Phase
Condition
Neoplasms
Treatment
BAY3713372
Clinical Study ID
Ages > 18 All Genders
Study Summary
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
Connect with a study center
Chris O'Brien Lifehouse
Camperdown, New South Wales 2050
AustraliaSite Not Available
Concord Repatriation General Hospital (CRGH) (Concord Hospital) - Concord Cancer Centre
Concord, New South Wales 2139
AustraliaSite Not Available
National Cancer Center Singapore
Singapore, 168583
SingaporeActive - Recruiting
National University Hospital Medical Centre
Singapore, 119074
SingaporeSite Not Available
The Royal Marsden NHS Foundation Trust
London, Greater London SW3 6JJ
United KingdomSite Not Available
The Royal Marsden NHS Foundation Trust | Sutton - Oak Foundation Drug Development Unit
London, Greater London SW3 6JJ
United KingdomSite Not Available
The Christie NHS Foundation Trust
Manchester, M20 5BX
United KingdomSite Not Available
The Christie NHS Foundation Trust | Christie Hospital - Experimental Cancer Medicine Team
Manchester, M20 5BX
United KingdomSite Not Available
Sarah Cannon Research Institute at HealthONE
Denver, Colorado 80218
United StatesSite Not Available
Florida Cancer Specialists & Research Institute - Lake Nona
Orlando, Florida 32827
United StatesSite Not Available
START | Midwest
Grand Rapids, Michigan 49546
United StatesSite Not Available
SCRI Oncology Partners
Nashville, Tennessee 37203
United StatesSite Not Available
NEXT Dallas
Irving, Texas 75039
United StatesSite Not Available
START | San Antonio
San Antonio, Texas 78229-3307
United StatesActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.