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Microsatellite Stable (MSS) Colorectal Cancer (CRC)Phase 2NCT06784947

Trial of Atezolizumab, Bevacizumab, and Tiragolumab in Patients With Microsatellite Stable, Metastatic Colorectal Cancer

A Phase 2 study testing Pre-Treatment Biopsy, On-Treatment Biopsy and Tiragolumab in people with Microsatellite Stable (MSS) Colorectal Cancer (CRC) and Metastatic Colorectal Cancer (CRC), run by University of Colorado, Denver at 1 site in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The goal of this study is to learn if a new combination treatment is effective for patients with microsatellite stable, advanced colorectal cancer. The study treatment combines 3 drugs: atezolizumab, bevacizumab, and tiragolumab. The main questions the study aims to answer are: 1. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Pre-Treatment Biopsy, On-Treatment Biopsy and Tiragolumab
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
13 participants
Where
1 siteUnited States
Study dates
25 Mar 2025to May 2028
Phase
Phase 2
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Able to sign the consent form.
  • Stated willingness and ability to comply with all study procedures and be available for the duration of the study.
  • ≥ 18 years at the time of informed consent.
  • Biopsy confirmed, unresectable, metastatic colorectal adenocarcinoma.
  • Measurable disease (disease that can be viewed and measured on scans), as assessed by the investigator per RECIST v1.1.
  • If in Cohort A, (1) the patient must state willingness to undergo pre- and on-treatment biopsies, and (2) the patient's disease must be amenable to biopsy.
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  • Eastern Cooperative Oncology Group performance status of 0-2.
  • Documented microsatellite stable and/or proficient mismatch repair status.
  • Documented testing for KRAS, NRAS, and BRAF mutation status.
  • Progression on or intolerance to prior therapy for unresectable, metastatic CRC including at least (1) fluoropyrimidine, oxaliplatin, and irinotecan chemotherapy AND (2) EGFR inhibitor therapy for patients with KRAS/NRAS/BRAF wild-type, left-sided disease.
  • Adequate hematologic and end organ function, defined by laboratory results obtained within 28 days prior to the first dose of study treatment.
  • ANC ≥ 1.2 × 10^9/L
  • Lymphocyte count ≥ 0.5 x 10^9/L
  • Platelet count ≥ 100 × 10^9/L, without transfusion in the prior week.
  • Hemoglobin ≥ 9 g/dL; patients may be transfused to meet this criterion.
  • Serum total bilirubin ≤ 1.5 x the upper limit of normal (ULN); patients with known Gilbert's disease may have a bilirubin ≤ 3.0 × ULN.
  • Aspartate transaminase, alanine transaminase, and alkaline phosphatase ≤ 2.5 × ULN with the following exceptions:
  • For patients with documented liver metastases, AST and/or ALT ≤ 5 × ULN.
  • For patients with documented liver or bone metastases, ALP ≤ 5 × ULN.
  • Serum albumin ≥ 25 g/L (2.5 g/dL)
  • Creatinine clearance ≥ 45 mL/min as calculated using the Cockcroft-Gault formula or measured using a 24-hour urine collection.
  • For patients not receiving therapeutic anticoagulation, international normalized ratio and activated partial thromboplastin time ≤ 1.5 × ULN.
  • Patients receiving therapeutic anticoagulation must be on a stable regimen, with INR and aPTT within the expected therapeutic range of intended use of the anticoagulant.
  • Negative HIV testing at screening, or, for those with known history of HIV, documented control of infection on anti-retroviral therapy with evidence of undetectable viral load and CD4 count of >500 cells/microL for a least 6 months prior to enrollment.
  • Negative hepatitis B surface antigen (HBsAg) test at screening.
  • Positive hepatitis B surface antibody (HBsAb) test at screening, or negative HBsAb test at screening accompanied by either of the following:
  • Negative total hepatitis B core antibody (HBcAb)
  • Positive total HBcAb test followed by quantitative hepatitis B virus (HBV) DNA < 500 IU/mL.
  • Negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody test followed by a negative HCV RNA test at screening.
  • For women of childbearing potential (WOCBP): agreement to refrain from heterosexual intercourse or use contraception.
  • For men: agreement to refrain from heterosexual intercourse or use a condom, and agreement to refrain from donating sperm.

Who cannot join

  • Illness or condition that may interfere with a patient's capacity to understand, follow, and/or comply with study procedures.
  • Known microsatellite instability-high or deficient mismatch repair status, or unknown status for both MSI and MMR.
  • Prior testing documenting a BRAF V600E mutation, or unknown testing results for KRAS, NRAS, and BRAF.
  • A limited number of patients with active liver metastases will be permitted in this trial. Those with a history of definitively treated liver metastases with treatment occurring at least 6 months prior to enrollment with no evidence of metastatic disease in the liver on subsequent imaging may be eligible to enroll as a patient without active liver disease.
  • Known symptomatic, untreated, or actively progressing central nervous system metastases. Asymptomatic patients with treated CNS lesions are eligible, provided that additional criteria are met.
  • History of leptomeningeal disease or carcinomatous meningitis.
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  • Spinal cord compression not definitively treated with surgery and/or radiation.
  • Uncontrolled tumor-related pain. Patients requiring pain medication must be on a stable regimen at study entry.
  • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures.
  • History of malignancy other than colorectal cancer within 3 years prior to screening, with the exception of malignancies with a negligible risk of metastasis or death, such as adequately treated carcinoma in situ of the cervix, basal or squamous cell skin cancer, localized prostate cancer, or ductal carcinoma in situ.
  • Active autoimmune disease, history of autoimmune disease requiring treatment with corticosteroids, disease modifying agents, and/or immunosuppressive therapy, or immune deficiency including, but not limited to, myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, antiphospholipid antibody syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain-Barré syndrome, or multiple sclerosis, with the exceptions listed below:
  • Patients with a history of autoimmune-related hypothyroidism who are on thyroid replacement hormone are eligible for the study.
  • Patients with controlled Type 1 diabetes mellitus who are on an insulin regimen are eligible for the study.
  • Patients with eczema, psoriasis, lichen simplex chronicus, or vitiligo with dermatologic manifestations only are eligible for the study provided all of following conditions are met:
  • Rash must cover < 10% of body surface area.
  • Disease is well controlled at baseline \& requires only low-potency topical corticosteroids.
  • There has been no occurrence of acute exacerbations of the underlying condition requiring psoralen plus ultraviolet A radiation, methotrexate, retinoids, biologic agents, oral calcineurin inhibitors, or high potency or oral corticosteroids within the previous 12 months.
  • Prior allogeneic stem cell or solid organ transplantation.
  • History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT scan.
  • Known history of tuberculosis and/or active tuberculosis.
  • Active bowel inflammation on imaging at the time of enrollment.
  • History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess.
  • Clinical signs or symptoms of GI obstruction or requirement for routine parenteral hydration, parenteral nutrition, or tube feeding.
  • Evidence of abdominal free air not explained by paracentesis or recent surgical procedure.
  • History of or active clinically significant cardiovascular dysfunction, including the following:
  • History of stroke or transient ischemic attack within 6 months prior to first dose of study treatment.
  • History of myocardial infarction within 6 months prior to first dose of study treatment.
  • Heart failure with New York Heart Association Class II or higher symptoms within 3 months prior to initiation of study treatment.
  • Unstable arrhythmia.
  • Coronary heart disease that is symptomatic or unstable angina.
  • Inadequately controlled hypertension. Anti-hypertensive therapy to achieve these parameters is allowed.
  • History of hypertensive crisis or hypertensive encephalopathy.
  • Grade ≥ 2 proteinuria, as demonstrated by ≥ 2+ protein on dipstick urinalysis and ≥ 1.0 g of protein in a 24-hour urine collection.
  • o All patients with ≥ 2+ protein on dipstick urinalysis at screening must undergo a 24-hour urine collection for protein. Patients with < 2+ protein on dipstick urinalysis are eligible for the study and do not require 24-hour urine collection.
  • Significant vascular disease within 6 months prior to initiation of study treatment.
  • History of Grade 4 venous thromboembolism.
  • History of Grade ≥ 2 hemoptysis, or other serious hemorrhage or bleeding risk, within 1 month prior to screening.
  • History or evidence of inherited bleeding diathesis or significant coagulopathy at risk of bleeding.
  • Major surgical procedure, or significant traumatic injury, within 4 weeks prior to initiation of study treatment, or anticipation of need for a major surgical procedure during the study.
  • o Study-related biopsies are not considered major surgical procedures in this study.
  • Minor surgical procedures, including placement of a vascular access device, within 7 days prior to initiation of study treatment, with the following exceptions:
  • Study-related biopsies are NOT considered as surgical procedures under the exclusion criteria. Pre-treatment study biopsies should be performed at least 3 days prior to study treatment initiation.
  • Patients must have sufficiently recovered from any prior surgery, including adequate wound healing.
  • Serious, non-healing wound, active ulcer, or untreated bone fracture.
  • Severe infection within 4 weeks prior to initiation of study treatment, including, but not limited to, hospitalization for complications of infection, bacteremia, or severe pneumonia, or any active infection that could impact patient safety.
  • Positive Epstein-Barr virus (EBV) viral capsid antigen immunoglobulin M (IgM) test at screening. An EBV polymerase chain reaction (PCR) test should be performed as clinically indicated to screen for acute infection or suspected chronic active infection. Patients with a positive EBV PCR test are excluded.
  • Current or recent (< 10 days prior to initiation of study treatment) use of aspirin (> 325 mg/day), or clopidogrel (> 75 mg/day), or recent (< 21 days prior to initiation of study treatment) use of therapeutic thrombolytic agents.
  • Recent (< 21 days prior to initiation of study treatment) initiation of full-dose oral or parenteral anticoagulants. The use of full-dose oral or parenteral anticoagulants is permitted as long as the following criteria are met:
  • The INR and/or aPTT are within therapeutic limits (according to the medical standard of the enrolling institution).
  • The patient has been on a stable dose of anticoagulants for at least 21 days prior to initiation of study therapy.
  • There is no evidence of or clinical concern for new or worsening thromboembolism within 21 days prior to initiation of study treatment.
  • The patient has no history of serious hemorrhage or bleeding risk.
  • The patient has no persisting bleeding diathesis or anatomic or pathologic condition that significantly increases the risk of hemorrhage.
  • Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to initiation of study treatment.
  • o Patients receiving prophylactic antibiotics (e.g., to prevent a urinary tract infection or chronic obstructive pulmonary disease exacerbation) are eligible for the study.
  • Treatment with a live, attenuated vaccine within 4 weeks prior to initiation of study treatment, or anticipation of need for such a vaccine during study treatment, within 90 days after the final dose of tiragolumab, or within 5 months after the final dose of atezolizumab.
  • Current treatment with anti-viral therapy for HBV.
  • Treatment with any systemic anti-cancer therapy within 21 days or 5 half-lives of starting study treatment, whichever is shorter.
  • Treatment with an investigational therapy within 42 days of initiation of study treatment.
  • Prior treatment with CD137 agonists or investigational immune checkpoint blockade therapies, including anti-LAG3, anti-CTLA-4, anti-PD-1, anti-PD-L1, or anti-TIGIT agents.
  • Prior radiation therapy within 14 days of Cycle 1, Day 1 of study treatment, and/or persistence of radiation-related adverse effects. Participants must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis prior to study treatment start. Palliative radiation therapy (as long as it does not involve target lesions) is permitted on the study.
  • Treatment with systemic immunostimulatory agents, including, but not limited to, interferon and IL-2, within 4 weeks or 5 drug-elimination half-lives (whichever is longer) prior to initiation of study treatment.
  • Treatment with systemic immunosuppressive medication (including, but not limited to, corticosteroids, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor-α [TNF- α] agents) within 2 weeks prior to initiation of study treatment, or anticipation of need for systemic immunosuppressive medication during study treatment, with the following exceptions:
  • Patients who received acute, low-dose systemic immunosuppressant medication or a one-time pulse dose of systemic immunosuppressant medication (e.g., 48 hours of corticosteroids for a contrast allergy) are eligible for the study.
  • Patients who received mineralocorticoids, corticosteroids for chronic obstructive pulmonary disease or asthma, or low-dose corticosteroids for orthostatic hypotension or adrenal insufficiency are eligible for the study.
  • Patients requiring chronic use of ≥ 10 mg prednisone per day or equivalent
  • Requirement for treatment with any medicinal product that contraindicates the use of any of the study treatments, may interfere with the planned treatment, impact patient compliance, or puts the patient at higher risk for treatment-related complications.
  • History of severe allergic anaphylactic reactions to chimeric or humanized antibodies or fusion proteins.
  • Known hypersensitivity to Chinese hamster ovary cell products or to any component of the atezolizumab, bevacizumab, or tiragolumab formulations.
  • Pregnancy or breastfeeding, or intention of becoming pregnant.
  • Any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding that contraindicates the use of an investigational drug, may affect the interpretation of the results, or may render the patient at high risk from treatment.

Trial locations and contacts

1 site in 1 country.

United States1 site

  • Universtiy of Colorado Hospital

    Aurora, Colorado, 80045

Other trials in United States

About this study

Official title: A Phase II Trial of Tiragolumab in Combination With Atezolizumab and Bevacizumab in Patients With Previously Treated, Microsatellite Stable, Metastatic Colorectal Adenocarcinoma

The goal of this study is to learn if a new combination treatment is effective for patients with microsatellite stable, advanced colorectal cancer. The study treatment combines 3 drugs: atezolizumab, bevacizumab, and tiragolumab. The main questions the study aims to answer are:

  1. Does the study treatment effectively treat colorectal cancer?
  2. Is the study treatment safe for patients with colorectal cancer?
  3. How does the study treatment effect the immune system in patients with colorectal cancer?

Participants in this study will receive the study treatment and undergo checkups, laboratory tests, and imaging tests for monitoring. Some participants will also undergo tumor biopsies.

Read the detailed description

This is a phase II study investigating the efficacy and safety of a triple-combination immunotherapy regimen in patients diagnosed with microsatellite stable metastatic colorectal cancer (MSS mCRC), refractory to fluorouracil, oxaliplatin, and irinotecan chemotherapy. The trial is designed as a single-arm, Simon two-stage study.

All participants will receive a fixed-dose regimen of the three agents: atezolizumab (1200 mg), bevacizumab (15 mg/kg), and tiragolumab (600 mg), administered intravenously on day 1 of 21-day cycles. Treatment response will be assessed by imaging using RECIST v1.1 every 9 weeks. Study treatment will be continued until disease progression, unacceptable toxicity, death, decision by the patient and/or treating physician to withdraw from the study, pregnancy, or study termination, whichever occurs first.

This study will enroll patients in 2 cohorts: A and B. Patients in Cohort A will undergo pre-treatment and on-treatment tumor biopsies for correlative studies. Patient in Cohort B will not receive study biopsies. Patients in Cohorts A and B will otherwise receive identical treatment.

Being tested
Pre-Treatment Biopsy, On-Treatment Biopsy, Tiragolumab, Atezolizumab, Bevacizumab
Keywords
immunotherapy, microsatellite stable colorectal cancer, tiragolumab, metastatic colorectal cancer, atezolizumab, bevacizumab
Medical subject headings
Spinocerebellar Degenerations, Colorectal Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Pre-Treatment BiopsyProcedure or surgery

    The pre-treatment biopsy should be performed at least 3 days prior to C1D1 of treatment.

  • On-Treatment BiopsyProcedure or surgery

    While the acceptable window for the C3D1 biopsy is ±3 days, it is preferred that the biopsy occurs following all treatments on C3D1.

  • TiragolumabDrug

    Tiragolumab is a human monoclonal antibody targeting the co-inhibitory molecule and immune checkpoint inhibitor T-cell immunoreceptor with immunoglobulin (Ig) and immunoreceptor tyrosine-based inhibitory motif (ITIM) domains (TIGIT), with potential immune checkpoint inhibitory activity. This treatment may help the immune system attack cancer cells.

  • AtezolizumabDrug

    Atezolizumab is a type of targeted therapy drug called an immune checkpoint inhibitor. It is a monoclonal antibody that works by binding to the protein PD-L1 (programmed death) on the surface of some cancer cells, which keeps cancer cells from suppressing the immune system. This allows the immune system to attack and kill the cancer cells.

  • BevacizumabDrug

    Bevacizumab works by blocking a protein called Vascular Endothelial Growth Factor (VEGF), which some cancer cells produce in large amounts. Blocking VEGF may prevent the growth of new blood vessels that tumors need to grow, and may help improve the immune response in the tumor. Bevacizumab is a type of targeted therapy called an angiogenesis inhibitor.

Study groups in NCT06784947
Study groupRoleWhat they receive
Treatment with BiopsyExperimentalPatients in Cohort A will undergo pre-treatment and on-treatment tumor biopsies for correlative analyses, with on-treatment biopsies obtained at cycle 3, day 1 (C3D1) +/- 3 days of treatment.
Receives: Procedure: Pre-Treatment Biopsy; Procedure: On-Treatment Biopsy; Drug: Tiragolumab; Drug: Atezolizumab; Drug: Bevacizumab
Treatment without BiopsyExperimentalIn Cohort B, no study-related biopsies will be obtained. Outside of pre- and on-treatment biopsies, patients in Cohort A and Cohort B will receive identical treatments and assessments.
Receives: Drug: Tiragolumab; Drug: Atezolizumab; Drug: Bevacizumab

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Objective Response Rate (ORR)

    The primary outcome of this trial is objective response rate (ORR), defined as the proportion of patients who achieve a complete or partial response to treatment according to RECIST v1.1 criteria.

    Measured: From time of study start to time of best response, up to 24 months

Secondary outcomes (6)

  1. Progression Free Survival (PFS)

    Progression free survival (PFS) measures the length of time from treatment start to disease progression or death, whichever comes first.

    Measured: From time of study start until disease progression or death, whichever comes first; up to 24 months

  2. Overall Survival (OS)

    Overall survival (OS) measures the duration of time from treatment start until death from any cause.

    Measured: From time of study start until death by any cause, up to 24 months

  3. Safety measured by adverse events

    Safety will be monitored by the reporting of types and grades of adverse events associated with the treatment regimen.

    Measured: From time of study start until time of study end, up to 24 months

  4. Impact of Liver Metastases on Treatment Response- ORR

    Objective response rate (ORR) will be assessed according to the presence or absence of liver metastases.

    Measured: From time of study start to time of best response (ORR), up to 24 months

  5. Impact of Liver Metastases on Treatment Response- PFS

    Progression free survival (PFS) will be assessed according to the presence or absence of liver metastases.

    Measured: From time of study start until disease progression or death, whichever comes first; up to 24 months

  6. Impact of Liver Metastases on Treatment Response- OS

    Overall survival (OS) will be assessed according to the presence or absence of liver metastases.

    Measured: From time of study start until death by any cause, up to 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Jan 2025
  2. Study start25 Mar 2025
  3. Primary completion18 Sep 2025
  4. Study completionMay 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
13 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06784947
Sponsor's protocol ID
24-0547.cc
Status last verified
Oct 2025
First submitted
8 Jan 2025
Last updated
2 Oct 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Pre-Treatment Biopsy, On-Treatment Biopsy and Tiragolumab in people with Microsatellite Stable (MSS) Colorectal Cancer (CRC) and Metastatic Colorectal Cancer (CRC), run by University of Colorado, Denver at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 31 inclusion and 71 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 2 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Objective Response Rate (ORR) (time frame: From time of study start to time of best response, up to 24 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06784947.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Oct 2025.

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