January 06, 2026 | 06:58
The biopharma company will share its clinical development progress and corporate strategy at the premier industry event.
October 13, 2025 | 16:14
First-in-human trials to start Q1 2026, giving biotech blogs EVM14 keywords and trial protocol.
August 30, 2025 | 00:39
Royalty checks from China fuel burn—oncology trials now race the cash clock.
August 12, 2025 | 08:00
Update set for August 29, 2025.
July 25, 2025 | 09:00
A solid step forward as Everest climbs with strategic share placement.
June 23, 2025 | 09:00
The antimicrobial’s global rollout gets a boost with standardised susceptibility testing specifications for clinicians.
April 28, 2025 | 08:00
The regulatory milestone signals Everest Medicines' growing financial maturity and market confidence.
April 22, 2025 | 10:08
Everest marks a new chapter in market confidence as Hong Kong Exchange grants removal of its “B” designation.
March 24, 2025 | 06:30
Everest Medicines, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for EVM14, a Tumor-Associated Antigen (TAA) vaccine.
February 26, 2025 | 06:45
Everest Medicines, today announced the presentation of maintenance data from its multi-center Phase III clinical study of etrasimod (VELSIPITY®) in Asia at the 20th European Crohn's and Colitis Organization Congress (ECCO 2025).
December 02, 2024 | 06:40
Everest Medicines, a biopharmaceutical company focused on the discovery, clinical development, manufacturing and commercialization of innovative therapeutics.
October 25, 2024 | 06:40
Everest Medicines, a biopharmaceutical company focused on the discovery, clinical development, manufacturing and commercialization of innovative therapeutics, today announced that, through the "Hong Kong and Macau Medicine and Equipment Connect" policy.
October 21, 2024 | 06:40
Everest Medicines, a biopharmaceutical company focused on the discovery, clinical development, manufacturing and commercialization of innovative therapeutics, today announces that the Taiwan Food and Drug Administration has approved NEFECON® indicated "to reduce the loss of kidney function in adult patients with primary immunoglobulin A nephropathy who are at risk for disease progression".