Phase 1 Kidney Cancer Trial, Recruiting NCT05752552 Sponsor: DeuterOncology Condition: Kidney Cancer
Back to Kidney Cancer

Phase 1 Kidney Cancer Trial, Recruiting

NCT05752552
Recruiting Phase 1

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:

  • Adults aged 18 years or older
  • People with a confirmed diagnosis of non-small cell lung cancer (NSCLC) that has spread or cannot be surgically removed, and where standard approved treatments are no longer an option
  • People whose cancer has tested positive for a specific genetic change called a "MET exon 14 skipping mutation," confirmed by a genetic test done within the last 3 months
  • People whose cancer can be measured on scans, according to a standard measurement system called RECIST 1.1
  • People who are reasonably active and able to carry out daily activities (assessed using a standard scale where a score of 0 or 1 is required)
  • People with adequate bone marrow, liver, and kidney function, meeting specific blood test thresholds
  • People who agree to follow the trial's contraception requirements during the study
  • People who have read and signed a consent form showing they understand the trial and are willing to take part

Who may not be able to join:

  • People whose cancer has other known genetic mutations that drive tumour growth
  • People who have had major surgery within the 3 weeks before joining the trial
  • People who have received chemotherapy, radiotherapy, immunotherapy, or another experimental drug within 3 weeks before starting the trial drug (or within 6 weeks for certain specific chemotherapy types)
  • People who have received antibody-based cancer treatment within 4 weeks before the first dose of the trial drug
  • People whose cancer got worse while they were previously treated with a type of drug called a MET-kinase inhibitor
  • People who have cancer that has spread to the brain, unless all of the following apply: the brain lesions are not causing symptoms and have already been treated; no steroids are currently needed to manage the brain lesions; and scans show the brain lesions have been stable for more than 28 days since the last treatment
  • People whose cancer has spread to the lining surrounding the brain and spinal cord
  • People with uncontrolled heart conditions, including unstable chest pain, heart failure, a heart attack within the past 12 months, significant irregular heart rhythms, a congenital condition affecting heart rhythm, reliance on a pacemaker, or abnormal heart electrical readings above specific thresholds on a screening test
  • People with high blood pressure that has not been controlled despite treatment
  • People with a positive pregnancy test at the time of screening (applicable to women of childbearing potential who are sexually active)
  • People with significantly altered mental status or a history of serious psychiatric illness that could affect their ability to follow the trial procedures
  • People with signs of an active infection currently requiring treatment with systemic medications
  • People with other medical conditions that, in the opinion of the treating doctor, make participation inadvisable (for example, pre-existing kidney problems)
  • People who are unable or unwilling to swallow capsules, or who have a condition that affects how the body absorbs medication taken by mouth

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 28 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Jaap Verweij, MD, CMO DeuterOncology

Phone: +32473558353

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
Phase 1
Sponsor
DeuterOncology
Registry
ClinicalTrials.gov
Start date
20 December 2022
Est. completion
1 September 2027

Where this trial is recruiting

🇧🇪 Belgium 🇫🇷 France 🇳🇱 Netherlands

Primary endpoints

Number of subjects who experience specific treatment-related adverse events (TRAEs)

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: 28 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