NCT07550088 · Darren Sigal, MD
BAL/BOT/agenT-797 in pMMR CRC With Liver Metastases
What this study is about
The goal of this clinical trial is to learn whether the combination of balstilimab, botensilimab, and agenT-797 is safe and effective in treating adults with previously treated metastatic colorectal cancer that is microsatellite stable (pMMR) and has spread to the liver.
View original scientific description
The goal of this clinical trial is to learn whether the combination of balstilimab, botensilimab, and agenT-797 is safe and effective in treating adults with previously treated metastatic colorectal cancer that is microsatellite stable (pMMR) and has spread to the liver. The main questions it aims to answer are: * What proportion of participants experience tumor shrinkage (objective response rate) based on imaging assessments? * What side effects occur with this combination treatment, including immune-related and cytokine-related reactions? All participants in this study will receive the combination treatment. There is no comparison group.
Interventions
DRUG
Balstilimab (BAL)
Administered at a fixed dose of 240mg intravenously (IV) on Days 1, 15, 29 of each 42-day cycle, for up to 9 cycles.
DRUG
Botensilimab (BOT)
Administered at a fixed dose of 75mg IV on Day 1 of Cycles 1 through 4. In the event of protocol-defined toxicity, the dose may be reduced to 50mg IV per protocol defined criteria.
DRUG
agenT-797
Administered at a dose of 1.4 x 107 cells/kg IV on Day 1 of Cycle 1 and Day 15 of Cycle 2.
Primary outcome measures
Overall Response Rate (ORR)
Time frame: From enrollment until first documented disease progression or end of study treatment (up to approximately 12 months).
ORR, defined as the proportion of participants whose best overall response (BOR) is either Complete Response (CR) or Partial Response (PR) per RECIST v1.1.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Adults ≥18 years of age with histologically confirmed metastatic colorectal cancer with liver metastases, including evidence of active liver disease if previously treated locally
- At least one measurable lesion per RECIST v1.1, with ≥1 target lesion in the liver
- Tumor confirmed as microsatellite stable (MSS)/proficient mismatch repair (pMMR) per a FDA-approved assay (Caris MI Cancer Seek®, FoundationOne® CDx, or Tempus xT CDx).
- Received ≥1 prior line of systemic therapy including fluorouracil, oxaliplatin, and irinotecan (not necessarily in combination), and prior EGFR inhibitor or bevacizumab if eligible, unless contraindicated
- ECOG performance status 0-1 and life expectancy ≥12 weeks
- Adequate organ and marrow function:
- ANC ≥1.5 × 10⁹/L
- Platelets ≥100 × 10⁹/L
- Hemoglobin ≥ 9 g/dL
- AST/ALT ≤2.5 × ULN
- Total bilirubin ≤1.5 × ULN
- Creatinine clearance ≥ 40 mL/min, as measured or calculated per local institutional standards.
- Albumin ≥3 g/dL
- PT/PTT ≤1.5 × ULN
- Willing and able to provide written informed consent
- Negative pregnancy test for women of childbearing potential
- Agreement to use effective contraception during study participation
Exclusion criteria
- Tumor is dMMR/MSI-high
- Prior treatment with PD-1, PD-L1, CTLA-4 inhibitors, or other immunotherapy agents
- Evidence of bowel obstruction, impending obstruction, or recent obstruction (within 3 months)
- Refractory ascites requiring frequent paracentesis or recent escalation of diuretics
- Clinically significant cardiovascular disease (e.g., recent myocardial infarction or stroke, unstable angina, NYHA class ≥III heart failure, uncontrolled arrhythmias) or QTc \>480 ms
- Active or untreated brain metastases or leptomeningeal disease
- Concurrent malignancy requiring treatment or active within 2 years (with protocol-specified exceptions)
- Receipt of prior anti-cancer therapy within protocol-defined washout periods, including:
- Cytotoxic, targeted therapy or other investigational therapy within 3 weeks.
- Monoclonal antibodies, antibody-drug conjugates, radioimmunoconjugates, or similar therapy, within 4 weeks, or 5 half-lives, whichever is shorter.
- Small molecules/tyrosine kinase inhibitors within 2 weeks or less than 5 circulating half-lives of investigational drug.
- Known hypersensitivity to study drugs or excipients
- History of or active interstitial lung disease or pneumonitis requiring systemic steroids
- Prior allogeneic transplant (organ, stem cell, or bone marrow)
- Active or recent autoimmune disease requiring systemic treatment
- Requirement for systemic corticosteroids (\>10 mg prednisone equivalent) or other immunosuppressive therapy within defined windows
- Active infection, including HIV, HTLV, HBV, HCV, or other infections requiring systemic therapy
- Recent SARS-CoV-2 infection within protocol-defined timeframe
- Uncontrolled hypertension, significant proteinuria (UPCR ≥1 g/g), or other clinically significant uncontrolled medical conditions
- Non-healing wounds, active bleeding, or uncontrolled thyroid dysfunction
- Psychiatric or substance use disorders that may interfere with study participation
- Receipt of live or attenuated vaccines within 30 days prior to treatment and while participating in the study
- Pregnant or breastfeeding women, or those planning pregnancy during the study
Where
- La Jolla, California
Collaborators
Scripps Health
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Aug 10, 2026 · Source of record for eligibility and locations