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

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Stemline Therapeutics

Status and phase

Enrolling
Phase 1

Conditions

Advanced Breast Cancer

Treatments

Drug: Elacestrant
Drug: MEN2312

Study type

Interventional

Funder types

Industry

Identifiers

NCT06638307
MEN2312-01
U1111-1308-5349 (Other Identifier)
2024-514661-19-00 (EU Trial (CTIS) Number)

Details and patient eligibility

About

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

Enrollment

240 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

240 participants in 2 patient groups

MEN2312: Monotherapy
Experimental group
Description:
Participants will receive MEN2312.
Treatment:
Drug: MEN2312
MEN2312: Combination Therapy (Elacestrant)
Experimental group
Description:
Participants will receive MEN2312 in combination with elacestrant.
Treatment:
Drug: MEN2312
Drug: Elacestrant

Trial contacts and locations

44

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Central trial contact

Stemline Trials

Data sourced from clinicaltrials.gov

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