Bristol Myers Squibb announces acceptance of U.S. and EU regulatory filings for Opdivo (nivolumab) plus Yervoy (ipilimumab) combined with limited chemotherapy in first-line lung cancer

8 April 2020 - Submissions based on results from Phase 3 CheckMate-9LA trial. ...

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Esperion Announces European Commission approval of the Nustendi (bempedoic acid and ezetimibe) tablet for the treatment of hypercholesterolaemia and mixed dyslipidaemia

6 April 2020 - First non-statin, LDL-C lowering combination medicine ever approved in Europe. ...

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Advanced Accelerator Applications announces Health Canada approval of Netspot diagnostic imaging agent kit to detect neuroendocrine tumours

7 April 2020 - Netspot is the first and only kit for the preparation of gallium (68 Ga) oxodotreotide injection for ...

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Submissions on whether the TGA should publish that a prescription medicine is under evaluation

8 April 2020 - Between 15 February and 29 March 2019, the TGA sought comments from interested parties on the ...

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Genentech provides regulatory update on risdiplam for the treatment of spinal muscular atrophy

7 April 2020 - U.S. FDA extends review time for risdiplam following agreed submission of additional data, including SUNFISH Part 2. ...

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Alnylam completes rolling submission of new drug application to the U.S. FDA and submits marketing authorisation application to the EMA for lumasiran for the treatment of primary hyperoxaluria type 1

7 April 2020 - Lumasiran is the first potential therapeutic to demonstrate substantial reduction in urinary oxalate excretion. ...

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Agenus receives fast track designation for balstilimab in advanced cervical cancer

7 April 2020 - Agenus today announced that the U.S. FDA has granted Agenus fast track designation for investigation of balstilimab ...

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FDA grants fast track designation to sacituzumab govitecan for urothelial cancer

7 April 2020 - Immunomedics today announced that the U.S. FDA has granted fast track designation for sacituzumab govitecan for the ...

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Blaze Bioscience announces FDA has granted fast track designation to BLZ-100 (tozuleristide) for paediatric central nervous system tumours

7 April 2020 - Phase 2/3 pivotal trial ongoing in patients up to 30 years of age undergoing surgery for paediatric ...

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Merck receives priority review from FDA for second application for Keytruda (pembrolizumab) based on biomarker, regardless of tumour type

7 April 2020 - Supplemental biologics license application accepted for Keytruda monotherapy in patients whose tumours are tumour mutational burden-high who ...

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Global regulators discuss observational studies of real world data for COVID-19 medicines

7 April 2020 - In a dedicated COVID-19 workshop, organised by the EMA under the umbrella of the International Coalition of ...

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India again allows export of anti-malarial drug touted for coronavirus

7 April 2020 - President Trump had urged the country, one of hydroxychloroquine’s biggest producers, to release supplies of the medicine. ...

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Scientists rush to find coronavirus cure—but it still isn’t fast enough

6 April 2020 - For drug companies, there is suddenly only one priority: the coronavirus. ...

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Mallinckrodt initiates rolling submission of biologics license application for StrataGraft regenerative skin tissue to U.S. FDA

6 April 2020 - Application is supported by data from pivotal phase 3 study for the treatment of deep partial-thickness thermal ...

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Bristol Myers Squibb expands patient support programs to help newly uninsured patients in the U.S.

7 April 2020 - Bristol Myers Squibb today announced an expansion of its existing patient support programs to help eligible ...

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