Last reviewed · How we verify

verteporfin PDT

QLT Inc. · FDA-approved active Small molecule Under review Quality 0/100

verteporfin PDT is a Photosensitizing agent Small molecule drug developed by QLT Inc.. It is currently FDA-approved for Age-related macular degeneration with predominantly classic choroidal neovascularization, Pathologic myopia with subfoveal choroidal neovascularization, Polypoidal choroidal vasculopathy. Also known as: Visudyne, vPDT.

Verteporfin is a photosensitizing agent that accumulates in abnormal blood vessels and is activated by light to generate reactive oxygen species that destroy those vessels.

Verteporfin is a small molecule DNA inhibitor used in photodynamic therapy for conditions such as choroidal neovascularization, macular degeneration, and chronic central serous chorioretinopathy. It is administered as part of a treatment regimen for these conditions, often in combination with other interventions like bevacizumab or ranibizumab.

At a glance

Generic nameverteporfin PDT
Also known asVisudyne, vPDT
SponsorQLT Inc.
Drug classPhotosensitizing agent
TargetLipoprotein receptors on neovascular endothelial cells
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved

Mechanism of action

Verteporfin is a benzoporphyrin derivative that preferentially localizes to neovascular endothelial cells. When exposed to non-thermal red light (689 nm wavelength) in photodynamic therapy (PDT), it generates singlet oxygen and reactive oxygen species that cause selective destruction of abnormal choroidal neovascularization and the endothelial cells lining these vessels, leading to vessel occlusion and regression.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about verteporfin PDT

What is verteporfin PDT?

verteporfin PDT is a Photosensitizing agent drug developed by QLT Inc., indicated for Age-related macular degeneration with predominantly classic choroidal neovascularization, Pathologic myopia with subfoveal choroidal neovascularization, Polypoidal choroidal vasculopathy.

How does verteporfin PDT work?

Verteporfin is a photosensitizing agent that accumulates in abnormal blood vessels and is activated by light to generate reactive oxygen species that destroy those vessels.

What is verteporfin PDT used for?

verteporfin PDT is indicated for Age-related macular degeneration with predominantly classic choroidal neovascularization, Pathologic myopia with subfoveal choroidal neovascularization, Polypoidal choroidal vasculopathy.

Who makes verteporfin PDT?

verteporfin PDT is developed and marketed by QLT Inc. (see full QLT Inc. pipeline at /company/qlt-inc).

Is verteporfin PDT also known as anything else?

verteporfin PDT is also known as Visudyne, vPDT.

What drug class is verteporfin PDT in?

verteporfin PDT belongs to the Photosensitizing agent class. See all Photosensitizing agent drugs at /class/photosensitizing-agent.

What development phase is verteporfin PDT in?

verteporfin PDT is FDA-approved (marketed).

What are the side effects of verteporfin PDT?

Common side effects of verteporfin PDT include Photosensitivity reactions, Vision decrease or blurred vision, Injection site reactions, Headache, Subretinal fibrosis.

What does verteporfin PDT target?

verteporfin PDT targets Lipoprotein receptors on neovascular endothelial cells and is a Photosensitizing agent.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing