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Eli Lilly and Company has expanded a licencing and partnership agreement with ProQR Therapeutics to discover, develop and market new geneticmedicines. The post Lilly and ProQR to expand geneticmedicine development agreement appeared first on Pharmaceutical Technology.
A four-year agreement between the companies comes with $170 million in cash and equity for Wave, which in recent years has dealt with clinical setbacks.
Biology is opening up new frontiers in medicine. We are witnessing a revolution in healthcare, driven by advances in genetics, Omics, RNA and CRISPR gene-editing technology, to deliver precision and personalised medicine, said Kiran Mazumdar-Shaw, executive chairperson, Biocon and Biocon Biologics.
The acquisition marks a significant bet by Lilly on gene therapy's potential to address tough-to-treat neurological disorders like Parkinson's disease.
The company, which is building a database of biological interactions found in nature, revealed $60 million in funding and a collaboration with David Liu’s lab.
The two drugmakers joined a long list of investors, including Pfizer and Sanofi, that have been funding the startup’s plan to develop a new type of lipid nanoparticle technology.
CARsgen Therapeutics has announced a col labor ation with Huadong Medicine to commercialise zevorcabtagene autoleucel (zevor-cel), CT053, in mainland China. It comprises autologous T cells that are modified genetically with a CAR including a complete human anti-BCMA single-chain fragment variant that has a high binding affinity.
Researchers see a greater need for new generation therapeutics to propel precision medicine. The development of innovative therapeutic approaches in healthcare encompass a variety of fields, including gene therapy, personalized medicine, immunotherapy, and advanced biologics.
Indian healthcare industry is of the view that emergence of genetic diagnostics will be a paradigm shift towards personalized medicine. Through the ever-evolving landscape of healthcare, the role of genetic diagnostics offers personalized insights and proactive solutions for disease management and prevention.
Moderna has entered a strategic partnership with Generation Bio for the development of non-viral geneticmedicines. Moderna’s biological and technical expertise will be combined with core technologies of the non-viral geneticmedicine platform from Generation Bio.
Facing mounting competition to its top-selling drug Eylea, Regeneron is teaming up with ViGeneron to develop a geneticmedicine for an inherited retinal disease.
CAH is a group of rare genetic disorders affecting the adrenal glands, which produce essential hormones like cortisol, aldosterone and androgens. Trial data for both the pediatric and adult trials were published in The New England Journal of Medicine. Crenessity marks the third approved drug for Neurocrine.
This intersection is where pharmacognosy meets drug patents, creating a unique landscape that shapes the future of medicine. Let’s embark on a journey to uncover the secrets of nature’s medicine cabinet and the legal frameworks that protect these discoveries.
Genetic mutations, both germline and acquired, are behind a large proportion of the most debilitating and sometimes life-threatening human diseases. But scientists have struggled to find effective treatments for many of these diseases since the dawn of modern medicine.
At a time when many startups have struggled to gain cash, the biotech has raised another $135 million to back its research, a new twist on geneticmedicine.
The partnership will use Intellia's "DNA writing” technology, and initially focus on people with the lung disease who have limited or no available treatment options.
Under the deal, Prevail obtains exclusive rights to use Scribe’s CRISPR X-Editing (XE) technologies to develop the medicines. The deal will see the integration of Scribe’s new CRISPR by Design approach and Prevail’s expertise in developing geneticmedicines for neurological disorders for specific genetic targets.
Spun out of research at Nationwide Children’s Hospital, Vironexis claims it will be the first company to start a study testing a cancer drug delivered via the adeno-associated viruses commonly used in geneticmedicines.
In a Policy Forum, Anna Lewis and colleagues argue that, for researchers and others who want to invoke genetic ancestry, there is a scientific and ethical imperative to move away from continental ancestry categories and to instead embrace a view of genetic ancestry that reflects continuous variation and historical depth.
An 11-year-old boy born deaf can hear after receiving Lilly's geneticmedicine. Others, including biotechs in China and Regeneron in the U.S., are taking aim at the same drug target.
The New York biotech will invest in and develop up to three drugs with Gensaic, an emerging startup aiming to use the viruses that infect bacteria to deliver geneticmedicines.
A deal with biotech startup Capsida, which recently raised $140 million, gives CRISPR access to a Caltech technology that aims to improve the delivery of geneticmedicines.
Taysha Gene Therapies is narrowing its research efforts and cutting around 35% of its workforce, the latest in a series of layoffs announced by makers of geneticmedicines.
Lysosomal storage disorders, diseases of cellular metabolism gone wrong, are the focus of a fast-expanding lineup of experimental geneticmedicines, a research boom that recalls biotech's roots.
The French pharma cited a "change in strategic direction" for ending a long-running pact focused on geneticmedicines for blood diseases, led by a sickle cell treatment in early testing.
He'll lead Tessera Therapeutics, a well-funded geneticmedicine startup. Severino left the pharma company in April after eight years as its chief scientist and then president.
Softbank and Fidelity joined a large group of investors in a $525 million Series C investment into Elevate, a high-powered geneticmedicine startup with an unusual business model.
The longtime partners believe that, by combining their technologies, they can create “in vivo” geneticmedicines for nervous system and muscular disorders.
The biotech is the latest in a growing list of geneticmedicine developers to sell themselves near record stock lows amid a challenging funding environment.
Trace Neuroscience aims to advance an RNA-binding therapy designed to preserve — and potentially improve — muscle function in people living with the nerve-destroying disorder.
The British pharma is deepening its investment in geneticmedicine through a deal for a group of Pfizer’s gene therapy delivery tools, while the New York giant cuts back.
The new facility cost nearly $70 million to build, and is part of a major push by the pharma giant to become a leader in geneticmedicine manufacturing.
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