Press Releases May 12, 2026 07:00 AM

Seres Therapeutics to Participate in H.C. Wainwright 4th Annual BioConnect Investor Conference

Seres Therapeutics to Present at H.C. Wainwright 4th Annual BioConnect Investor Conference

By Caleb Monroe MCRB

Seres Therapeutics, a clinical-stage biotechnology company focused on live biotherapeutics, announced its participation in the H.C. Wainwright 4th Annual BioConnect Investor Conference, where it will present a company overview. The company is advancing several therapies, including SER-155 and SER-603, targeting inflammatory and immune diseases.

Seres Therapeutics to Participate in H.C. Wainwright 4th Annual BioConnect Investor Conference
MCRB

Key Points

  • Seres Therapeutics will present at an investor conference to discuss its clinical progress and pipeline.
  • The company has FDA-approved VOWST™, the first orally administered microbiome therapeutic, now divested to Nestlé Health Science.
  • SER-155, with Breakthrough Therapy and Fast Track designations, is Phase 2 ready for allogeneic hematopoietic stem cell transplant patients, pending funding; SER-603 targets inflammatory bowel disease.
  • The company’s work impacts the biotechnology, pharmaceutical, and healthcare sectors, especially in microbiome therapeutics and immune-related diseases.

CAMBRIDGE, Mass., May 12, 2026 (GLOBE NEWSWIRE) -- Seres Therapeutics, Inc. (Nasdaq: MCRB), a leading live biotherapeutics company, today announced that management will attend the upcoming H.C. Wainwright 4th Annual BioConnect Investor Conference and will present a company overview at 3:30 p.m. ET on May 19, 2026.

A live webcast of the presentation will be accessible through the “Events and Presentations” tab on the “Investors and News” section of the Company’s website at http://www.serestherapeutics.com and will be available for replay following the event.

About Seres Therapeutics
Seres Therapeutics, Inc. (Nasdaq: MCRB) is a clinical-stage biotechnology company developing novel live biotherapeutics, with a focus on inflammatory and immune diseases. The Company led the development and FDA approval of VOWST™, the first orally administered microbiome therapeutic, which was subsequently divested to Nestlé Health Science. SER-155, which has received Breakthrough Therapy and Fast Track designations, is being advanced for patients undergoing allogeneic hematopoietic stem cell transplant, and is Phase 2 ready, pending receipt of funding. An investigator-sponsored trial of SER-155 is ongoing in immune checkpoint inhibitor–related enterocolitis to further evaluate the potential breadth of the Company’s live biotherapeutic platform. SER-603, in development for inflammatory bowel disease, is designed to modulate the gastrointestinal microbiome and support mucosal barrier integrity by targeting inflammatory bacteria and associated metabolites. For more information, please visit www.serestherapeutics.com.  

Investor and Media Contact:  
[email protected]

Carlo Tanzi, Ph.D.
Kendall Investor Relations
[email protected]


Risks

  • The advancement of SER-155 to Phase 2 is contingent on securing additional funding, presenting financial risk.
  • Clinical trials like the investigator-sponsored trial for SER-155 and development of SER-603 carry typical biotech risks including trial outcomes and regulatory approvals.
  • Divestiture of VOWST™ to Nestlé Health Science may limit future revenue from this product, impacting financial projections.

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