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Study of ECI830 Single Agent or in Combination in Patients With Advanced HR+/HER2- Breast Cancer and in Patients With Other Advanced Solid Tumors

NCT06726148 · Novartis
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Official title
An Open-label, Multi-center, Phase I/II Study of ECI830 as a Single Agent and in Combination With Ribociclib and Endocrine Therapy in Patients With Advanced Hormone Receptor Positive, HER2-negative Breast Cancer and Advanced Solid Tumors
About this study
This is a first-in-human, open-label, phase I/II, multi-center study consisting of an ECI830 single agent treatment arm in patients with advanced HR+/HER2- breast cancer or other advanced solid tumors harboring CCNE1 amplification or extensive-stage small cell lung cancer (ES-SCLC), and a combination treatment arm of ECI830 with ribociclib and fulvestrant in patients with advanced breast cancer. Single agent escalation may be followed by an expansion part stratified by disease indication. The escalation of the combination arm may continue into a randomized, open label, Phase II with optional dose optimization in advanced breast cancer patients.
Eligibility criteria
Inclusion Criteria: Age ≥ 18 years old. Patients with one of the following indications: Phase I: HR+/HER2- aBC with disease progression on or following at least one line of hormone-based therapy in combination with a CDK4/6i and at least one additional line of systemic therapy for metastatic disease. Histologically and/or cytologically confirmed diagnosis of locally advanced or metastatic cancer with a CCNE1 amplification. For dose expansion only: no more than 3 prior lines of therapy for advanced or metastatic disease. Patients with ES-SCLC and disease progression on or after standard of care (SoC). For dose expansion only: no more than 2 prior lines of therapy for advanced or metastatic disease are allowed. Phase II: HR+/HER2- aBC with disease progression on an aromatase inhibitor or tamoxifen in combination with a CDK4/6 inhibitor for unresectable/metastatic disease with no more than 2 lines of endocrine therapy. Measurable disease as determined by RECIST v1.1. BC only: If no measurable disease is present, then at least one predominantly lytic bone lesion must be present that can be accurately assessed at baseline and is suitable for repeated assessment. Exclusion Criteria: Previous treatment with a CDK2 inhibitor at any time. Patients with inadequate bone marrow and/or organ functions with out-of-range laboratory values. Clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormality including MI, CABG, long QT syndrome, or risk factors for TdP. Presence of symptomatic CNS metastases or CNS metastases that require local therapy or increasing doses of corticosteroids within 2 weeks prior to study entry. For the combination treatment: Patients with symptomatic visceral disease or any disease burden that makes the patient ineligible for endocrine-based therapy. Patients who could not tolerate the prescribed dose of ribociclib during a previous course of treatment, requiring dose reduction or permanent discontinuation due to adverse events. For patients with BC: Patient is concurrently using hormone replacement therapy. WOCBP who are unwilling to use highly effective contraception methods, pregnant or nursing women. Other protocol-defined inclusion/exclusion criteria may apply.
Study design
Enrollment target: 280 participants
Allocation: randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2025-04-03
Estimated completion: 2028-09-25
Last updated: 2026-08-27
Interventions
Drug: ECI830Drug: ribociclibDrug: fulvestrant
Primary outcomes
  • Phase I: Incidence of dose-limiting toxicities (DLTs) (2 years)
  • Phase I: Incidence of adverse events (AEs) and serious adverse events (SAEs) (2 years)
  • Phase I: Number of participants with dose interruptions, reductions and discontinuations (2 years)
Sponsor
Novartis Pharmaceuticals · industry
Contacts & investigators
ContactNovartis Pharmaceuticals · contact · novartis.email@novartis.com · 1-888-669-6682
ContactNovartis Pharmaceuticals · contact · novartis.email@novartis.com · +41613241111
All locations (33)
University of California LARecruiting
Los Angeles, California, United States
Florida Cancer SpecialistsRecruiting
Fort Myers, Florida, United States
Dana Farber Cancer InstituteRecruiting
Boston, Massachusetts, United States
WA Uni School Of MedRecruiting
St Louis, Missouri, United States
Memorial Sloan KetteringRecruiting
New York, New York, United States
SCRI Oncology PartnersRecruiting
Nashville, Tennessee, United States
MD Anderson Cancer Center Uni of TeRecruiting
Houston, Texas, United States
Fred Hutch Cancer ResearchRecruiting
Seattle, Washington, United States
Novartis Investigative SiteRecruiting
Clayton, Victoria, Australia
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Melbourne, Victoria, Australia
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Toronto, Ontario, Canada
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Montreal, Quebec, Canada
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Nanjing, Jiangsu, China
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Xian, Shanxi, China
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Brno, Czechia
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Copenhagen, Denmark
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Odense C, Denmark
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Bordeaux, France
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Saint-Herblain, France
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Freiburg im Breisgau, Baden-Wurttemberg, Germany
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Heidelberg, Germany
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Ulm, Germany
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Haifa, Israel
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Tel Aviv, Israel
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Milan, MI, Italy
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Modena, MO, Italy
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Chuo Ku, Tokyo, Japan
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Singapore, Singapore
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Seoul, Seoul, South Korea
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Barcelona, Spain
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Barcelona, Spain
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Tainan, Taiwan
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London, Oxford, United Kingdom