Ireland
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Recruiting Phase 1

A First-in-Human Study of MEN2312 in Adults With Advanced Breast Cancer

NCT06638307 · tracked via the Priya Life Science USA tracker
Phase
Phase 1
Started
2024-10-25
Last updated
2026-08-07

Condition(s) studied

Advanced Breast Cancer

Investigational drug(s) / intervention(s)

MEN2312Elacestrant →

MEN2312: MEN2312 administered as oral tablets.

Elacestrant: Elacestrant administered as oral tablets.

Study summary

This is a first-in-human study of MEN2312, a lysine acetyltransferase 6 (KAT6) inhibitor, in adult participants with advanced breast cancer.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria: * Participant has advanced (locoregionally recurrent or metastatic) breast cancer not amenable to curative therapy. * Presence of genetic alterations in PIK3CA/AKT1/PTEN in participants' tumor tissue. * Participant must have received at least 1 prior line of endocrine therapy for advanced/metastatic disease or participant who has radiological evidence of breast cancer recurrence or progression during or within 12 months from the end of adjuvant treatment with endocrine therapy, as these participants are considered as first-line relapsed participants. * Progression on previous cyclin-dependent kinase 4 and 6 inhibitor treatment in combination with fulvestrant or aromatase inhibitor is required. Key Exclusion Criteria: * Active or newly diagnosed central nervous system metastases. * Participants with advanced, symptomatic visceral spread, who are at risk of life-threatening complications in the short term, including massive uncontrolled effusions (peritoneal, pleural, pericardial), pulmonary lymphangitis, or liver involvement \>50%. * Participants with any toxicities related to prior radiation therapy that have not resolved to baseline or to National Cancer Institute Common Terminology Criteria for Adverse Events v5.0 Grade ≤1, except alopecia and peripheral sensory neuropathy (Grade ≤2). Note: Other inclusion/exclusion criteria may apply.

Primary outcome measure(s)

  • Number of Participants Experiencing Dose-limiting Toxicity When Administered MEN2312 — Baseline through Day 28
  • Recommended Phase 2 Dose (RP2D) of MEN2312 — Baseline through Month 6

Trial sites (45)

FacilityCityRegionStatus
Highlands Oncology Group Springdale Arkansas Recruiting
City of Hope Duarte California Recruiting
UC San Diego Moores Cancer Center La Jolla California Recruiting
Stanford Cancer Center Palo Alto California Recruiting
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California Recruiting
UCLA Hematology Oncology - Parkside Santa Monica California Recruiting
Yale Comprehensive Cancer Center New Haven Connecticut Recruiting
Advent Health Orlando Altamonte Springs Florida Recruiting
Sarah Cannon Research Institute at Florida Cancer Specialists Orlando Florida Recruiting
Florida Cancer Specialists & Research Institute (FCS) - Sarasota Sarasota Florida Recruiting
Moffitt Cancer Center Tampa Florida Recruiting
Winship Cancer Institute, Emory University Atlanta Georgia Recruiting
University of Illinois Hospital and Health Sciences System (Outpatient Cancer Center) Chicago Illinois Recruiting
University of Chicago Medical Center Chicago Illinois Recruiting
University of Iowa Health Care Iowa City Iowa Recruiting
The University of Kansas Cancer Center Fairway Kansas Recruiting
Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland Recruiting
Massachusetts General Hospital Cancer Center Boston Massachusetts Recruiting
Dana-Farber Cancer Institute Boston Massachusetts Recruiting
START Midwest - Oncology Grand Rapids Michigan Recruiting
Mayo Clinic Rochester Minnesota Recruiting
Astera Cancer Care East Brunswick New Jersey Recruiting
Perlmutter Cancer Center - Sunset Park Brooklyn New York Recruiting
Perlmutter Cancer Center at NYU Langone Hospital - Long Island Mineola New York Recruiting
Laura & Isaac Perlmutter Cancer Center at NYU Langone Health New York New York Recruiting
Memorial Sloan Kettering Cancer Center New York New York Recruiting
Providence Cancer Institute Franz Clinic Portland Oregon Recruiting
The West Clinic, PC dba West Cancer Center Germantown Tennessee Recruiting
SCRI Oncology Partners Group Nashville Tennessee Recruiting
University of Texas Southwestern Medical Center Dallas Texas Recruiting
The University of Texas M.D. Anderson Cancer Center Houston Texas Recruiting
START San Antonio, LLC San Antonio Texas Recruiting
University of Texas Health Science Center San Antonio San Antonio Texas Recruiting
START Mountain West Valley City Utah Recruiting
NEXT Virginia Fairfax Virginia Recruiting
University of Wisconsin Carbone Cancer Center Madison Wisconsin Recruiting
Froedtert Hospital & the Medical College of Wisconsin Milwaukee Wisconsin Recruiting
Hospital Universitario Vall d'Hebron - Vall d'Hebron Institute of Oncology (VHIO) Medical Oncology Department Barcelona Spain Recruiting
IOB - Madrid Fundacion Hermanas Hospitalarias (Hospital Beata Maria Ana) Madrid Spain Recruiting
START Madrid - Hospital Universitario Fundacion Jimenez Diaz Madrid Spain Recruiting

+ 5 more sites — see the full list on the official registry below.

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 NCT06638307 on ClinicalTrials.gov ↗ ← All trials in the USA