Phase 1 Bladder Cancer Trial, Recruiting NCT07140315 Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Condition: Bladder Cancer
Back to Bladder Cancer

Phase 1 Bladder Cancer Trial, Recruiting

NCT07140315
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 must be willing and able to sign a consent form agreeing to take part in the trial.
  • You must be 18 years of age or older and able to understand and agree to the consent process.
  • You must have been diagnosed with a specific type of lung cancer (non-small cell lung cancer) or bladder cancer, confirmed by a laboratory test on tissue, and be a candidate for a type of immunotherapy treatment.
  • A specific protein test (called PD-L1) must have already been done on your cancer tissue, or there must be enough tissue available to do this test.
  • You must be reasonably active and able to care for yourself — this is measured by a standard scale where a score of 0, 1, or 2 is required (confirm with trial site).
  • Your blood, kidney, and liver levels must be within an acceptable range, based on blood tests done within 28 days before joining the trial.
  • If you are a woman who could become pregnant, you must have a negative pregnancy blood test within 24 hours before receiving the study scan drug.
  • Women who cannot become pregnant may join if they have had a surgical procedure to prevent pregnancy or have been through menopause for at least 1 year.
  • If you are a woman who could become pregnant, or a man whose partner could become pregnant, you must agree to use an appropriate form of contraception during the trial.

Who may not be able to join:

  • You may not be eligible if you have recently been treated with certain immunotherapy drugs (anti-PD-L1 or anti-PD-L2 treatments) — at least 4 months must have passed since that treatment ended.
  • You may not be eligible if you are still experiencing significant side effects from a previous cancer treatment that have not improved to a mild level.
  • You may not be eligible if you have been taking increasing doses of steroid medications (such as dexamethasone) in the 7 days before starting the trial treatment — stable or low doses, as well as inhaled or skin-applied steroids, may be acceptable (confirm with trial site).
  • You may not be eligible if you have had a serious allergic reaction to a similar type of drug (monoclonal antibody) in the past, or if you are known to be allergic to any ingredients in the study drugs.
  • You may not be eligible if you have another serious medical condition or active infection that the trial doctor believes could make it unsafe for you to participate.
  • You may not be eligible if you are pregnant, based on a test taken within 24 hours before the study scan.
  • You may not be eligible if you are currently breastfeeding.
  • You may not be eligible if you are unable to follow the requirements and schedule of the trial.

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 27 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: Seyed Ali Mosallaie, MD, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Phone: 14109296586

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
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
1 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety of [18F]DK222 as assessed by number of grade 3-5 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: 27 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