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NCT Number: NCT06638307

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

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

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Hospital Universitario Vall d'Hebron - Vall d'Hebron Institute of Oncology (VHIO) Medical Oncology Department, Barcelona, Spain

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

MEN2312

Drug

MEN2312 administered as oral tablets.

Elacestrant

Drug

Elacestrant administered as oral tablets.

Other names: Orserdu

Primary outcomes

  1. Number of Participants Experiencing Dose-limiting Toxicity When Administered MEN2312

    Time frame: Baseline through Day 28

  2. Recommended Phase 2 Dose (RP2D) of MEN2312

    Time frame: Baseline through Month 6

Secondary outcomes

  1. Overall Response Rate (ORR)

    Time frame: Baseline through 28 days after the last treatment administration (up to approximately 7 months)

  2. Duration of Response (DOR)

    Time frame: Baseline through 28 days after the last treatment administration (up to approximately 7 months)

  3. Clinical Benefit Rate (CBR)

    Time frame: Baseline through 28 days after the last treatment administration (up to approximately 7 months)

  4. Progression-free Survival (PFS)

    Time frame: Baseline through 28 days after the last treatment administration (up to approximately 7 months)

  5. Overall Survival (OS)

    Time frame: Baseline through 3 months after the last treatment administration (up to approximately 9 months)

  6. Time to Response (TTR)

    Time frame: Baseline through 28 days after the last treatment administration (up to approximately 7 months)

  7. Area Under the Plasma Concentration-time Curve (AUC) of MEN2312 When Administered as Monotherapy

    Time frame: Up to 6 months post dose

  8. AUC of MEN2312 When Administered as Combination Therapy

    Time frame: Up to 6 months post dose

  9. Amount of MEN2312 Excreted in Urine When Administered as Monotherapy

    Time frame: Up to 2 months post dose

  10. Comparison of Plasma Concentration of MEN2312 Monotherapy With MEN2312 Combination Therapy

    Time frame: Up to 6 months post dose

Study contacts

Contact information is provided by the study sponsor or research team.

Stemline Trials

CONTACT

[email protected]

1-877-332-7961

Sponsors and collaborators

Lead sponsor

Stemline Therapeutics, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2027
Study completion
2029
First posted
Oct 15, 2024
Registry last updated
Jul 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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