# Safety and Efficacy Study of ARQ 501 in Adult Patients With Leiomyosarcoma

> **NCT00310518** · PHASE2 · COMPLETED · sponsor: **ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)** · enrollment: 30 (—)

## Conditions studied

- Cancer

## Interventions

- **DRUG:** ARQ 501

## Key facts

- **NCT ID:** NCT00310518
- **Lead sponsor:** ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2006-02
- **Primary completion:** 2007-07
- **Final completion:** 2007-07
- **Target enrollment:** 30 (—)
- **Last updated:** 2009-04-29


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00310518

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00310518, "Safety and Efficacy Study of ARQ 501 in Adult Patients With Leiomyosarcoma". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT00310518. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*