RecruitingPhase 1

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

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

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests MEN2312 in humans for the first time. It is for adults with advanced breast cancer. MEN2312 blocks a protein called KAT6.

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

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • You have breast cancer that has come back near its starting point or spread to other parts of the body, and treatment cannot cure it.
  • Your tumor has changes in the PIK3CA, AKT1, or PTEN genes.
  • You had at least one hormone therapy for advanced cancer, OR scans show your cancer came back or grew during or within 12 months after hormone therapy given after your main treatment.
  • Your cancer grew while you were taking a CDK4/6 inhibitor with fulvestrant or an aromatase inhibitor. These are medicines that block cancer growth and hormone effects.

Who can't join

  • You have active or newly found cancer spread to the brain or spinal cord.
  • Cancer has spread to internal organs, causes symptoms, and could soon be life-threatening. Examples include large, uncontrolled fluid buildup around the lungs, heart, or belly; spread through the lungs’ lymph vessels; or cancer in more than half of the liver.
  • Side effects from past radiation have not returned to your usual level or become mild. Hair loss and up to moderate nerve damage that affects feeling are exceptions.

Simplified for readability. The official criteria below are what the study team uses.

Official 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.

Study sites (37)

AR

CA

CT

  • Yale Comprehensive Cancer Center · New Haven, CT 06511Patricia LoRusso, DO · Principal investigatorMore trials in New Haven

FL

  • Advent Health Orlando · Altamonte Springs, FL 32701Wassim Mchayleh, MD · Principal investigatorMore trials in Altamonte Springs
  • Sarah Cannon Research Institute at Florida Cancer Specialists · Orlando, FL 32827Cesar Perez Batista, MD · Principal investigatorMore trials in Orlando
  • Florida Cancer Specialists & Research Institute (FCS) - Sarasota · Sarasota, FL 34232Judy Wang, MD · Principal investigatorMore trials in Sarasota
  • Moffitt Cancer Center · Tampa, FL 33612Hatem Soliman · Principal investigatorMore trials in Tampa

GA

  • Winship Cancer Institute, Emory University · Atlanta, GA 30322Manali Bhave · Principal investigatorMore trials in Atlanta

IA

IL

  • University of Illinois Hospital and Health Sciences System (Outpatient Cancer Center) · Chicago, IL 60612Oana Danciu · Principal investigatorMore trials in Chicago
  • University of Chicago Medical Center · Chicago, IL 60637Nan Chen · Principal investigatorMore trials in Chicago

KS

  • The University of Kansas Cancer Center · Fairway, KS 66205Priyanka Sharma · Principal investigatorMore trials in Fairway

MA

  • Massachusetts General Hospital Cancer Center · Boston, MA 02114Seth Wander, MD, PhD · Principal investigatorMore trials in Boston
  • Dana-Farber Cancer Institute · Boston, MA 02215Antonio Giordano, MD, PhD · Principal investigatorMore trials in Boston

MD

  • Sidney Kimmel Comprehensive Cancer Center · Baltimore, MD 21287Jessica Tao, MD · Principal investigatorMore trials in Baltimore

MI

MN

NJ

NY

  • Perlmutter Cancer Center - Sunset Park · Brooklyn, NY 11220Nancy Chan · Principal investigatorMore trials in Brooklyn
  • Perlmutter Cancer Center at NYU Langone Hospital - Long Island · Mineola, NY 11501Nancy Chan · Principal investigatorMore trials in Mineola
  • Laura & Isaac Perlmutter Cancer Center at NYU Langone Health · New York, NY 10016Nancy Chan · Principal investigatorMore trials in New York
  • Memorial Sloan Kettering Cancer Center · New York, NY 10065Sherry Shen · Principal investigatorMore trials in New York

OR

  • Providence Cancer Institute Franz Clinic · Portland, OR 97213David Page · Principal investigatorMore trials in Portland

TN

  • The West Clinic, PC dba West Cancer Center · Germantown, TN 38138Gregory Vidal · Principal investigatorMore trials in Germantown
  • SCRI Oncology Partners Group · Nashville, TN 37203Erika P Hamilton, MD · Principal investigatorMore trials in Nashville

TX

  • University of Texas Southwestern Medical Center · Dallas, TX 75390Heather McArthur · Principal investigatorMore trials in Dallas
  • The University of Texas M.D. Anderson Cancer Center · Houston, TX 77030Jason Mouabbi, MD · Principal investigatorMore trials in Houston
  • START San Antonio, LLC · San Antonio, TX 78229Amita Patnaik, MD · Principal investigatorMore trials in San Antonio
  • University of Texas Health Science Center San Antonio · San Antonio, TX 78229Virginia Kaklamani, MD · Principal investigatorMore trials in San Antonio

UT

VA

WI

  • University of Wisconsin Carbone Cancer Center · Madison, WI 53792Kari Wisinksi · Principal investigatorMore trials in Madison
  • Froedtert Hospital & the Medical College of Wisconsin · Milwaukee, WI 53226Lubna Chaudhary · Principal investigatorMore trials in Milwaukee