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Seres Therapeutics to Participate in 2025 J.P. Morgan Healthcare Conference

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Seres Therapeutics (MCRB) announced its participation in the 43rd Annual J.P. Morgan Healthcare Conference, where CEO Eric Shaff will present on January 16, 2025. The presentation will focus on the company's biotherapeutics pipeline, particularly SER-155, which recently received FDA Breakthrough Therapy designation for reducing bloodstream infections in adults undergoing allogeneic hematopoietic stem cell transplant.

The Phase 1b study results showed SER-155 achieved a 77% relative risk reduction in bloodstream infections, significant reduction in antibiotic exposure, and lower febrile neutropenia incidence. Seres is actively seeking partners to explore SER-155's development for additional vulnerable populations, including autologous-HSCT patients, cancer patients, CAR-T recipients, and others.

Seres Therapeutics (MCRB) ha annunciato la sua partecipazione alla 43陋 Conferenza Sanitaria Annuale J.P. Morgan, dove il CEO Eric Shaff presenter脿 il 16 gennaio 2025. La presentazione si concentrer脿 sul pipeline di bioterapici dell'azienda, in particolare su SER-155, che ha recentemente ricevuto la designazione di Terapia Innovativa da parte della FDA per ridurre le infezioni del flusso sanguigno negli adulti sottoposti a trapianto di cellule staminali ematopoietiche allogeniche.

I risultati dello studio di Fase 1b hanno dimostrato che SER-155 ha raggiunto una riduzione relativa del rischio del 77% nelle infezioni del flusso sanguigno, una significativa riduzione dell'esposizione agli antibiotici e una minore incidenza di neutropenia febbrile. Seres sta attivamente cercando partner per esplorare lo sviluppo di SER-155 per ulteriori popolazioni vulnerabili, inclusi pazienti sottoposti a HSCT autologo, pazienti oncologici, riceventi di CAR-T e altri.

Seres Therapeutics (MCRB) anunci贸 su participaci贸n en la 43陋 Conferencia Anual de Salud J.P. Morgan, donde el CEO Eric Shaff presentar谩 el 16 de enero de 2025. La presentaci贸n se centrar谩 en la l铆nea de bioterap茅uticos de la compa帽铆a, especialmente en SER-155, que recientemente recibi贸 la designaci贸n de Terapia Innovadora por parte de la FDA para reducir las infecciones en el torrente sangu铆neo en adultos que se someten a un trasplante de c茅lulas madre hematopoy茅ticas alog茅nicas.

Los resultados del estudio de Fase 1b mostraron que SER-155 logr贸 una reducci贸n del riesgo relativo del 77% en infecciones en el torrente sangu铆neo, una reducci贸n significativa en la exposici贸n a antibi贸ticos y una menor incidencia de neutropenia febril. Seres est谩 buscando activamente socios para explorar el desarrollo de SER-155 para poblaciones vulnerables adicionales, incluidos pacientes de HSCT aut贸logo, pacientes con c谩ncer, receptores de CAR-T y otros.

Seres Therapeutics (MCRB)電 鞝43須 J.P. Morgan 項姢旒鞏 旎嵓霟办姢鞐 彀胳棳頃滊嫟瓿 氚滍憸頄堨溂氅, CEO 鞐愲Ν 靸ろ攧臧 2025雲 1鞗 16鞚检棎 氚滍憸頃 鞓堨爼鞚措嫟. 鞚 氚滍憸電 須岇偓鞚 靸濍旃橂鞝 韺岇澊頂勲澕鞚, 韸鬼瀳 SER-155鞐 齑堨爯鞚 毵烄稖 瓴冹澊氅, 鞚措姅 斓滉芳 FDA 順侅嫚 旃橂鞝 歆鞝鞚 氚涭晞 鞎岆瓴愳爜 臁绊槇 欷勱赴 靹疙彫 鞚挫嫕鞚 氚涬姅 靹膘澑鞚 順堧 臧愳椉鞚 欷勳澊電 雿 霃勳泙鞚 欷雼.

1b靸 鞐瓣惮 瓴瓣臣鞐 霐半ゴ氅 SER-155電 順堧 臧愳椉鞐愳劀 77% 靸侂寑鞝 鞙勴棙 臧愳唽毳 雼劚頄堨溂氅, 頃儩鞝 雲胳稖鞚 靸侂嫻頃 臧愳唽鞕 氚滌棿靹 順胳甑 臧愳唽歃濎潣 氚滌儩毳 臧愳唽毳 氤挫榾雼. Seres電 鞛愱皜 HSCT 頇橃瀽, 鞎 頇橃瀽, CAR-T 靾橅槣鞛 霌 於旉皜鞝侅澑 旆暯頃 鞚戈惮 歆戨嫧鞚 鞙勴暅 SER-155鞚 臧滊皽鞚 韮愳儔頃橁赴 鞙勴暣 鞝侁饭鞝侅溂搿 韺岉姼雱堧ゼ 彀娟碃 鞛堧嫟.

Seres Therapeutics (MCRB) a annonc茅 sa participation 脿 la 43e Conf茅rence annuelle sur la sant茅 J.P. Morgan, o霉 le PDG Eric Shaff pr茅sentera le 16 janvier 2025. La pr茅sentation mettra l'accent sur le pipeline de bioth茅rapeutiques de l'entreprise, en particulier SER-155, qui a r茅cemment re莽u la d茅signation de th茅rapie innovante par la FDA pour r茅duire les infections sanguines chez les adultes subissant une greffe de cellules souches h茅matopo茂茅tiques allog茅niques.

Les r茅sultats de l'茅tude de phase 1b ont montr茅 que SER-155 a atteint une r茅duction du risque relatif de 77% des infections sanguines, une r茅duction significative de l'exposition aux antibiotiques et une incidence plus faible de neutrop茅nie f茅brile. Seres recherche activement des partenaires pour explorer le d茅veloppement de SER-155 pour d'autres populations vuln茅rables, y compris les patients ayant subi une HSCT autologue, les patients atteints de cancer, les receveurs de CAR-T et d'autres.

Seres Therapeutics (MCRB) gab die Teilnahme an der 43. j盲hrlichen J.P. Morgan Healthcare-Konferenz bekannt, bei der CEO Eric Shaff am 16. Januar 2025 einen Vortrag halten wird. Die Pr盲sentation wird sich auf die Biotherapeutika-Pipeline des Unternehmens konzentrieren, insbesondere auf SER-155, das k眉rzlich von der FDA die Breakthrough-Therapie-Bezeichnung erhalten hat, um Blutstrominfektionen bei Erwachsenen, die sich einer allogenen h盲matopoetischen Stammzelltransplantation unterziehen, zu reduzieren.

Die Ergebnisse der Phase 1b-Studie zeigten, dass SER-155 eine 77% relative Risikominderung bei Blutstrominfektionen erreichte, eine signifikante Reduzierung der Antibiotikaexposition und eine geringere Inzidenz von febriler Neutropenie. Seres sucht aktiv nach Partnern, um die Entwicklung von SER-155 f眉r weitere gef盲hrdete Bev枚lkerungsgruppen zu erkunden, einschlie脽lich Patienten mit autologischer HSCT, Krebspatienten, CAR-T-Empf盲ngern und anderen.

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CAMBRIDGE, Mass., Dec. 16, 2024 (GLOBE NEWSWIRE) -- Seres Therapeutics, Inc. (Nasdaq: MCRB), a leading live biotherapeutics company, today announced that management will participate in the 43rd Annual J.P. Morgan Healthcare Conference. Eric Shaff, President and Chief Executive Officer, will present a corporate overview on January 16, 2025 at 7:30 a.m. PT.

Seres will highlight its plans to advance its biotherapeutics pipeline, focusing on SER-155, the Company鈥檚 lead program. The Company recently announced that SER-155 received Breakthrough Therapy designation for the reduction of bloodstream infections (BSIs) in adults undergoing allogeneic hematopoietic stem cell transplant, to treat hematological malignancies, from the US Food and Drug Administration聽(FDA). This designation was supported by Phase 1b placebo-controlled study results in patients undergoing allo-HSCT demonstrating that SER-155 was associated with a significant reduction in BSIs (77% relative risk reduction), a significant reduction in systemic antibiotic exposure, and lower incidence of febrile neutropenia. In addition to allo-HSCT, bloodstream infections are a common and serious complication in many other medically vulnerable populations, including autologous-HSCT patients, cancer patients with neutropenia, CAR-T recipients, individuals with chronic liver disease, solid organ transplant recipients, as well as patients in the intensive care unit and long-term acute care facilities. Seres is actively seeking a partner to provide financial resources and other capabilities to more fully explore the development of SER-155 and additional pipeline candidates for these populations.

A live video webcast of the presentation will be accessible under the 鈥淓vents and Presentations鈥 tab on the 鈥淚nvestors and News鈥 section of the Company鈥檚 website at www.serestherapeutics.com聽and will be available for replay following the event.

About聽Seres Therapeutics
Seres Therapeutics, Inc.聽(Nasdaq: MCRB) is a clinical-stage company focused on improving patient outcomes in medically vulnerable populations through novel live biotherapeutics. Seres led the successful development and approval of VOWST鈩, the first FDA-approved orally administered microbiome therapeutic, which was sold to Nestl茅 Health Science in聽September 2024. The Company is developing SER-155, which has received both Breakthrough Therapy and Fast Track designation, and which has demonstrated a significant reduction in bloodstream infections and related complications (as compared to placebo) in a clinical study in patients undergoing allo-HSCT. SER-155 and the Company's other pipeline programs are designed to target multiple disease-relevant pathways and are manufactured from standard clonal cell banks via cultivation, rather than from the donor-sourced production process used for VOWST. In addition to allo-HSCT, the Company intends to evaluate SER-155 and other cultivated live biotherapeutic candidates in other medically vulnerable patient populations including autologous-HSCT patients, cancer patients with neutropenia, CAR-T recipients, individuals with chronic liver disease, solid organ transplant recipients, as well as patients in the intensive care unit and long-term acute care facilities. For more information, please visit聽.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including statements about: our clinical development plans; the ability for SER-155 and other product candidates to improve patient outcomes in medically vulnerable populations; our ability to secure a partnership and/or generate additional capital; and other statements which are not historical fact.

These forward-looking statements are based on management鈥檚 current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: (1) we have incurred significant losses, are not currently profitable and may never become profitable; (2) our need for additional funding; (3) our history of operating losses; (4) our novel approach to therapeutic intervention; (5) our reliance on third parties to conduct our clinical trials and manufacture our product candidates; (6) the competition we will face; (7) our ability to protect our intellectual property; (8) our ability to retain key personnel and to manage our growth; (9) the effect of the VOWST sale on our ability to retain and hire key personnel and maintain relationships with our customers, suppliers, advertisers, partners and others with whom we do business, or on our operating results and businesses generally途 (10) the risks associated with the disruption of management鈥檚 attention from ongoing business operations due to the obligation to provide transition services途 (11) our failure to receive the installment payments or the milestone payments in the future途 (12) the uncertainty of impact of the 50/50 profit and loss sharing arrangement on our reported results and liquidity; and (13) we may not be able to realize the anticipated benefits of the VOWST sale. These and other important factors discussed under the caption 鈥淩isk Factors鈥 in our Quarterly Report on Form 10-Q filed with the聽Securities and Exchange Commission聽(SEC), on聽November 13, 2024, and our other reports filed with the聽SEC聽could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management鈥檚 estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.

Investor and Media Contacts:

Carlo Tanzi, Ph.D.
Kendall Investor Relations
ctanzi@kendallir.com


FAQ

What results did SER-155 show in Seres Therapeutics' Phase 1b study for MCRB?

SER-155 demonstrated a 77% relative risk reduction in bloodstream infections, significant reduction in systemic antibiotic exposure, and lower incidence of febrile neutropenia in patients undergoing allogeneic hematopoietic stem cell transplant.

When will Seres Therapeutics (MCRB) present at the J.P. Morgan Healthcare Conference 2025?

Seres Therapeutics will present on January 16, 2025, at 7:30 a.m. PT during the 43rd Annual J.P. Morgan Healthcare Conference.

What breakthrough designation did MCRB's SER-155 receive from the FDA?

SER-155 received FDA Breakthrough Therapy designation for reducing bloodstream infections in adults undergoing allogeneic hematopoietic stem cell transplant to treat hematological malignancies.

What additional patient populations could benefit from MCRB's SER-155 treatment?

Additional potential populations include autologous-HSCT patients, cancer patients with neutropenia, CAR-T recipients, individuals with chronic liver disease, solid organ transplant recipients, and patients in intensive care and long-term acute care facilities.

What is Seres Therapeutics (MCRB) seeking regarding SER-155 development?

Seres is actively seeking partners to provide financial resources and capabilities to explore SER-155's development and additional pipeline candidates for various vulnerable populations.

Seres Therapeutics, Inc.

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Biotechnology
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