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NCT00622063 · ClinicalTrials.gov registry record · Phase 1

An Extension Study for Patients Previously Treated With ARQ 501

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
1
Enrollment target

NCT00622063: Completed Phase 1 study, sponsored by ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA).

NCT00622063 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 1 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00622063, 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
1 participants
Enrollment target

Study Summary

To provide ongoing treatment with ARQ 501 for patients who have benefited from prior treatment with ARQ 501

Interventions

  • DRUG ARQ 501

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2006-12
Phase Phase 1

What the finished NCT00622063 record still lists

NCT00622063 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (98% lower).

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

NCT00622063 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00622063 about?

NCT00622063 is a clinical study titled "An Extension Study for Patients Previously Treated With ARQ 501". To provide ongoing treatment with ARQ 501 for patients who have benefited from prior treatment with ARQ 501

What is the current status of trial NCT00622063?

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

What interventions are being tested in trial NCT00622063?

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

Who is sponsoring clinical trial NCT00622063?

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.

How this trial's enrollment target compares

Where NCT00622063's enrollment target sits among peer trials

1 2001st of 2000 the lowest of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00622063, the US trial registry maintained by the National Library of Medicine. NCT00622063 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.