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New treatment option for Refractory Metastatic Microsatellite Stable Colorectal Cancer (MSS-CRC)
Official title Phase 2 Study of SR-8541A in Combination With Botensilimab and Balstilimab in Subjects With Refractory Metastatic Microsatellite Stable Colorectal Cancer (MSS-CRC)
ClinicalTrials.gov ID: NCT06589440
What this study is testing
What is SR-8541A?
SR-8541A is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for refractory metastatic microsatellite stable colorectal cancer (mss-crc).
Also referred to as Botensilimab, Balstilimab.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This is an open-label, dose escalation and expansion, multi-center phase 2 study evaluating the safety and efficacy of SR-8541A administered orally in combination with intravenous botensilimab and balstilimab in subjects with MSS-CRC with and without active liver metastases.
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Written informed consent from subject
- Age ≥ 18 years old on the date of consent
- Histologically confirmed diagnosis of unresectable and metastatic adenocarcinoma of the colon or rectum
- Non-microsatellite instability high or non-deficient mismatch repair (non-MSI-H/non-dMMR) tumor status per a standard local testing method
- Must have received at least 1 prior chemotherapy regimen for metastatic or recurrent CRC
You likely can't join if
- Hypersensitivity or allergy to any of the study drugs or their excipients.
- In Part 2, Cohort A, active liver metastases by computed topography (CT) or magnetic resonance imaging (MRI).
- Treatment with one of the following classes of drugs within the delineated time window prior to first dose:
- Small molecule/tyrosine kinase inhibitors within 2 weeks
- Any other systemic therapy for CRC within 3 weeks
- Received another investigational drug within 30 days or active participation in another clinical trial (follow-up is permitted)
See the full eligibility criteria
- Written informed consent from subject
- Age ≥ 18 years old on the date of consent
- Histologically confirmed diagnosis of unresectable and metastatic adenocarcinoma of the colon or rectum
- Non-microsatellite instability high or non-deficient mismatch repair (non-MSI-H/non-dMMR) tumor status per a standard local testing method
- Must have received at least 1 prior chemotherapy regimen for metastatic or recurrent CRC
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
- Measurable disease per RECIST v1.1 (Eisenhauer et al., 2009)
- Able to provide archival or fresh tumor tissue during screening (required) and post-treatment (optional)
- Adequate renal function defined as creatinine clearance ≥ 60mL/min
- Adequate liver function
- Adequate hematologic function
- No growth factor support, transfusions, or albumin administration within 14 days of first dose of study treatment
- Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures
- Male and female people of childbearing potential must agree to use a highly medically effective method of contraception and refrain from sperm/egg donation throughout the study starting with the first dose of study...
- Hypersensitivity or allergy to any of the study drugs or their excipients.
- In Part 2, Cohort A, active liver metastases by computed topography (CT) or magnetic resonance imaging (MRI).
- Treatment with one of the following classes of drugs within the delineated time window prior to first dose:
- Small molecule/tyrosine kinase inhibitors within 2 weeks
- Any other systemic therapy for CRC within 3 weeks
- Received another investigational drug within 30 days or active participation in another clinical trial (follow-up is permitted)
- Medications/products which are known strong inhibitors or inducers of the CYP enzymes within 5 x T1/2
- Received programmed cell death protein 1, PD-(L)1, or CTLA-4 therapies including any immune checkpoint inhibitor or experimental immunologic agents.
- Partial or complete bowel obstruction within the last 3 months, signs/symptoms of bowel obstruction, or known radiologic evidence of impending obstruction.
- Refractory ascites.
- Current evidence of interstitial lung disease (ILD) or pneumonitis, or prior history of ILD or non-infectious pneumonitis requiring glucocorticoids.
- Continuous systemic treatment with either corticosteroids (\>10 mg daily prednisone equivalents) or other immunosuppressive medications within 28 days prior to Day 1.
- Active autoimmune disease that has required systemic treatment in past 2 years
- Patients with adrenal / pituitary insufficiency
- History of documented congestive heart failure; unstable angina; poorly controlled hypertension; clinically significant valvular heart disease; high-risk uncontrolled arrhythmias (including sustained ventricular...
- History of allogeneic organ transplant, stem cell transplant, or bone marrow transplant
- Previous SARS-CoV-2 infection within 10 days for mild or asymptomatic infections or 20 days for severe/critical illness prior to first dose
- Requirement for treatment with strong cytochrome P450 3A4 inducers or inhibitors
- Presence of gastrointestinal condition, for example, malabsorption, that might affect the absorption of Investigational Product(s).
- Troponin I \> ULN
- Uncontrolled hypertension
- Corrected QT interval by Fridericia (QTcF) ≥ 470 ms per the central mean average of triplicate electrocardiograms (ECGs)
- Left Ventricular Ejection Fraction (LVEF) \< 50% using echocardiogram or multigated acquisition (MUGA)
- Symptomatic uncontrolled central nervous system (CNS) disease requiring treatment with steroids or anti-seizure medications within 2 months prior to Day 1. However, people with brain metastases that have been previously...
- Leptomeningeal disease
- Spinal cord compression not definitively treated with surgery and/or radiation
- Bleeding diathesis due to underlying medical condition or anticoagulation medication which is unable to be promptly reversed by medical treatment
- Prior additional malignancy that is progressing or has received treatment the previous 3 years prior to first dose except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin...
- History of uncontrolled seizures, central nervous disorders, substance abuse disorder or psychiatric disability judged by the Investigator to be clinically significant and would interfere with cooperation with...
- Active infection requiring systemic treatment at time of first dose
- Positive for human immunodeficiency virus (HIV) (HIV antibodies) or active hepatitis B (e.g., HbsAg reactive) or active hepatitis C (e.g., HCV ribonucleic acid [RNA] qualitative) infection with detectable viral load
- Pregnant or lactating females who plan to nurse a child during or within 3 months of the last dose of study treatment
- Major surgery within 28 days prior to first dose and/or minor surgery (excluding biopsy) within 7 days prior to first dose. Note: If the subject had major surgery, the subject must have recovered adequately from the...
- Prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality that, in the Investigator's opinion, could affect the safety of the subject or impair the...
- Planned use of any of the prohibited concomitant medications
The study team makes the final eligibility decision.
Where it's taking place
- Morristown, New Jersey, United States
- Austin, Texas, United States
- Dallas, Texas, United States
- Houston, Texas, United States
- Tyler, Texas, United States
- Seattle, Washington, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Morristown, New Jersey, United States; Austin, Texas, United States; Dallas, Texas, United States; Houston, Texas, United States; Tyler, Texas, United States; Seattle, Washington, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.