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Double-Masked Study of Photrex (Rostaporfin) Photodynamic Therapy in the Treatment of Age-Related Macular Degeneration

A Phase III Randomized, Multicenter, Multinational, Double-Masked, Placebo-Controlled Study of Photrex (Rostaporfin) Photodynamic Therapy in the Treatment of Classic and Occult Subfoveal Choroidal Neovascularization Associated With AMD

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00157976
Enrollment
660
Registered
2005-09-12
Start date
2005-09-30
Completion date
Unknown
Last updated
2005-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Macular Degeneration

Keywords

Macular Degeneration, AMD, Visual Acuity

Brief summary

The purpose of this study is to confirm the efficacy and safety of rostaporfin (PHOTREX) photodynamic therapy (PDT) in the treatment of classic and occult subfoveal choroidal neovascularization (CNV) associated with age-related macular degeneration (AMD).

Interventions

DRUGPhotrex (rostaporfin)

Sponsors

Miravant Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients with age greater than or equal to 50 years with at least one subfoveal CNV membrane secondary to AMD that can be demonstrated by fluorescein angiography.

Design outcomes

Primary

MeasureTime frame
Visual Acuity

Secondary

MeasureTime frame
Angiographic changes

Countries

Bulgaria, Czechia, Poland, Romania

Contacts

Primary ContactMiravant Pharmaceuticals
ctinfo@miravant.com1-800-685-2959

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026