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Basic Research: Building a Firm Foundation for Biomedicine

NIH Director's Blog: Drug Development

In an analysis of more than 28 million papers in the PubMed.gov database , researchers found NIH contributed to published research that was associated with every single one of the 210 new drugs approved by the Food and Drug Administration from 2010 through 2016 [1]. This first exercise resulted in a list of 210 new drugs.

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Overcoming the complexity of free energy perturbation calculations

Drug Target Review

However, the high computing power, associated costs, and complexity of FEP mean it is not as widely adopted within the drug development industry as it should be. As a result, drug developers can expedite the path to clinical and commercial stages, meaning patients will receive essential treatments at accelerated rates.

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Advanced 3D cell-based technologies

Drug Target Review

The first successful chip adaptation to a lung model was first described in 2010 by Donald Ingber, a bioengineer at Wyss institute. 1,2 This miniature organ chip devices emulate 3D structures with tissue-specific cell types and recreating organ functional units in an in vitro setting to test the effects of drugs and detailed reviewed.

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The evolution of cell therapy to address unmet medical needs

Drug Target Review

MSTX), from 2010, and was also a member of its board of directors from 2011, until Mast’s merger with Savara, Inc. Culley previously served as Chief Executive Officer of Mast Therapeutics, Inc. SVRA) in April 2017. Mr Culley served on the Board of Orphagen Pharmaceuticals, Inc. from May 2017 until December 2022.

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GMAX Zhengzhou Manufacturing Site Breaks Ground

The Pharma Data

About GMA301: the first Mab drug developed for PAH, GMA301 is a humanized mAb (IgG4) against endothelin receptor type A (ETa). Its long half-life makes it a promising candidate to optimize drug convenience (1MQ). About Gmax Biopharm LLC: Gmax is a clinical stage company established in 2010 and headquartered in Hangzhou, China.

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GMAX Biopharm gives first does of anti-body drug treating PAH in phase 1B trial

The Pharma Data

. “Also, its long-lasting half-life makes monthly dosing possible and this will substantially improve convenience and compliance of drug use for patients.” ” About GMA301: a humanized mAb (IgG4) against endothelin receptor type A (ETa), is the first mAb drug developed for PAH.

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The art and science of drug formulation

Drug Target Review

The science behind drug formulation The formulation of a drug is both an art and a science, requiring a deep understanding of the drug’s chemical and physical properties. 1 Challenges in drug formulation Developing a successful drug formulation is fraught with challenges.

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