Globe Newswire
Remittix prepares to remove 20% of its original token supply as JPMorgan expands institutional access to Solana through two tokenized money market funds.
MAJURO, Marshall Islands, Oct. 25, 2026 (GLOBE NEWSWIRE) -- Remittix has announced plans to burn 300 million RTX tokens at launch, removing 20% of its original supply as the project approaches its November 24, 2026 market debut. The burn brings a major tokenomics milestone into the final launch window alongside... (continue reading...)
- 44.8% ORR at 6mg/kg dose in late-line CRC patients
- ARR-217 was generally well-tolerated
- ArriVent to host virtual webinar on Monday, October 26, 2026, at 8 am ET to discuss the data from the ARR-217 program
NEWTOWN SQUARE, Pa., Oct. 25, 2026 (GLOBE NEWSWIRE) -- ArriVent BioPharma, Inc. (Company or ArriVent) (Nasdaq: AVBP), a clinical-stage company dedicated to accelerating the global development of innovative biopharmaceutical therapeutics, today announced initial... (continue reading...)
Pre-specified and Statistically Powered Key Endpoints Included Progression-free Survival (PFS) and Overall Survival (OS). Although Primary Endpoint of PFS Was Not Met, The Key Secondary Endpoint of OS Was Improved With VAZKEPA/VASCEPA
Patients Taking VASCEPA Prior to and Following Liver Resection for CRCLM Were Estimated to Have an Approximately 32% Reduction in the Risk of Death at 5 Years Relative to the Control Arm
DUBLIN and BRIDGEWATER, N.J., Oct. 25, 2026 ... (continue reading...)
GERMANTOWN, Md., Oct. 25, 2026 (GLOBE NEWSWIRE) -- AirTripMaker, a growing travel platform focused on connecting travelers with convenient international air travel options, is expanding its USA and Canada to India travel network to serve passengers traveling from the United States or Canada to India’s most important metropolitan, business, technology, cultural and tourism destinations.
In 2026, finding a “deal” to India is no longer just about price—it’s about... (continue reading...)
- Updated Phase 1b dataset provides nearly 18 months of median follow-up and shows the durability of clinical benefit observed with givastomig
- Clinical activity observed across CLDN18.2 expression levels, including in patients with lower-expression tumors not eligible for currently approved CLDN18.2-targeted therapies
- Totality of efficacy, safety and long-term follow-up data supports selection of the 8 mg/kg dose for registrational development
- Ongoing U.S. Food and Drug... (continue reading...)
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