Subcutaneous Drug Delivery Market Is Booming Worldwide 2021-2028 | Becton Dickinson and Company, Novo Nordisk A/S, Johnson & Johnson, Sanofi S.A.

Prefilled syringes are plastic syringes of premeasured dose that are ready to use. It improves patient compliance, dosing accuracy, usability, and protection while lowering dosing errors. Healthcare practitioners are increasingly using combination devices, especially injectable drug delivery systems such as prefilled syringes, as the number of injectable biological drugs grows.

According to Fisher Clinical Service's report, "Growth and Benefits of Pre-Filled Syringes," about 13 biotechnology drugs were commercially available in 1989, rising to 210 in 2012. According to Fisher Clinical Service, the prefilled syringes market was projected to account for a quarter of all injectable drug delivery systems in 2013 which included around 35 of the 100 top-selling drugs, which were to be incorporated in the form of injection.

In April 2020, Teva Pharmaceuticals USA, Inc. dispatched the autoinjector gadget for AJOVY (fremanezumab-vfrm) injection in the U.S. market. AJOVY is shown for the preventive treatment of migraine in adults and is offered subcutaneously to the patients. Likewise, in December 2016, Becton, Dickinson and Company declared the dispatch of BD Neopak 2.25 mL prefillable glass needle, which is produced for biopharmaceutical makers zeroed in on assembling of touchy biologic medications for the therapy of ongoing sicknesses like rheumatoid joint inflammation, psoriasis, lupus, and serious asthma. The needle offers higher volume subcutaneous injections, in this manner assisting with improving security and comfort for patients.

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Impact of Coronavirus (Covid-19) Pandemic:

• The pandemic of COVID-19 has had a major impact on clinical trials. According to a survey conducted on April 23, 2020 by Medidata Solutions, Inc. (an American technology firm that produces and markets applications as a service for clinical trials), 63 percent of survey respondents have avoided hiring new patients for existing clinical trials, while 43 percent have delayed their studies.

• Additionally, in March 2020, the US Food and Drug Administration (FDA) issued recommendations for administering clinical testing of medicinal drugs during the COVID-19 public health emergency. On June 3, 2020, the recommendations were revised again.

• Clinical trials for the treatment of COVID-19 are being conducted by research institutes by delivering possible medicines subcutaneously.

• For example, on April 13, 2020, the University Hospital of La Princesa began a phase 2 clinical trial to assess the safety and effectiveness of Sarilumab delivered subcutaneously for the treatment of COVID-19. The research will be finished in June 2020.

• Furthermore, healthcare institutions and researchers are conducting current clinical trials using the following safety precautions:

• Patients' approval is obtained over the internet or via video calls by healthcare providers. According to a survey conducted on April 23, 2020 by Medidata Solutions, Inc., 45 percent of respondents choose virtual/telemedicine for consulting.

• Before scheduling in-person appointments, patients get a phone call to check for COVID-19 symptoms.

• Study evaluations are carried out in isolated outpatient settings.

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In order to broaden their product offerings in the industry, key players are focusing on implementing numerous inorganic growth initiatives such as partnership alliances, and agreements. Insulet Corporation, for example, announced an agreement with a dealer in May 2019 of its Omnipod System in Finland, Italy, Norway, Sweden and other European countries.

In addition, small businesses are concentrating on the production of novel epinephrine auto injectors that are thermally stable. Manufacturers in the global subcutaneous drug delivery industry have a growth potential because currently available drugs perform well at particular temperatures. For patients suffering from anaphylaxis due to an acute allergic attack, Windgap Medical is working on a handheld kit that can blend a dry version of the drug into solution, allowing temperature consistency and a longer shelf-life of treatment.

Key Takeaways:

Due to increased product releases and approvals, the global subcutaneous drug delivery market is projected to develop at a CAGR of 9.7% over the forecast period. For example, Becton, Dickinson and Company obtained FDA approval for the second generation BD Nano pen needle in January 2019, which is designed for more accurate subcutaneous injection in diabetic patients.

Because of the substantial rise in self-administration of medications to cure chronic disorders, the disposable segment is projected to have a larger market share in 2020.

Because of the increasing prevalence of autoimmune diseases such as multiple sclerosis and new approvals for injector implants, the auto-immune disorders segment held a higher market share among disease indications in 2018.

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