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$2M Grant Drives Research on Novel Insulin in Type 1 Diabetes
[UC San Diego] Pettus, an associate professor of medicine and board-certified endocrinologist who specializes in treating diabetes at UC San Diego Health, is leading a study on Liver Targeted Insulin in type 1 diabetes. The Leona M. and Harry B. Helmsley Charitable Trust recently provided a grant of more than $2 million to UC San Diego to support the research effort.
Mammary Cell News
QHS Researchers Collaborate on New Terry Fox New Frontiers Program Project
[Queen's University] Queen’s Health Sciences researchers are part of a multi-institutional research team that will receive $2.4 million to advance cancer research and treatment. The collaborative team – led by principal investigators at Sunnybrook Research Institute and Princess Margaret Cancer Centre – is behind one of five projects to receive funding in the 2023 Terry Fox New Frontiers Program Project Grant competition.
Muscle Cell News
Curi Bio Awarded Over $4.4M in NIH Grants to Advance Translational Science
[Curi Bio] Curi Bio announced two recent SBIR grants worth $4.4 million from the National Institutes of Health (NIH) to support its pioneering work on implementing human models to advance discovery of the next generation of medicines.
Hematopoiesis News
Fulcrum’s Sickle Cell Disease Program Is Back in Business After FDA Lifts 6-Month Hold
[Fierce Biotech] After a six-month wait, Fulcrum Therapeutics’ sickle cell disease plans are back on track after the FDA lifted a hold on the biotech’s candidate. The regulator instigated the full clinical hold on the therapy, dubbed FDX-6058, back in February.
Cancer Stem Cell News
US Extends Science Pact with China: What It Means for Research
[Nature] The US government has extended for six months a key symbolic agreement to cooperate with China in science and technology.
Cell Therapy News
Taysha Gene Therapies Announces Fast Track Designation Granted by US FDA for TSHA-102 in Rett Syndrome
[Taysha Gene Therapies, Inc.] Taysha Gene Therapies, Inc. announced the U. FDA has granted Fast Track Designation to TSHA-102, a self-complementary intrathecally delivered AAV9 gene transfer therapy in clinical evaluation for Rett syndrome.