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A Phase 1a/1b Study of ELVN-001 for the Treatment Chronic Myeloid Leukemia

NCT05304377 · Enliven Therapeutics
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Official title
A Phase 1a/1b Study of ELVN-001 for the Treatment of Chronic Myeloid Leukemia
About this study
This first-in-human trial with ELVN-001 is a dose escalation study with the primary purpose to identify the recommended dose(s) for expansion (RDEs) of single agent ELVN-001 in chronic phase CML with or without T315I mutations. The safety, tolerability and pharmacokinetic profile of ELVN-001 will be assessed together with an evaluation of changes in BCR-ABL1 transcript. An understanding of the safety profile, PK and preliminary evidence of anti-CML activity will be used to inform future development of ELVN-001 in adults with CML. By virtue of its predicted pharmacological profile ELVN-001 has the potential to be tolerable and achieve a deep molecular response in patients with CML with or without T315I mutations who do not tolerate or benefit from available TKIs.
Eligibility criteria
Inclusion Criteria: * BCR-ABL1 positive CML in chronic phase, with or without T315I mutation. * US: The patient has failed or is intolerant to at least one prior second-generation tyrosine kinase inhibitor (TKI) or asciminib. Rest of World: The patient has failed, is intolerant to, or not a candidate for, available therapies known to be active for treatment of their CML (country-specific criteria may vary). * ECOG performance status of 0 to 2. * Adequate hematologic, hepatic and renal function. * Prior bone marrow transplant allowed if ≥ 6 months prior to the first dose of ELVN-001. Exclusion Criteria: * Treatment with anti-cancer or anti-CML therapy within 7 days or 5 half-lives, whichever is longer. * History of acute tyrosine kinase inhibitor (TKI)-related pancreatitis within 6 months of study entry. Active chronic pancreatitis, or pancreatic disease due to any cause. * QTc \>470 ms.
Study design
Enrollment target: 250 participants
Allocation: non_randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2022-05-22
Estimated completion: 2027-12
Last updated: 2026-04-01
Interventions
Drug: ELVN-001
Primary outcomes
  • Phase 1a: Incidence of dose limiting toxicities (28 days)
  • Phase 1a: Incidence of adverse events (AEs) (up to 28 days)
  • Phase 1a: Incidence of clinically significant laboratory abnormalities (up to 28 days)
Sponsor
Enliven Therapeutics · industry
Contacts & investigators
ContactStudy Contact · contact · ELVN-001-101@enliventherapeutics.com · 707-799-3272
All locations (45)
Memorial Sloan Kettering Cancer CenterRecruiting
New York, New York, United States
Montefiore Medical CenterRecruiting
The Bronx, New York, United States
Oregon Health & Science University-Knight Cardiovascular InstituteRecruiting
Portland, Oregon, United States
The University of Texas MD Anderson Cancer CenterRecruiting
Houston, Texas, United States
Royal Adelaide HospitalRecruiting
Adelaide, Australia
UZ GentRecruiting
Ghent, Belgium
UZ LeuvenRecruiting
Leuven, Belgium
CHU LiegeRecruiting
Liège, Belgium
University Health Network (UHN) - Princess Margaret Cancer CentreRecruiting
Toronto, Ontario, Canada
CHU Amiens Picardie Site SudRecruiting
Amiens, France
Institut Bergonie - Centre Regional de Lutte Contre Le Cancer de Bordeaux et Sud OuestRecruiting
Bordeaux, France
CHRU de Lille - Hopital Calmette-Boulevard du Pr Leclercq CHRU LilleRecruiting
Lille, France
Centre Hospitalier Universitaire (CHU) De Limoges Hopital DupuytrenRecruiting
Limoges, France
Centre Leon BerardRecruiting
Lyon, France
Centre Hospitalier Lyon SudWithdrawn
Pierre-Bénite, France
Uniklinik RWTH Aachen MedizinischeRecruiting
Aachen, Germany
Charite Campus VirchowRecruiting
Berlin, Germany
Klinikum der Goethe UniversitatRecruiting
Frankfurt, Germany
Universitaetsklinikum Des Saarlandes Und Medizinische Fakultaet Der Universitaet Des SaarlandesRecruiting
Homburg, Germany
Universitaetsklinikum JenaRecruiting
Jena, Germany
Medizinische Universitatsklinik Mannheim der Universitat HeidelbergRecruiting
Mannheim, Germany
Universitaetsmedizin RostockRecruiting
Rostock, Germany
Semmelweis Egyetem, Belgyogyaszati es Onkologiai KlinikaRecruiting
Budapest, Hungary
Pecsi Tudomanyegyetem Klinikai Kozpont (University of Pecs, Clinical Centre)Recruiting
Pécs, Hungary
Hadassah Medical CenterRecruiting
Jerusalem, Israel
The Galilee Medical CenterRecruiting
Nahariya, Israel
Rabin Medical CenterRecruiting
Petah Tikva, Israel
Azienda Ospedaliero Universitaria Delle MarcheRecruiting
Ancona, Italy
Radboud University Medical CenterRecruiting
Nijmegen, Netherlands
Szpital Specjalistycnzy im. Jedrzeja Sniadeckiego w Nowym SaczuRecruiting
Nowy Sącz, Poland
MICS Centrum Medyczne TorunRecruiting
Torun, Poland
Instytut Hematologii I TransfuzjologiiRecruiting
Warsaw, Poland
Chonbuk National University HospitalWithdrawn
Jeonju, Jeollabuk-do, South Korea
Keimyung University Dongsan HospitalWithdrawn
Daegu, South Korea
Uijeongbu Eulji Medical CenterRecruiting
Gyeonggi-do, South Korea
Chonnam National University Hwasun HospitalWithdrawn
Hwasun, South Korea
Samsung Medical CenterWithdrawn
Seoul, South Korea
Hospital Del MarRecruiting
Barcelona, Spain
Hospital Universitario de Gran Canaria Dr. Negrin, Servicio Canario e Salud (SCS)Withdrawn
Las Palmas de Gran Canaria, Spain
Hospital Universitario La PazRecruiting
Madrid, Spain
Complejo Hospitalario de Toledo - Hospital Virgen de la SaludTerminated
Toledo, Spain
Universitat de Valencia - Hospital Universitari i Politecnic La Fe de Valencia (Hospital La Fe Bulevar Sur)Recruiting
Valencia, Spain
Beatson West of Scotland Cancer Centre, Gartnavel General HospitalRecruiting
Glasgow, United Kingdom
Hammersmith Hospital Imperial College Healthcare NHS TrustRecruiting
London, United Kingdom
The Christie NHS Foundation TrustRecruiting
Manchester, United Kingdom
A Phase 1a/1b Study of ELVN-001 for the Treatment Chronic Myeloid Leukemia · TrialPath