Verteporfin Market Growth Is Driven by Increasing Incidence of Severe Eye Conditions


Verteporfin is a medication used to eliminate the abnormal blood vessels in the eye associated with conditions such as the wet form of macular degeneration. Along with laser light treatment, it is used for the treatment of severe eye conditions, such as ocular histoplasmosis, pathologic myopia, and macular degeneration. Moreover, verteporfin is extensively used to help prevent decreased vision and blindness. It is administered intravenously before 15-20 minutes of photo dynamic treatment. After the injection of verteporfin, doctor will use laser light treatment on the affected eye(s). The laser light will convert the drug into a form that works by damaging only the cells that cause serious eye problems.

Thus, with the increasing incidence of severe eye conditions, such as ocular histoplasmosis, pathologic myopia, and macular degeneration, demand for verteporfin is also increasing with a rapid pace, driving the growth of the verteporfin market. According to the World Health Organization (WHO), pathologic myopia causes more vision impairment/blindness in Asians than in Caucasians. Overall vision impairment due to pathologic myopia occurs in 5 to 10 Asian people per 100,000 annually. Asia accounts for around 60% of the world population, and thus, will see the largest projected number of cases of age-related macular degeneration (AMD) and will increase more rapidly than other regions, despite having the lowest prevalence currently.

This in turn is expected to augment the growth of the verteporfin market, especially in the Asia Pacific. Verteporfin is used in combination with photodynamic therapy (PDT) for the treatment of abnormal growth of leaky blood vessels in the eye caused by wet AMD, pathologic myopia, or histoplasmosis of the eye. Moreover, the demand for verteporfin has also increased due to diversified use of verteporfin in various applications of ophthalmology, driving the verteporfin market growth. Thus, to meet the increasing demand, market players are focusing on launching new products for the use of verteporfin in ophthalmology.

For instance, in 2019, CIBA Corporation received authorization, from the European Medicine Evaluation Agency, for the marketing of verteporfin therapy for choroidal neovascularization. The European Medicines Agency is an agency of the European Union (EU) in charge of the evaluation and supervision of medicinal products. Photodynamic therapy with verteporfin has been tested for treatment of several human cancer, such as metastatic breast cancer, pancreatic cancer, and posterior uveal melanoma. Furthermore, research institutes are focused on applying verteporfin in oncology treatments, which in turn is also expected to accelerate the growth of the verteporfin market.

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