🔎 Trials Near Me

Home › NCT06638307

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

RecruitingPhase 1

A Phase 1, First-in-Human Study of MEN2312, a KAT6 Inhibitor, as Monotherapy and in Combination in Participants With Advanced Breast Cancer

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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.

About the study

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

What is being tested

Sponsor: Stemline Therapeutics, Inc. · Participants: 240 · Started: Oct 25, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06638307

Locations in the U.S.

ArkansasHighlands Oncology Group, Springdale
CaliforniaCity of Hope, Duarte
UC San Diego Moores Cancer Center, La Jolla
Stanford Cancer Center, Palo Alto
UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco
UCLA Hematology Oncology - Parkside, Santa Monica
ConnecticutYale Comprehensive Cancer Center, New Haven
FloridaAdvent Health Orlando, Altamonte Springs
Sarah Cannon Research Institute at Florida Cancer Specialists, Orlando
Florida Cancer Specialists & Research Institute (FCS) - Sarasota, Sarasota
Moffitt Cancer Center, Tampa
GeorgiaWinship Cancer Institute, Emory University, Atlanta
IllinoisUniversity of Chicago Medical Center, Chicago
University of Illinois Hospital and Health Sciences System (Outpatient Cancer Center), Chicago
IowaUniversity of Iowa Health Care, Iowa City
KansasThe University of Kansas Cancer Center, Fairway
MarylandSidney Kimmel Comprehensive Cancer Center, Baltimore
MassachusettsDana-Farber Cancer Institute, Boston
Massachusetts General Hospital Cancer Center, Boston
MichiganSTART Midwest - Oncology, Grand Rapids
MinnesotaMayo Clinic, Rochester
New JerseyAstera Cancer Care, East Brunswick
New YorkPerlmutter Cancer Center - Sunset Park, Brooklyn
Perlmutter Cancer Center at NYU Langone Hospital - Long Island, Mineola
Laura & Isaac Perlmutter Cancer Center at NYU Langone Health, New York
Memorial Sloan Kettering Cancer Center, New York
OregonProvidence Cancer Institute Franz Clinic, Portland
TennesseeThe West Clinic, PC dba West Cancer Center, Germantown
SCRI Oncology Partners Group, Nashville
TexasUniversity of Texas Southwestern Medical Center, Dallas
The University of Texas M.D. Anderson Cancer Center, Houston
START San Antonio, LLC, San Antonio
University of Texas Health Science Center San Antonio, San Antonio
UtahSTART Mountain, West Valley City
VirginiaNEXT Virginia, Fairfax
WisconsinUniversity of Wisconsin Carbone Cancer Center, Madison
Froedtert Hospital & the Medical College of Wisconsin, Milwaukee

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.