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NCT00302172 · ClinicalTrials.gov registry record · Phase 1
ARQ 197 in Subjects With Metastatic 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
- 78
- Enrollment target
NCT00302172: Completed Phase 1 study, sponsored by ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA).
NCT00302172 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 78 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00302172, 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
- 78 participants
- Enrollment target
Study Summary
To determine the safety, tolerability and recommended Phase 2 dose (RP2D) of ARQ 197.
Interventions
- DRUG ARQ 197
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 78 participants |
| Start Date | 2006-01 |
| Phase | Phase 1 |
What the finished NCT00302172 record still lists
NCT00302172 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 78 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% higher).
The record links to 0 conditions, and to 1 intervention - of which ARQ 197 is the first listed.
NCT00302172 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00302172 about?
NCT00302172 is a clinical study titled "ARQ 197 in Subjects With Metastatic Solid Tumors". To determine the safety, tolerability and recommended Phase 2 dose (RP2D) of ARQ 197.
What is the current status of trial NCT00302172?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 78 participants. The study started on 2006-01.
What interventions are being tested in trial NCT00302172?
The interventions under investigation include: ARQ 197 (DRUG).
Who is sponsoring clinical trial NCT00302172?
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00302172's enrollment target sits among peer trials
78 697th of 2000 higher than 1,298 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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