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NCT05221827

Clinical Performance Evaluation of the C2i-Test

Terminated Last updated 27 February 2023
What this trial tests

trial testing C2i Test in Muscle-Invasive Bladder Carcinoma in 3 participants. Terminated before completion.

Timeline
24 February 2022
Primary endpoint
27 July 2022
27 July 2022

Quick facts

Lead sponsorC2i Genomics
StatusTerminated
Study typeOBSERVATIONAL
Enrollment3
Start date24 February 2022
Primary completion27 July 2022
Estimated completion27 July 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

C2i Genomics — full company profile →

Who can join

Adults 22 to 100, any sex, with Muscle-Invasive Bladder Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The C2i-WGS-MRD Test (hereinafter referred to as C2i-Test), a personalized molecular circulating tumor DNA (ctDNA) test, is an in vitro qualitative test that uses next generation sequencing (NGS) based whole-genome sequencing (WGS) data for detecting molecular residual disease (MRD) in patients diagnosed with muscle-invasive bladder cancer (MIBC) and histopathologically classified as stage II-IIIA. The C2i-Test is a single site assay performed in the C2i Genomics' CLIA-certified laboratory. This is a prospective non-interventional study to collect definitive evidence of the safety and effectiveness of C2i-Test for the intended use, in a statistically justified number of subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Muscle-Invasive Bladder Carcinoma

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05221827.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing