Colorectal Cancer Trial, Recruiting NCT06787105 Sponsor: iOMEDICO AG Condition: Colorectal Cancer
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Colorectal Cancer Trial, Recruiting

NCT06787105
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 years or older.
  • People who have been diagnosed with metastatic colorectal cancer (cancer of the bowel that has spread to other parts of the body) and whose treating doctor has decided that treatment with a medicine called fruquintinib is appropriate, in line with the current approved prescribing guidelines in Germany.
  • People who have already received standard chemotherapy treatments, including specific drug combinations (fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapies), as well as treatment targeting a process called blood vessel growth (anti-VEGF therapy), and — for those whose tumour has a specific genetic profile called RAS wild-type — treatment targeting a protein called EGFR (anti-EGFR therapy).
  • People whose cancer got worse during, or who could not tolerate, treatment with either of two specific medicines: trifluridine/tipiracil or regorafenib (or both).
  • People who meet any additional requirements listed in the current approved prescribing guidelines for fruquintinib (confirm with trial site).
  • People who have signed a written consent form agreeing to take part in the trial.

Who may not be able to join:

  • People who took part in another interventional clinical trial (a trial involving a medical treatment or procedure) within the 30 days before enrolling in this trial or before starting fruquintinib, whichever happens first.
  • People who have medical reasons that make fruquintinib unsuitable for them, as listed in the current approved prescribing guidelines (confirm with trial site).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Professor Dr. med. Sebastian Stintzing, Charité Campus Mitte Medizinische Klinik Hämatologie/Onkologie und Tumorimmunologie

Phone: +49 761 152420

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
iOMEDICO AG
Registry
ClinicalTrials.gov
Start date
17 February 2025
Est. completion
1 December 2027

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Real-world disease control rate (RW DCR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov