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NCT07823322Not yet recruitingPhase 2

A Study to Evaluate INCA33890 in the Treatment of Circulating Tumor DNA-Positive Stage II/III Microsatellite Stable Colorectal Cancer After Curative Resection and Chemotherapy

A Phase 2 Study of INCA33890 in the Treatment of Circulating Tumor DNA-Positive Stage II/III Microsatellite Stable Colorectal Cancer After Curative Resection and Chemotherapy (NEXERA-204)

Source: ClinicalTrials.gov · Last updated 22 Sept 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate INCA33890 in the treatment of circulating tumor DNA-positive stage II/III microsatellite stable colorectal cancer after curative resection and chemotherapy.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
First submitted
11 Sept 2026
Start date
Oct 2026
Primary completion date
May 2029
Lead sponsor
Incyte Corporation
NCT number
NCT07823322

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 40
  • From Oct 2026 to the primary completion date, May 2029
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with an anti-PD-(L)1 or anti-CTLA-4 for any indication within the last 3 years.
  • Significant concurrent and/or uncontrolled medical condition.

Other illness

  • History of metastatic (Stage IV) colorectal adenocarcinoma, including oligometastatic disease or metastatic recurrence, even if all metastatic sites and the primary tumor were completely resected and the patient is currently without evidence of disease.
  • History of other malignancy within 2 years.
  • Active autoimmune disease that has required systemic treatment in the past 2 years.
  • History of organ transplant, including allogeneic stem cell transplantation.
    • Other protocol-defined inclusion/exclusion criteria apply.

Other

  • MSI-H/dMMR per historical data in the medical record.

Who the study is looking for

  • Received curative-intent (R0) resection of histologically confirmed Stage II or III colorectal adenocarcinoma.
  • Completed all neoadjuvant and/or adjuvant chemotherapy, including at least 3 months of fluoropyrimidine-based chemotherapy.
  • Has minimal residual disease (MRD), defined as ctDNA positive by the Signatera™ assay (whole exome sequencing \[WES\] or whole genome sequencing \[WGS\]) in a blood sample collected between:
    • 2 weeks and 12 months after completion of adjuvant chemotherapy or
    • 4 weeks and 12 months after curative resection following total neoadjuvant therapy.
    • Note: If the participant received any investigational therapy for MRD, ctDNA positivity must be confirmed in a blood sample collected at least 4 weeks after completion of that investigational therapy and within the applicable 12-month window described above.
  • Has no clinical or radiographic evidence of disease confirmed by chest, abdominal, and pelvic PET-CT scan and by brain imaging (MRI or CT scan with contrast) within 4 weeks prior to C1D1 study drug administration.
  • ECOG performance status of 0 or 1.
  • Adequate organ function determined by laboratory results.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.