Ownership
Public
Employees
~354
Therapeutic Areas
HematologyRare DiseasesNeurology
Stage
Phase 3
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Modalities
Gene therapy (AAV-based gene transfer)Genome editing (Zinc Finger Nucleases - ZFN)Epigenetic regulation (Zinc Finger Protein Transcription Factors - ZFP-TF)

Sangamo Therapeutics General Information

Sangamo is a pioneer in genomic medicine using proprietary zinc finger technology platforms. Its lead wholly owned programs target serious neurological and rare genetic diseases. The company has advanced its neurology pipeline toward the clinic and secured major licensing deals with Genentech and Astellas for novel capsid delivery technologies. The Fabry disease program is on an accelerated regulatory path after positive Phase I/II data; a pivotal BLA submission is anticipated in the second half of 2025. An IND was cleared for ST‑503 in iSFN pain with first patient dosing expected mid‑2025. Nonclinical proof-of-concept was demonstrated in prion disease models.[6][8]

Contact Information

Primary Industry
Biotech
Corporate Office
Brisbane, California
United States

Drug Pipeline

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Drug Asset 2
Phase X
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Drug Asset 3
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Key Partnerships

Genentech/Roche – global epigenetic regulation & capsid delivery license agreement for neurodegenerative diseases[6], Astellas – capsid license agreement targeting up to five neurological indications[6], Previous or ongoing collaborations have included Pfizer, Biogen, Kite/Gilead, Lilly, Alexion, Takeda.[5][10]

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Sangamo Therapeutics Funding

Deal TypeDateAmountStatusStage
InvestmentFeb 4, 2026$25.0MCompletedPhase 3
Early Stage VC (Series A)04-Jun-2020$38MCompletedPhase 1
Seed Round12-Feb-2019$8.5MCompletedStartup

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Sangamo Therapeutics Financial Metrics

Market Cap
$91.8M
Total Revenue
$14.2M
Enterprise Value
$95.9M