DTIL
Precision BioSciences, Inc.4.8200
+0.0200+0.42%
Dec 16, 4:00:00 PM EST
Earnings Call Transcripts
This Quarter (Q1 '26)
No earnings call transcript available yet
Last Quarter (Q4 '25)
No earnings call transcript available
Key Stats
Market Cap
116.03MP/E (TTM)
-Basic EPS (TTM)
-8.96Dividend Yield
0%Recent Filings
8-K
PBGENE-DMD KOL event details
Precision BioSciences hosted a KOL event on March 17, 2026, detailing its PBGENE-DMD gene editing therapy for Duchenne muscular dystrophy, targeting 60% of patients via ARCUS excision of exons 45-55 to restore near full-length dystrophin. Preclinical data showed durable muscle function gains in DMD mice and strong NHP transduction; FUNCTION-DMD Phase 1/2 trial, post-FDA IND clearance, targets 3-5 patients with safety data and early efficacy by year-end. Initial data across multiple patients expected late 2026. Risks include clinical translation uncertainties.
8-K
Q4 profit, $137M cash
Precision BioSciences posted Q4 2025 net income of $20.1M on $34.2M revenue, versus $17.8M loss prior year, fueled by $26.2M Novartis termination and $8M Imugene milestone. Cash hit $137.2M after $75M November raise, funding runway through 2028 amid PBGENE-HBV dosing in 13 patients showing safety and antiviral activity. Data catalysts loom in 2026. Milestones drive momentum.
10-K
FY2025 results
Precision BioSciences posted a $45.7M net loss for FY2025 ended December 31, 2025, with revenue dropping to $34.3M from $68.7M in 2024 after Novartis terminated its hemoglobinopathy collaboration. R&D expenses fell 9% to $54.2M as PBGENE-HBV advanced to Phase 1/2a ELIMINATE-B with positive safety data from nine patients across 22 doses, while PBGENE-DMD gained FDA IND clearance for its Phase 1/2 FUNCTION-DMD trial targeting 60% of DMD patients. Q4 momentum built with $75M gross proceeds from a November equity offering, $8M Imugene milestone, and $7.5M TG Therapeutics payment, bolstering cash to $137M (sufficient through 2028). Debt stands at $22.5M under a secured term loan. Novartis termination reclaims ARCUS rights for hemoglobinopathies. Clinical trial delays threaten pipeline progress.
8-K
FDA clears PBGENE-DMD IND
Precision BioSciences secured FDA IND clearance for PBGENE-DMD on February 11, 2026, greenlighting site activation for the FUNCTION-DMD Phase 1/2 trial in DMD patients with exons 45-55 mutations, affecting 60% of cases. This wholly-owned in vivo gene editor aims to restore near full-length dystrophin via one-time therapy. First U.S. site activation targets first half of 2026. Trial risks loom large.
8-K
Cash runway to 2028
Precision BioSciences reports $137M in preliminary cash as of December 31, 2025, funding operations through 2028 amid clinical advances. ELIMINATE-B trial for PBGENE-HBV eyes biopsy data in H1 2026 and Part 2 expansion; FUNCTION-DMD Phase 1/2 dosing starts late Q1/early Q2 2026, with initial data by year-end. Cash bolsters key milestones. Audit ongoing, figures unaudited.
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