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Scientists seek new clues to tame tough colorectal cancer

NCT ID NCT03699111

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study looked at 29 patients with a hard-to-treat form of advanced colorectal cancer. The goal was to find new ways to group these patients based on the biology of their tumors. This could help doctors choose more effective treatments in the future. The study did not test any new drugs, but focused on analyzing tumor samples.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this research could lead to better personalized treatment strategies for patients with this hard-to-treat form of colorectal cancer.
What could go wrong
This was a small, observational study (29 participants) focused on data analysis, not testing a new treatment. The findings are exploratory and may not directly change patient care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

29 people

The number who actually took part.

Started

Sep 2018

Finished

Apr 2022

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

All patients with stage IV MSS RAS mutant colorectal cancer

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria Patient Status 1. Ability to give signed informed consent prior to any study specific procedures and willing and able to comply with the protocol, 2. Age ≥ 18 years, 3. ECOG status of ≤ 2, 4. At least 16 weeks of life expectancy at time of entry into the study. Disease-related 5. Histologically confirmed stage IV MSS RAS mt mCRC as per standard diagnostic tests, 6. Unresectable and measurable disease (at least one measurable target lesion) as per clinical and radiologic criteria (RECIST v.1.1), 7. No prior chemotherapy and/or radiation therapy for CRC administered in the metastatic setting, 8. Scheduled to receive or receiving SOC chemotherapy with fluoropyrimidines and oxaliplatin +/- bevacizumab (baseline blood sample should be collected and questionnaires completed during pre-screening and before chemotherapy initiation), 9. Availability of archival formalin-fixed paraffin-embedded (FFPE) tissue from: 1. Preferred: surgical resection of the primary or metastatic tumour or 2. Biopsy samples (biopsy taken at endoscope, needle core or surgical incision or excision) obtained from the primary or metastatic tumour. The archival FFPE tissue blocks must be obtained during initial diagnosis (before patient was exposed to any chemotherapy and/or radiation therapy). Exclusion Criteria 1. Patient with CRC that has received any therapy for CRC before: 1. surgical resection of tissue that would be utilised in this study or 2. biopsy procedure for tissue that would be utilised in this study, 2. Patient who has received any investigational product within 28 days of the first day of palliative chemotherapy administration, 3. Patient with any significant history of non-compliance to medical treatments or with inability to grant reliable informed consent, 4. Patient with clinical or laboratory contraindication to receive SOC chemotherapy with fluoropyrimidines and oxaliplatin.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Beaumont Hospital

    Dublin, Ireland

  • Bon Secours Hospital, Cork

    Cork, Ireland

  • Hospital Universitari Vall d'Hebron

    Barcelona, Spain

  • Institut Catala d'Oncologia

    Barcelona, Spain

  • Private Practice Oncology, Heidelberg

    Heidelberg, Germany

  • Private Practice Oncology, Speyer

    Speyer, Germany

  • St Vincent's University Hospital

    Dublin, Ireland

  • Tallaght University Hospital

    Dublin, Ireland

  • University Hospital Galway

    Galway, Ireland

  • University Hospital, Mannheim

    Mannheim, Germany

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