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NCT00099190 · ClinicalTrials.gov registry record · Phase 1

ARQ 501 in Combination With Docetaxel in Patients With Cancer

A Phase 1 study, sponsored by ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA).

Completed
Registry status
Phase 1
Development phase
50
Enrollment target

NCT00099190 is a Phase 1 study that has completed, run by ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA). The registered enrollment target is 50 participants.

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The verdict

NCT00099190, a Phase 1 study, has completed, sponsored by ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA).

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety of ARQ 501 in combination with docetaxel in patients with advanced or metastatic cancer. In addition, the study is designed to observe the potential the combination of ARQ 501 and docetaxel have in treating cancer.

Interventions

  • DRUG ARQ 501

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2004-12
Est. Completion 2006-11
Phase Phase 1

What the Registry Record Tells You About NCT00099190

The ClinicalTrials.gov registry entry for NCT00099190 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA), which has 27 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which ARQ 501 is the first listed.

NCT00099190 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00099190 about?

NCT00099190 is a clinical study titled "ARQ 501 in Combination With Docetaxel in Patients With Cancer". The purpose of this study is to determine the safety of ARQ 501 in combination with docetaxel in patients with advanced or metastatic cancer. In addition, the study is designed to observe the potential the combination of ARQ 501 and docetaxel have in treating cancer.

What is the current status of trial NCT00099190?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2004-12. Estimated completion is 2006-11.

What interventions are being tested in trial NCT00099190?

The interventions under investigation include: ARQ 501 (DRUG).

Who is sponsoring clinical trial NCT00099190?

This trial is sponsored by ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA), which has 27 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.