Seres Therapeutics Pauses SER-155 Investment, Cuts Workforce by 30%
Seres Therapeutics announced that, following advancement of key startup activities for the SER-155 Phase 2 study in allo-HSCT, including the submission of a final protocol to the FDA, study site evaluation and qualification with its CRO, and manufacturing of Phase 2 study drug substance, Seres is pausing additional investment in that program and will shift its operational focus to high-value earlier-stage pipeline programs while continuing to seek funding for the SER-155 Phase 2 study. Seres also announced additional measures to reduce operating costs, including a workforce reduction of approximately 30%. As a result of these and other runway extension actions, and based on current operating plans, the Company expects to extend its cash runway through the third quarter of 2026, thereby providing additional opportunities to advance development of its live biotherapeutic programs for inflammatory and immune diseases, and pursue potential collaborations. The company said, "The SER-155 program has meaningfully advanced Seres' understanding of how microbes in the GI tract functionally modulate pathways at the mucosal barrier-immune interface associated with inflammatory and immune-related diseases. Accordingly, the Company's strategy moving forward will prioritize advancing its early-stage programs, including SER-603 that targets inflammatory and immune indications such as ulcerative colitis, Crohn's disease, and immune checkpoint related enterocolitis. Discussions are ongoing with counterparties related to potential collaborations in these areas." "Seres has taken extensive steps to prepare for a robust SER-155 Phase 2 study in allo-HSCT, including submission of a final protocol to the FDA, advancement of drug substance manufacturing, selection of a CRO and engagement with prospective study sites. As we shift our operational focus to our promising earlier-stage pipeline, we are now in a position to streamline our organization and cost structure," said Thomas DesRosier and Marella Thorell, co-CEOs of Seres. "These cost reduction initiatives and other actions are expected to extend our cash runway through the end of the third quarter of this year, supporting continued development of our programs for inflammatory and immune-related diseases, with targets validated by our previously reported preclinical and clinical datasets, and providing additional time to secure funding for our SER-155 Phase 2 study. In addition, as we pursue earlier stage programs with the greatest opportunity, such as those targeting inflammatory bowel disease, we are exploring collaborations to provide additional capital to the Company. We are very grateful for the many contributions of our departing team members."
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- Executive Changes: Seres Therapeutics announced the appointment of Richard Kenderas as Executive Chair and interim CEO, who has been on the board since September 2014, suggesting his extensive experience will guide the company's strategic direction.
- Management Stability: Former co-CEOs Thomas DesRosier and Marella Thorell will continue as Chief Legal Officer and Chief Financial Officer, respectively, ensuring continuity and stability in management, which is crucial for maintaining investor confidence.
- Investment Pause Impact: Following the pause in investments for its lead program, Seres faces market concerns regarding its future growth potential, leading to a decline in stock price, reflecting investor caution towards the company's strategic adjustments.
- Market Reaction: Despite strong SER-155 data, the increased dilution risk has prompted analysts to adjust Seres' rating to 'Hold', which may affect the company's future financing capabilities and market performance.
- Investment Pause: Seres Therapeutics announced a pause on additional investments for its mid-stage trial, resulting in a ~25% drop in premarket trading, indicating significant funding challenges for its lead asset SER-155.
- Focus on Early Programs: The company will shift its focus to earlier-stage programs, including a fully enrolled study for SER-155 in immune checkpoint-related enterocolitis, expected to generate data by early Q2 2026, highlighting potential market demand for cancer therapies.
- Layoff Plans: Seres plans to lay off nearly 30% of its workforce to extend its cash runway through Q3 2026, a move aimed at streamlining operations and reducing costs to support the development of its early-stage pipeline.
- Regulatory Preparedness: CEO Marella Thorell stated that the company has taken extensive steps to prepare for a robust SER-155 Phase 2 study, including submitting a final protocol to the FDA, demonstrating commitment and confidence in future research.
- Study Pause Reason: Seres announced the pause of the SER-155 Phase 2 study following the completion of site evaluation and qualification with its contract research organization, despite the drug substance already being manufactured, which could hinder future R&D progress.
- Strategic Shift: The company will refocus its operations on high-value early-stage pipeline programs, particularly those targeting inflammatory bowel disease (IBD), aiming to seek greater market opportunities amid limited resources.
- Cash Runway Extension: Through cost-cutting measures, including a 30% workforce reduction, Seres expects to extend its cash runway into Q3 2026, which will support the continued development of immune-related disease programs while seeking additional funding for the SER-155 Phase 2 study.
- Market Reaction: While retail sentiment on Stocktwits remains in the 'bullish' territory, MCRB stock has fallen 51% year-to-date and 75% over the past 12 months, indicating investor concerns about the company's future prospects.
- Strategic Shift: Seres Therapeutics announced a pivot towards emerging programs in inflammatory and immune diseases, resulting in a 16.25% drop in stock price during Thursday's premarket session, raising investor concerns about its current pipeline and funding strategies.
- Clinical Trial Update: The company has finalized the protocol for its Phase 2 study of SER-155 and is pausing further investment in this program, with results from the investigator-sponsored study expected in early Q2 2026, indicating a focus on early-stage programs.
- Workforce Reduction: Seres announced a 30% workforce reduction aimed at extending its cash runway through Q3 2026, allowing it to concentrate on advancing early-stage live biotherapeutic programs and pursue potential collaborations, highlighting financial constraints.
- Technical Trend Analysis: Currently trading at $11.80, Seres stock is 24.4% below its 20-day simple moving average, indicating a bearish trend and ongoing operational challenges, as the stock has decreased by 13.86% over the past 12 months.

FDA Feedback on SER-155: Seres Therapeutics received constructive feedback from the FDA regarding the Phase 2 study protocol for SER-155, aimed at preventing bloodstream infections in adults undergoing stem cell transplants, which will aid in finalizing the protocol.
Workforce Reduction and Financial Outlook: The company is reducing its workforce by approximately 25%, which is expected to incur cash payments of $1.0 - $1.4 million in Q4 2025, while extending its cash runway into the second quarter of 2026.







