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NCT05062317 · ClinicalTrials.gov registry record · Phase 2

ctDNA-Directed Post-Hepatectomy Chemotherapy for Patients With Resectable Colorectal Liver Metastases

A Phase 2 study of Liver Metastases, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
Phase 2
Development phase
120
Enrollment target
1
Study location

NCT05062317 is a Phase 2 study of Liver Metastases that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 120 participants, above the 64-participant average among 27 other Liver Metastases trials with a reported enrollment target (88% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT05062317, a Phase 2 study of Liver Metastases, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
Phase 2
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

To determine if the detection of ctDNA after surgical resection of CLM can stratify patients into high and low-risk cohorts for early disease recurrence in order to inform post-operative adjuvant therapy.

Conditions Studied

Interventions

  • DRUG Capecitabine
  • DRUG Leucovorin
  • DRUG Oxaliplatin
  • DRUG Irinotecan
  • DRUG 5-FLUOROURACIL

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2022-04-26
Est. Completion 2027-02-28
Phase Phase 2

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT05062317

The ClinicalTrials.gov registry entry for NCT05062317 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 64-participant average among 27 other Liver Metastases trials with a reported enrollment target (88% higher). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Liver Metastases appearing as the primary indexed condition, and to 5 interventions - of which Capecitabine is the first listed.

NCT05062317 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05062317 about?

NCT05062317 is a clinical study titled "ctDNA-Directed Post-Hepatectomy Chemotherapy for Patients With Resectable Colorectal Liver Metastases". To determine if the detection of ctDNA after surgical resection of CLM can stratify patients into high and low-risk cohorts for early disease recurrence in order to inform post-operative adjuvant therapy.

What is the current status of trial NCT05062317?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 2022-04-26. Estimated completion is 2027-02-28.

What conditions does trial NCT05062317 study?

This clinical trial studies the following conditions: Liver Metastases.

What interventions are being tested in trial NCT05062317?

The interventions under investigation include: Capecitabine (DRUG), Leucovorin (DRUG), Oxaliplatin (DRUG), Irinotecan (DRUG), 5-FLUOROURACIL (DRUG).

Who is sponsoring clinical trial NCT05062317?

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

Where is trial NCT05062317 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.