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Senti Biosciences Participates in Virtual Investor CEO Connect Segment to Discuss the Company’s Groundbreaking AML Data at the American Society of Hematology Annual Meeting and Recently Granted RMAT Designation

Key Takeaway: Senti Biosciences participated in a Virtual Investor CEO Connect Segment, where CEO Timothy Lu discussed the FDA's granting of RMAT designation to SENTI-202, a CAR-NK cell therapy. This investigational therapy is aimed at treating relapsed/refractory AML and builds on previous Orphan Drug Designation. Recent clinical trial data from 20 patients was also shared at the ASH Annual Meeting.
Price reaction · baseline $1.1 (2026-01-14 close) · hit pre-market · clean, no other SNTI news in the window
day 0 close · peak
-3.6%

Market Sentiment Analysis

POSITIVE FACTORS

  • Senti Biosciences received RMAT designation for SENTI-202.
  • Promising data from clinical trials presented at ASH Annual Meeting.
  • Senti Bio is advancing innovative therapies for hematologic malignancies.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+84%
120-day peak, hindsight
Typical move
76.7%
average across 4 past catalysts
Cash runway
~5 mo
High dilution risk
Lead asset
SENTI-202
Phase 1 · AML/MDS

Full Press Release Details

Access the segmenthere
SOUTH SAN FRANCISCO, Calif., Jan. 14, 2026 (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 aVirtual Investor CEO Connect Segment.
As part of the segment,Timothy Lu, MD, PhD, CEOof Senti, discussed itsrecent news releaseannouncing that the U.S. Food and Drug Administration (FDA) granted Regenerative Medicine Advanced Therapy (RMAT) designation to SENTI-202, the Company’s potential first-in-class Logic Gated off-the-shelf chimeric antigen receptor natural killer (CAR-NK) investigational cell therapy, that is currently in development for the treatment of relapsed/refractory hematologic malignancies, including AML. The RMAT designation builds on the Orphan Drug Designation that the FDA granted SENTI-202 in June. Dr. Lu also discussed the new data from 20 patients (18 with evaluable responses) in its ongoing multinational, multicenter clinical trial of SENTI-202 in patients with relapsed or refractory AML that were recently presented at the American Society of Hematology (ASH) Annual Meeting in Orlando.
About Senti BioSenti 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 comprises 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.
Availability of Other Information About Senti BioFor more information, please visit the Senti Bio website at https://www.sentibio.com or follow Senti Bio on X (formerly Twitter) (@SentiBio) and LinkedIn (Senti Biosciences). Investors and others should note that we communicate with our investors and the public using our company website (www.sentibio.com), 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 X and LinkedIn. The information that we post on our website or on X or LinkedIn 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.

Senti Bio Contacts:Investors:investors@sentibio.comMedia:media@sentibio.com

Investor Contact:Jenene ThomasChief Executive OfficerJTC Team, LLCT: 908.824.0775snti@jtcir.com

Frequently Asked Questions

What is SENTI-202?

SENTI-202 is an investigational CAR-NK cell therapy developed by Senti Biosciences for treating relapsed/refractory AML.

What designation did the FDA grant to SENTI-202?

The FDA granted Regenerative Medicine Advanced Therapy (RMAT) designation to SENTI-202.

Where was the new data on SENTI-202 presented?

The new data on SENTI-202 was presented at the American Society of Hematology Annual Meeting.

How many patients were involved in the clinical trial data shared?

The clinical trial data shared involved 20 patients, with 18 having evaluable responses.

Last updated: Jan 15, 2026