Press release
Navigating Growth: Orphan Drugs Market Set to Hit $355 Billion by 2030
Orphan Drugs Market Overview -The orphan drugs market refers to medications developed to treat rare diseases, affecting a small portion of the population. Due to the limited market potential, traditional pharmaceutical companies often neglect these conditions. However, orphan drugs play a crucial role in addressing unmet medical needs for patients with rare diseases.
These drugs undergo a specialized regulatory process, often receiving incentives such as extended market exclusivity and tax credits to encourage their development. The market has grown substantially over the years, driven by advancements in biotechnology and increased awareness of rare diseases.
Despite their relatively small target population, orphan drugs can be lucrative for pharmaceutical companies due to premium pricing and reduced competition. The market is characterized by a diverse range of therapies, including biologics, gene therapies, and small molecules.
The orphan pharmaceuticals market was valued at USD 160.78 billion in 2021 and is expected to rise from USD 175.57 billion in 2022 to USD 355.00 billion by 2030, representing a compound annual growth rate (CAGR) of 9.20% during the forecast period (2022- 2030).
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Market Competitive Landscape:
The essential competitors shaping the global orphan drugs market:
Hoffmann-La Roche AG (Switzerland)
Mylan (US)
Celgene Corporation (US)
Novartis AG (Switzerland)
Biogen (US)
Takeda Pharmaceutical Company Limited (Japan)
Merck KGaA (Germany)
Eli Lilly And Company (US)
Sanofi (France)
Janssen Services LLC (US)
Orphan Drugs Market Segmentation
According to the survey carried out by QuintilesIMS Institute, 6,084 rare diseases were conveyed in the US in 2016. Some situations of rare diseases can affect only a minority of people, while others may affect hundreds or thousands, which counts as cystic fibrosis, which marks approximately 30,000 people in the United States. Overall, rare disease patients comprise about 6% to 8% of the population depending upon the factors that are responsible for the rising prevalence of the rare disease is owing to swelling paternal and maternal ages and increased usage of fertility therapies. Therefore, there are many various causes of rare diseases, the majority of which are genetic, directly caused by changes in genes or chromosomes. The future of the global orphan drug looks good and have a successful venture by the year 2023. Upon this, Market Research Future Reports offers a comprehensive segmental analysis of the global orphan drugs market, which has been segmented into drug type, sale, drug, and therapy class.
By the mode of drug type, the global orphan drugs market is further categorized as biologics and non-biologics. Wherein, the biologics accounted for the market value of USD 75,103.32 million in 2017.
By the mode of sale, the global orphan drugs market has been categorized into generics and prescribed.
By the mode of drug, the global orphan drugs market has been categorized into Revlimid, Rituxan, opdivo, keytruda, imbruvica, soliris, jakaf, pomalyst, darzalex, spinraza, adcetris.
Lastly, the global Orphan Drugs Market is categorized by therapy class, which has been segmented into oncology, blood, central nervous systems, endocrine, cardiovascular and respiratory.
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Market Synopsis:
Currently, awareness of the orphan drug market is spreading rapidly around the world, which is leading to the growing adoption of the orphan drug act, particularly in countries such as Japan, Australia, Europe, and others, in order to stimulate more and more research and development in the orphan drug field. Even the government in some regions is offering incentives to manufacture orphan drugs. Furthermore, with the rising occurrence of rare diseases, many governments have raised healthcare spending, resulting in the expansion of the worldwide orphan pharmaceuticals market. On the other hand, the expense of creating medications is often high, and their availability is limited when compared to traditional drugs.
To address medicine supply chain gaps, governments in many regions are pushing the development of orphan drugs through increased investments and strategies. As a result, this factor is driving higher CAGR demand for the orphan pharmaceuticals market, which is expected to grow at a faster rate throughout the forecast period.
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Orphan Drugs Market Regional Insights
The global orphan drug market is evaluated regionally, with regions including the Americas, Europe, Asia-Pacific, and the Middle East and Africa. The Americas had the biggest market share (39.98%) in 2017. The Americas is also expected to lead the global orphan medicines market over the assessment period. As a result, the expansion of the orphan medication market in this region is primarily driven by the increasing prevalence of uncommon illnesses.
The European orphan pharmaceuticals market is now predicted to be the second-largest over the evaluation period, owing to an increase in the number of pharmaceutical companies exporting drugs both inside and outside of Europe. This is projected to help boost the orphan medicine industry in the coming years. While the majority of European companies are engaged in the research and development of orphan drugs based on patient needs, this is expected to expand in the coming years due to favorable factors such as the introduction of innovative technologies, stable pricing, reimbursement, unmet medical needs, and a strong clinical pipeline.
The Asia-Pacific region is also expected to be the fastest expanding market for orphan pharmaceuticals due to its emerging healthcare infrastructure. Because of its growing population, Asia has significant long-term potential for orphan medicine medications and treatments, which are available in a variety of countries. Furthermore, due to the rising occurrence of other diseases such as endocrinology, cardiovascular and lymphatic systems, as well as respiratory disorders, the orphan drugs market in this region is experiencing tremendous growth, which will continue to rise in the coming years as healthcare projects and investments expand.
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