Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07282912 · ClinicalTrials.gov registry record · Phase 2

Trial Comparing Standard of Care Therapy With and Without Sequential Cytoreductive Intervention for Patients With Metastatic Foregut Adenocarcinoma and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid (ctDNA) Levels

A Phase 2 study of Gastric Adenocarcinoma and Esophageal Adenocarcinoma, sponsored by Yale University.

Recruiting
Registry status
Phase 2
Development phase
54
Enrollment target
1
Study location

NCT07282912 is a Phase 2 study of Gastric Adenocarcinoma and Esophageal Adenocarcinoma that is actively recruiting participants, run by Yale University. The registered enrollment target is 54 participants, below the 244-participant average among 47 other Gastric Adenocarcinoma trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07282912, a Phase 2 study of Gastric Adenocarcinoma and Esophageal Adenocarcinoma, is actively recruiting participants, sponsored by Yale University.

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

Study Summary

This is a randomized, open label, single-center, phase 2, randomized controlled trial of sequential cytoreductive intervention versus standard of care therapy for patients with intervenable oligometastatic (stage IV) cancer of the upper gastrointestinal (GI) tract and undetectable ctDNA at the time of randomization after a three-month induction chemotherapy period.

Interventions

  • PROCEDURE Sequential cytoreductive intervention
  • DIAGNOSTIC_TEST Signatera Genome ultra-sensitive ctDNA blood test

Study Locations (1)

Connecticut

  • Smilow Cancer Center - New Haven

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2026-03
Est. Completion 2028-06
Phase Phase 2

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT07282912

The ClinicalTrials.gov registry entry for NCT07282912 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 244-participant average among 47 other Gastric Adenocarcinoma trials with a reported enrollment target (78% lower). The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 9 conditions, with Gastric Adenocarcinoma appearing as the primary indexed condition, and to 2 interventions - of which Sequential cytoreductive intervention is the first listed.

NCT07282912 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT07282912 about?

NCT07282912 is a clinical study titled "Trial Comparing Standard of Care Therapy With and Without Sequential Cytoreductive Intervention for Patients With Metastatic Foregut Adenocarcinoma and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid (ctDNA) Levels". This is a randomized, open label, single-center, phase 2, randomized controlled trial of sequential cytoreductive intervention versus standard of care therapy for patients with intervenable oligometastatic (stage IV) cancer of the upper gastrointestinal (GI) tract and undetectable ctDNA at the time ...

What is the current status of trial NCT07282912?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 54 participants. The study started on 2026-03. Estimated completion is 2028-06.

What conditions does trial NCT07282912 study?

This clinical trial studies the following conditions: Gastric Adenocarcinoma, Esophageal Adenocarcinoma, Pancreas Adenocarcinoma, Gastroesophageal Adenocarcinoma, Gallbladder Adenocarcinoma.

What interventions are being tested in trial NCT07282912?

The interventions under investigation include: Sequential cytoreductive intervention (PROCEDURE), Signatera Genome ultra-sensitive ctDNA blood test (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT07282912?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07282912 being conducted?

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

Similar trials for Gastric Adenocarcinoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

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.