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Patent: 11,041,020
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Summary for Patent: 11,041,020
Title: | Methods for the treatment of active Psoriatic Arthritis |
Abstract: | The present invention relates to compositions and methods utilizing anti-TNF antibodies having a heavy chain (HC) comprising SEQ ID NO:36 and a light chain (LC) comprising SEQ ID NO:37 for use in the safe and effective treatment of active Psoriatic Arthritis (PsA). |
Inventor(s): | Harrison Diane D., Hsia Elizabeth C., Kim Lee-Lian, Lo Kim Hung |
Assignee: | JANSSEN BIOTECH, INC. |
Application Number: | US16517594 |
Patent Claims: | see list of patent claims |
Patent landscape, scope, and claims summary: | Comprehensive Analysis of the Claims and Patent Landscape for United States Patent 11,041,020 IntroductionUnderstanding the intricacies of a U.S. patent, such as the recently granted United States Patent 11,041,020, involves a detailed analysis of its claims, the patent landscape, and the broader legal and procedural context. This article will delve into these aspects, providing insights into the patent's validity, the challenges it may face, and the implications for inventors and policymakers. Patent Claims and Subject Matter EligibilityUnderstanding the ClaimsTo analyze the claims of United States Patent 11,041,020, it is crucial to determine whether they meet the criteria for patent eligibility under U.S. law. The Supreme Court's Alice/Mayo test, as outlined in the Alice Corp. v. CLS Bank International decision, is a key framework here. This test involves two steps: first, determining whether the claims are directed to an abstract idea, law of nature, or natural phenomenon; and second, if so, whether the claims contain an inventive concept that transforms the nature of the claim into a patent-eligible application[3]. Example from Similar CasesFor instance, in the case of Electric Power Group, LLC v. Alstom S.A., the court found that the claims were directed to the abstract idea of monitoring and analyzing data from disparate sources without any inventive concept that would make them patent-eligible[2]. Allowance Rates and Examination ProcessOverview of the Examination ProcessThe U.S. Patent and Trademark Office (USPTO) employs a rigorous examination process to evaluate patent applications. This process includes multiple stages, such as the first-action allowance rate, progenitor allowance rate, and family allowance rate. These metrics help in understanding the likelihood of a patent being granted and the complexity of the examination process[1]. Impact of Entity Size on Allowance RatesStudies have shown that applications filed by small firms are less likely to be granted than those filed by large firms. This disparity can have significant implications for inventors and policymakers, highlighting the need for support mechanisms for smaller entities[1]. Patent Trial and Appeal Board (PTAB) and Inter Partes ReviewRole of PTABThe Leahy-Smith America Invents Act (AIA) of 2011 introduced significant changes to U.S. patent law, including the creation of the Patent Trial and Appeal Board (PTAB). PTAB is empowered to hear administrative challenges to the validity of patents, such as Inter Partes Review (IPR). These mechanisms provide a post-grant review process that can impact the validity of patents like 11,041,020[3]. Challenges to Patent ValidityPTAB reviews focus on whether patent claims are directed to ineligible subject matter and whether they meet the novelty and nonobviousness requirements. If a patent is challenged through IPR, the PTAB will assess whether the claims are supported by sufficient evidence and whether they are novel and nonobvious compared to prior art[3]. Competitive Intelligence and Patent Landscape AnalysisUsing Patent File WrappersReviewing patent file wrappers can provide valuable insights into the prosecution history of a patent. This includes understanding the arguments made by examiners, the reasons for any rejections, and how the applicant responded. For example, a non-final rejection might highlight specific prior art that anticipates the claimed invention, which could be crucial in assessing the patent's validity[4]. Novelty and Nonobviousness RequirementsNovelty RequirementFor a patent to be granted, the claimed invention must be novel, meaning it must not have been patented, described in a printed publication, or in public use, on sale, or otherwise available to the public before the effective filing date of the claimed invention. If every element of the claimed invention is already disclosed in prior art, no valid patent can be issued[3]. Nonobviousness RequirementEven if an invention is novel, it must also be nonobvious. This means that the invention must be significantly different from existing knowledge in the field. The USPTO assesses whether the claimed invention would have been obvious to a person of ordinary skill in the relevant field at the time of the invention[3]. Implications for Inventors and PolicymakersSupport for Small EntitiesThe disparity in allowance rates between small and large firms highlights the need for policies that support smaller entities. This could include reduced fees, access to resources, and educational programs to help small inventors navigate the complex patent system[1]. Legal and Procedural ChallengesInventors must be aware of the legal and procedural challenges that can arise during the patent application process. Understanding the Alice/Mayo test, the role of PTAB, and the importance of novelty and nonobviousness can help in drafting robust patent claims and preparing for potential challenges[2][3]. Case Study: Electric Power Group, LLC v. Alstom S.A.Abstract Ideas and Inventive ConceptsThe case of Electric Power Group, LLC v. Alstom S.A. serves as a cautionary tale for inventors. The court found that the claims were too broad and lacked an inventive concept, leading to a summary judgment against the patent holder. This underscores the importance of ensuring that patent claims are specific and transformative[2]. "The claims therefore do not state an arguably inventive concept in the realm of application of the information-based abstract ideas." - _Electric Power Group, LLC v. Alstom S.A._[2] Key Takeaways
FAQsWhat is the Alice/Mayo test, and how does it impact patent eligibility?The Alice/Mayo test is a two-step framework used to determine whether patent claims are eligible for patenting. It first checks if the claims are directed to an abstract idea, law of nature, or natural phenomenon, and then determines if the claims contain an inventive concept that transforms the nature of the claim into a patent-eligible application[3]. How does the size of the entity filing a patent application affect the allowance rate?Studies have shown that applications filed by small firms are less likely to be granted than those filed by large firms. This disparity highlights the need for support mechanisms for smaller entities[1]. What is the role of the Patent Trial and Appeal Board (PTAB) in patent law?PTAB is a tribunal within the USPTO that hears administrative challenges to the validity of patents, including Inter Partes Review (IPR). It assesses whether patent claims are directed to ineligible subject matter and whether they meet the novelty and nonobviousness requirements[3]. Why is it important to review patent file wrappers?Reviewing patent file wrappers provides valuable insights into the prosecution history of a patent, including arguments made by examiners, reasons for rejections, and applicant responses. This can be crucial in assessing the patent's validity and preparing for potential challenges[4]. What are the novelty and nonobviousness requirements for patentability?For a patent to be granted, the claimed invention must be novel (not previously patented, published, or publicly available) and nonobvious (significantly different from existing knowledge in the field). These requirements ensure that only truly innovative inventions are patented[3]. Sources
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Details for Patent 11,041,020
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Janssen Biotech, Inc. | SIMPONI ARIA | golimumab | Injection | 125433 | July 18, 2013 | ⤷ Subscribe | 2039-07-20 |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |