News by Europäische Kommission pharma => bionity.com (2024)

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First immunotherapy for rare and aggressive skin cancer in the European Union approved Initial launches planned in Germany and the UK 22-Sep-2017 - Merck and Pfizer Inc. announced that the European Commission (EC) has granted marketing authorization for BAVENCIO® (avelumab) as a monotherapy for the treatment of adult patients with metastatic Merkel cell carcinoma (mMCC), a rare and aggressive skin cancer. BAVENCIO will have marketing ... avelumab cancer drugs immunotherapies +3 Loading...

EU project to find vaccine against ticks 09-Sep-2013 - European Union-funded researchers are launching a five-year project to find a vaccine against ticks to prevent them transmitting the diseases they carry to people they bite. The €3 million project is funded under the Seventh Framework Programme for Research and Technological Development (FP7). ... babesiosis encephalitis Lyme disease +1 Loading...

European Commission authorizes EU-wide marketing and distribution of Biofrontera's Ameluz 20-Dec-2011 - Biofrontera was informed by the European Commission that its product Ameluz® (in development called BF-200 ALA) was approved for distribution throughout the entire EU, Norway, Island and Liechtenstein. Already in October had the responsible "European Medicines Agency" recommended the approval ... actinic keratosis photo-dynamic therapies Loading...

Takeda’s Edarbi receives European marketing authorisation for the treatment of essential hypertension 12-Dec-2011 - Takeda Pharmaceutical Company Limited announced that the European Commission has granted marketing authorisation for Edarbi® (azilsartan medoxomil), a new once-daily angiotensin receptor blocker (ARB) (also known as angiotensin II receptor antagonist [AIIRA]) for the treatment of essential ... cardiovascular diseases hypertension phase III studies Loading...

S*BIO’s JAK2 Inhibitor SB1518 Granted Orphan Drug Designation by European Commission for the Treatment of Myelofibrosis 20-Oct-2010 - S*BIO Pte Ltd announced that the European Commission (EC)has granted orphan drug designation to SB1518, its potent and orally active JAK2 inhibitor for thetreatment of primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (PPV-MF) and postessentialthrombocythemia myelofibrosis ... diseases food inhibitors +4 Loading...

Novartis receives approval in the European Union for Menveo 22-Mar-2010 - Novartis announced that the European Commission (EC) granted a Marketing Authorization for Menveo® (Meningococcal Group A, C, W135 and Y conjugate vaccine) in all 27 European member states. Menveo is indicated for the active immunization of adolescents (from 11 years of age) and adults at risk of ... bacteria bacterial meningitis clinical trials +5 Loading...

The European Commission grants Orphan Drug Designation for Intravenous CP-4126 for the Treatment of Pancreatic Cancer 03-Nov-2009 - Clavis Pharma ASA announced that the European Commission has granted Orphan Drug Designation (Orphan Medicinal Product) for Intravenous CP-4126 for the treatment of pancreatic cancer. The designation follows the recommendation given by the European Medicines Agency (EMEA) in September this ... Expression food Orphan Drug Designation +3 Loading...

Movetis obtains EU authorisation for the commercialisation of Resolor (prucalopride) 26-Oct-2009 - Movetis announced that it has obtained approval from the European Commission for the commercialisation of its lead product Resolor (prucalopride – a 1mg and 2mg once a day oral tablet) for the symptomatic treatment of chronic constipation (CC) in women in whom laxatives fail to provide adequate ... chronic constipation clinical trials Iceland +2 Loading...

European Commission Approves Genzyme’s Mozobil Product Provides Significant New Option for Certain Cancer Patients Requiring a Stem Cell Transplant 06-Aug-2009 - Genzyme Corporation announced that the European Commission has granted marketing authorization for Mozobil® (plerixafor injection), providing a significant new option for patients with the blood cancers lymphoma and multiple myeloma who require an autologous stem cell transplant.“Mozobil has ... blood cancer bone marrow chemotherapy +7 Loading...

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S*BIO’s JAK2 Inhibitor SB1518 Granted Orphan Drug Designation by European Commission for the Treatment of Myelofibrosis View news

Novartis receives approval in the European Union for Menveo View news

The European Commission grants Orphan Drug Designation for Intravenous CP-4126 for the Treatment of Pancreatic Cancer View news

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Movetis obtains EU authorisation for the commercialisation of Resolor (prucalopride) view news

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