Modern Immunotherapy in BCG-Unresponsive, BCG-Relapsing and High Risk BCG-Naive Non-Muscle Invasive Urothelial Carcinoma of the Bladder

Upon successful screening and registration, enrollment to durvalumab monotherapy (cohort 1) will begin. If DLT criteria outlined in the protocol are exceeded with durvalumab monotherapy (cohort 1), the study will close. Provided the safety of durvalumab monotherapy is established, enrollment to combination regimen cohorts will proceed. Cohorts will simultaneously enroll in parallel to each other with patients assigned to cohorts based on patient slot availability and study site choice of radiation arm participation. Patient assignment to future phase 1 arms would proceed similarly. Within BCG

Trial Details

NCT ID
NCT03317158
Phase
PHASE1 / PHASE2
Sponsor
Noah Hahn, M.D.
Status
RECRUITING
Cancer Type
Non-Muscle-Invasive Bladder Cancer
Interventions
  • Durvalumab (Cohort 1-3)
  • External Beam Radiotherapy (EBRT)
  • Bacillus Calmette-Guérin (BCG)
  • Gemcitabine
  • Docetaxel
  • Tremelimumab
Locations (sample)
  • Phoenix, Arizona, United States|33.44838,-112.07404
  • Stanford, California, United States|37.42411,-122.16608
  • Chicago, Illinois, United States|41.85003,-87.65005
  • Indianapolis, Indiana, United States|39.76838,-86.15804
  • Iowa City, Iowa, United States|41.66113,-91.53017

Key Eligibility Criteria

  • Subject must meet all of the following applicable criteria to participate in this study:
  • Histologically confirmed non-muscle invasive urothelial carcinoma of the bladder (Ta, T1, or Tis stage) on TURBT obtained within 60 days of registr…
  • NOTE: Mixed histologies are permitted, provided a component of urothelial carcinoma is present. Patients with histologically confirmed non- muscle …
  • ECOG (WHO) performance status 0 or 1

For full eligibility, visit ClinicalTrials.gov.

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