Trial Watch: A Study of TAR-200 in Combination With Cetrelimab Versus Concurrent Chemoradiotherapy in Participants With Muscle-invasive Bladder Cancer (MIBC) of the Bladder

Research type: Registered later-phase trialRegulatory status: InvestigationalGuideline status: Not addressed

Important context

In plain English

The 30-second version

What happened?

ClinicalTrials.gov confirms that this Phase 3 study is registered and currently listed as Active Not Recruiting. This establishes the study's existence and registry-reported design/status, not a treatment benefit.

Why does it matter?

Phase 3 trials can contribute later-stage human evidence. CancerDiscoveries can track this record as results and regulatory information emerge.

What does this not prove?

A registered trial is not proof that the intervention works, is not FDA approval for this cancer or use, and is not a clinical-guideline recommendation.

Keep reading for evidence stage, limitations, study details, and sources.

What changed: ClinicalTrials.gov lists A Study of TAR-200 in Combination With Cetrelimab Versus Concurrent Chemoradiotherapy in Participants With Muscle-invasive Bladder Cancer (MIBC) of the Bladder (NCT04658862) as a Phase 3 interventional cancer study. The registry status is Active Not Recruiting, with the record last updated 2026-08-28.

Study snapshot: Phase 3; Active Not Recruiting; planned enrollment 518. Conditions listed: Urinary Bladder Neoplasms. A primary outcome listed by the registry is: Time from Randomization to the First Bladder Intact Event-free Survival (BI-EFS) event.

This entry tracks verified trial-registry facts. Trial registration by itself does not show that an intervention is effective, safe for a particular person, FDA-approved for this use, or recommended by clinical guidelines.

Population / Applicability

Studied in: Participants age 18 Years and older with Urinary Bladder Neoplasms who meet the study-specific registry eligibility criteria. (Adults)

Eligibility is study-specific. Registry information does not determine whether any individual should enroll in or receive the intervention.

Full evidence details
Study design
Not specified in this summary
Sample size
518
Primary outcome
Time from Randomization to the First Bladder Intact Event-free Survival (BI-EFS) event
Replication
Unknown

Funding & Conflicts

ClinicalTrials.gov lists the lead sponsor as Janssen Research & Development, LLC. Sponsorship is reported for transparency and does not establish efficacy.

Regulatory status by jurisdiction

Country or region not specified

Status
Investigational
Last verified
2026-08-28

Cancer-type scope for this record is not yet recorded.

Guideline positions

Guideline

Position
Not addressed
Last verified
2026-08-28

Primary evidence supporting this story

Last reviewed

Trial Watch: A Study of TAR-200 in Combination With Cetrelimab Versus Concurrent Chemoradiotherapy in Participants With Muscle-invasive Bladder Cancer (MIBC) of the Bladder

https://cancerdiscoveries.com/discoveries/trial-watch-a-study-of-tar-200-in-combination-with-cetrelimab-versus-concurrent-chemoradiotherapy-in-participants-with-muscle-invasive-bladder-cancer-mibc-of-the-bladder/

Research type: Registered later-phase trial

What This Means

ClinicalTrials.gov confirms that this Phase 3 study is registered and currently listed as Active Not Recruiting. This establishes the study's existence and registry-reported design/status, not a treatment benefit.

What This Doesn't Mean

A registered trial is not proof that the intervention works, is not FDA approval for this cancer or use, and is not a clinical-guideline recommendation.

Why It Matters

Phase 3 trials can contribute later-stage human evidence. CancerDiscoveries can track this record as results and regulatory information emerge.

Important Limitations

  • Clinical-trial participation has study-specific eligibility criteria; registry listing does not mean a person qualifies or should enroll.

Primary sources

  • ClinicalTrials.gov — NCT04658862 — https://clinicaltrials.gov/study/NCT04658862 (NCT04658862)

Date verified: 2026-08-28

Correction status: No correction or retraction