Welcome to our dedicated page for Senti Bioscience news (Ticker: SNTI), a resource for investors and traders seeking the latest updates and insights on Senti Bioscience stock.
Senti Biosciences, Inc. (Senti Bio) (NASDAQ: SNTI) is a clinical-stage biotechnology company developing cell and gene therapies that incorporate engineered Gene Circuits. This news page aggregates company announcements, scientific updates, and corporate disclosures so readers can follow how Senti Bio advances its Gene Circuit platform and clinical programs over time.
A major focus of Senti Bio’s news flow is SENTI-202, its first-in-class Logic Gated off-the-shelf CAR-NK cell therapy product candidate. Company releases describe ongoing Phase 1 clinical evaluation of SENTI-202 in adults with relapsed or refractory CD33 and/or FLT3 expressing hematologic malignancies, including acute myeloid leukemia and myelodysplastic syndrome. Updates have highlighted clinical and pharmacodynamic data, presentations at the American Society of Hematology (ASH) Annual Meeting, and FDA designations such as Orphan Drug Designation and Regenerative Medicine Advanced Therapy (RMAT) designation.
Visitors can also expect news on Senti Bio’s participation in investor and scientific conferences, quarterly financial result announcements, and communications about its broader Gene Circuit platform. These items provide context on how the company positions its synthetic biology approach, preclinical work in NK and T cells, and efforts to explore Gene Circuits in other modalities and disease areas through partnerships.
For investors and observers tracking SNTI, this page offers a centralized view of press releases and related information, from clinical data readouts and regulatory milestones to corporate presentations. Checking this feed periodically can help users understand the evolution of Senti Bio’s pipeline and its activities within the cell and gene therapy landscape.
Senti Biosciences (Nasdaq: SNTI), a clinical-stage biotechnology company, participated in Nasdaq's Amplify Spotlight Series. CEO and Co-Founder Timothy Lu presented a corporate overview highlighting the company's proprietary Gene Circuit platform for developing next-generation cell and gene therapies.
The company's lead program, SENTI-202, is a first-in-class off-the-shelf CAR NK cell therapy targeting CD33 and/or FLT3-expressing hematologic malignancies, including AML and myelodysplastic syndrome (MDS). The therapy is currently in Phase 1 clinical trials and has shown positive preliminary data. Notably, SENTI-202 has received Orphan Drug Designation from the FDA for treating relapsed/refractory hematologic malignancies including AML.
Senti Biosciences (Nasdaq: SNTI), a clinical-stage biotechnology company focused on developing next-generation cell and gene therapies, will present at the 2025 SEED Conference in Houston, TX. The company's Co-Founder and CEO, Timothy Lu, MD, PhD, will deliver a presentation titled "Solving the Grand Challenge of Tumor-Specific Therapies with Logic-Gated Cells" on June 24, 2025 at 1:20 PM CT.
The SEED Conference, established in 2014, is a premier technical event for synthetic biology professionals that has attracted over 5,000 attendees since its inception. The conference serves as a platform for sharing research, networking, and discussing advances in synthetic biology.
Senti Biosciences (NASDAQ: SNTI), a clinical-stage biotechnology company focused on developing next-generation cell and gene therapies through its proprietary Gene Circuit platform, has announced an upcoming presentation. Timothy Lu, M.D., Ph.D., the company's Co-Founder and Chief Executive Officer, will present at the LIVE! with Webull Corporate Connect: Virtual Biotech Investment Webinar on Thursday, May 29, 2025, at 2:40 PM ET.
Senti Biosciences (NASDAQ: SNTI) has received an additional $1.0 million from the California Institute for Regenerative Medicine (CIRM) after achieving clinical study enrollment milestones. This brings the total received to $7.4 million of the $8.0 million grant supporting SENTI-202 development.
SENTI-202, a first-in-class Logic Gated off-the-shelf CAR-NK cell therapy, targets CD33 and/or FLT3-expressing hematologic malignancies while sparing healthy bone marrow cells. In its ongoing Phase 1 trial, preliminary results showed the therapy was well-tolerated with no dose-limiting toxicities. The preliminary recommended Phase 2 dose was set at 1.5 x 109 CAR NK cells.
Notable efficacy results include: 2 of 3 patients achieving composite Complete Remission (cCR) in the preliminary RP2D cohort, 5 of 7 patients achieving Overall Response Rate across all dose levels, and 4 of 4 cCR patients achieving MRD-negative status, with the longest response lasting 8+ months.
The trial showed SENTI-202 was well-tolerated with 4 out of 7 patients achieving composite Complete Remission (cCR). All cCR patients were MRD negative and maintained responses ranging from 4+ to 8+ months. The preliminary recommended Phase 2 dose was identified at 1.5 x 109 CAR NK cells.
Financial results for Q1 2025 showed cash and cash equivalents of $33.8 million. R&D expenses increased to $9.3 million from $8.8 million year-over-year, while G&A expenses decreased to $7.1 million from $7.5 million. The company reported a net loss of $14.1 million ($1.41 per share).
Senti Biosciences (NASDAQ: SNTI) has released a Virtual Investor segment featuring Dr. Kanya Rajangam, President, Head of R&D and Chief Medical Officer, discussing recently presented positive preliminary Phase 1 clinical trial data for SENTI-202 at AACR Annual Meeting 2025.
SENTI-202 is a pioneering off-the-shelf Logic Gated selective CD33 OR FLT3 NOT EMCN chimeric antigen receptor natural killer (CAR-NK) cell therapy being developed for treating relapsed/refractory hematologic malignancies, including acute myeloid leukemia (AML).