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Precision BioSciences (DTIL) investor relations material
Precision BioSciences Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Report covers the quarter ended September 30, 2025, for a clinical-stage gene editing company focused on in vivo therapies using the ARCUS platform.
Key programs include PBGENE-HBV (Hepatitis B) in Phase 1 and PBGENE-DMD (Duchenne muscular dystrophy) preparing for IND filing, with new clinical and preclinical data presented.
Initiated dosing in Cohort 3 of the ELIMINATE-B Phase 1 trial for chronic hepatitis B, with additional data readouts planned for early 2026.
Novartis terminated its collaboration agreement effective January 2026; milestone payment received from Imugene.
Cost reduction initiatives and operating efficiencies implemented in Q3 2025 to extend cash runway into the second half of 2027.
Financial highlights
Revenue for Q3 2025 was $13,000, down from $576,000 in Q3 2024; nine-month revenue was $60,000, down from $68.1 million in 2024, mainly due to prior period milestone and license revenue.
Net loss for Q3 2025 was $21.8 million ($1.84 per share), compared to $16.4 million ($2.25 per share) in Q3 2024; nine-month net loss was $65.9 million.
Operating expenses for Q3 2025 were $20.7 million, down slightly from $21.9 million in Q3 2024.
Cash, cash equivalents, and restricted cash totaled $71.2 million as of September 30, 2025, compared to $121.3 million a year earlier.
Accumulated deficit reached $548.3 million as of September 30, 2025.
Outlook and guidance
Cash runway expected to fund operations into the second half of 2027, supporting potential Phase 2 for PBGENE-HBV and pivotal study for PBGENE-DMD.
Phase 1 initiation for PBGENE-DMD anticipated in H1 2026, with initial data expected in H2 2026.
Additional data readouts for PBGENE-HBV planned in early 2026.
Data from the OTC-HOPE trial (partnered program) expected in H1 2026.
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