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Senti Bio Participates in Virtual Investor “What This Means� Segment Discussing The Phase 2 Dose and Schedule Selection for SENTI-202 in its Clinical Trial for Acute Myeloid Leukemia

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Senti Biosciences (NASDAQ:SNTI) participated in a Virtual Investor segment to discuss the Phase 2 dose selection for SENTI-202, their Logic Gated off-the-shelf CAR-NK cell therapy. The presentation was led by Dr. Kanya Rajangam, President, Head of R&D and Chief Medical Officer.

SENTI-202 is being developed as a potential first-in-class treatment for relapsed/refractory hematologic malignancies, including acute myeloid leukemia (AML). The discussion focused on the recently announced recommended Phase 2 dosing schedule for the clinical trial.

Senti Biosciences (NASDAQ:SNTI) ha partecipato a un segmento Virtual Investor per discutere la selezione del dosaggio per la Fase 2 di SENTI-202, la loro terapia cellulare CAR-NK 'Logic Gated' pronta all'uso. La presentazione è stata condotta da Dr. Kanya Rajangam, Presidente, Responsabile R&S e Direttore Medico.

SENTI-202 è in sviluppo come possibile trattamento first-in-class per le malattie ematologiche recidivanti/refrattarie, inclusa la leucemia mieloide acuta (LMA). La discussione si è concentrata sul regime posologico raccomandato per la Fase 2, annunciato di recente.

Senti Biosciences (NASDAQ:SNTI) participó en un segmento Virtual Investor para abordar la selección de dosis de fase 2 de SENTI-202, su terapia celular CAR-NK 'Logic Gated' lista para usar. La presentación estuvo a cargo de Dr. Kanya Rajangam, Presidente, Jefe de I&D y Director Médico.

SENTI-202 se está desarrollando como un posible tratamiento first-in-class para las neoplasias hematológicas en recaída/refractarias, incluida la leucemia mieloide aguda (LMA). La discusión se centró en el esquema posológico recomendado para la Fase 2, anunciado recientemente.

Senti Biosciences (NASDAQ:SNTI)가 Virtual Investor 세션� 참여� SENTI-202� 2� 투여� 선정� 대� 논의했습니다. 해당 'Logic Gated' 즉시 사용 가능한 CAR‑NK 세포 치료제의 발표� Dr. Kanya Rajangam (President, Head of R&D � Chief Medical Officer)� 진행했습니다.

SENTI-202� 급성 골수� 백혈�(AML)� 포함� 재발/불응� 혈액�� 대� 잠재� first-in-class 치료법으� 개발 중입니다. 논의� 최근 발표� 2� 권고 투여 스케줄에 초점� 맞췄습니�.

Senti Biosciences (NASDAQ:SNTI) a participé à un segment Virtual Investor pour discuter de la sélection de dose de Phase 2 pour SENTI-202, sa thérapie cellulaire CAR‑NK 'Logic Gated' prête à l'emploi (off‑the‑shelf). La présentation a été menée par Dr. Kanya Rajangam, President, Head of R&D et Chief Medical Officer.

SENTI-202 est en cours de développement comme traitement potentiellement first‑in‑class pour les malignités hématologiques en rechute/réfractaires, y compris la leucémie myéloïde aiguë (LMA). La discussion a porté sur le calendrier posologique recommandé pour la Phase 2, annoncé récemment.

Senti Biosciences (NASDAQ:SNTI) nahm an einem Virtual Investor‑Segment teil, um die Dosiswahl für die Phase�2‑Studie von SENTI-202 zu besprechen, ihrer 'Logic Gated' Off‑the‑Shelf CAR‑NK‑Zelltherapie. Die Präsentation wurde von Dr. Kanya Rajangam, President, Head of R&D und Chief Medical Officer, geleitet.

SENTI-202 wird als potenzielle First‑in‑Class‑Behandlung für rezidivierte/refraktäre hämatologische Malignome, einschließlich akuter myeloischer Leukämie (AML), entwickelt. Die Diskussion konzentrierte sich auf den kürzlich bekannt gegebenen empfohlenen Dosierungsplan für Phase 2.

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SOUTH SAN FRANCISCO, Calif., Aug. 12, 2025 (GLOBE NEWSWIRE) -- Senti Biosciences, Inc. (Nasdaq: SNTI) (“Senti Bio�), a clinical-stage biotechnology company developing next-generation cell and gene therapies using its proprietary Gene Circuit platform, today announced that it participated in a .

For the segment,  of Senti, discussed the Company’s recently announced recommended Phase 2 dose selection for its potential first-in-class Logic Gated off-the-shelf chimeric antigen receptor natural killer (CAR-NK) cell therapy, SENTI-202, in development for the treatment of relapsed/refractory hematologic malignancies including acute myeloid leukemia (AML).

The “What This Means� segment can be accessed .

About Senti Bio

Senti Bio is a biotechnology company developing a new generation of cell and gene therapies for patients living with incurable diseases. To achieve this, Senti Bio is leveraging its synthetic biology platform to engineer Gene Circuits into new medicines with enhanced precision and control. These Gene Circuits are designed to precisely kill cancer cells, to spare healthy cells, to increase specificity to target tissues, and/or to be controllable even after administration. The Company’s wholly-owned pipeline is comprised of cell therapies engineered with Gene Circuits to target challenging liquid and solid tumor indications. Senti’s Gene Circuits have been shown preclinically to work in both NK and T cells. Senti Bio has also preclinically demonstrated the potential breadth of Gene Circuits in other modalities and diseases outside of oncology, and continues to advance these capabilities through partnerships.

Forward-Looking Statements

This press release and document contain certain statements that are not historical facts and are considered forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements generally are identified by the words “believe,� “could,� “predict,� “continue,� “ongoing,� “project,� “expect,� “anticipate,� “estimate,� “intend,� “strategy,� “future,� “opportunity,� “plan,� “may,� “should,� “will,� “would,� “will be,� “will continue,� “will likely result,� “forecast,� “seek,� “target� and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. Forward-looking statements are predictions, projections, and other statements about future events that are based on current expectations of Senti Bio’s management and assumptions, whether or not identified in this document, and, as a result, are subject to risks and uncertainties. Forward-looking statements include, but are not limited to, expectations regarding Senti Bio’s growth, strategy, progress and timing of its clinical trials for SENTI-202;the timing of availability of data from the ongoing Phase 1 clinical trial of SENTI-202; the ability of any product candidate to perform in humans in a manner consistent with nonclinical, preclinical or previous clinical study data; expectations regarding the anticipated dosing of patients and availability of data from clinical trials, and the timing thereof. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as and must not be relied on by any investor as, a guarantee, an assurance, a prediction, or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and will differ from assumptions. Many actual events and circumstances are beyond the control of Senti Bio. Many factors could cause actual future results to differ materially from the forward-looking statements in this document, including but not limited to: (i) changes in domestic and foreign business, market, financial, political and legal conditions, (ii) changes in the competitive and highly regulated industries in which Senti Bio operates, variations in operating performance across competitors, changes in laws and regulations affecting Senti Bio’s business, (iii) the ability to implement business plans, forecasts and other expectations, (iv) the risk of downturns and a changing regulatory landscape in Senti Bio’s highly competitive industry, (v) risks relating to the uncertainty of any projected financial information with respect to Senti Bio, (vi) risks related to uncertainty in the timing or results of Senti Bio’s clinical trial start up, clinical studies, patient enrollment, and GMP manufacturing startup activities, (vii) Senti Bio’s dependence on third parties in connection with clinical trial startup, clinical studies, and GMP manufacturing activities, (viii) risks related to delays and other impacts from macroeconomic and geopolitical events, increasing rates of inflation and rising interest rates on business operations, (ix) risks related to the timing and utilization of the grant from CIRM, and (x) the success of any future research and development efforts by Senti Bio. The foregoing list of factors is not exhaustive. You should carefully consider the foregoing factors and the other risks and uncertainties described in the “Risk Factors� section of Senti Bio’s most recent periodic report filed with the U.S. Securities and Exchange Commission (“SEC�), and other documents filed by Senti Bio from time to time with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements in this document. There may be additional risks that Senti Bio does not presently know, or that Senti Bio currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements in this document. Forward-looking statements speak only as of the date they are made. Senti Bio anticipates that subsequent events and developments may cause Senti Bio’s assessments to change. Except as required by law, Senti Bio assumes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events, or otherwise.

Availability of Other Information About Senti Biosciences, Inc.

For more information, please visit the Senti Bio website at or follow Senti Bio on (@SentiBio) and (Senti Biosciences). Investors and others should note that we communicate with our investors and the public using our company website (), including, but not limited to, company disclosures, investor presentations and FAQs, Securities and Exchange Commission filings, press releases, public conference call transcripts and webcast transcripts, as well as on and . The information that we post on our website or on or could be deemed to be material information. As a result, we encourage investors, the media and others interested to review the information that we post there on a regular basis. The contents of our website or social media shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended.

Investor Contact:
JTC Team, LLC
Jenene Thomas
(908) 824-0775


FAQ

What is SENTI-202 and what is it being developed for?

SENTI-202 is a Logic Gated off-the-shelf CAR-NK cell therapy being developed as a potential first-in-class treatment for relapsed/refractory hematologic malignancies, including acute myeloid leukemia (AML).

Who presented Senti Biosciences' (SNTI) Phase 2 dose selection update?

Dr. Kanya Rajangam, President, Head of Research & Development and Chief Medical Officer of Senti Bio, presented the Phase 2 dose selection update.

What type of technology platform does Senti Biosciences use?

Senti Biosciences uses its proprietary Gene Circuit platform for developing next-generation cell and gene therapies.

What stage of development is SENTI-202 currently in?

SENTI-202 has reached the Phase 2 clinical trial stage, where the recommended dose and schedule have been recently selected for treating hematologic malignancies.
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Biotechnology
Biological Products, (no Disgnostic Substances)
United States
SOUTH SAN FRANCISCO