Phase 1 Kidney Cancer Trial, Recruiting NCT06582017 Sponsor: Nammi Therapeutics Inc Condition: Kidney Cancer
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Phase 1 Kidney Cancer Trial, Recruiting

NCT06582017
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:

  • You have been diagnosed with an advanced, inoperable, or spreading solid tumor (such as ovarian, pancreatic, bladder, kidney, liver, gastrointestinal, lung, prostate, or breast cancer) confirmed by a lab test, OR you have been diagnosed with multiple myeloma.
  • Your cancer has continued to grow or spread despite standard treatments, or standard treatments are no longer working or cannot be tolerated.
  • If you have multiple myeloma, you must have already tried at least 3 previous treatments, including specific types known as a proteasome inhibitor, an IMiD, and an anti-CD38 therapy (confirm with trial site).
  • You are 18 years of age or older.
  • You are generally able to carry out daily activities, with your overall health rated on a standard scale as 0, 1, or 2 (meaning you are fully active to capable of limited self-care).
  • You have at least one area of cancer that can be measured or tracked using standard medical imaging or lab criteria.
  • Your liver, kidneys, bone marrow, and other organs are working well enough to meet the trial's requirements (confirm specific levels with trial site).
  • Your heart is pumping blood adequately, as measured by a standard heart function test.
  • If you are a woman who could become pregnant, you must have a negative pregnancy test before starting and agree to use at least one highly effective form of birth control during the study and for 120 days after your last dose.
  • If you are a man who could father a child, you must agree to use at least one highly effective form of birth control during the study and for 120 days after your last dose, and you must not donate sperm during this time.

Who may not be able to join:

  • You have serious heart problems, such as severe heart failure, a heart attack in the last 6 months, an unstable irregular heartbeat, a personal or family history of a specific heart rhythm condition called long QT syndrome, or signs of reduced blood flow to the heart on a heart tracing (ECG).
  • You have chest pain caused by heart disease, or you have previously had a procedure such as a heart stent, balloon procedure, or bypass surgery.
  • You are currently taking medications that are known to affect heart rhythm in a way that may be risky (confirm specific medications with trial site).
  • You have an active, uncontrolled infection (bacterial, viral, or fungal) that requires treatment.
  • You have a known allergy or sensitivity to the study drug or any of its ingredients (confirm with trial site).
  • You are currently breastfeeding.
  • You have other significant health conditions that the trial team considers a concern (confirm with trial site).
  • You have received cancer treatment within the past 28 days, or within a timeframe based on how long your last treatment stays in the body — whichever is shorter.
  • You have had a large area of your body treated with radiation within the past 4 weeks, or a smaller area treated within the past 2 weeks.
  • You have had major surgery within the past 30 days.
  • You are regularly taking a high dose of steroid medication (more than 20 mg per day of prednisone or an equivalent drug).
  • You have an active, significant liver disease such as hepatitis B or C, autoimmune hepatitis, or advanced liver scarring (cirrhosis).
  • You have had a serious mood disorder such as major depression within the past two years that is not currently well managed with treatment.
  • You have an autoimmune condition (where the immune system attacks the body) that is not currently well controlled.
  • You have an uncontrolled hormone or metabolism-related condition, such as thyroid problems, diabetes, or blood sugar issues that are not currently well managed.

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: Dennis Kim, MD, Nammi Therapeutics Inc

Phone: 818-926-3428

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
Nammi Therapeutics Inc
Registry
ClinicalTrials.gov
Start date
28 August 2024
Est. completion
31 December 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of Adverse Events

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