
Nuala Moran
Articles
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1 week ago |
bioworld.com | Nuala Moran
Home » Brink’s recombinase enzymes offer new gene editing approachBrink’s recombinase enzymes offer new gene editing approachNewco Brink Therapeutics SAS is poised to work on the next chapter in genome editing after raising €3.5 million (US$4 million) in seed funding to discover and develop programmable recombinase enzymes. BioWorld Financings Newco news Cancer CAR T Seed Europe
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1 week ago |
bioworld.com | Nuala Moran
M42 enters R&D with investment in longevity firm JuvenescenceThe Abu Dhabi health care company M42 is to make an investment in U.K.-based longevity specialist Juvenescence as a route to moving into drug discovery and development, with the two forming a partnership to work together on products that extend the healthy lifespan and improve the treatment of chronic diseases. BioWorld Science Deals and M&A Financings Aging Series B Europe
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1 week ago |
bioworld.com | Nuala Moran
Home » Cyprumed, Merck ink $493M peptide pill licensing deal BioWorld briefs for April 15, 2025. BioWorld MedTech briefs for April 15, 2025. At first glance, it appears that biopharmaceuticals dodged the latest U.S. tariff bullet; med-tech, not so much. According to the executive order President Donald... U.S. tariffs on biopharmaceuticals have advanced beyond administration talking points.As a precursor to tariffs, Commerce Secretary Howard Lutnick initiated an...
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1 week ago |
bioworld.com | Nuala Moran
Cyprumed, Merck ink $493M peptide pill licensing deal Oral peptide delivery specialist Cyprumed GmbH is about to find out if the high bioavailability of its tablet formulations seen in animal models will translate across to humans, after signing a $493 million license and option agreement with Merck & Co. Inc. BioWorld Deals and M&A Endocrine/metabolic Peptide Europe U.S.
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1 week ago |
bioworld.com | Nuala Moran
New UK law aims for ‘faster, fairer and more inclusive’ clinical trialsAs new clinical trials regulations were signed into law in the U.K., an analysis of 4,616 submissions to conduct studies has highlighted what is required for the updated law to translate into a more efficient, streamlined and adaptable regulatory framework. BioWorld Regulatory Cancer Europe MHRA Policy
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