A First-in-human Study to Learn How Safe BAY 3713372 is and How it Works in Participants With MTAP-deleted Solid Tumors

Last updated: April 22, 2025
Sponsor: Bayer
Overall Status: Active - Recruiting

Phase

1

Condition

Neoplasms

Treatment

BAY3713372

Clinical Study ID

NCT06914128
22931
2025-520623-24-00
  • Ages > 18
  • All Genders

Study Summary

The study treatment, BAY 3713372, is under development to treat MTAP (methylthioadenosine phosphorylase)-deleted solid tumors. It is thought to work by blocking the protein arginine N-methyltransferase 5 (PRMT5). This may kill the MTAP-deleted cancer cells while sparing the normal cells.

The main objective of this first-in-human study is to check if BAY 3713372 is safe for further testing and find the dose that could be used to treat different cancer types that are also MTAP-deleted in future studies.

For this, the researchers will study and analyze:

  • the number of participants who have adverse events after receiving different doses of BAY 3713372 and their severity.

  • the number of participants who experience dose-limiting toxicities (DLTs) after receiving different doses of BAY 3713372, their severity and how often they happened. A DLT is a pre-defined medical problem caused by a specific dose of a drug that is too severe to continue using that dose.

  • the total amount of BAY 3713372 in participants' blood (also called AUC) over time after single and multiple doses.

  • the highest level of BAY 3713372 in participants' blood (also called Cmax) after single and multiple doses.

Other than the main objective, researchers will also check for the number of participants who show a response to treatment and how long they live without the cancer getting worse.

The study participants will receive BAY 3713372 (starting from low to high doses) in the study, to find the highest safe dose for further testing.

Participants may take the study treatment as long as they benefit from the treatment without any severe medical problems.

Participants will visit the study site:

  • at least twice before the treatment starts

  • multiple times when they start taking the treatment

  • once after 30 days of receiving the last dose and every 9 weeks after that until the cancer worsens, or the participant stops for any other reason

During the study, the doctors and their study team will:

  • check participants' health by performing tests such as blood and urine tests, and checking heart health using an electrocardiogram

  • check if the participants' cancer has grown and/or spread using computed tomography (CT) or magnetic resonance imaging (MRI) and, if needed, bone scan

  • take tumor samples

The study doctors and their team will contact the participants every 3 months until 2 years after the last participant's last dose or the end of the study to learn about the participant's health.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Participant age >= 18 years old with solid tumor and at least 1 evaluable lesion asper Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1)

  • Homozygous MTAP-deletion identified through molecular testing from a locallycertified laboratory.

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

  • Participants must have exhausted available standard of care treatments known to bebeneficial for this tumor type or for whom these treatments are not acceptable andfor whom this trial is a reasonable option

Exclusion

Exclusion Criteria:

  • Previous additional cancer else than the one evaluated in this study within the past 2 years except for basal or squamous cell carcinoma of the skin, carcinoma in situof the cervix, superficial bladder tumors, localized prostate cancer or other tumorsthat in the opinion of the investigator, are considered cured or not immediatelylife-threatening, and will not interfere with the scientific goals of this study.

  • Presence of central nervous system (CNS) tumors including progressing, novel and/orsymptomatic metastatic brain disease.

  • Presence of glioblastoma multiforme (GBM).

  • A marked prolongation of QT/QTc interval at screening (e.g., repeated demonstrationof a QTc interval >450 ms). Participants with permanent pacemakers (i.e., a pacedrhythm) may be eligible after discussion with the sponsor.

  • Cardiac history comprising:

  • History of congestive heart failure Class >II according to the New York HeartAssociation Functional Classification.

  • Myocardial infarction less than 6 months before the start of studyintervention.

  • Serious cardiac arrhythmias requiring treatment or any clinically importantabnormalities in rhythm, conduction or morphology on resting ECG with theexception of atrial fibrillation which is well-controlled and requires onlydigoxin or beta blockers.

  • Unstable angina or new-on major surgery, open biopsy, or significant trauma within 4weeks before start of study intervention.

Study Design

Total Participants: 70
Treatment Group(s): 1
Primary Treatment: BAY3713372
Phase: 1
Study Start date:
March 21, 2025
Estimated Completion Date:
June 17, 2029

Connect with a study center

  • Chris O'Brien Lifehouse

    Camperdown, New South Wales 2050
    Australia

    Site Not Available

  • Concord Repatriation General Hospital (CRGH) (Concord Hospital) - Concord Cancer Centre

    Concord, New South Wales 2139
    Australia

    Site Not Available

  • National Cancer Center Singapore

    Singapore, 168583
    Singapore

    Active - Recruiting

  • National University Hospital Medical Centre

    Singapore, 119074
    Singapore

    Site Not Available

  • The Royal Marsden NHS Foundation Trust

    London, Greater London SW3 6JJ
    United Kingdom

    Site Not Available

  • The Royal Marsden NHS Foundation Trust | Sutton - Oak Foundation Drug Development Unit

    London, Greater London SW3 6JJ
    United Kingdom

    Site Not Available

  • The Christie NHS Foundation Trust

    Manchester, M20 5BX
    United Kingdom

    Site Not Available

  • The Christie NHS Foundation Trust | Christie Hospital - Experimental Cancer Medicine Team

    Manchester, M20 5BX
    United Kingdom

    Site Not Available

  • Sarah Cannon Research Institute at HealthONE

    Denver, Colorado 80218
    United States

    Site Not Available

  • Florida Cancer Specialists & Research Institute - Lake Nona

    Orlando, Florida 32827
    United States

    Site Not Available

  • START | Midwest

    Grand Rapids, Michigan 49546
    United States

    Site Not Available

  • SCRI Oncology Partners

    Nashville, Tennessee 37203
    United States

    Site Not Available

  • NEXT Dallas

    Irving, Texas 75039
    United States

    Site Not Available

  • START | San Antonio

    San Antonio, Texas 78229-3307
    United States

    Active - Recruiting

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