Close Menu

    Subscribe to Updates

    Get the latest creative news from FooBar about art, design and business.

    What's Hot

    Heat intensifies severe drought across European nations

    July 24, 2026

    Amazon wildfires in Brazil fall to lowest level in four decades

    July 23, 2026

    Private sector wage growth hits six year low in latest UK data

    July 22, 2026
    • Home
    • Contact Us
    Amman ObserverAmman Observer
    • Automotive
    • Business
    • Entertainment
    • Health
    • Lifestyle
    • Luxury
    • News
    • Sports
    • Technology
    • Travel
    Amman ObserverAmman Observer
    Home » Halia Therapeutics Completes Enrollment in Phase 2a Clinical Trial of HT-6184 for Myelodysplastic Syndrome (MDS)
    PR Newswire

    Halia Therapeutics Completes Enrollment in Phase 2a Clinical Trial of HT-6184 for Myelodysplastic Syndrome (MDS)

    June 4, 2025
    Facebook WhatsApp Twitter Pinterest LinkedIn Telegram Tumblr Email Reddit VKontakte

    LEHI, Utah, June 4, 2025 /PRNewswire/ — Halia Therapeutics, a clinical-stage biopharmaceutical company pioneering therapies inspired by genetic resilience, today announced the completion of enrollment for its open-label Phase 2a clinical trial evaluating HT-6184 (Ofirnoflast) in patients with lower-risk Myelodysplastic Syndrome (MDS) who are refractory to, intolerant of, or ineligible for erythropoiesis-stimulating agents (ESA).

    The Genetic Resilience Company

    The study (CTRI/2023/11/059758) is designed to evaluate the efficacy, safety, and biomarker response of HT-6184, a novel allosteric modulator of NEK7 that disrupts NEK7–NLRP3 protein interaction, thereby preventing the formation of the NLRP3 inflammasome. This mechanism also promotes the disassembly of pre-formed NLRP3 inflammasomes, targeting a key inflammatory pathway implicated in bone marrow dysfunction in myelodysplastic syndromes (MDS). The two-stage study enrolled 18 evaluable patients in Stage 1 and has now completed enrollment of an additional 15 participants in Stage 2.

    “Completing enrollment in our Phase 2a MDS study is a major milestone as we continue to validate our mechanism of action targeting innate immune dysregulation,” said Dr. David Bearss, CEO of Halia Therapeutics. “This study provides important proof-of-concept data to support the therapeutic potential of HT-6184 in reducing clonal inflammation and improving hematologic outcomes for patients with symptomatic anemia.”

    The trial consists of a 16-week treatment period, followed by a response-based continuation phase. Responders may continue on therapy, while non-responders showing a greater than 30% reduction in variant allele frequency (VAF) clone size may receive up to 16 additional weeks of treatment, either as monotherapy or in combination with prior ESA therapy. Key study objectives include evaluating efficacy through hematological improvement, clonal suppression, and VAF reduction, assessing safety and patient tolerance, monitoring changes in inflammasome-related biomarkers, and measuring quality of life using patient-reported outcome tools.

    An interim analysis was conducted following Stage 1, and topline results from the complete study are expected later this year.

    About Halia Therapeutics
    Halia Therapeutics is redefining treatment paradigms by targeting the innate immune system and harnessing genetic resilience. Founded on breakthrough research identifying protective mutations in individuals genetically predisposed to severe diseases, Halia’s therapies aim to restore immune balance in inflammatory and neurodegenerative conditions.

    The company’s pipeline includes:

    • HT-6184, currently in a Phase 2a trial for Myelodysplastic Syndrome (MDS)
    • HT-6184, in combination with semaglutide, a planned Phase 2a trial in obese and Type 2 diabetes (T2D) patients, is expected to initiate in 3Q25.
    • HT-4253, a neuroinflammation-targeted candidate, is currently in an ongoing Phase 1 clinical trial (NCT06537817), expected to conclude in 3Q25.

    For more information about Ofirnoflast (HT-6184), HT-4253, or ongoing clinical trials, please visit www.haliatx.com.

    Media Contact

    Taylor Avei
    Director of Business Development
    Halia Therapeutics
    info@haliatx.com

    Photo – https://mma.prnewswire.com/media/2702932/Halia_Therapeutics_Logo.jpg

    Cision View original content:https://www.prnewswire.co.uk/news-releases/halia-therapeutics-completes-enrollment-in-phase-2a-clinical-trial-of-ht-6184-for-myelodysplastic-syndrome-mds-302472862.html


    Related Posts

    ThreatBook Launches Best-of-Breed Advanced Threat Intelligence Solution

    September 29, 2025

    2025 Yidan Prize spotlights changemakers advancing complex systems literacy and multilingual education

    September 29, 2025

    KingSmith Celebrates 10 Years of Innovation with Global "One Endless Journey" Campaign

    September 19, 2025

    Vantage Celebrates 4.5-Star Rating on Trustpilot, Strengthening Client Confidence

    September 19, 2025

    Huawei Releases 4+10+N SME Intelligence Solutions, Powering the Last Mile of the Intelligent World

    September 18, 2025

    The New QUATRA 100M 5G Enhances Nextivity Enterprise DAS Platform, Supporting Public, Private and IoT Networks

    September 16, 2025
    Editor's Pick

    Heat intensifies severe drought across European nations

    July 24, 2026

    Amazon wildfires in Brazil fall to lowest level in four decades

    July 23, 2026

    Private sector wage growth hits six year low in latest UK data

    July 22, 2026

    UN urges fair rules for artificial intelligence worldwide

    July 18, 2026

    Indonesia begins building $20.9 billion Masela LNG project

    July 18, 2026

    IOM launches $98 million appeal for Venezuela quake recovery

    July 18, 2026

    DR Congo Ebola outbreak reaches 2,267 cases and 893 deaths

    July 18, 2026

    Northern Ontario wildfires trigger evacuations and closures

    July 16, 2026
    © 2026 Amman Observer | All Rights Reserved
    • Home
    • Contact Us

    Type above and press Enter to search. Press Esc to cancel.