Phase 2 Bladder Cancer Trial, Recruiting NCT07030257 Sponsor: Tasca Therapeutics Condition: Bladder Cancer
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Phase 2 Bladder Cancer Trial, Recruiting

NCT07030257
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 whose cancer can be measured or tracked by researchers to see if it changes over time
  • People for whom existing standard cancer treatments are not suitable or are no longer an option
  • People who have a tumor tissue sample available for lab testing, or who are willing to have a biopsy taken safely
  • People diagnosed with locally advanced, recurring, or metastatic cancer that cannot be cured
  • (Part 1) People with most types of solid tumors — except brain cancer — where the cancer has continued to grow, stopped responding to standard treatment, or where treatment side effects were too severe, and a clinical trial is being considered as a next step
  • (Part 1) People with specific advanced or metastatic cancers including colorectal cancer, small cell lung cancer, head and neck cancer, non-small cell lung cancer, pancreatic cancer, or bladder cancer — some requiring a specific gene mutation in the cancer
  • (Part 1) People with selected solid tumor types — except brain cancers — where the cancer carries a specific gene mutation
  • (Part 2) People with specific advanced or metastatic cancers including colorectal cancer, small cell lung cancer, or head and neck cancer — some requiring a specific gene mutation in the cancer
  • (Part 2) People with selected solid tumor types — except brain cancers — where the cancer carries a specific gene mutation
  • People whose blood and urine test results meet the required levels
  • People of childbearing potential who are using adequate contraception
  • People who are willing and able to provide written informed consent and follow the study requirements

Who may not be able to join:

  • People who are unable to swallow pills
  • People with a known history of HIV, hepatitis C (HCV), or hepatitis B (HBV), unless the condition has been cured or is well controlled with an undetectable viral load
  • People with an active tumor in the brain
  • People with significant liver disease
  • People with significant diseases affecting the stomach or digestive system
  • People who have had another type of cancer within the past 5 years, with some exceptions for cancers considered likely to be cured
  • People with significant heart disease
  • People with other poorly controlled health conditions that could make taking the study drug unsafe
  • People who are pregnant or currently breastfeeding
  • People who have recently received certain anti-cancer or other specific medications within a set period before the study drug would begin (confirm with trial site for exact timeframes)

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 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

Phone: 617-430-7109

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
Sponsor
Tasca Therapeutics
Registry
ClinicalTrials.gov
Start date
27 August 2025
Est. completion
15 August 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Part 1: Determine the maximum tolerated dose (MTD); Part 2: Evaluate the efficacy of CP-383 at the recommended phase 2 dose in selected tumor types

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