Legend Biotech announces submission of European marketing authorisation application for BCMA CAR-T therapy ciltacabtagene autoleucel (cilta-cel) for the treatment of relapsed and/or refractory multiple myeloma

30 April 2021 - Submission follows accelerated assessment granted by the Committee for Medicinal Products for Human Use of the European ...

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FDA approves higher dosage of naloxone nasal spray to treat opioid overdose

30 April 2021 - The U.S. FDA announced today the approval of a higher dose naloxone hydrochloride nasal spray product to ...

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FDA approves treatment for chronic kidney disease

30 April 2021 - Approval is first to cover many causes of disease. ...

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U.S. Food and Drug Administration accepts for priority review Bristol Myers Squibb’s application for Opdivo (nivolumab) as adjuvant treatment for patients with muscle-invasive urothelial carcinoma

30 April 2021 - Application based on Phase 3 CheckMate-274 trial, in which Opdivo nearly doubled disease-free survival compared to placebo. ...

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Update on U.S. FDA review of LEO Pharma’s biologics license application for tralokinumab for the treatment of adults with moderate to severe atopic dermatitis

29 April 2021 - FDA has requested additional data relating to a device component of tralokinumab. ...

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Bristol Myers Squibb statement on FDA Advisory Committee meeting on Opdivo post sorafenib hepatocellular carcinoma U.S. indication

29 April 2021 - As part of its industry-wide review of accelerated approvals in oncology without confirmatory benefit, the U.S ...

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AstraZeneca struggles with data needed for COVID-19 vaccine’s approval

29 April 2021 - Company is assembling data for FDA review, hoping for another stamp of regulatory backing in global rollout ...

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Ilaris receives Health Canada approval as first of its kind treatment for rare, inflammatory disorder, adult-onset Still's disease

29 April 2021 - The approval of Ilaris (canakinumab) in the treatment of adult-onset Still's disease brings hope for Canadians living ...

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Cerapedics announces FDA breakthrough device designation granted for P-15L bone graft for the treatment of degenerative disc disease

29 April 2021 - P-15L bone graft is currently being studied in the Company's ASPIRE IDE clinical trial. ...

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FDA Advisory Committee votes in favour of maintaining accelerated approval of Genentech’s Tecentriq for previously untreated metastatic bladder cancer

28 April 2021 - Genentech today announced the U.S. FDA Oncologic Drugs Advisory Committee voted 10 to 1 in favour of ...

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Australia accused of delaying campaign to allow generic COVID vaccines

29 April 2021 - Australia is among a group of rich countries accused of standing in the way of some ...

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EMA starts evaluating use of Olumiant in hospitalised COVID-19 patients requiring supplemental oxygen

29 April 2021 - EMA has started evaluating an application to extend the use of Olumiant (baricitinib) to include treatment ...

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Biogen provides regulatory update on the supplemental biologic license application for subcutaneous administration of Tysabri (natalizumab)

28 April 2021 - Biogen today announced that it has received a complete response letter from the U.S. FDA for ...

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COVID-19 vaccine weekly safety report - 28-04-2021

29 April 2021 - The TGA has been closely monitoring suspected adverse events from the use of COVID-19 vaccines since the ...

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FDA takes action for failure to submit required clinical trial results information to ClinicalTrials.gov

28 April 2021 - Being transparent about the results of completed clinical trials enables important advances in the development of medical ...

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