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NCT00102505 · ClinicalTrials.gov registry record · Phase 1

A Study of Motexafin Gadolinium (MGd) in Combination With Docetaxel and Cisplatin for Treatment of Non-Small Cell Lung Cancer (NSCLC)

A Phase 1 study of Non-Small-Cell Lung Carcinoma and Carcinoma, Bronchogenic, sponsored by Pharmacyclics.

Completed
Registry status
Phase 1
Development phase
36
Enrollment target
1
Study location

NCT00102505 is a Phase 1 study of Non-Small-Cell Lung Carcinoma and Carcinoma, Bronchogenic that has completed, run by Pharmacyclics. The registered enrollment target is 36 participants, below the 235-participant average among 30 other Non-Small-Cell Lung Carcinoma trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00102505, a Phase 1 study of Non-Small-Cell Lung Carcinoma and Carcinoma, Bronchogenic, has completed, sponsored by Pharmacyclics.

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

Study Summary

The purpose of the study is to determine the dose limiting toxicities and maximum tolerated dose of motexafin gadolinium when administered with docetaxel and cisplatin in patients with Non-small Cell Lung Cancer. A cycle consists of 3 weeks. During week 1, patients receive MGd, docetaxel, and cisplatin treatment followed by 2 weeks without treatment. Eligible patients will receive 1 or 2 doses of MGd, depending on cohort, and a single dose of docetaxel and cisplatin at 75 mg/m² during the first week of each cycle. Additionally, tumor response will be evaluated at the end of even numbered cycles (2, 4, and 6). Patients may stay on the study a maximum of 6 cycles.

Interventions

  • DRUG Motexafin Gadolinium Injection

Study Locations (1)

Texas

  • The University of Texas MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2004-11
Phase Phase 1

Sponsor

Pharmacyclics

54 total trials

What the Registry Record Tells You About NCT00102505

The ClinicalTrials.gov registry entry for NCT00102505 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 235-participant average among 30 other Non-Small-Cell Lung Carcinoma trials with a reported enrollment target (85% lower). The listed sponsor is Pharmacyclics, which has 54 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Non-Small-Cell Lung Carcinoma appearing as the primary indexed condition, and to 1 intervention - of which Motexafin Gadolinium Injection is the first listed.

NCT00102505 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT00102505 about?

NCT00102505 is a clinical study titled "A Study of Motexafin Gadolinium (MGd) in Combination With Docetaxel and Cisplatin for Treatment of Non-Small Cell Lung Cancer (NSCLC)". The purpose of the study is to determine the dose limiting toxicities and maximum tolerated dose of motexafin gadolinium when administered with docetaxel and cisplatin in patients with Non-small Cell Lung Cancer. A cycle consists of 3 weeks. During week 1, patients receive MGd, docetaxel, and cispl...

What is the current status of trial NCT00102505?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2004-11.

What conditions does trial NCT00102505 study?

This clinical trial studies the following conditions: Non-Small-Cell Lung Carcinoma, Carcinoma, Bronchogenic.

What interventions are being tested in trial NCT00102505?

The interventions under investigation include: Motexafin Gadolinium Injection (DRUG).

Who is sponsoring clinical trial NCT00102505?

This trial is sponsored by Pharmacyclics, which has 54 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00102505 being conducted?

This trial has 1 study location across Texas. 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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