Global Ankylosing Spondylitis Market, by Drug Type (Nonsteroidal Anti-inflammatory Drugs (NSAIDs), Disease-modifying Anti-rheumatic Drugs (DMARDs), TNF Inhibitors, Corticosteroids, and Others), by Route of Administration (Oral and Parentral), by Distribution Channel (Hospital Pharmacies, Retail Pharmacies, and Online Pharmacies), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) is estimated to be valued at US$ 4,864.3 Mn in 2021 and is expected to exhibit a CAGR of 8.2% during the forecast period (2021-2028), as highlighted in a new report published by Coherent Market Insights.
The increasing regulatory approvals for ankylosing spondylitis drugs is expected to propel growth of the global ankylosing spondylitis market over the forecast period. For instance, in October 2021, the U.S. Food and Drug Administration approved the first interchangeable biosimilar product, Cyltezo by Boehringer Ingelheim, a pharmaceutical company headquartered in Germany, to treat certain inflammatory diseases such as ankylosing spondylitis, active psoriatic arthritis, and others. In August 2017, cyltezo (adalimumab-adbm), was approved by U.S. Food and Drug Administration (FDA) for treating a number of chronic inflammatory diseases. It is the first monoclonal antibody that has been granted ‘interchangeable’ status for multiple indications including ankylosing spondylitis and others. Cyltezo is interchangeable with as well as biosimilar to its reference product, Humira (adalimumab), which is the second interchangeable biosimilar product that has been approved by the agency. Cyltezo is the first interchangeable monoclonal antibody.
Global Ankylosing Spondylitis Market – Impact of Coronavirus (COVID-19) Pandemic
Patients with ankylosing spondylitis are generally prescribed immunosuppressants to manage their symptoms. These medications suppress the immune system, and hence such patients are at a higher risk of acquiring infections, including COVID-19. This may hamper the ankylosing spondylitis market, as people might stop taking immunosuppressants, due to the fear of being contacted by the infection.
Moreover, various clinical trials have been paused as researchers are facing multiple challenges in visiting places and carrying out clinical trials effectively. For instance, according to a survey conducted on April 23, 2020, by Medidata Solutions, Inc., a U.S. based technology company (which develops and markets software as a service for clinical trials, 63% of survey respondents reported that they stopped recruiting new patients for ongoing clinical trials and 43% of the respondents have postponed their studies.
Even though regulatory agencies, such as European Medicines Evaluation Agency (EMEA) and the U.S. Food and Drug Administration (FDA), have promoted measures and guidelines for maintaining the integrity of the trials that attempt to guarantee the safety, rights, and wellbeing of patients as well as healthcare staff during this COVID-19 pandemic, finding it challenging to carry on clinical trials and keeping them on track.