Acg Advocacy: Newsguard Technologies
Alexander, Borovicka & O Shea Government Solutions (Fka Alexander & Borovicka Go: Volan Technology Inc.
Alpine Group Partners, LLC.: Enviva Holdings, Lp
Alpine Group Partners, LLC.: Takeda Pharmaceuticals America, Inc.
Alston & Bird LLP: USagainstalzheimers Action
Arent Fox LLP: Grand Street Settlement, Inc.
Bracewell LLP: Sustainable Opportunities Acquisition Corporation
Bramer Group, LLC: Ducommun Inc.
Capitol Counsel LLC: American Association Of Settlement Consultants
Capitol Counsel LLC: Rebuild Local News Coalition
Capitol Counsel LLC: United Spinal Association
Cavarocchi Ruscio Dennis Associates, L.L.C.: Cure Epilepsy
G2G Consulting: Lead Safe Cleveland Coalition
Grayrobinson Pa: City Of Apopka Fl
Hogan Lovells US LLP: Prodigy Education
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Presented by Coalition for App Fairness
With Daniel Lippman and Zach Warmbrodt
VENUES STILL WAITING FOR CASH AFTER LOBBYING VICTORY: When the pandemic hit last year, concert and performing arts venues banded together to form the National Independent Venue Association, which spent months lobbying Congress to help them. They succeeded in December: Congress included a grant program for shuttered venues in the Covid relief.
Alembic Pharmaceuticals announced that it has received approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Midodrine Hydrochloride Tablets USP, 2.5 mg, 5 mg, and 10 mg.
The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), ProAmatine Tablets, 2.5 mg, 5 mg, and 10 mg, of Takeda Pharmaceuticals USA, Inc. (Takeda). Midodrine Hydrochloride Tablets are indicated for the treatment of symptomatic orthostatic hypotension (OH).
Midodrine Hydrochloride Tablets USP 2.5 mg, 5 mg, and 10 mg have an estimated market size of US$ 60 million for twelve months ending September 2020 according to IQVIA.
Alembic has a cumulative total of 138 ANDA approvals (120 final approvals and 18 tentative approvals) from USFDA.
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EAGAN, Minn., Dec. 16, 2020 /PRNewswire/ In an effort to help assess the value of hemophilia A treatments relative to total health care costs and emergency department visits, Prime Therapeutics LLC (Prime) has finalized an arrangement with Takeda Pharmaceuticals America, Inc., a wholly-owned subsidiary of Takeda Pharmaceutical Company Limited (NYSE:TAK) ( Takeda ) for the factor replacement product ADVATE
® [Antihemophilic Factor (Recombinant)], which is used in the treatment and prevention of bleeding episodes in patients with hemophilia A (congenital factor VIII deficiency).
Hemophilia treatment options have increased in recent years, including innovative therapies. However, these innovations come at a high price. Therefore, it is important to establish integrated medical and pharmacy benefit contracts between payers and product manufacturers on existing treatments. The arrangement between Prime and Takeda provides: