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European Commission approves Teysuno in metastatic colorectal cancer

Latest Corporate news updates; Pharma Feb 3rd 2022...
Feb 03

GSK and Vir Biotechnology announce joint procurement agreement with European Commission for COVID-19 treatment, Sotrovimab

Latest pharma news update...
Aug 02

Roche’s Tecentriq approved by European Commission for metastatic non-small cell lung cancer

Tecentriq is now the first and only single-agent cancer immunotherapy with three dosing options...
May 08

Xeris Pharmaceuticals receives approval from the European Commission for Ogluo

Ogluo (Glucagon) is indicated treatment of severe hypoglycemia...
Feb 15

AtraZeneca's Imfinzi approved in the EU for less-frequent, fixed-dose use in unresectable non-small cell lung cancer

New option extends dosing from two to four weeks, reducing medical visits and improving patient convenience ...
Jan 15

Elevar Therapeutic collaborates with Inceptua Group for commercialization of Apealea in Europe

Inceptua will have exclusive rights to distribute and commercialize Apealea in Europe...
Dec 28

European Commission approves Roche’s Phesgo for people with HER2-positive breast cancer

Subcutaneous administration is preferred by patients, physicians and healthcare providers, and is associated with a reduction in healthcare costs ...
Dec 23

Blueprint Medicines submits sNDA to USFDA for AYVAKIT for the treatment of advanced systemic mastocytosis

Blueprint Medicines requested priority review for this application, which, if granted, could result in a six-month review process...
Dec 18

Eisai receives approval for indication expansion of anti-epileptic agent fycompa for use in pediatric patients

Dec 01

European Commission approves Supemtek® (quadrivalent recombinant influenza vaccine) for the prevention of influenza in adults aged 18 years and older

The European Commission has granted marketing authorization for Supemtek®, a quadrivalent (four-strain) recombinant influenza vaccine, for the prevention of influenza in adults aged 18 ...
Nov 20

Eisai receives approval for indication expansion of anti-epileptic agent fycompa for use in pediatric patients

The approval was based on the results of Phase III and Phase II clinical studies conducted globally to evaluate Fycompa as an adjunctive therapy in ...
Nov 16

Bristol Myers Squibb Receives European Commission approval for Opdivo plus Yervoy for treatment of Lung Cancer

European Commission decision marks the first time a dual immunotherapy with limited chemotherapy is approved for patients with non-small cell lung cancer in the ...
Nov 09

European Commission approves Roche’s Tecentriq in combination with Avastin for the treatment of people with the most common form of liver cancer

European Commission approves Roche’s Tecentriq in combination with Avastin for the treatment of people with the most common form of liver cancer....
Nov 02

Passage Bio’s PBGM01 receives Orphan Drug Designation from EMA for treatment of GM1 Gangliosidosis

Oct 27

Novartis gets European Commission approval for Enerzair Breezhaler

Novartis gets European Commission approval For Enerzair Breezhaler asthma treatment ...
Jul 09

AbbVie submits regulatory applications to FDA and EMA for RINVOQ

RINVOQ will be used for the treatment of adults with Active Psoriatic Arthritis...
Jun 08

EC approves subcutaneous formulation of Entyvio for maintenance therapy in adults with Crohn's disease or Ulcerative Colitis

May 08

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