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Clinical Trial News

The Foundation for the National Institutes of Health Announces Study Results Published in ... - FNIH

FNIH study in Radiology identifies variations in ultrasound elastography measurements, aiding interpretation of liver disease progression. Findings suggest a 30.7% difference in SWE and 35.6% in VCTE may reflect technical variability, not true changes in liver stiffness, guiding future clinical trials and reducing reliance on liver biopsies.

Phase 3 Trial Shows Superior Survival With Rilertinib for EGFR-Mutated NSCLC

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TREMFYA® (guselkumab) receives U.S. FDA approval for adults with moderately to ... - PR Newswire

FDA approves TREMFYA®, the first dual-acting IL-23 inhibitor for active ulcerative colitis, showing significant endoscopic remission rates in QUASAR program. TREMFYA® is also approved for plaque psoriasis and psoriatic arthritis.

Ascendis Pharma Receives Orphan Drug Exclusivity in the U.S. for YORVIPATH ... - Morningstar

FDA grants 7-year market exclusivity to YORVIPATH for treating hypoparathyroidism in adults.

Conventional, Complementary, and Integrative Pain Therapies in a Military Population with ...

Study compares effectiveness of starting chronic pain treatment with standard rehabilitative care (SRC) vs. complementary and integrative health (CIH) therapies using a Sequential Multiple Assignment Randomized Trial (SMART) Design. Both groups showed significant improvement up to six months, with CIH initially showing more improvement. Findings support expanding access to CIH approaches.

FDA clears brain mapping tool for neuromodulation therapies - Parkinson's News Today

FDA clears Turing Medical's Bullsai Identify, an AI-driven brain mapping tech for personalized neuromodulation therapy in Parkinson's disease, aiming to enhance treatment precision and reduce side effects.

TRILUMINATE update: TEER with Abbott's TriClip device still safe, effective after 3 years

TEER with TriClip reduced TR to moderate or less in 79% of patients, with sustained benefits including TR reduction and QOL improvements at three years. The proportion of patients with NYHA class III or IV dropped from 76% to 19%. The safety profile remains favorable, though the impact on mortality or hospitalization for heart failure is unclear.

Norton Cancer Institute patient receives first-in-world clinical trial medicine dos | Louisville ...

John T. Hamm, M.D., is the first to administer a Phase 1 clinical trial medication for solid tumors, sponsored by OncoC4 Inc., at Norton Cancer Institute. The trial aims to reduce tumor size and slow spread in advanced/metastatic solid tumors.

Studies show safety, efficacy of RSV preventive drug in kids - CIDRAP

Two studies in *Pediatrics* show nirsevimab's safety and efficacy in preventing RSV in infants and children, with Spain's universal RSV prevention via nirsevimab reducing hospitalizations by 63%. Additionally, Oregon research finds a strong correlation between viral wastewater concentration and community respiratory tests for flu, RSV, and COVID-19.

Biopharma Company Sues DEA for 'Unjustified Delays' in Approving Cannabis Research

MMJ BioPharma Cultivation sues DEA for delays in cannabis research approval for MS and HD treatments, alleging financial harm and patient suffering. The lawsuit questions DEA's use of Administrative Law Judges and accuses DEA Administrator Anne Milgram of bias against cannabis research.
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