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Looking for participantsPhase3

A Study 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

Sponsor: Incyte Corporation

NCT ID: NCT07284849

View on ClinicalTrials.gov ↗

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.

CRC (Colorectal Cancer)

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

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

MSIBRAF

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
Inclusion Criteria: * Stage IV colorectal adenocarcinoma not amenable to curative resection. * No prior systemic treatment for unresectable or metastatic disease. Participants who received adjuvant or neoadjuvant therapy may enroll if there was no recurrence within 12 months of the end of treatment. * Measurable disease per RECIST v1.1. * ECOG performance status of 0 or 1. * Adequate organ function determined by laboratory results. Exclusion Criteria: * 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 malignancy within 2 years. * Treatment with an anti-PD-(L)1 or other immune checkpoint inhibitor for any indication within the last 3 years. * Active autoimmune disease that has required systemic treatment in the past 2 years. * Significant concurrent and/or uncontrolled medical condition. * History of organ transplant, including allogeneic stem cell transplantation. Other protocol-defined inclusion/exclusion criteria apply.

Where Is This Study? (9 UK sites)

Bristol Haematology and Oncology Centre

Bristol BS2 8ED, United Kingdom

Recruiting

Velindre Cancer Centre

Cardiff CF14 2TL, United Kingdom

NOT_YET_RECRUITING
Hospital R&D contact (matched)

Sarah Townsend

Velindre.R&Doffice@wales.nhs.uk02920 196165

St James University Hospital

Leeds LS9 7TF, United Kingdom

NOT_YET_RECRUITING

Barts Hospital

London EC1A 7BE, United Kingdom

Recruiting
Hospital R&D contact (matched)

Dr Mays Jawad

research.governance@qmul.ac.uk020 7882 6826

Guys Hospital

London SE1 9RT, United Kingdom

NOT_YET_RECRUITING
Hospital R&D contact (matched)

Main Email: gstt.research.rbhh@nhs.net

gstt.research.rbhh@nhs.netn/a

Royal Marsden Hospital - Fulham

London SW3 6JJ, United Kingdom

Recruiting
Hospital R&D contact (matched)

Mark Brandon-Grove

research.development@rmh.nhs.uk020 3186 5416

Kent Oncology Centre - Maidstone Hospital

Maidstone ME16 9QQ, United Kingdom

Recruiting

The Christie Nhs Foundation Trust Uk

Manchester M20 4BX, United Kingdom

Recruiting
Hospital R&D contact (matched)

Research and Innovation Office

the-christie.ri@nhs.net---

The Royal Marsden Nhs Foundation Trust - Sutton

Sutton SM2 5PT, United Kingdom

Recruiting
Hospital R&D contact (matched)

Mark Brandon-Grove

research.development@rmh.nhs.uk020 3186 5416

How to Get in Touch

Incyte Corporation Call Center (US)

Sponsor contact

CONTACT

1.855.463.3463 medinfo@incyte.com

Incyte Corporation Call Center (ex-US)

Sponsor contact

CONTACT

+800 00027423 eumedinfo@incyte.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-10