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Active, not recruiting Phase 3 Interventional

BCG in Combination With Durvalumab in Adult BCG-naïve, High-risk NMIBC Participants

ClinicalTrials.gov ID: NCT05943106

Public ClinicalTrials.gov record NCT05943106. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 6:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase IIIb Open-Label, Single-Arm, Multi-Center, US Study of Bacillus Calmette-Guerin (BCG) Administered in Combination With Durvalumab in Adult BCG-naïve, High-risk Non-Muscle- Invasive Bladder Cancer Participants (PATAPSCO)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety, tolerability, and efficacy profile of durvalumab + BCG (induction and maintenance) combination therapy in adult United States participants with a histologically confirmed diagnosis of high-risk non-muscle-invasive bladder cancer (NMIBC), who have received no prior systemic therapy for NMIBC, and who are BCG-naïve.

Study identification

NCT ID
NCT05943106
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 11, 2023 (Actual)
Primary completion
Jun 16, 2025 (Actual)
Completion
Mar 31, 2027 (Estimated)
Last update posted
Aug 13, 2026

2023 – 2027

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Research Site Phoenix Arizona 85054 —
Research Site Little Rock Arkansas 72211 —
Research Site San Diego California 92123 —
Research Site Lakewood Colorado 80228 —
Research Site Hialeah Florida 33016 —
Research Site Jacksonville Florida 32209 —
Research Site Greenwood Indiana 46143 —
Research Site Wichita Kansas 67226 —
Research Site Baltimore Maryland 21203 —
Research Site Hanover Maryland 21076 —
Research Site Royal Oak Michigan 48073 —
Research Site Troy Michigan 48084 —
Research Site Syracuse New York 13210 —
Research Site Cincinnati Ohio 45212 —
Research Site Bala-Cynwyd Pennsylvania 19004-1017 —
Research Site Myrtle Beach South Carolina 29572 —
Research Site Nashville Tennessee 37209 —
Research Site Austin Texas 78759 —
Research Site Spokane Washington 99202 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05943106, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 13, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05943106 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →