SEC Form 10-Q filed by Seres Therapeutics Inc.
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Date | Price Target | Rating | Analyst |
---|---|---|---|
5/8/2025 | $6.00 | Buy → Neutral | Chardan Capital Markets |
10/24/2024 | Neutral → Underweight | JP Morgan | |
6/26/2023 | $12.00 | Outperform | Oppenheimer |
4/21/2023 | $7.00 | Neutral | JP Morgan |
7/23/2021 | $42.00 → $29.00 | Buy | Canaccord Genuity |
7/23/2021 | $30.00 → $16.00 | Buy | Chardan Capital |
7/23/2021 | $36.00 → $18.00 | Outperform | Oppenheimer |
7/23/2021 | $46.00 → $25.00 | Buy | HC Wainwright & Co. |
SCHEDULE 13G/A - Seres Therapeutics, Inc. (0001609809) (Subject)
S-8 - Seres Therapeutics, Inc. (0001609809) (Filer)
10-Q - Seres Therapeutics, Inc. (0001609809) (Filer)
Chardan Capital Markets downgraded Seres Therapeutics from Buy to Neutral and set a new price target of $6.00
JP Morgan downgraded Seres Therapeutics from Neutral to Underweight
Oppenheimer resumed coverage of Seres Therapeutics with a rating of Outperform and set a new price target of $12.00
CAMBRIDGE, Mass., May 27, 2025 (GLOBE NEWSWIRE) -- Seres Therapeutics, Inc. (NASDAQ:MCRB) (Seres or the Company), a leading live biotherapeutics company, today announced the Company will be presenting new exploratory biomarker data from its SER-155 Phase 1b study in a poster session at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting, taking place May 30 –June 3 in Chicago. The Company previously reported exploratory biomarker data from the SER-155 Phase 1b study showing evidence of improved intestinal epithelial barrier integrity and modulation of systemic inflammatory responses. The results are consistent with SER-155's intended therapeutic mechanisms to reduce the r
In line with recent FDA feedback, Seres expects to submit a Phase 2 study protocol to FDA in the coming weeks for SER-155 for the prevention of bloodstream infections (BSIs) in adults undergoing allogeneic hematopoietic stem cell transplant (allo-HSCT) for the treatment of hematological malignancies SER-155 Phase 1b placebo-controlled study exploratory translational biomarker data reinforce intended mechanisms of action, consistent with clinical results that showed a significant reduction (77% relative risk reduction) in BSIs, and support broader potential for Seres' live biotherapeutics to address inflammatory and immune diseases Seres advancing SER-155 strategic partnership discussions i
CAMBRIDGE, Mass., April 29, 2025 (GLOBE NEWSWIRE) -- Seres Therapeutics, Inc. (NASDAQ:MCRB), a leading live biotherapeutics company, today announced that it will present three related posters at the upcoming 2025 Digestive Disease Week (DDW) Conference being held May 3-6, 2025, in San Diego, CA. Seres previously reported exploratory translational biomarker data from its SER-155 Phase 1b study, which provided evidence supporting the intended therapeutic mechanisms. These included promoting intestinal epithelial barrier integrity to reduce the translocation of bacteria and inflammatory bacterial products into the bloodstream, as well as modulating systemic inflammatory responses. New resu
For Immediate Release: April 26, 2023 Today, the U.S. Food and Drug Administration approved Vowst, the first fecal microbiota product that is taken orally. Vowst is approved for the prevention of recurrence of Clostridioides difficile (C. difficile) infection (CDI) in individuals 18 years of age and older, following antibacterial treatment for recurrent CDI. “Today’s approval provides patients and healthcare p
4 - Seres Therapeutics, Inc. (0001609809) (Issuer)
4 - Seres Therapeutics, Inc. (0001609809) (Issuer)
4 - Seres Therapeutics, Inc. (0001609809) (Issuer)