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NCT00827177 · ClinicalTrials.gov registry record · Phase 1

Dose Escalation Study of ARQ 197 in Combination With Sorafenib in Adult Patients With Advanced Solid Tumors

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
87
Enrollment target

NCT00827177 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 87 participants.

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The verdict

NCT00827177, 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
87 participants
Enrollment target

Study Summary

This is an open-label, dose-escalation study of ARQ 197 administered orally in combination with sorafenib.

Interventions

  • DRUG Treatment with ARQ 197 in combination with sorafenib

Trial Details

FieldValue
Enrollment Target 87 participants
Start Date 2009-09
Est. Completion 2013-05
Phase Phase 1

What the Registry Record Tells You About NCT00827177

The ClinicalTrials.gov registry entry for NCT00827177 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 87 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 Treatment with ARQ 197 in combination with sorafenib is the first listed.

NCT00827177 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00827177 about?

NCT00827177 is a clinical study titled "Dose Escalation Study of ARQ 197 in Combination With Sorafenib in Adult Patients With Advanced Solid Tumors". This is an open-label, dose-escalation study of ARQ 197 administered orally in combination with sorafenib.

What is the current status of trial NCT00827177?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 87 participants. The study started on 2009-09. Estimated completion is 2013-05.

What interventions are being tested in trial NCT00827177?

The interventions under investigation include: Treatment with ARQ 197 in combination with sorafenib (DRUG).

Who is sponsoring clinical trial NCT00827177?

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

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