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NCT00802555 · ClinicalTrials.gov registry record · Phase 1

Safety Study of ARQ 197 in Cirrhotic Patients With Hepatocellular Carcinoma (HCC)

A Phase 1 study of Hepatocellular Carcinoma and Cirrhosis, 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
21
Enrollment target
5
Study locations

NCT00802555 is a Phase 1 study of Hepatocellular Carcinoma and Cirrhosis 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 21 participants, below the 257-participant average among 145 other Hepatocellular Carcinoma trials with a reported enrollment target (92% lower). The trial reports 5 study locations across 2 states.

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The verdict

NCT00802555, a Phase 1 study of Hepatocellular Carcinoma and Cirrhosis, 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
21 participants
Enrollment target
5
Study locations

Study Summary

Multi-center, single-arm Phase 1b study designed to evaluate safety and tolerability of ARQ 197 in cirrhotic patients with HCC.

Interventions

  • DRUG ARQ 197

Study Locations (5)

Other

  • - Bologna
  • - Milan
  • - Barcelona

Texas

  • - Dallas
  • - Houston

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2009-01
Est. Completion 2011-12
Phase Phase 1

What the Registry Record Tells You About NCT00802555

The ClinicalTrials.gov registry entry for NCT00802555 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 257-participant average among 145 other Hepatocellular Carcinoma trials with a reported enrollment target (92% lower). 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 2 conditions, with Hepatocellular Carcinoma appearing as the primary indexed condition, and to 1 intervention - of which ARQ 197 is the first listed.

NCT00802555 reports 5 study locations spanning 2 distinct geographic areas - top geographies include Other, Texas.

Frequently Asked Questions

What is clinical trial NCT00802555 about?

NCT00802555 is a clinical study titled "Safety Study of ARQ 197 in Cirrhotic Patients With Hepatocellular Carcinoma (HCC)". Multi-center, single-arm Phase 1b study designed to evaluate safety and tolerability of ARQ 197 in cirrhotic patients with HCC.

What is the current status of trial NCT00802555?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2009-01. Estimated completion is 2011-12.

What conditions does trial NCT00802555 study?

This clinical trial studies the following conditions: Hepatocellular Carcinoma, Cirrhosis.

What interventions are being tested in trial NCT00802555?

The interventions under investigation include: ARQ 197 (DRUG).

Who is sponsoring clinical trial NCT00802555?

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.

Where is trial NCT00802555 being conducted?

This trial has 5 study locations 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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