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ebook: Never Miss A Hit – Unleash Your Drug Discovery With A Label-Free Playlist

Drug Target Review

This ebook deep dives into adoption and optimization of label-free hit-to-lead (HTL) technologies, including advanced surface plasmon resonance (SPR) applications for hit identification and validation.

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The Cost of Knowledge: Evaluating Open vs. Paid Data for Pharma

DrugBank

These data sources are known for being highly referenced and usable for specific research activities; further yet, a number of recognizable open sources, along with their identifiers, are considered industry standard resources.

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An Evolving Regulatory Environment for Rare and Orphan Diseases

Advarra

The Orphan Drug Act of 1983 was instrumental in changing the number of orphan drugs approved in the U.S. The law established the Office of Orphan Products Development , providing financial incentives for pharmaceutical companies to develop orphan drugs and making it more viable to invest in orphan drug research and development.

Disease 52
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Deliberate Dysentery

Codon

People are hesitant to do this because it's not a particularly flashy disease to research, nor is this population the focus of major pharmaceutical companies. So if you're a researcher, you can pour your heart and soul into a hepatitis C vaccine, and it probably won't ever get tested. So you have to do a field study.

Vaccine 126
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Innovation Drives Excellence, Innovent Successfully Held 2020 Virtual R&D Day

The Pharma Data

Dr. Liu shared his over 30 years of R&D experience in drug development both in the global pharmaceutical companies and world renowned scientific research institutions. Yong-Jun Liu , the newly appointed President of Innovent also made his first public appearance on the virtual R&D day.

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Accelerating Drug Discovery Through Repurposing

DrugBank

CMap utilizes gene expression profiles to connect drugs, genes, and diseases, enabling researchers to identify potential repurposing candidates based on their transcriptional signatures. We invite researchers, pharmaceutical companies, and academic institutions to join us to unlock the full potential of drug repurposing.

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Using clinical genomics and AI in drug development to elevate success

Drug Target Review

Drug development: addressing complexity and success rates Drug development is a complex and expensive process, requiring multidisciplinary expertise and high-risk financial investments. The major hurdles that pharmaceutical companies face are long lead times, high costs and a low probability of success (PoS).