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NCT01930006 · ClinicalTrials.gov registry record · Phase 1
Safety Study of Two Oral Formulations of MGCD265 Administered in Healthy Subjects in the Fasting State
A Phase 1 study of Advanced Malignancies, sponsored by Mirati Therapeutics.
- Completed
- Registry status
- Phase 1
- Development phase
- 14
- Enrollment target
- 1
- Study location
NCT01930006 is a Phase 1 study of Advanced Malignancies that has completed, run by Mirati Therapeutics. The registered enrollment target is 14 participants, below the 88-participant average among 10 other Advanced Malignancies trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01930006, a Phase 1 study of Advanced Malignancies, has completed, sponsored by Mirati Therapeutics.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 14 participants
- Enrollment target
- 1
- Study location
Study Summary
In this study two MGCD265 oral formulations at dose level of 100 mg are administered to healthy male and female subjects under fasting conditions.
Conditions Studied
Interventions
- DRUG MGCD265
Study Locations (1)
Kansas
- Vince & Associates Clinical Research, Inc. - Overland Park
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 14 participants |
| Start Date | 2013-08 |
| Est. Completion | 2013-12 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01930006
The ClinicalTrials.gov registry entry for NCT01930006 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 14 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 88-participant average among 10 other Advanced Malignancies trials with a reported enrollment target (84% lower). The listed sponsor is Mirati Therapeutics, which has 49 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Advanced Malignancies appearing as the primary indexed condition, and to 1 intervention - of which MGCD265 is the first listed.
NCT01930006 reports 1 study location spanning 1 distinct geographic area - top geographies include Kansas.
Frequently Asked Questions
What is clinical trial NCT01930006 about?
NCT01930006 is a clinical study titled "Safety Study of Two Oral Formulations of MGCD265 Administered in Healthy Subjects in the Fasting State". In this study two MGCD265 oral formulations at dose level of 100 mg are administered to healthy male and female subjects under fasting conditions.
What is the current status of trial NCT01930006?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2013-08. Estimated completion is 2013-12.
What conditions does trial NCT01930006 study?
This clinical trial studies the following conditions: Advanced Malignancies.
What interventions are being tested in trial NCT01930006?
The interventions under investigation include: MGCD265 (DRUG).
Who is sponsoring clinical trial NCT01930006?
This trial is sponsored by Mirati Therapeutics, which has 49 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01930006 being conducted?
This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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