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NCT00220649 · ClinicalTrials.gov registry record · Phase 1

Safety Study of Combination Chemotherapy in Patients With Metastatic Solid Tumors or Adenocarcinoma of the Pancreas

A Phase 1 study of Pancreatic Neoplasms, sponsored by St. Luke's-Roosevelt Hospital Center.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target
1
Study location

NCT00220649 is a Phase 1 study of Pancreatic Neoplasms that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 25 participants, below the 601-participant average among 30 other Pancreatic Neoplasms trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00220649, a Phase 1 study of Pancreatic Neoplasms, has completed, sponsored by St. Luke's-Roosevelt Hospital Center.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target
1
Study location

Study Summary

The purpose of this trial is to determine the maximum tolerated dose and the dose-limiting toxicity of biweekly oxaliplatin in combination with fixed doses of irinotecan, 5-fluorouracil/leucovorin and gemcitabine in patients with metastatic solid tumors or adenocarcinoma of the pancreas.

Conditions Studied

Interventions

  • DRUG gemcitabine; irinotecan; leucovorin; 5-fluorouracil; oxaliplatin

Study Locations (1)

New York

  • St. Luke's-Roosevelt Hospital Center - New York

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2004-03
Phase Phase 1

What the Registry Record Tells You About NCT00220649

The ClinicalTrials.gov registry entry for NCT00220649 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 601-participant average among 30 other Pancreatic Neoplasms trials with a reported enrollment target (96% lower). The listed sponsor is St. Luke's-Roosevelt Hospital Center, which has 57 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pancreatic Neoplasms appearing as the primary indexed condition, and to 1 intervention - of which gemcitabine; irinotecan; leucovorin; 5-fluorouracil; oxaliplatin is the first listed.

NCT00220649 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT00220649 about?

NCT00220649 is a clinical study titled "Safety Study of Combination Chemotherapy in Patients With Metastatic Solid Tumors or Adenocarcinoma of the Pancreas". The purpose of this trial is to determine the maximum tolerated dose and the dose-limiting toxicity of biweekly oxaliplatin in combination with fixed doses of irinotecan, 5-fluorouracil/leucovorin and gemcitabine in patients with metastatic solid tumors or adenocarcinoma of the pancreas.

What is the current status of trial NCT00220649?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2004-03.

What conditions does trial NCT00220649 study?

This clinical trial studies the following conditions: Pancreatic Neoplasms.

What interventions are being tested in trial NCT00220649?

The interventions under investigation include: gemcitabine; irinotecan; leucovorin; 5-fluorouracil; oxaliplatin (DRUG).

Who is sponsoring clinical trial NCT00220649?

This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00220649 being conducted?

This trial has 1 study location across New York. 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

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