treatment News

AyuVis Research Inc., a TechFW client, has been granted Orphan Drug Designation from the U.S. Food and Drug Administration (FDA) for its small molecule drug AVR-48 for the prevention of bronchopulmonary dysplasia or BPD. AVR-48 works to modulate the immune system by decreasing the inflammatory response to MV and oxygen...
BEERSE, BELGIUM, March 10, 2026 (GLOBE NEWSWIRE) — Johnson & Johnson today announced the submission of a Type II variation application to the European Medicines Agency (EMA) seeking approval for an indication extension of TECVAYLI®▼(teclistamab) as monotherapy for the treatment of adult patients with relapsed/refractory multiple myeloma (RRMM) who have received...
A unique and innovative telemedicine project is providing distant nursing home patients with Parkinson’s disease access to neurologists at the University of Rochester Medical Center. A pilot study of the project – the results of which were released this month at the International Congress of Parkinson’s Disease and Movement Disorders...
MELBOURNE, Australia — Telix Pharmaceuticals Limited (ASX: TLX; NASDAQ: TLX, Telix, the Company) today announces that a first patient has been dosed in the Phase 1 ZOLAR1 trial of TLX300-CDx (89Zr-olaratumab) in patients with advanced, metastatic soft tissue sarcoma (STS) at the Melbourne Theranostic Innovation Centre (MTIC) in Melbourne, Australia. ZOLAR...
MELBOURNE, Australia and INDIANAPOLIS, Ind. — Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that the first patient has been dosed with TLX101-Tx (¹³¹I-iodofalan) in Telix’s pivotal IPAX BrIGHT trial1, marking the first radiopharmaceutical therapy to enter Phase 3 development for glioblastoma, an aggressive form of brain cancer....
MELBOURNE, Australia — Telix Pharmaceuticals Limited (ASX: TLX) today announces that the  U.S. Food and Drug Administration (FDA) has granted Fast Track designation for the Company’s investigational glioma imaging product, TLX101-CDx (Pixclara™2, 18F-floretyrosine or 18F-FET). The granted Fast Track designation is for the characterisation of progressive or recurrent glioma using...
MELBOURNE, Australia and INDIANAPOLIS — Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, “Telix”) today announces that it has submitted a marketing authorization application (MAA) in Europe for TLX101-Px (O-(2-[18F]fluoroethyl)-L-tyrosine, 18F-FET), its glioma (brain cancer) imaging candidate. Telix has been preparing the European and U.S. regulatory packages for TLX101-Px concurrently, bringing forward...