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Senti Biosciences

Gene medicines whose dose can be tuned after treatment

Raised to date

$10M

of $40M offered across 1 Form D filing

Still open
$30M
Investors
1
Last filed
Jun 4, 2026

About

Senti Biosciences Holdings is a clinical-stage biopharmaceutical company in South San Francisco, California, traded on Nasdaq as SNTI, that engineers synthetic biology into cell and gene therapies. Its original Gene Circuit platform builds proprietary DNA logic into therapeutic cells so they sense their environment, compute a decision, and kill cancer cells while sparing healthy tissue, applied in both NK and T cells. In July 2026 the company announced a strategic transaction transferring its gene-circuit-enabled pipeline, including the lead allogeneic NK cell therapy SENTI-202 for acute myeloid leukemia, to a newly formed private company controlled by its largest investor Celadon, with up to $60 million in milestone payments flowing back to Senti stockholders. Senti is now refocused on its earlier-stage Regulator Dial platform for controllable genetic medicines. It was co-founded in 2016 and is led by CEO Timothy Lu, M.D., Ph.D., a former tenured MIT faculty member in biological and electrical engineering.

Regulator Dial combines synthetic biology with AI to give clinicians dynamic control over a genetic medicine after it has been administered - dialing expression up or down in the patient - addressing the one-way, irreversible dosing that constrains conventional gene and cell therapy.

Funding

  • DebtFiled Jun 4, 2026Form D
    $10M/ $40M

Product

Regulator Dial platform

Genetic medicine platform

A proprietary technology platform integrating synthetic biology and AI to enable dynamic, post-administration control of genetic medicines, letting the expression of a delivered therapy be tuned after it is already in the patient. It is the company's go-forward focus following the July 2026 spin-out of the gene-circuit pipeline.

  • Post-administration control of therapeutic gene expression
  • Synthetic biology circuits combined with AI-guided design
  • Applicable across gene therapy and engineered cell therapy modalities

Built for

Patients with hematologic and solid tumor cancers and monogenic disorders such as Rett syndrome, reached through clinical development, biopharma partnerships and eventual prescribers

People on file