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Sangamo Therapeutics (SGMO) investor relations material
Sangamo Therapeutics Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Advanced clinical and preclinical pipeline in Fabry disease, chronic neuropathic pain, and prion disease, with first neurology clinical study patient recruitment and enrollment.
Fabry disease program (ST-920) achieved positive registrational data, with durable kidney and cardiac outcomes, and is on a clear path to potential accelerated approval.
Productive regulatory interactions with FDA and MHRA for Fabry and prion disease programs, with FDA reaffirming eGFR slope as endpoint.
Neurology pipeline includes ST-503 (chronic neuropathic pain, Phase 1/2 trial initiated) and ST-506 (prion disease, CTA submission expected mid-2026).
Ongoing business development efforts to secure Fabry commercialization partner and advance industry partnerships.
Financial highlights
Q3 2025 net loss of $34.9 million, or $0.11 per share; nine-month net loss of $85.5 million.
Revenues for Q3 2025 were $0.6 million, down sharply from $49.4 million in Q3 2024, mainly due to prior year Genentech collaboration revenue.
Cash and cash equivalents as of September 30, 2025: $29.6 million, with $6 million from Pfizer and $9.1 million from at-the-market offering received after quarter-end.
Non-GAAP operating expenses for Q3 2025 were $33.0 million; GAAP OpEx was $36.1 million.
Up to $5.9 billion in potential future milestones and exercise fees from partnerships.
Outlook and guidance
Cash runway expected to fund operations into Q1 2026, including recent Pfizer license fee and stock sale proceeds, but additional capital is required.
Preparing for a BLA submission for Fabry disease gene therapy as early as Q1 2026, contingent on funding and regulatory agreement.
Prion disease CTA submission expected as early as mid-2026; preliminary clinical data for neurology programs anticipated from early 2027.
2025 GAAP operating expenses expected to be $135–$155 million; non-GAAP OpEx expected at $125–$145 million.
Actively seeking new capital through equity, debt, and strategic collaborations.
- Genentech deal and strong clinical results drive funding, but cash runway ends Q1 2025.SGMO
Q2 20242 Feb 2026 - Genentech deal, Fabry fast track, and clinical wins drive Q3 profit, but funding risk persists.SGMO
Q3 202414 Jan 2026 - Pipeline advances and partnerships drive progress, but urgent funding needed by mid-2025.SGMO
Q4 202426 Dec 2025 - Up to $500M in securities offered, with $194.5M in common stock via Jefferies at-the-market.SGMO
Registration Filing16 Dec 2025 - Board seeks approval for director elections, equity plan amendment, and auditor ratification.SGMO
Proxy Filing1 Dec 2025 - Fabry and Hemophilia A BLAs advance, with Nav1.7 gene therapy entering clinic in 2024.SGMO
Barclays 27th Annual Global Healthcare Conference 202525 Nov 2025 - Fabry program advances, but urgent capital and partnership needs threaten operations past Q4 2025.SGMO
Q2 202524 Nov 2025 - Lilly deal, pipeline progress, and cost cuts extend cash runway to late Q3 2025, but funding risks remain.SGMO
Q1 202517 Nov 2025 - Neurology-focused genomic medicines advance with strong clinical and financial momentum.SGMO
Corporate Presentation6 Nov 2025
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