BENITIONSClinical Trial Intelligence

A Study of TAR-200 in Combination With Cetrelimab, TAR-200 Alone, or Cetrelimab Alone in Participants With Non-Muscle Invasive Bladder Cancer (NMIBC) Unresponsive to Intravesical Bacillus Calmette-Guérin Who Are Ineligible for or Elected Not to Undergo Radical Cystectomy

Phase 2 Active, not recruiting NCT04640623

ConditionUrinary Bladder Neoplasms
PhasePhase 2
SponsorJanssen Research & Development, LLC
StatusActive, not recruiting
Enrollment220 participants
InterventionsTAR-200, Cetrelimab
Start dateDec 18, 2020
Completion dateJul 3, 2025
Results postedJul 29, 2026

Summary

The purpose of this study is to evaluate the overall complete response (CR) rate in participants treated with TAR-200 in combination with cetrelimab (Cohort 1), or TAR-200 alone (Cohort 2), or cetrelimab alone (Cohort 3) with Carcinoma in Situ (CIS), with or without concomitant high-grade Ta or T1 papillary disease; and disease-free survival (DFS) in participants treated with TAR-200 alone with papillary disease only (Cohort 4).

Cohorts 1, 2, and 3: Overall Complete Response (CR) Rate

From date of first dose up to clinical cut-off date 3rd July 2025 (up to 50 months) · percentage of participants

Cohort 1: TAR-200 + Cetrelimab (CIS With or Without Papillary Disease)67.9 percentage of participants
Cohort 2: TAR-200 Monotherapy (CIS With or Without Papillary Disease)82.4 percentage of participants
Cohort 3: Cetrelimab IV Monotherapy (CIS With or Without Papillary Disease)46.4 percentage of participants

Cohort 4: Disease-free Survival (DFS)

From date of first dose up to clinical cut-off date 3rd July 2025 (up to 50 months) · months

Cohort 4: TAR-200 Monotherapy (Papillary Disease Only)NA months

Open in BENITIONS View on ClinicalTrials.gov

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