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NCT05394337 · ClinicalTrials.gov registry record · Phase 1

Neoadjuvant PD-1 Plus TIGIT Blockade in Patients With Cisplatin-Ineligible Operable High-Risk Urothelial Carcinoma

A Phase 1 study of Metastatic Malignancy, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
Phase 1
Development phase
10
Enrollment target
1
Study location

NCT05394337: Recruiting Phase 1 study of Metastatic Malignancy, sponsored by M.D. Anderson Cancer Center.

NCT05394337 is a Phase 1 study of Metastatic Malignancy that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05394337, a Phase 1 study of Metastatic Malignancy, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
Phase 1
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

To learn if the combination of atezolizumab and tiragolumab can help to control bladder cancer when it is given before surgery to remove the bladder and tumor.

Conditions Studied

Interventions

  • DRUG Atezolizumab
  • DRUG Tiragolumab

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2023-02-23
Est. Completion 2025-12-31
Phase Phase 1
M.D. Anderson Cancer Center

2,692 total trials

What NCT05394337 shows while recruiting

NCT05394337 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

The record links to 1 condition, with Metastatic Malignancy appearing as the primary indexed condition, and to 2 interventions - of which Atezolizumab is the first listed.

NCT05394337 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT05394337 about?

NCT05394337 is a clinical study titled "Neoadjuvant PD-1 Plus TIGIT Blockade in Patients With Cisplatin-Ineligible Operable High-Risk Urothelial Carcinoma". To learn if the combination of atezolizumab and tiragolumab can help to control bladder cancer when it is given before surgery to remove the bladder and tumor.

What is the current status of trial NCT05394337?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2023-02-23. Estimated completion is 2025-12-31.

What conditions does trial NCT05394337 study?

This clinical trial studies the following conditions: Metastatic Malignancy.

What interventions are being tested in trial NCT05394337?

The interventions under investigation include: Atezolizumab (DRUG), Tiragolumab (DRUG).

Who is sponsoring clinical trial NCT05394337?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05394337 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT05394337's enrollment target sits among peer trials

10 1914th of 2000 higher than 46 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05394337, the US trial registry maintained by the National Library of Medicine. NCT05394337 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.