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Intracellular Drug Delivery – A Potential Treatment for Lethal Orphan Diseases

Roots Analysis

We have put in our best effort to make it easily graspable what are the intracellular drug delivery technologies and how it can ensure effective treatment for fatal disease. Below are the highlights that we feel would be helpful to understand about the intracellular drug delivery / intracellular non-viral drug delivery approach.

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Top 20 Most Innovative Pharma & Biotech Companies of 2025, According to Fast Company

XTalks

The rankings are based on each companys ability to tackle critical challenges from drug delivery and diagnostics to personalized therapies using cutting-edge science. 10x Genomics 10x Genomics reported $707 million in 2024 revenue. Here are 20 companies leading the way in 2025.

Genome 59
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Metagenomics revolution: Empress Therapeutics on drug discovery breakthroughs

Outsourcing Pharma

Dr Dawn Thompson has over 20 years of experience in building technology platforms that leverage genomics at scale to produce novel products.

Genome 109
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The cluster effect: Connectivity and collaboration in life sciences hubs

Pharmaceutical Technology

From the Human Genome Project to contemporary drug development, collaboration is critical to the life sciences. The company is using the site to produce medical-grade silicones designed for a range of healthcare applications, from drug delivery to implantables.

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Technological Innovation: The Medicine of Healthcare

Delveinsight

AI is able to mine records, design treatment studies, find out targets of drug delivery in a way more drastic manner than a human can. Genome Sequencing. Nanodevices are used to improve medical imaging and some nanoparticle-based drug delivery systems are currently being used in research and studies.

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mRNA Therapeutics and mRNA Vaccines Industry: Current Scenario and Future Trends

Roots Analysis

In the last few years, researchers have become interested in using in vitro transcribed (IVT) mRNA as a drug delivery agent. mRNA drugs are considered to offer an effective alternative to gene therapies, specifically for protein replacement, as they avoid the risk of genome integration and offer strong transient expression.

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Rheumatoid arthritis treated with implanted cells that release drug

The Pharma Data

The approach allows those cells to remain in the body for a long time and secrete a drug whenever there is a flare of inflammation.” The researchers used CRISPR-Cas9 genome editing technology to make cells that secrete a biologic drug in response to inflammation. ” The new findings are published online Sept.

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