Four months after receiving a complete response letter from the U.S. FDA for tolebrutinib to treat non-relapsing secondary progressive multiple sclerosis, Sanofi SA received a positive opinion ...
Minimal residual disease (MRD) has become a central concept in modern oncology, reshaping how clinicians evaluate response, ...
Children and adults with a type of congenital hearing loss now have a free treatment option, with the U.S. FDA’s accelerated approval of Regeneron Pharmaceuticals Inc.’s DB-OTO, an AAV-mediated gene ...
New Approach Methodologies (NAMs) for drug development are transforming biomedical research by replacing or complementing ...
Researchers in the U.K. have developed an AI-driven method of identifying viruses in wild animals with the potential to ...
Optimism rose for what could be the first CAR T therapy in autoimmune disease as Kyverna Therapeutics Inc. made public a ...
A modified version of CRISPR-Cas9 has enabled, for the first time, the efficient integration of a large transgene capable of ...
Flagship Pioneering Inc. has announced the launch of Serif Biomedicines Inc., a biotechnology company pioneering modified DNA as a new class of medicines. Modified DNA brings together the best ...
When a tumor migrates and colonizes another tissue or organ, it can be identified as a metastasis, but its origin is not ...
Clinical updates for biopharma and med tech, including data readouts and publications: Abbott, Agenus, Astrazeneca, Briacell, Clearmind, Greenwich, Intodna, Kyverna ...
With rezpegaldesleukin (rezpeg) phase IIb data in alopecia areata holding strong over time, backers of Nektar Therapeutics ...
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