The European Commission has granted Orphan Medicinal Product Designation in the EU for MIV-818
Medivir today announced that the European Commission, in accordance with the opinion from the European Medicines Agency (EMA), has granted orphan medicinal product designation in the EU for MIV-818 for the treatment of patients with hepatocellular carcinoma (HCC), the most common type of primary liver cancer
Biotechnology | 05/07/2020 | By Darshana | 443
NPPA fixes retail prices of 14 formulations under DPCO 2013
NPPA has fixed retail prices of 14 formulations under Drugs Prices Control Order (DPCO)- 2013 relating to 76th Authority meeting dated June 22, 2020.
Biotechnology | 03/07/2020 | By Darshana | 809
Selumetinib granted orphan drug designation in Japan for neurofibromatosis type 1
AstraZeneca today announced that selumetinib has been granted orphan drug designation (ODD) in Japan for the treatment of neurofibromatosis type 1 (NF1), a rare and debilitating genetic disease
Biotechnology | 01/07/2020 | By Darshana | 428
'COVAXIN': India's first Covid vaccine gets DGCI's approval for clinical trials
Bharat Biotech, has successfully developed Covaxin, India's 1st vaccine candidate for COVID-19, in collaboration with the Indian Council of Medical Research (ICMR) and the National Institute of Virology (NIV). The SARS-CoV-2 strain was isolated in NIV, Pune and transferred to Bharat Biotech
Biotechnology | 30/06/2020 | By Darshana | 353
Hetero Healthcare set to supply 20,000 vials of generic remdesivir across country
Following the approval of "Covifor", the generic of remdesivir by DCGI, Hetero Healthcare Limited, a group company of Hetero is set to deliver the first set of 20,000 vials in two equal lots of 10,000 each
Biotechnology | 25/06/2020 | By Darshana | 497
Novartis discontinues hydroxychloroquine trial for COVID-19 due to acute enrollment challenges
Novartis has made the decision to stop and discontinue its sponsored hydroxychloroquine(HCQ) clinical trial for COVID-19 due to acute enrollment challenges that have made trial completion infeasible
Biotechnology | 22/06/2020 | By Darshana | 280
Merck Animal Health, known as MSD Animal Health outside the United States and Canada, announced the completion of its acquisition of Quantified Ag, a leading data and analytics company that monitors cattle body temperature and movement in order to detect illness early
Biotechnology | 19/06/2020 | By Darshana | 367
Neurocrine Biosciences Inc and Takeda Pharmaceutical Company Limited announced a strategic collaboration to develop and commercialise compounds in Takeda's early-to-mid-stage psychiatry pipeline. Specifically, Takeda granted an exclusive license to Neurocrine Biosciences for seven pipeline programmes, including three clinical stage assets
Biotechnology | 18/06/2020 | By Darshana | 242
Bayer announced today the initiation of the FINEARTS-HF study, a multicenter, randomized, double-blind, placebo-controlled Phase III study to evaluate the efficacy and safety of finerenone on morbidity and mortality in patients suffering from symptomatic heart failure
Biotechnology | 16/06/2020 | By Darshana | 606
Following National Pharmaceutical Pricing Authority (NPPA) directive to address the demand of tocilizumab injection in government hospitals in Gujarat for the treatment of COVID-19 patients, the Mumbai-based pharmaceutical major Cipla Ltd has renewed its supply by releasing another batch of 700 tocilizumab injections to Gujarat
Biotechnology | 11/06/2020 | By Darshana | 1015
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