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NCT00016367 · ClinicalTrials.gov registry record · Phase 2

Cisplatin and Gemcitabine Plus Trastuzumab in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer

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

Completed
Registry status
Phase 2
Development phase
22
Enrollment target

NCT00016367: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00016367 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 22 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00016367, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
22 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining chemotherapy with monoclonal antibody therapy may kill more tumor cells. PURPOSE: Phase II trial to study effectiveness of combining cisplatin, gemcitabine, and trastuzumab in treating patients who have stage IIIB or stage IV non-small cell lung cancer.

Interventions

  • DRUG Cisplatin
  • DRUG Gemcitabine Hydrochloride
  • BIOLOGICAL Trastuzumab

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 1999-05-13
Est. Completion 2004-12-14
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00016367 record still lists

NCT00016367 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 3 interventions - of which Cisplatin is the first listed.

NCT00016367 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00016367 about?

NCT00016367 is a clinical study titled "Cisplatin and Gemcitabine Plus Trastuzumab in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining chemothera...

What is the current status of trial NCT00016367?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 22 participants. The study started on 1999-05-13. Estimated completion is 2004-12-14.

What interventions are being tested in trial NCT00016367?

The interventions under investigation include: Cisplatin (DRUG), Gemcitabine Hydrochloride (DRUG), Trastuzumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00016367?

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

How this trial's enrollment target compares

Where NCT00016367's enrollment target sits among peer trials

22 1790th of 2000 higher than 207 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00016367, the US trial registry maintained by the National Library of Medicine. NCT00016367 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.