Intellia Therapeutics (NTLA) Q4 2025 earnings summary
Event summary combining transcript, slides, and related documents.
Q4 2025 earnings summary
8 Jul, 2026Executive summary
Achieved rapid enrollment in key phase 3 trials for ATTR amyloidosis (MAGNITUDE, MAGNITUDE-2) and hereditary angioedema (HAELO), with MAGNITUDE-2 resuming after FDA hold was lifted following protocol amendments.
Lonvo-z and Nex-z, both one-time gene-editing therapies, continue to show durable efficacy with no waning of effect up to three years in trials.
Strong patient and physician interest in lonvo-z, with market research indicating high likelihood of adoption if approved.
Commercial readiness efforts for lonvo-z are well underway, including field team expansion, payer engagement, and launch strategy development.
Addressed clinical holds on nex-z Phase 3 trials, with MAGNITUDE-2 hold lifted and enrollment resuming; MAGNITUDE trial for ATTR-CM remains on hold pending FDA alignment.
Financial highlights
Cash, cash equivalents, and marketable securities totaled $605.1 million as of December 31, 2025, down from $861.7 million a year prior.
Collaboration revenue for Q4 2025 was $23 million, up from $12.9 million in Q4 2024, driven by contract terminations and increased reimbursements.
R&D expenses decreased to $88.7 million in Q4 2025 from $116.9 million in Q4 2024, mainly due to lower employee and material costs.
Net loss for Q4 2025 was $95.8 million, a significant improvement from $128.9 million in the prior-year quarter; full-year net loss was $412.7 million versus $519.0 million in 2024.
Operating loss for Q4 2025 was $98.7 million, compared to $136.4 million in Q4 2024.
Outlook and guidance
Cash runway expected to extend into the second half of 2027, covering key milestones including MAGNITUDE-2 completion and lonvo-z launch.
Top-line data for lonvo-z in HAE expected mid-2026, with BLA submission planned for the second half of 2026 and U.S. launch targeted for first half of 2027.
MAGNITUDE-2 enrollment expected to complete in the second half of 2026; ongoing FDA engagement for MAGNITUDE trial.
Commercial launch preparations for lonvo-z continue, with focus on sales, reimbursement, and distribution infrastructure.
Latest events from Intellia Therapeutics
- Accelerated phase III progress in ATTR and HAE, with major data and milestones expected by 2027.NTLA
BofA Securities 2025 Healthcare Conference9 Jul 2026 - A single 50 mg dose achieved 81% attack reduction and 73% attack-free rate in HAE patients.NTLA
Study Update9 Jul 2026 - Late-stage pipeline progress, restructuring, and cash runway extend operational momentum into 2027.NTLA
Q4 20249 Jul 2026 - Nexi/nex-z achieved deep, durable TTR reduction and clinical stabilization in ATTR amyloidosis.NTLA
Study Update9 Jul 2026 - Strong CRISPR trial progress, $944.7M cash, Q3 net loss $135.7M, late-stage pipeline advancing.NTLA
Q3 20248 Jul 2026 - All proposals, including director elections and auditor ratification, were approved unanimously.NTLA
AGM 20269 Jun 2026 - Single-dose gene editing therapy delivers robust, durable HAE control with U.S. launch targeted for 2027.NTLA
Jefferies Global Healthcare Conference 20263 Jun 2026 - First phase III in vivo CRISPR trial completed, with strong HAE results and global TTR progress.NTLA
RBC Capital Markets Global Healthcare Conference 202620 May 2026 - Phase III data show superior efficacy for lonvo-z, with commercial launch targeted for next year.NTLA
Bank of America Global Healthcare Conference 202615 May 2026