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Fixing drug discovery’s most persistent problem with AI

Drug Target Review

Absorption, distribution, metabolism, excretion and toxicity – collectively known as ADMET – are among the most critical and challenging hurdles in small molecule drug discovery. Before a compound can become a viable therapy, it must pass a series of tests – not just for potency, but for how it behaves in the body.

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The First Weight Loss Drugs

Codon

government could do until the 1938 Federal Food, Drug, and Cosmetic Act gave authority to the FDA to regulate drugs. Rivus Pharmaceuticals raised over $100m to take their DNP prodrug, HU6, into clinical trials for obesity in 2022. Still, there wasn’t much the U.S. The agency promptly used its new powers to ban DNP.

Drugs 71
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Bayer and Broad Institute extend cancer therapy research collaboration

Broad Institute

Our joint goal is to bring innovation to cancer patients by building a robust, sustainable pipeline in oncology,” said Dominik Ruettinger, Global Head of Research and Early Development for Oncology, Pharmaceuticals Division, Bayer AG. The research is guided by joint project and governance teams.

Therapies 105
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Extension Of Innovation Partnering Office at Monash University In Collaboration With Victorian State Government To Accelerate The Life-Sciences Hub

The Pharma Data

– Victorian State Government extends financing of JJIPO@Monash for an additional two years. Johnson & Johnson Innovation announced today the extension of the Johnson & Johnson Innovation Partnering Office at Monash University’s Clayton Campus in Melbourne (JJIPO@Monash) in collaboration with the Victorian State Government.

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Concurrent Validation for Breakthrough and Orphan Drugs: Meeting the Needs for Accelerated Manufacturing

The Premier Consulting Blog

Process validation is a critical regulatory requirement in pharmaceutical manufacturing. In the case of urgent or immediate public interest, process validation may be conducted concurrently with manufacturing the commercial small molecule or biologic product to expedite product availability for patients.

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Women in Stem with Lidia Pieri

Drug Target Review

Sibylla’s scientific founders come from very different scientific fields that do not usually speak to each other, such as theoretical physics, molecular biology and pharmaceutical chemistry. We also have collaborations with pharmaceutical companies where we leverage the best of our unique platform and pharma expertise on the target.

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Pfizer and BioNTech receive CHMP positive opinion for COVID-19 vaccine booster in the European Union

The Pharma Data

The companies do not expect the introduction of booster doses in the United States and the EU, if authorized, to impact the existing supply agreements in place with governments and international health organizations around the world. For more than 170 years, we have worked to make a difference for all who rely on us. Source link: [link].

Vaccine 52