The confirmation came from two separate sets of in vitro studies conducted at leading institutions. Research led by Professor Tim Bull at City St George's University of London demonstrated that RHB-204 could kill Mycobacterium avium subspecies paratuberculosis, commonly called MAP, in long-term intracellular culture …
PRKAG2 syndrome is a rare, hereditary condition caused by mutations in the PRKAG2 gene, which produces a regulatory subunit of an enzyme called AMPK. Mutations in this gene cause AMPK to remain abnormally active, leading to the accumulation of glycogen within heart muscle cells. …
One of the more consequential milestones reported for the quarter was the outcome of a Phase 1 driving simulation trial of GlyphAllo, Seaport's allopregnanolone-based drug candidate. Sleep-disrupting side effects, particularly residual sedation that affects next-day functioning, have been a limitingFactorfor neuroactive steroid therapies in …
Oncology testing volumes accelerated to 32% growth in the quarter, underpinned by expanding adoption of the company's diagnostic platform. The Minimal Residual Disease segment — which involves detecting traces of cancer remaining after treatment — saw particularly rapid expansion, with approximately 12,000 tests performed …
The INFORM-MS trial evaluated intranasal foralumab, a fully human anti-CD3 monoclonal antibody, in patients with non-active secondary progressive MS (na-SPMS) — a disease state characterized by the gradual accumulation of neurological disability independent of acute relapses. The dual primary endpoints required the trial to …
George Lederman, Ph.D., joins Tonix as Executive Vice President of Strategy and Transformation, a newly defined role that combines responsibilities more typically held by separateBusinessfunctions — operational AI deployment and business development deal-making. His prior experience includes an associate partner role at McKinsey and …
The Phase 1 study is designed as an open-label, dose-escalation trial with the primary objectives of evaluating the safety, tolerability, and pharmacokinetics of intravesically administered UGN-501. The trial will also aim to determine a recommended Phase 2 dose. Eligible participants include adults with recurrent …
Invex released its September quarter report and Appendix 4C on 30 October 2026. Subsequent to quarter end, as announced on 26 October, the company entered a binding share purchase agreement to acquire 100% of Rekover Therapeutics, a New Zealand biotechnology company.
Argenica released its quarterly update and Appendix 4C on 30 October 2026. The company said it had completed a Phase 2 clinical trial of xaranetide in acute ischaemic stroke patients at Australian hospitals during 2025, and it is now designing a targeted late-stage trial …
BCAL released its quarterly activities report and Appendix 4C on 30 October 2026. The company completed clinical validation of BREASTESTplus 2 for women aged 30 and over across all breast densities. In the validation study the test showed a sensitivity of 80.3% and a …