Business Wire

MRM Health’s Lead Candidate MH002 Granted Fast Track Designation by U.S. FDA for the Treatment of Mild-to-Moderate Ulcerative Colitis

30.4.2026 22:17:00 CEST | Business Wire | Press Release

Share

MRM Health, a clinical-stage biopharmaceutical company developing therapeutics for immune-mediated diseases, which unlock the power of the microbiome to restore immune balance, today announced that MH002, the Company’s lead rationally designed Live Biotherapeutic Product (LBP) candidate, has been granted Fast Track designation by the U.S. Food and Drug Administration (FDA) for the treatment of mild-to-moderate ulcerative colitis (UC). MH002 today is the most advanced LBP targeting inflammatory bowel disease (IBD)-specific mechanisms and is composed of a rationally designed microbial consortium of six well-characterized commensal strains.

The FDA’s Fast Track is a process designed to facilitate the development and expedite the review of drugs to treat serious conditions and fill an unmet medical need. The purpose is to get important drugs to patients earlier. Fast Track designation enables frequent communication with the FDA to discuss the drug's development plan and ensure collection of appropriate data needed to support drug approval. Products granted Fast Track status may also qualify for Accelerated Approval and Priority Review, and companies may be eligible to submit completed sections of the New Drug Application (NDA) on a rolling basis.

“The FDA’s decision to grant Fast Track designation to MH002 recognizes the potential of this promising Live Biotherapeutic Product to address the significant unmet need for innovative and more effective therapies for patients with ulcerative colitis, who have become resistant to standard treatments or for whom conventional therapies have little or no effect,” said Dr. Sam Possemiers, CEO of MRM Health. “This designation enables us to work closely with the agency to further accelerate the development of MH002 with the goal of getting it to patients in need of well-tolerated therapies with sustained efficacy as quickly as possible.”

“Live biotherapeutic approaches are opening entirely new avenues for treating immune-mediated diseases such as ulcerative colitis,” said Professor Geert D’Haens, MD gastroenterologist and investigator at Amsterdam UMC. “While several treatments are available for UC, this is mostly the case for moderate-to-severe UC patients and many patients still fail to achieve durable remission or require treatment escalation, underscoring the need for novel treatment options. The Fast Track designation for MH002 confirms the growing recognition of microbiome-based therapies as a scientifically grounded strategy to restore gut homeostasis and achieve more durable remission in IBD patients.”

Fast Track designation supported by Phase 2a excellent safety and encouraging efficacy signals

The designation was supported by results from a completed Phase 2a clinical trial in mild-to-moderate UC. Over eight weeks of treatment, MH002 demonstrated excellent safety and encouraging efficacy signals, consistent with mucosal healing and anti-inflammatory activity, recovery of microbiome balance, and induction of clinical remission. No safety signals or adverse reactions were observed. MH002 also showed positive outcomes in an open-label study in acute pouchitis, further underscoring its broad therapeutic potential.

MH002 is an orally administered capsule for mild-to-moderate ulcerative colitis and pouchitis, designed to restore microbiome balance and promote mucosal healing and immune rebalancing without immunosuppression. The product candidate will be evaluated in a clinical Phase 2b study (STARFISH-UC; NCT07296315) in patients with mild-to-moderate UC. The study will enroll approximately 204 patients and includes a 12-week induction phase comparing two MH002 dosing regimens versus placebo, followed by a 40-week open-label extension phase. The trial will be conducted across sites in Europe and the United States, with first results expected in Q4 2027.

Upcoming event:

MRM Health will be presenting at the Digestive Disease Week (DDW) 2026, taking place May 2 – 5, 2026 in Chicago, IL, USA.

Poster Session:

Date & time

Presenter

Title

Tuesday, May 5th
12:30pm – 1:30pm CDT
Track: Inflammatory
Bowel Diseases

Sam Possemiers, PhD
CEO, MRM Health

Tu1533: Studying treatment of mild-to-moderate ulcerative colitis with MH002, an optimized live biotherapeutic product: insights from analyzing first clinical data for the design of a confirmatory trial

***

About MRM Health

MRM Health is a clinical-stage biotech developing innovative microbiome-based Live Biotherapeutic Products for chronic inflammatory diseases with high unmet need. Its CORAL® platform enables the design and manufacture of disease-focused microbial consortia with enhanced efficacy and scalability. In addition to advancing lead program MH002 into pivotal clinical development in ulcerative colitis and the orphan disease indication, pouchitis, MRM Health has ongoing preclinical programs in other inflammatory diseases and immune-oncology. In September 2025, MRM Health successfully closed a 55M€ Series B round led by Biocodex, with strong support from ATHOS, BNP Paribas Fortis Private Equity and existing investors SFPIM, AvH, OMX Europe VF, QBic and VIB.

For more information, please follow us on LinkedIn or visit the website at www.mrmhealth.com.

View source version on businesswire.com: https://www.businesswire.com/news/home/20260430814717/en/

Contacts

Corporate
MRM Health NV
Dr. Sam Possemiers – CEO
info@mrmhealth.com

Media relations
International & DACH
MC Services AG
Anne Hennecke
Phone: +49.151.125.557.59
anne.hennecke@mc-services.eu

Media relations
BeNeLux/France
Backstage Communication
Gunther De Backer
Phone: +32.475.903.909
gunther@backstagecom.be

(c) 2024 Business Wire, Inc., All rights reserved.

Business Wire, a Berkshire Hathaway company, is the global leader in multiplatform press release distribution.

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

SES Announces Extraordinary General Meeting of Shareholders15.5.2026 08:30:00 CEST | Press Release

SES: Société Anonyme RCS Luxembourg B 81267 Notice is hereby given of the Extraordinary General Meeting of SES, Société Anonyme, to be held at the Company's registered office at Château de Betzdorf, L-6815 Betzdorf (the "Company"), Luxembourg, on Wednesday 17 June 2026 at 3:00 p.m. CET AGENDA Attendance list, quorum and adoption of the agenda Nomination of a secretary and of two scrutineers Cancellation of shares purchased in connection with the buy-back programme of 2 November 2023, as amended on 2 May 2024, in accordance therewith and pursuant thereto - Reduction of the share capital in accordance with article 450-5 of the law of 10 August 1915 on commercial companies, as amended, by forty-four million nine hundred ten thousand seven hundred eighty euro (EUR 44,910,780) through the cancellation of thirty-five million nine hundred and twenty-eight thousand six hundred and twenty-four (35,928,624) shares divided into (i) twenty-three million nine hundred and fifty-two thousand four hun

Cinemo Honored with 2026 AutoX Award for Automotive Infotainment Innovation15.5.2026 08:05:00 CEST | Press Release

Cinemo, global leader in AI-powered, fully integrated in-vehicle entertainment and digital media solutions, delivering seamless multi-screen experiences for drivers and passengers, has been recognized as an Automotive Infotainment Innovator at the 2026 AutoX Innovator Awards by Compass Intelligence, highlighting its role in shaping the next generation of in-vehicle experiences. The AutoX Innovator Awards recognize companies that move the industry forward. Winners are selected based on criteria including technological advancement, differentiation, integration capabilities, user experience, industry partnerships, and feasibility. Additional emphasis is placed on real-world outcomes, such as improving driver safety, enhancing passenger experiences, delivering positive market impact, and transforming mobility. “Cinemo exemplifies the future of automotive infotainment, where innovation is defined not just by technology, but by the experiences it enables,” said Stephanie Atkinson, CEO of Com

Experian Partners With ServiceNow to Scale Trusted Decisioning to Agentic AI15.5.2026 08:00:00 CEST | Press Release

Experian, the global data and technology company, and ServiceNow (NYSE: NOW), the AI control tower for business reinvention, today unveil a new global multi-year partnership which harnesses the power of autonomous AI agents across platforms, helping businesses make faster and smarter decisions at scale. Through this partnership, autonomous AI agents can gain the ability to act faster, and more consistently, starting with employee onboarding, third-party risk management and model life cycle governance use cases. A major challenge for global organisations adopting agentic AI is achieving scale, with deployments often constrained by a lack of trusted data. In fact, industry research shows that data limitations are the primary barrier for eight in ten organisations. By connecting trusted intelligence directly into enterprise workflows, this partnership enables agentic AI to scale well beyond pilot deployments. With the Experian Ascend Platform natively connected to the ServiceNow AI Platfo

Meiji Seika Pharma: Positive Results from the Phase III Integral-1 Trial of Nacubactam, a Novel β-Lactamase Inhibitor, in Complicated Urinary Tract Infections or Acute Uncomplicated Pyelonephritis ― Published in The Lancet15.5.2026 03:00:00 CEST | Press Release

Meiji Seika Pharma Co., Ltd. (headquartered in Tokyo; President and Representative Director: Toshiaki Nagasato) today announced that the results of the Integral-1 study, one of two global Phase III clinical trials evaluating the efficacy and safety of its novel β-lactamase inhibitor nacubactam (development code: OP0595), have been published in The Lancet. The article is entitled “---Efficacy and safety of cefepime–nacubactam and aztreonam–nacubactam compared with imipenem–cilastatin for complicated urinary tract infection or acute uncomplicated pyelonephritis (Integral-1): a double-blind, randomised phase 3 trial” (https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(26)00596-9/fulltext) Integral-1 is a global, double-blind, randomized Phase III trial (jRCT2031230075) in patients with complicated urinary tract infection or acute uncomplicated pyelonephritis that compared the efficacy and safety of nacubactam co-administered with either cefepime or aztreonam versus imipenem-c

Boomi Teams up With Gong to Bring Revenue AI to Boomi Agentstudio14.5.2026 18:00:00 CEST | Press Release

Boomi, the data activation company for AI, today announced a collaboration withGong, the leader in Revenue AI, to bring revenue signals captured in Gong natively into the Boomi Enterprise Platform. This collaboration enables enterprises to establish an active data foundation designed to transform customer conversations into coordinated, automated actions across systems and functions enterprise-wide with Boomi Agentstudio. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260514443012/en/ Boomi Teams Up with Gong to Bring Revenue AI to Boomi Agentstudio Gong goes beyond capturing deal activity to surface real-time insights into risk, buyer intent, competitive dynamics, and key engagement signals. That intelligence moves from conversation to coordinated action, flowing across CRM, ERP, product, and operational systems with the governance and security that enterprises require. Through this collaboration, these signals can be serve

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye