Remove p applicant Glaxosmithkline
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Novartis announces NEJM publication of Phase III ASCLEPIOS trials demonstrating superior efficacy of ofatumumab in patients with relapsing multiple sclerosis

The Pharma Data

vs 0.25) in ASCLEPIOS I and II, respectively ( P < 001 in both studies) (primary endpoints) 1. Showed a relative risk reduction of 34% ( P =.002) 002) in 3-month confirmed disability worsening (CDW) and 32% ( P =.01) Ofatumumab was originally developed by Genmab and licensed to GlaxoSmithKline. vs 0.22) and 58% (0.10

Trials 52
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Rising Need of Autoinjectors

Roots Analysis

Notable examples of other autoinjector-based combination products include Fasenra® Pen (AstraZeneca), Gvoke® Hypopen (Xeris Pharmaceuticals), NUCALA Autoinjector (GlaxoSmithKline), and Vyleesi Autoinjector (AMAG Pharmaceuticals® / Palatin Technologies). The generic version of EpiPen received the FDA approval in 2018.

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European Commission approves Benlysta for adult patients with active lupus nephritis

The Pharma Data

GlaxoSmithKline plc (GSK) today announced the European Commission has approved the expanded use of intravenous and subcutaneous BENLYSTA (belimumab) in combination with background immunosuppressive therapies for the treatment of adult patients with active lupus nephritis (LN) in Europe, in addition to systemic lupus erythematosus (SLE).

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GSK and Vir Biotechnology announce the start of the EMA rolling review of VIR-7831 (sotrovimab) for the early treatment of COVID-19

The Pharma Data

Review will support a formal Marketing Authorisation Application. GlaxoSmithKline plc and Vir Biotechnology, Inc. The rolling review will continue until enough evidence is available to support a formal marketing authorisation application. About the COMET-ICE Study Design.

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Emergency Use Authorization request to FDA for VIR-7831 for the early treatment of COVID-19

The Pharma Data

GlaxoSmithKline plc and Vir Biotechnology, Inc. today announced the submission of an application to the U.S. Data from the registrational COMET-ICE trial also will form the basis for a Biologics License Application (BLA) submission to the FDA.

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How GSK, Chiesi Farmaceutici, Regeneron/Sanofi, Novartis, and AB Science are trying to benefit patients afflicted with Inadequately Controlled Asthma?

Delveinsight

GlaxoSmithKline’s Trelegy Ellipta for the treatment of Inadequately Controlled Asthma. GlaxoSmithKline is worth mentioning here, as it is presenting key posters and studies on Trelegy Ellipta in uncontrolled asthma patients.

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COVID-19 Pandemic Coverage

XTalks

For example, the S&P 500 is just 100 points below its pre-pandemic peak while NASDAQ had fully recovered its losses by early June and is now reporting record highs. percent of applicants have apparently been defrauding the program by “double-dipping”, a no-no that the federal government is threatening to punish. billion in June.