Recruiting
Phase 2

Cemiplimab, Fianlimab, REGN7075

Sponsor:

NSABP Foundation Inc

Code:

NCT07058012

Conditions

Colo-rectal Cancer

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Cemiplimab

cemiplimab plus fianlimab

cemiplimab + REGN7075

ctDNA testing

Study Details

Brief summary:

The NSABP FC-13 study is being done to determine if using immunotherapies alone or in combination with other drugs will delay or prevent colorectal cancer from coming back in patients with colorectal cancer who are ctDNA-positive after their treatment. Immunotherapeutic drugs (immunotherapies) act on different proteins on the surface of cells of the immune system and trigger the immune system to destroy cancer cells. The drugs being studied in NSABP FC-13 are cemiplimab, fianlimab, and REGN7075.

Conditions

Colo-rectal Cancer

Study ID

NCT07058012

Start date

Apr 17, 2026

Status verified date

Sep, 2026

Completion date

Jun 1, 2029

Anticipated

Primary completion date

Apr 17, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • The patient must have consented to participate and, prior to beginning specific study procedures, must have signed and dated appropriate Institutional Review Board (IRB) -approved consent forms that conform to federal and institutional guidelines for study treatment.
  • Patients must be greater than or equal to18 years old.
  • The ECOG performance status must be 0-1.
  • Patients must have confirmed histologic and pathologic stage II/III colon, stage II/III rectal, or oligometastatic stage IV colorectal adenocarcinoma (per AJCC 8th edition).
  • There must be documentation by CT scan with contrast that the patient has no definitive evidence of (non-resected or non-ablated) metastatic disease including assessment of chest, abdomen, and pelvis at the time of study enrollment
  • All patients must have had a complete (R0) resection of their primary tumor and resected or ablated (radiofrequency ablation, stereotactic body radiation therapy \[SBRT\], microwave ablation, etc.\]) oligometastatic disease if present AND at least 3 months of a standard systemic chemotherapy regimen (e.g., FOLFOX or CAPOX or fluoropyrimidine monotherapy). This includes either adjuvant chemotherapy for colon cancer or perioperative (adjuvant or neoadjuvant) chemotherapy for rectal cancer or oligometastatic colon or rectal cancer. Chemoradiotherapy for rectal cancer (as a component of curative treatment) is acceptable. NOTE: Patients who achieve a clinical complete response and opt for a non-operative approach to their primary tumor management are not eligible.

  • Patients must be ctDNA-positive by an assay run in any CLIA-certified lab obtained within 2 weeks to 12 months following completion of definitive all curative therapy for colorectal cancer.
  • Tumor status of microsatellite stability (MSS) or Proficient mismatch repair (pMMR) is confirmed through a standard of care assay through a CLIA-certified lab.
  • At the time of study entry, blood counts performed within 28 days prior to study entry must meet the following criteria:

  • ANC must be greater than or equal to (≥) 1000/mm3,
  • Platelet count must be ≥ to 80,000/mm3; and
  • Hemoglobin must be ≥ 8 g/dL. (Note: transfusions may be used to correct hemoglobin for patients experiencing anemia from therapy who otherwise would be eligible for the study.)
  • Albumin greater than (>) 3.0 g/dL.
  • The following criteria for evidence of adequate hepatic function performed within 28 days prior to study entry must be met:

  • Total bilirubin less than or equal to (≤) 1.5 x ULN
  • AST and ALT must be ≤ 3.0 x ULN for the lab. (Note: In patients with elevated ALT or AST, the values must be stable for at least 2 weeks and with no evidence of biliary obstruction on imaging.)
  • Creatinine must be ≤ 1.5 x upper limit of normal (ULN) or calculated creatinine clearance ≥ 40mL/min.
  • All prior chemotherapy toxicities (excluding alopecia, amenorrhea, and peripheral neuropathy) must be less than (<) Grade 2 at the time study therapy is to begin unless AE(s) are clinically stable on supportive therapy.
  • Patients must have no evidence of opportunistic infections.
  • Patients of childbearing potential must have a negative pregnancy per institutional policies prior to receiving the first dose of study therapy.
  • Male and female patients with reproductive potential must agree to use accepted effective methods of contraception while receiving study therapy and for at least 180 days (6 months) after the completion of study therapy. Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the patient.

Exclusion Criteria:

  • Colon cancer other than adenocarcinoma, e.g., sarcoma, lymphoma, carcinoid.
  • Patients with MSI-high (dMMR) tumors.
  • Use and/or receipt of the last dose of anti-cancer therapy (chemotherapy, immunotherapy, targeted therapy, biologic therapy, monoclonal anti-bodies) or radiation therapy within 4 weeks prior to receiving first dose of study therapy or associated with immune-mediated adverse events (imAEs) that were Grade ≥1 within 90 days prior to the first dose of study therapy or associated with toxicity that resulted in discontinuation of the immune-modulating agent.
  • History of active or latent tuberculosis (TB) infection. If the presence of TB (active or latent) is established, then treatment for TB must be completed according to local guidelines prior to the screening.
  • Active untreated or uncontrolled systemic fungal, bacterial, or viral infections, or active infection requiring systemic anti-infectious therapy.
  • Current or history of systemic autoimmune disease requiring systemic immunosuppressive therapy will not be allowed. Note: the following will not be exclusionary: 1) the presence of laboratory evidence of autoimmune disease (e.g., positive antinuclear antibody titer or lupus anticoagulant) without associated symptoms; 2) clinical evidence of vitiligo or other forms of depigmenting illness; 3) mild autoimmunity not impacting the function of major organs (e.g., controlled Hashimoto thyroiditis, limited psoriasis), Type I diabetes.
  • Patients will be excluded if they are on systemic steroid therapy that cannot be discontinued (except for the use of prednisone or equivalent <0.125mg/kg/day as replacement therapy). Inhaled or topical steroids are permitted.
  • Receipt of live attenuated vaccination within 30 days prior to study entry.
  • Known active or chronic hepatitis B virus (HBV) or hepatitis C virus (HCB) infections.

Note: Patients with a history of hepatitis C virus (HCV) infection must have been treated and with confirmation of cure, can be eligible.

  • History of allogeneic organ or bone marrow transplantation.
  • Any of the following cardiovascular conditions:

  • Documented NYHA Class II, III or IV congestive heart failure,
  • History of myocardial infarction (MI), angina pectoris, or coronary artery bypass graft (CABG) within 6 months prior to starting study treatment
  • Transient ischemic attack (TIA) or stroke within 1 year.
  • History of myocarditis
  • Troponin T (TnT) or troponin I (TnI) > 2x institutional ULN at baseline. Patients with TnT or TnI levels between > 1 to 2x ULN are permitted if repeat levels within 24 hours are ≤ 1x ULN. If TnT or TnI levels are > 1 to 2x ULN within 24 hours, the subject may undergo a cardiac evaluation and be considered for treatment by the investigator based on medical judgement in the patient's best interest.
  • Active, documented inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis).
  • Major surgical procedure within 28 days prior to study entry.
  • Other malignancies: unless the patient is considered disease-free and has completed therapy for the malignancy greater than or equal to 36 months prior to study entry. Patients with the following cancers are eligible if diagnosed and definitively treated within the past 12 months: carcinoma in situ of the cervix, and basal cell and squamous cell carcinoma of the skin. Other in situ neoplasms will be reviewed by the Protocol Officer and/or Protocol Chair.
  • Psychiatric or addictive disorders or other conditions that in the opinion of the investigator would preclude the patient from meeting the study requirements or interfering with interpretation of study results.
  • Pregnancy or lactation at the time of study entry.
  • Use of any investigational agent within 28 days prior to the first dose of study therapy.

Study Design

Enrollment

79 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Other

Interventions and Outcome Measures

Arms

active comparator: Arm 1

cemiplimab

active comparator: Arm 2

cemiplimab plus fianlimab

experimental: Arm 3

cemiplimab plus REGN7075

Interventions

Cemiplimab

Cemiplimab 350mg intravenously

cemiplimab plus fianlimab

Cemiplimab 350mg + Fianlimab 1600mg intravenously

cemiplimab + REGN7075

Cemiplimab 350mg + REGN7075 2700mg intravenously

ctDNA testing

Eligible patients using results for ctDNA-positivity as obtained from a commercial assay run in any CLIA-certified lab will proceed to enrollment and begin treatment. All patients will have confirmation of ctDNA-positivity via the Signatera\^TM assay (Clinical Trial Assay), but treatment may proceed while awaiting confirmatory results.

Primary outcome measure

  • Clearance of cDNA [ Time Frame: From enrollment to 12 weeks ]

Central Contacts and Locations

Central contacts

Department of Site and Study Management (DSSM)

1-800-270-3165industry.trials@nsabp.org

Locations

University of Florida

Recruiting

Gainesville, Florida, United States, 32611

University of Iowa - Holden Comprehensive Cancer Center

Recruiting

Iowa City, Iowa, United States, 52242

University of Kansas Cancer Center

Recruiting

Kansas City, Kansas, United States, 66160

University of Maryland Greenbaum

Recruiting

Baltimore, Maryland, United States, 21201

Missouri Baptist

Recruiting

St Louis, Missouri, United States, 63131

First Health of the Carolinas

Recruiting

Pinehurst, North Carolina, United States, 28374

Allegheny General Hospital

Recruiting

Pittsburgh, Pennsylvania, United States, 15212

Magee-Womens Hospital of UPMC

Recruiting

Pittsburgh, Pennsylvania, United States, 15213

Ballad Health Cancer Center - Kingsport

Recruiting

Kingsport, Tennessee, United States, 37660

Huntsman Cancer Institute - University of Utah

Recruiting

Salt Lake City, Utah, United States, 84112

University of Virginia Health

Recruiting

Charlottesville, Virginia, United States, 22903

Bon Secours St. Francis Medical Center

Recruiting

Midlothian, Virginia, United States, 23114

Virginia Commonwealth University - Massey

Recruiting

Richmond, Virginia, United States, 23298

More Information

Sponsor

NSABP Foundation Inc

Last update posted

Sep 3, 2026

Last verified

Sep, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by NSABP Foundation Inc on 2026-09-03.