Trials / Completed
CompletedNCT01023295
Study Evaluating the Safety and Response of Fosbretabulin in Asian Patients With Polypoidal Choroidal Vasculopathy (PCV)
OXiGENE OXC402-201: A Phase 2, Randomized, Double-Masked, Placebo-Controlled Study of the Safety, Pharmacokinetics, and Biological Effects of Intravenous Fosbretabulin in Asian Subjects With Polypoidal Choroidal Vasculopathy (PCV)
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Mateon Therapeutics · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this study is to examine effects of fosbretabulin tromethamine (fosbretabulin) on PCV as reflected by a change from baseline in the number of polypoid lesions on indocyanine green angiography (ICGA).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | fosbretabulin | single dose, intravenous infusion |
| DRUG | Saline | single dose, intravenous infusion |
Timeline
- Start date
- 2009-07-01
- Primary completion
- 2010-08-01
- Completion
- 2010-08-01
- First posted
- 2009-12-02
- Last updated
- 2011-11-01
Locations
5 sites across 5 countries: United States, Hong Kong, Singapore, South Korea, Taiwan
Source: ClinicalTrials.gov record NCT01023295. Inclusion in this directory is not an endorsement.