Proliferative Vitreoretinopathy (PVR) – Market Outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2021 To 2032

Proliferative Vitreoretinopathy (PVR) Market Outlook

Thelansis’s “Proliferative Vitreoretinopathy (PVR) Market Outlook, Epidemiology, Competitive Landscape, and Market Forecast Report – 2021 To 2032" covers disease overview, epidemiology, drug utilization, prescription share analysis, competitive landscape, clinical practice, regulatory landscape, patient share, market uptake, market forecast, and key market insights under the potential Proliferative Vitreoretinopathy (PVR) treatment modalities options for eight major markets (USA, Germany, France, Italy, Spain, UK, Japan, and China).

Proliferative Vitreoretinopathy (PVR) Overview

Proliferative vitreoretinopathy (PVR) is the most common cause of failure of rhegmatogenous retinal detachment repair. It is characterised by the growth and contraction of cellular membranes within the vitreous cavity and on both sides of the retinal surface and intraretinal fibrosis. Contraction of these membranes can cause the retina to redetach and transform a rhegmatogenous detachment into a tractional detachment. It is most common as a clinical complication of surgical procedures to correct rhegmatogenous retinal detachments, which are detachments that follow the formation of a retinal tear or hole. Tractional forces produced by the scar tissue-like PVR membranes can be transmitted to the retina, resulting in complete retinal detachment, retinal degeneration, and permanent blindness. PVR has also been reported to be common following posterior segment procedures or disorders such as giant retinal tears, macular relocation surgery, tumors endoresection, and chip implantation. PVR has been developed in 29% of cytomegalovirus retinitis-related retinal detachment patients infected with the human immunodeficiency virus.

• PVR is reported to account for 5-10% of all rhegmatogenous retinal detachments (RRD) and is the most common cause of surgery failure for RRD.

Geography Covered:

North America- the United States and Canada

Europe- EU5 (Germany, France, Italy, Spain, and the United Kingdom)

Other countries- Japan & China

Study Period: 2021-2032

Current Clinical Practice and Treatment Algorithm

This section of the study covers country-specific current clinical practice, the standard of care, and significant limitations around addressing the unmet needs. Retrospective analysis and bench-marking of clinical study outcomes are presented in terms of Pre-treatment & post-treatment clinical and demographic patient characteristics. Essentially, this section will cover the evolution of the current competitive landscape and its impact on the future treatment paradigm.

KOL Insights:

KOLs across 8 MM markets from the center of Excellence/ Public/ Private hospitals participated in the study. Insights around current treatment landscape, epidemiology, clinical characteristics, future treatment paradigm, and Unmet needs

Market Forecast: Patient Based Forecast Model (MS. Excel Based Automated Dashboard)

- Data Inputs with sourcing

- Market Event and Product Event

- Country-specific Forecast Model

- Market uptake and patient share uptake

- Attribute Analysis

- Analog Analysis

- Disease burden and pricing scenario

- Summary and Insights

NPV/ IRR Calculator-

Optimization of cash flow/ revenue flow concerning all fixed and variable investments throughout the product development process. The rate of return on an investment is a critical indicator to ensure the profitability and break-even of the project.

Competitive Landscape:

The competitive landscape includes country-specific approved as well as pipeline therapies. Any asset/product-specific designation or review such as Orphan drug designation, Fast track, Priority Review, Breakthrough Therapy Designation, Rare Pediatric Disease Designation, and Accelerated Approval are tracked and supplemented with analyst commentary.

Clinical Trial Assessment-

Detailed clinical trial data analysis and critical product positioning include trial design, primary outcomes, secondary outcomes, dosing and schedules, inclusion and exclusion criteria, recruitment status and essentially covers the reported adverse events. Majorly the trial analysis helps determine the potential of the critical assets and their probable filing and launch date.

Unmet Medical Needs Overview-

This report presents the most important clinical unmet needs in the treatment, according to Thelansis research and analysis. Other essential unmet needs identified through our study include decreased cost burden on patients, improved administration convenience, and improved patient compliance.

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