clinical development program for its fixed-dose combination treatment of levodopa, carbidopa and entacapone for enteral infusion in advanced Parkinson s disease patients. The product is currently marketed as Lecigon in the Nordic countries and certain European markets.
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RIDGEFIELD, Conn., April 23, 2021 /PRNewswire/ Boehringer Ingelheim today announced results from a phase III, randomized study that concluded that switching several times from Humira® (adalimumab) to Cyltezo® (adalimumab-adbm) produced similar clinical outcomes in terms of pharmacokinetics, efficacy, immunogenicity, and safety in people with moderate-to-severe chronic plaque psoriasis. The 32-week data will be presented at the American Academy of Dermatology 2021 virtual meeting experience. We are proud to present the results from Voltaire-X, a landmark study that supports Boehringer Ingelheim s application for interchangeability between Cyltezo® and Humira®, said Thomas Seck, Senior Vice President, Medicine and Regulatory Affairs at Boehringer Ingelheim. This first-of-its-kind switching study further reinforces our goal to broaden access to biosimilar treatment options while contributing to the quality and sustainability of healt
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4 hours ago On Tuesday in the District of Delaware, Boehringer Ingelheim Pharmaceuticals Inc. (BIPI) and its affiliates filed a complaint against a generic drug manufacturer with allegations that the generic company has infringed the plaintiffs’ patents covering diabetes drug Trijardy XR.
The plaintiffs own or are assignees of United States Patent Nos. 8,551,957; 9,155,705; 9,415,016; 9,949,998; 10,022,379; 10,258,637; and 10,406,172 covering Trijardy XR, all of which were issued by the U.S. Patent and Trademark Office between 2013 and 2019, the complaint said. BIPI also holds New Drug Application (NDA) No. 212614 for empagliflozin-linagliptin-metformin hydrochloride extended-release tablets in various dosages, sold under the brand name product. The plaintiffs’ drug patent information is listed in the Food and Drug Administration (FDA)’s database
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