Phase 1 Bladder Cancer Trial, Recruiting NCT04389632 Sponsor: Seagen, a wholly owned subsidiary of Pfizer Condition: Bladder Cancer
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Phase 1 Bladder Cancer Trial, Recruiting

NCT04389632
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 a specific type of cancer that has spread or cannot be surgically removed, confirmed by a lab test — eligible cancer types include non-small cell lung cancer, head and neck squamous cell cancer, HER2-negative breast cancer, esophageal squamous cell carcinoma, esophageal/gastro-esophageal junction adenocarcinoma, cutaneous squamous cell cancer, pancreatic cancer, bladder cancer, cervical cancer, gastric (stomach) cancer, or high-grade serous ovarian cancer.
  • Depending on which part of the trial you join, your cancer has come back or stopped responding to standard treatments, or you were unable to tolerate them (confirm with trial site for specific part requirements).
  • For some parts of the trial, you must be starting treatment for your advanced or spread cancer for the first time (no prior treatment for this stage of disease).
  • You are well enough to carry out basic daily activities, with only mild limitations at most (a doctor's assessment score of 0 or 1 on a standard scale).
  • Your cancer can be measured using scans at the start of the study.
  • Depending on which part of the trial you join, you may need to agree to have a small sample of your tumor taken (a biopsy) before and/or during treatment.

Who may not be able to join:

  • You have had another type of cancer within the past 3 years, or there are still signs of a previous cancer in your body (with some exceptions for low-risk cancers — confirm with trial site).
  • You currently have active cancer that has spread to your brain; however, if brain spread was previously treated and has been stable for at least 4 weeks, you may still be eligible (confirm with trial site).
  • Cancer has spread to the membranes surrounding your brain or spinal cord.
  • You have previously received a specific type of drug called an MMAE-containing agent, or a drug that targets a protein called integrin beta-6.
  • You already have nerve damage (such as tingling, numbness, or pain in hands or feet) — the level of nerve damage that disqualifies you depends on which part of the trial you are joining (confirm with trial site).
  • You have had a serious uncontrolled infection (viral, bacterial, or fungal) in the 2 weeks before starting the study drug.
  • You have severe lung disease that is not caused by your cancer.
  • For some parts of the trial: you previously received certain immune-based cancer treatments and had to stop because of a serious immune-related side effect (grade 3 or higher).
  • You have a history of a non-infectious lung condition called interstitial lung disease (ILD) or pneumonitis that needed steroid treatment, or you currently have or are suspected to have this condition.
  • Your lungs' ability to absorb oxygen is significantly reduced (below 50% of the expected level on a specific breathing test — confirm with trial site).
  • You or your close family members work directly on this trial at the study site or for the company running 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: Pfizer CT.gov Call Center, Pfizer

Phone: 1-800-718-1021

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
Seagen, a wholly owned subsidiary of Pfizer
Registry
ClinicalTrials.gov
Start date
8 June 2020
Est. completion
16 June 2027

Where this trial is recruiting

🇫🇷 France 🇰🇷 South Korea 🇪🇸 Spain 🇨🇭 Switzerland 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Number of participants with adverse events (AEs); Number of patients with laboratory abnormalities; Number of participants with dose-limiting toxicities (DLTs)

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