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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

TypeNameDescription
DRUGfosbretabulinsingle dose, intravenous infusion
DRUGSalinesingle 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.

Study Evaluating the Safety and Response of Fosbretabulin in Asian Patients With Polypoidal Choroidal Vasculopathy (PCV) (NCT01023295) · Clinical Trials Directory