Wockhardt receives US FDA qualified infectious disease product designation for WCK 6777, a first ever once-a-day β-lactam enhancer class antibiotic

20 April 2020 -  WCK 6777 is a once-a-day combination antibiotic based on Wockhardt’s NCE zidebactam, which imparts WCK 6777 ...

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Director of U.S. agency key to vaccine development leaves role suddenly amid coronavirus pandemic

21 April 2020 - Rick Bright, one of the nation’s leading vaccine development experts and the director of the Biomedical ...

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Myovant Sciences Submits new drug application to the FDA for once daily, oral relugolix for the treatment of men with advanced prostate cancer

21 April 2020 - Myovant expects to submit a second application for relugolix combination tablet for women with uterine fibroids in ...

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DOJ clears U.S. drug companies to distribute hydroxychloroquine to coronavirus patients

21 April 2020 - The U.S. Department of Justice on Monday cited "extreme urgency" in clearing U.S. pharmaceutical distributors from ...

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Here’s why a COVID-19 vaccine could end up costing you a small fortune

21 April 2020 - Things have gone from bad to worse for Brian Helstien. For a decade, he’s been grappling ...

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Imbruvica (ibrutinib) receives 11th FDA approval

21 April 2020 - Granted under FDA's real-time oncology review pilot program, Project Orbis and priority review. ...

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Coronavirus puts big pharma’s IP regime to the test

21 April 2020 - “Chaotic” is how Jorge Contreras, a law professor at the University of Utah, describes a struggle ...

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If pharma helps quench the COVID-19 pandemic, what will it want in return?

21 April 2020 - Make no mistake: the only long-term solution to the COVID-19 pandemic is a safe and effective ...

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Hydroxychloroquine and other auto-immune drugs don’t fully protect against coronavirus, early data suggest

18 April 2020 - Data compiled by rheumatology researchers show dozens of patients who were taking Plaquenil and other drugs became ...

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Big pharma has the chance to come to the world’s rescue

20 April 2020 - The pandemic may finally do for the pharmaceutical industry what relentless TV advertising cannot: show off its ...

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FDA and EMA accept applications for Genentech’s Ocrevus (ocrelizumab) shorter two hour infusion time

19 April 2020 - Reduces infusion time to 2 hours from the current 3.5 hours for patients with relapsing or primary ...

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Novartis to sponsor large clinical trial of hydroxychloroquine in hospitalised COVID-19 patients

20 April 2020 - Novartis has reached an agreement with the US FDA to proceed with a Phase III clinical trial ...

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NIH to launch public-private partnership to speed COVID-19 vaccine and treatment options

17 April 2020 - The National Institutes of Health (NIH) and the Foundation for the NIH are bringing together more than ...

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Finding effective treatments for COVID-19: scientific integrity and public confidence in a time of crisis

16 April 2020 - Everyone wants new treatments and vaccines to address the devastation of coronavirus disease 2019 (COVID-19). ...

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FDA approves first targeted treatment for patients with cholangiocarcinoma, a cancer of bile ducts

17 April 2020 - Today, the U.S. FDA granted accelerated approval to Pemazyre (pemigatinib), the first treatment approved for adults with ...

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