At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- INCA33890 (drug), Placebo (drug), Bevacizumab (drug), FOLFOX (drug)
- How long the study runs
- Study runs about 42 months (dates as stated)
- About the drug or intervention
- INCA33890 — drug: INCA33890 will be administered at protocol defined dose. · Placebo — drug: Placebo will be administered at protocol defined dose. · Bevacizumab — drug: Bevacizumab will be administered at protocol defined dose. · FOLFOX — drug: FOLFOX will be administered at protocol defined dose.
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 700
- Started
- 2026-03-05
- Last checked
- 2026-10
Plain English Summary
What is this study?
- • Testing a new treatment for crc (colorectal cancer)
- • Phase3 - 700 participants
- • The purpose of this study is to evaluate the efficacy and safety of standard-of-care chemotherapy and bevacizumab with or without INCA33890 in the first-line treatment of metastatic microsatellite stable colorectal cancer
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with crc (colorectal cancer)
Where?
- • Bristol - Bristol Haematology and Oncology Centre
- • Cardiff - Velindre Cancer Centre
- • Leeds - St James University Hospital
- • London - Barts Hospital
- • +5 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The purpose of this study is to evaluate the efficacy and safety of standard-of-care chemotherapy and bevacizumab with or without INCA33890 in the first-line treatment of metastatic microsatellite stable colorectal cancer.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
- How fit you need to be: ECOG 0 or better
Biomarkers mentioned
What the study is looking for
- ✓Stage IV colorectal adenocarcinoma not amenable to curative resection.
- ✓cancer that can be measured on scans v1.1.
- ✓Fit enough for normal activity (ECOG 0) or 1.
- ✓healthy organ determined by laboratory results.
Who cannot take part
- ✗MSI-H/dMMR per historical data in the medical record.
- ✗BRAF V600E mutation per historical data in the medical record.
- ✗Untreated and/or progressing CNS metastases.
- ✗History of other cancer within 2 years.
- ✗Treatment with an anti-PD-(L)1 or other immune checkpoint inhibitor for any indication within the last 3 years.
See the full criteria
Where Is This Study? (9 UK sites)
Bristol Haematology and Oncology Centre
Bristol BS2 8ED, United Kingdom
Velindre Cancer Centre
Cardiff CF14 2TL, United Kingdom
St James University Hospital
Leeds LS9 7TF, United Kingdom
Barts Hospital
London EC1A 7BE, United Kingdom
Guys Hospital
London SE1 9RT, United Kingdom
Royal Marsden Hospital - Fulham
London SW3 6JJ, United Kingdom
Kent Oncology Centre - Maidstone Hospital
Maidstone ME16 9QQ, United Kingdom
The Christie Nhs Foundation Trust Uk
Manchester M20 4BX, United Kingdom
The Royal Marsden Nhs Foundation Trust - Sutton
Sutton SM2 5PT, United Kingdom
How to Get in Touch
Incyte Corporation Call Center (US)
Sponsor contactCONTACT
Incyte Corporation Call Center (ex-US)
Sponsor contactCONTACT
