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NCT00033241 · ClinicalTrials.gov registry record · Phase 1

Erlotinib Combined With Gemcitabine in Treating Patients With Newly Diagnosed Locally Advanced or Metastatic Pancreatic Cancer or Other Solid Tumors

A Phase 1 study of Pancreatic Cancer and Unspecified Adult Solid Tumor, Protocol Specific, sponsored by OSI Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
2
Study locations

NCT00033241: Completed Phase 1 study of Pancreatic Cancer and Unspecified Adult Solid Tumor, Protocol Specific, sponsored by OSI Pharmaceuticals.

NCT00033241 is a Phase 1 study of Pancreatic Cancer and Unspecified Adult Solid Tumor, Protocol Specific that has completed, run by OSI Pharmaceuticals. The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00033241, a Phase 1 study of Pancreatic Cancer and Unspecified Adult Solid Tumor, Protocol Specific, has completed, sponsored by OSI Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
2
Study locations

Study Summary

RATIONALE: Erlotinib may interfere with the growth of tumor cells and slow the growth of the tumor. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining erlotinib with gemcitabine may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of combining erlotinib with gemcitabine in treating patients who have newly diagnosed locally advanced or metastatic pancreatic cancer or other solid tumors.

Interventions

  • DRUG gemcitabine hydrochloride
  • DRUG erlotinib hydrochloride

Study Locations (2)

Arizona

  • Arizona Cancer Center at University of Arizona Health Sciences Center - Tucson

Texas

  • Cancer Therapy and Research Center - San Antonio

Trial Details

FieldValue
Start Date 2001-07-23
Est. Completion 2004-04-22
Phase Phase 1
OSI Pharmaceuticals

16 total trials

What the finished NCT00033241 record still lists

NCT00033241 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 2 conditions, with Pancreatic Cancer appearing as the primary indexed condition, and to 2 interventions - of which gemcitabine hydrochloride is the first listed.

NCT00033241 reports a single indexed study location in Arizona, Texas.

Frequently Asked Questions

What is clinical trial NCT00033241 about?

NCT00033241 is a clinical study titled "Erlotinib Combined With Gemcitabine in Treating Patients With Newly Diagnosed Locally Advanced or Metastatic Pancreatic Cancer or Other Solid Tumors". RATIONALE: Erlotinib may interfere with the growth of tumor cells and slow the growth of the tumor. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining erlotinib with gemcitabine may kill more tumor cells. PURPOSE: Phase I trial to ...

What is the current status of trial NCT00033241?

This trial is currently completed. It is a Phase 1 study. The study started on 2001-07-23. Estimated completion is 2004-04-22.

What conditions does trial NCT00033241 study?

This clinical trial studies the following conditions: Pancreatic Cancer, Unspecified Adult Solid Tumor, Protocol Specific.

What interventions are being tested in trial NCT00033241?

The interventions under investigation include: gemcitabine hydrochloride (DRUG), erlotinib hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00033241?

This trial is sponsored by OSI Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00033241 being conducted?

This trial has 2 study locations across Arizona, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT00033241, the US trial registry maintained by the National Library of Medicine. NCT00033241 (unsized enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.