A Bioequivalence Study of Docetaxel for Injectable Emulsion (ANX-514) in Patients With Advanced Cancer
NCT00664170 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 39
Last updated 2009-05-28
Summary
The purpose of this study is to compare an injectable emulsion form of docetaxel to Taxotere in patients with advanced cancer.
Conditions
Interventions
- DRUG
-
ANX-514
75 mg/m\^2
- DRUG
-
75 mg/m\^2
Sponsors & Collaborators
-
Mast Therapeutics, Inc.
lead INDUSTRY
Principal Investigators
-
Jeff Stewart, MBA · Mast Therapeutics, Inc.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-04-30
- Primary Completion
- 2009-04-30
- Completion
- 2009-04-30
Countries
- United States
- Argentina
- Estonia
Study Locations
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