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

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

PFS is defined as the time from randomization to first documented disease progression by Resist 1.1 criteria or death from any cause, whichever occurs first.

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
Yale University

1,492 total trials

What NCT07282912 shows while recruiting

NCT07282912 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 244-participant average among 47 other Gastric Adenocarcinoma trials with a reported enrollment target (78% lower).

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 a single indexed study location in 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.

Where NCT07282912's enrollment target sits among peer trials

54 26th of 47 higher than 22 of 47 other Gastric Adenocarcinoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Gastric Adenocarcinoma 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 NCT07282912, the US trial registry maintained by the National Library of Medicine. NCT07282912 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.