Phase 2 Kidney Cancer Trial, Recruiting NCT05985161 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Kidney Cancer
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Phase 2 Kidney Cancer Trial, Recruiting

NCT05985161
Recruiting Phase 2

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 6 years or older at the time of signing consent forms. Children aged 12 months to under 6 years may also be eligible depending on which part of the trial is currently open (confirm with trial site).
  • People (or their parents or legal guardians) who are able and willing to sign a consent form agreeing to take part. For younger children, age-appropriate agreement will also be sought where guidelines require it.
  • People who are well enough to carry out at least 60% of normal daily activities, as measured by a standard medical scoring scale appropriate for their age.
  • People diagnosed with a Wilms tumor or nephroblastoma (a type of kidney cancer) who meet at least one of these conditions: they are in their second or later relapse; they have a high-risk tumour type and are in their first relapse or the tumour has not responded to treatment; or they have relapsed after receiving a more intensive treatment regimen than the standard first-line options (confirm with trial site for specific regimens).
  • People diagnosed with any type of rhabdoid tumour — including those in the brain, kidney, soft tissue, liver, or ovary — who have already received at least one course of treatment that did not work.
  • People with a type of nerve sheath tumour called a malignant peripheral nerve sheath tumour (MPNST) that has grown, come back, cannot be surgically removed, or has spread, and who have already received at least one course of treatment that did not work.
  • People with a solid tumour (not a blood cancer or lymphoma) that is not covered by the groups above, but where there is specific scientific evidence suggesting their tumour may respond to the study drug selinexor — this requires approval from the lead study doctor and supporting documentation (confirm with trial site).
  • People with a solid tumour that has a specific type of genetic change involving a gene called BCOR — for example certain fusions or duplications — as confirmed by genetic testing. Other BCOR changes may qualify with lead study doctor approval (confirm with trial site).
  • People whose cancer can be measured on scans (for the main phase of the trial). People in the early drug-level testing part of the trial may have disease that is either measurable or detectable.
  • People who have fully recovered from the side effects of any previous cancer treatment, and who have waited the required amount of time since their last treatment — ranging from 7 days (for some non-intensive drugs) up to 84 days (for a bone marrow transplant from a donor), depending on the treatment type.
  • People with adequate liver function, as shown by blood tests taken within the two weeks before starting the study drug.
  • People with adequate kidney function, confirmed by kidney tests taken within the two weeks before starting the study drug, showing the kidneys are filtering at an acceptable level.
  • People with adequate blood cell counts, confirmed by blood tests taken within the two weeks before starting the study drug, and who have not received blood platelet transfusions or certain blood-boosting injections in the 7 days before those tests.

Who may not be able to join:

  • People who have previously been treated with selinexor or any other drug in the same class (called XPO1 inhibitors).
  • People who currently have an infection that is not under control. People on preventative antibiotics or with a recently controlled infection may still be considered (confirm with trial site).
  • People who have previously received a solid organ transplant (such as a kidney or liver transplant).
  • People who have had a bone marrow transplant using cells from a donor and are currently receiving active treatment for graft-versus-host disease (a complication of that transplant).
  • People whose medical, mental health, or personal circumstances mean, in the treating doctor's judgement, they may not be able to follow the study's safety monitoring or care requirements.
  • People who are pregnant or breastfeeding. Girls who have started their periods will need to take a pregnancy test before joining.
  • People of reproductive age who are not willing to use two effective methods of contraception (such as barrier methods like condoms) for the duration of the study. Abstinence is considered an acceptable method.

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 20 July 2026
Phase 2: approximately ~30% 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: Michael Ortiz, MD, Memorial Sloan Kettering Cancer Center

Phone: 1-833-MSK-KIDS

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 2
Registry
ClinicalTrials.gov
Start date
1 August 2023
Est. completion
1 August 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Overall Response Rate

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: 20 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