Earnings summaries and quarterly performance for Intellia Therapeutics.
Executive leadership at Intellia Therapeutics.
John Leonard
President and Chief Executive Officer
Birgit Schultes
Executive Vice President, Chief Scientific Officer
David Lebwohl
Executive Vice President, Chief Medical Officer
Edward Dulac
Executive Vice President, Chief Financial Officer and Treasurer
Eliana Clark
Executive Vice President, Chief Technology Officer
James Basta
Executive Vice President, General Counsel and Corporate Secretary
Board of directors at Intellia Therapeutics.
Research analysts who have asked questions during Intellia Therapeutics earnings calls.
Yanan Zhu
Wells Fargo Securities
6 questions for NTLA
Brian Cheng
JPMorgan Chase & Co.
5 questions for NTLA
Alec Stranahan
Bank of America
4 questions for NTLA
Joseph Thome
TD Cowen
4 questions for NTLA
Luca Issi
RBC Capital Markets
4 questions for NTLA
Silvan Tuerkcan
Citizens JMP
4 questions for NTLA
David Lebowitz
Citigroup Inc.
3 questions for NTLA
Jay Olson
Oppenheimer & Co. Inc.
3 questions for NTLA
Jonathan Miller
Evercore ISI
3 questions for NTLA
Maurice Raycroft
Jefferies Financial Group
3 questions for NTLA
Rick Bienkowski
Cantor Fitzgerald
3 questions for NTLA
William Pickering
Sanford C. Bernstein & Co.
3 questions for NTLA
Andy Chen
Wolfe Research, LLC
2 questions for NTLA
Emma
Piper Sandler
2 questions for NTLA
Huidong Wang
Barclays
2 questions for NTLA
Jack Allen
Robert W. Baird & Co.
2 questions for NTLA
Jake
Craig-Hallum Capital Group
2 questions for NTLA
Konstantinos Biliouris
BMO Capital Markets
2 questions for NTLA
Lidiya Rizova
Leerink Partners
2 questions for NTLA
Mani Foroohar
Leerink Partners
2 questions for NTLA
Mark
Stifel
2 questions for NTLA
Maury Raycroft
Jefferies
2 questions for NTLA
Mike
Northland Securities
2 questions for NTLA
Mitchell Kapoor
H.C. Wainwright & Co.
2 questions for NTLA
Myles Minter
William Blair & Company
2 questions for NTLA
Salveen Richter
Goldman Sachs
2 questions for NTLA
Shelby
RBC Capital Markets
2 questions for NTLA
Troy Langford
TD Cowen
2 questions for NTLA
Aaron
Bank of America Corporation
1 question for NTLA
Brandon Frith
Wolfe Research, LLC
1 question for NTLA
Cheng Li
Oppenheimer & Co. Inc.
1 question for NTLA
Dae Gon Ha
Stifel
1 question for NTLA
Farzin Haque
Jefferies
1 question for NTLA
Gena Wang
Barclays
1 question for NTLA
Hang Hu
Barclays
1 question for NTLA
Hannah Tran
Wolfe Research
1 question for NTLA
Joon Lee
Truist Securities
1 question for NTLA
Kostas Biliouris
BMO Capital Markets
1 question for NTLA
Liisa Bayko
Evercore ISI
1 question for NTLA
Lili Nsongo
iA Capital Markets
1 question for NTLA
Lut Ming Cheng
JPMorgan Chase & Co.
1 question for NTLA
Mark Aleynick
Goldman Sachs
1 question for NTLA
Matthew Guggenbiller
Bank of America
1 question for NTLA
Matthew Harrison
Bank of America
1 question for NTLA
Mehdi Goudarzi
Truist Securities
1 question for NTLA
Ry Forseth
Guggenheim Securities
1 question for NTLA
Terence Flynn
Morgan Stanley
1 question for NTLA
Whitney Ijem
Canaccord Genuity Inc.
1 question for NTLA
William Sanger
Leerink Partners
1 question for NTLA
Yuriy Slutskyy
BMO Capital Markets
1 question for NTLA
Recent press releases and 8-K filings for NTLA.
- Intellia Therapeutics reported $605.1 million in cash, cash equivalents, and marketable securities as of December 31, 2025, with a cash runway expected into the second half of 2027.
- For the fourth quarter of 2025, collaboration revenue increased to $23 million from $12.9 million in the prior year quarter, while net loss significantly decreased to $95.8 million from $128.9 million.
- The company anticipates top-line data for its lonvo-z Phase 3 HAELO trial for hereditary angioedema (HAE) by mid-2026, with a Biologics License Application (BLA) submission planned for the second half of 2026 and a potential launch in the first half of 2027.
- Enrollment for the Nex-z Phase 3 trials (MAGNITUDE and MAGNITUDE-2) for ATTR amyloidosis was suspended and subsequently placed on clinical hold by the FDA in October 2025 due to elevated liver transaminases and total bilirubin in a patient; the company expects to restart enrollment in MAGNITUDE and complete enrollment in MAGNITUDE-2 in 2026.
- Intellia Therapeutics reported a net loss of $95.8 million for Q4 2025, an improvement from $128.9 million in the prior-year quarter, with collaboration revenue increasing to $23 million for Q4 2025.
- As of December 31, 2025, the company held $605.1 million in cash, cash equivalents, and marketable securities, which is expected to fund operations into the second half of 2027.
- Enrollment for the lonvo-z HAELO Phase 3 clinical trial for hereditary angioedema (HAE) was completed in September 2025, with top-line data anticipated by mid-2026 and a Biologics License Application (BLA) submission planned for the second half of 2026.
- The FDA lifted the clinical hold on the MAGNITUDE-2 trial for nex-z (ATTR amyloidosis with polyneuropathy) in late January 2026, with enrollment expected to be completed in the second half of 2026, while discussions with the FDA regarding the MAGNITUDE trial (cardiomyopathy) are ongoing.
- Intellia Therapeutics reported a cash, cash equivalents, and marketable securities balance of $605.1 million as of December 31, 2025, and expects this to be sufficient to fund operations into the second half of 2027.
- The FDA lifted the clinical hold on the MAGNITUDE-2 trial for nex-z in ATTR amyloidosis (polyneuropathy) in late January 2026, with enrollment expected to complete in the second half of 2026; however, the hold on the larger MAGNITUDE trial (cardiomyopathy) remains ongoing.
- The HAELO phase 3 clinical trial for lonvo-z in hereditary angioedema (HAE) completed enrollment with 80 patients in September 2025, ahead of schedule, with top-line data expected by mid-2026 and a potential launch in 2027.
- For the fourth quarter of 2025, collaboration revenue increased to $23 million from $12.9 million in the prior-year quarter, and the net loss significantly decreased to $95.8 million from $128.9 million in Q4 2024.
- Intellia Therapeutics reported its fourth quarter and full-year 2025 financial results, showing an increased collaboration revenue and a reduced net loss compared to the prior year.
- The company ended 2025 with $605.1 million in cash, cash equivalents, and marketable securities, which is expected to fund operations into the second half of 2027.
- For its lonvo-z program for HAE, Intellia expects to report topline Phase 3 clinical data by mid-2026, with a Biologics License Application (BLA) submission planned for the second half of 2026 and an anticipated U.S. launch in the first half of 2027.
- Regarding its nex-z program, the FDA lifted the clinical hold on the MAGNITUDE-2 Phase 3 trial for ATTRv-PN, with enrollment completion expected in the second half of 2026. Engagement with the FDA is ongoing for the clinical hold on the MAGNITUDE Phase 3 trial for ATTR-CM.
| Metric | Q4 2024 | FY 2024 | Q4 2025 | FY 2025 |
|---|---|---|---|---|
| Collaboration Revenue ($USD Thousands) | 12,874 | 57,877 | 23,017 | 67,671 |
| R&D Expenses ($USD Thousands) | 116,877 | 466,311 | 88,652 | 388,861 |
| G&A Expenses ($USD Thousands) | 32,444 | 125,829 | 33,075 | 119,800 |
| Net Loss ($USD Thousands) | (128,898) | (519,021) | (95,786) | (412,694) |
| Cash, cash equivalents and marketable securities (as of period end) ($USD Thousands) | 861,730 | 861,730 | 605,134 | 605,134 |
- Intellia Therapeutics ended 2025 with approximately $605.1 million in cash, cash equivalents, and marketable securities, which is expected to fund operations into the second half of 2027.
- For the fourth quarter of 2025, the company reported collaboration revenue of $23.0 million and a net loss of $95.8 million.
- HAELO Phase 3 clinical data for lonvo-z in HAE is expected by mid-2026, with a Biologics License Application (BLA) submission planned for the second half of 2026 and an anticipated U.S. launch in the first half of 2027.
- The FDA lifted the clinical hold on the MAGNITUDE-2 Phase 3 trial for nex-z in ATTRv-PN on January 27, 2026, with enrollment completion expected in the second half of 2026; however, engagement with the FDA is ongoing to resolve the clinical hold on the MAGNITUDE Phase 3 trial for ATTR-CM.
- The FDA has removed the clinical hold on Intellia Therapeutics' Investigational New Drug application (IND) for the MAGNITUDE-2 Phase 3 clinical trial of nexiguran ziclumeran (nex-z) for patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN).
- Intellia plans to resume patient enrollment and dosing for the MAGNITUDE-2 trial, having aligned with the FDA on study modifications and enhanced safety monitoring of liver laboratory tests.
- The clinical holds on both MAGNITUDE and MAGNITUDE-2 were initially imposed on October 29, 2025, following the observation of Grade 4 liver transaminases and increased total bilirubin in a patient dosed with nex-z in the MAGNITUDE trial.
- Engagement with the FDA is ongoing regarding the clinical hold on the MAGNITUDE Phase 3 clinical trial for transthyretin amyloidosis with cardiomyopathy (ATTR-CM), with an update expected once alignment is achieved.
- Intellia Therapeutics' Lombozi program for hereditary angioedema (HAE) has completed enrollment for its Phase 3 HAELO trial, with top-line data anticipated by mid-2026, a Biologics License Application (BLA) submission in H2 2026, and a commercial launch expected in H1 2027.
- The Nexi program for transthyretin amyloidosis (TTR) is currently under a clinical hold by the FDA, which was triggered by a patient death due to septicemia from a perforated duodenal ulcer, not liver failure. Intellia is actively engaged with the FDA to resolve the hold.
- The company reports a strong financial position, with capital to fund operations into mid-2027.
- Intellia Therapeutics announced the completion of enrollment for its Lombozi (HAE) Phase 3 Halo trial, with top-line data expected by mid-2026, a Biologics License Application (BLA) submission in H2 2026, and a commercial launch targeted for H1 2027.
- The company's Nexi (TTR amyloidosis) Phase 3 trials (Magnitude and Magnitude-2) are currently on clinical hold, with Intellia actively engaged with the FDA for resolution.
- Intellia clarified that the patient death which led to the Nexi clinical hold was attributed to septicemia from a perforated duodenal ulcer, not liver failure.
- Intellia maintains a strong capital position, providing funding for operations into mid-2027.
- Intellia Therapeutics, a leader in CRISPR medicine, is advancing two late-stage clinical programs: Lombozi for hereditary angioedema (HAE) and Nexi for transthyretin amyloidosis (TTR).
- For Lombozi, the Phase 3 Halo trial enrollment is complete, with top-line data anticipated by mid-2026, BLA submission in H2 2026, and a commercial launch targeted for H1 2027.
- The Nexi Phase 3 programs for TTR amyloidosis are currently under clinical hold, with resolving this hold being a top priority for 2026. The hold was triggered by a patient who succumbed to septicemia due to a perforated duodenal ulcer, not liver failure.
- The company maintains a strong capital position, providing funding for operations into mid-2027.
- Intellia Therapeutics' nexiguran ziclumeran (nex-z) MAGNITUDE and MAGNITUDE-2 Phase 3 clinical trials for transthyretin (ATTR) amyloidosis are on clinical hold following a Grade 4 liver transaminase elevation in a patient who subsequently passed away on November 5, 2025, due to septic shock secondary to a perforated duodenal ulcer.
- The company is working to resolve the clinical holds and plans to provide an update after finalizing a path forward with regulators for nex-z.
- Intellia expects to present topline Phase 3 HAELO data for lonvoguran ziclumeran (lonvo-z) by mid-2026, with a Biologics License Application (BLA) submission planned for the second half of 2026 and a U.S. commercial launch in the first half of 2027.
- Intellia anticipates its existing capital will fund operations into mid-2027.
Quarterly earnings call transcripts for Intellia Therapeutics.
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