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Active, not recruiting Phase 1

Phase 1b Study of OP-1250 (Palazestrant) in Combination With Ribociclib, Alpelisib, Everolimus, or Atirmociclib in ER+, HER2- Breast Cancer

NCT05508906 · tracked via the Priya Life Science USA tracker
Phase
Phase 1
Started
2022-08-31
Last updated
2026-09-15

Condition(s) studied

Metastatic Breast CancerER-positive Breast CancerHER2-negative Breast CancerBreast CancerLocally Advanced Breast Cancer

Investigational drug(s) / intervention(s)

Palazestrant →Ribociclib →Alpelisib →Everolimus →Atirmociclib →

Palazestrant: Complete estrogen receptor antagonist (CERAN)

Ribociclib: All subjects in Treatment Group 1 will receive palazestrant in combination with ribociclib.

Alpelisib: All subjects in Treatment Group 2 will receive palazestrant in combination with alpelisib.

Everolimus: All subjects in Treatment Group 3 will receive palazestrant in combination with everolimus.

Atirmociclib: All subjects in Treatment Group 4 will receive palazestrant in combination with atirmociclib.

Study summary

This is a Phase 1b open-label, 2-part study in 4 treatment groups. The 4 treatment groups are as follows:

Treatment Group 1: Palazestrant (OP-1250) in combination with ribociclib (KISQALI®, Novartis Pharmaceuticals Corporation).

Treatment Group 2: Palazestrant (OP-1250) in combination with alpelisib (PIQRAY®, Novartis Pharmaceuticals Corporation).

Treatment Group 3: Palazestrant (OP-1250) in combination with everolimus.

Treatment Group 4: Palazestrant (OP-1250) in combination with atirmociclib.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Female or male aged \>18 years. * Willing and able to participate and comply with all study requirements. * Histologically- or cytologically-confirmed advanced or metastatic Breast Cancer (mBC). * ER+/HER2- disease, as determined in the most recently obtained archival tumor tissue sample from a metastatic site, using locally accepted criteria by the local pathology report. * Evaluable disease with one of the following: Measurable disease, ie, at least 1 measurable lesion as per RECIST 1.1 (a lesion at a previously irradiated site may only be counted as a target lesion if there is clear sign of progression since the irradiation) OR patients with predominantly bone disease (with or without other non-measurable lesions) are allowed if it is possible to evaluate on radiological examinations (eg. bone scan, PET/CT, CT, MRI) even if lesions are non-measurable according to RECIST 1.1. * Life expectancy ≥6 months, as judged by the investigator. * Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1. * Has received no more than 1 prior hormonal regimen (Treatment Group 1). Has received no more than 2 prior hormonal regimens (Treatment Group 2 and Treatment Group 3) . Has received no more than 2 prior hormonal regimens for metastatic disease in Part 1 (Dose Escalation) and no more than 1 prior hormonal regimes in Part 2 (Dose Expansion) for metastatic disease, regardless of type of endocrine agent (Treatment Group 4) for advanced or metastatic disease. Prior hormonal regimens in combination with CDK4/6 inhibitors are allowed in all treatment groups. For subjects in Treatment Group 4, no prior chemotherapy for metastatic breast cancer is allowed. * Has received no more than 1 prior chemotherapy (which includes antibody drug conjugates) for locally advanced or metastatic breast cancer. Exclusion Criteria: * Prior or concurrent malignancy whose natural history or treatment may interfere with the safety or efficacy assessment of the investigational regimen. * Clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormality. * History of cerebral vascular disease within 6 months prior to the first administration of study drug dose. * History of a pulmonary embolism, or deep venous thrombosis within the last 6 months, or subject has an increased risk of thrombosis as determined by the investigator. * History of pneumonitis or interstitial lung disease. * Leptomeningeal disease or spinal cord compression. * Medical history or ongoing gastrointestinal disorders that could affect absorption of oral therapeutics. * Known human immunodeficiency virus infection. * Known clinically significant history of liver disease consistent with Child-Pugh Class B or C, including active viral or other hepatitis (eg, hepatitis B or hepatitis C virus), current alcohol abuse, or cirrhosis. * History of severe cutaneous reaction, such as Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, or drug reaction with eosinophilia and systemic symptoms. * Active infection or at a high risk of developing a serious infection (e.g. participants with immunodeficiencies, uncontrolled diabetes mellitus, uncontrolled heart disease, poor general health, poor nutritional status). * Has clinically significant co-morbidities, such as, psychiatric disease, or any other condition that could impact the ability of the subject to participate in this study or otherwise has the potential to confound the study results. * Have received prior treatment with OP-1250. * Have received prior treatment with approved or investigational PI3K inhibitor (Treatment Group 2) or mTOR inhibitor (Treatment Group 3).

Primary outcome measure(s)

  • Dose Limiting Toxicities (DLTs) — The first 28 days of treatment
    To determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D), and/ or recommended dose expansion (RDE) of palazestrant when administered with ribociclib (Treatment Group 1), alpelisib (Treatment Group 2), or everolimus (Treatment Group 3), or atirmociclib (Treatment Group 4). The incidence of DLTs will be assessed in the Dose Escalation part (Part 1) of the study.
  • Characterize the incidence, nature and severity of treatment emergent adverse events (TEAEs) and serious adverse events (SAEs) of palazestrant when administered with ribociclib, alpelisib, everolimus, or atirmociclib. — Up to 30 days after last dose of study drug(s) treatment
    Characterize the incidence, nature and severity of TEAEs and SAEs of palazestrant when administered with ribociclib (Treatment Group 1), alpelisib (Treatment Group 2), everolimus (Treatment Group 3), or atirmociclib (Treatment Group 4) according to NCI-CTCAE version 5.0.
  • Pharmacokinetics (PK) of palazestrant when administered with ribociclib (Treatment Group 1) or alpelisib (Treatment Group 2), everolimus (Treatment Group 3), or atirmociclib (Treatment Group 4) . — Every 28 days
    To assess the PK of palazestrant (and potential metabolites) in combination with ribociclib (Treatment Group 1), alpelisib (Treatment Group 2), everolimus (Treatment Group 3), or atirmociclib (Treatment Group 4). Plasma levels of palazestrant will be assessed at predefined intervals to establish PK parameters (including: Cmax, Cmin, Tmax, AUC, and t1⁄2 as data permit) and palazestrant trough concentration at steady state).

Trial sites (16)

FacilityCityRegionStatus
Banner MD Anderson Cancer Center Gilbert Arizona
University of California San Francisco Health San Francisco California
University of Colorado Cancer Center Aurora Colorado
Advent Health Hematology and Oncology Orlando Florida
University of Iowa Iowa City Iowa
Dana Farber Cancer Institute Boston Massachusetts
Henry Ford Health Detroit Michigan
Regents of the University of Minnesota Minneapolis Minnesota
Washington University, School of Medicine St Louis Missouri
Ichan School of Medicine at Mount Sinai New York New York
Atrium Health Levine Cancer Institute Charlotte North Carolina
Vanderbilt-Ingram Cancer Center Nashville Tennessee
MD Anderson Cancer Center Houston Texas
Northwest Medical Specialties Tacoma Washington
Macquarie Health Sydney New South Wales
Breast Cancer Research Center- Western Australia Nedlands Western Australia
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05508906 on ClinicalTrials.gov ↗ ← All trials in the USA