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Enliven Therapeutics (ELVN)

Earnings summaries and quarterly performance for Enliven Therapeutics.

Research analysts covering Enliven Therapeutics.

Recent press releases and 8-K filings for ELVN.

EnLiven Therapeutics Updates on 001 Clinical Development and Financial Position
ELVN
New Projects/Investments
Guidance Update
  • EnLiven Therapeutics (ELVN) is developing 001, an ATP-competitive, highly selective BCR-ABL inhibitor for chronic myeloid leukemia (CML), which is designed to address primary resistance to allosteric inhibitors like SCEMBLIX.
  • Early data for 001 showed 32% achievement of Major Molecular Response (MMR) in heavily pretreated late-line CML patients, including those resistant to asciminib.
  • The company plans to initiate a Phase III study for 001 next year (2026), enrolling 400-500 patients in a second-line plus trial design.
  • EnLiven ended the last quarter with approximately $480 million in cash, providing a runway into the first half of 2029, which is expected to cover the top-line data for the pivotal trial.
Nov 18, 2025, 4:00 PM
Enliven Provides Update on CML Program 001 and Financial Runway
ELVN
New Projects/Investments
Guidance Update
  • Enliven (ELVN) is developing 001, an ATP-competitive BCR-ABL inhibitor for chronic myeloid leukemia (CML), with early data showing 32% achievement of MMR in heavily pretreated late-line patients.
  • The company plans to initiate a Phase 3 study for 001 in 2026, enrolling 400-500 patients in a second-line plus trial design.
  • Enliven's financial runway extends into the first half of 2029, with approximately $480 million in cash as of the last quarter.
  • The company is also exploring combination studies and expects to disclose new non-oncology assets in 2026.
Nov 18, 2025, 4:00 PM
Enliven Therapeutics Details Phase 3 Plans and Financial Runway for CML Drug 001
ELVN
New Projects/Investments
Guidance Update
  • Enliven Therapeutics (ELVN) is developing 001, an ATP-competitive, highly selective BCR-ABL inhibitor for the treatment of patients with chronic myeloid leukemia (CML).
  • Early data for 001 showed 32% achievement of Major Molecular Response (MMR) in heavily pretreated late-line CML patients, including those previously treated with and resistant or refractory to asciminib (Semblix).
  • The company plans to initiate a Phase 3 study in 2026 with a second-line plus trial design, aiming to enroll 400-500 patients for a head-to-head study.
  • Enliven differentiates its mechanism from allosteric inhibitors like Semblix and TURN701, positioning 001 to address primary resistance to these drugs, and is interested in exploring combination therapies in the future.
  • Enliven ended the last quarter with approximately $480 million in cash and projects a financial runway into the first half of 2029, which is expected to cover well through the top-line data for the pivotal trial.
Nov 18, 2025, 4:00 PM
Enliven Therapeutics Reports Q3 2025 Financial Results and Business Update
ELVN
Earnings
Guidance Update
New Projects/Investments
  • Enliven Therapeutics reported a net loss of $20.1 million for the third quarter of 2025, compared to a net loss of $23.2 million for the third quarter of 2024.
  • Research and development expenses for the third quarter of 2025 were $18.2 million, while general and administrative expenses were $6.9 million.
  • As of September 30, 2025, the company had $477.6 million in cash, cash equivalents, and marketable securities, which is expected to provide a cash runway into the first half of 2029.
  • The company completed enrollment of the randomized Phase 1b cohorts of the ENABLE trial for ELVN-001 in CML and remains on track to initiate a Phase 3 pivotal trial for ELVN-001 in 2026.
Nov 12, 2025, 9:10 PM
Enliven Therapeutics Reports Q3 2025 Financial Results and Provides Business Update
ELVN
Earnings
New Projects/Investments
Guidance Update
  • Enliven Therapeutics reported a net loss of $20.1 million for the third quarter ended September 30, 2025, compared to a net loss of $23.2 million for the same period in 2024.
  • As of September 30, 2025, the company held $477.6 million in cash, cash equivalents, and marketable securities, which is expected to provide a cash runway into the first half of 2029.
  • The company completed enrollment of the randomized Phase 1b cohorts of the ENABLE trial for ELVN-001 and remains on track to initiate a Phase 3 pivotal trial in 2026.
Nov 12, 2025, 9:05 PM

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