BiotechChinaCourt CasesInvalidationPharma
23 November 2018

No % homology? How to craft allowable claim scope around sequences to comply with China’s strict written description requirements

Since 2010, the Patent Re-examination Board (PRB) has published the top 10 patent invalidation cases of the year in April of each year. The selection criteria are high social concern, significant impact on the related industry, or involve difficult legal issues and important examination criteria. Below is one of the top 10 cases that discusses what is considered allowable claim scope around sequences.

It is well known that China has strict requirements when it comes to adequate written description and support in the specification. Chinese Patent Law Article 26(4) says that “all claims must be supported by the description and shall define the extent of the patent protection sought for in a clear and concise manner.”

In the unpredictable arts, such as chemistry and biology, the breadth of protection is highly dependent on the number and scope of the specific examples in the specification. The resultant narrow claims that are often issued in China are easy to design-around, thus making Chinese patents less attractive for biotech inventions with few actual examples.

Invalidation Request: Novozymes CN98813338.5

We summarize a Top 10 IP Cases of 2016 regarding an invalidation request of Novozymes’ Chinese invention patent (CN98813338.5) by Jiangsu Boli Biological Products Co. Ltd. Novozyme’s patent relates to an isolated glucoamylase with improved thermal stability and many uses, such as converting starch into glucose. The claims were written in a way that included a functional limitation (having “glucoamylase activity”) plus a scope defined in one or more of the following ways: “comprising” a SEQ ID, consisting of a SEQ ID plus 99% homology, and source, e.g., derived from a particular strain.

For support, the specification described two sequences, SEQ ID NO: 7 and 14, both of which were isolated enzymes from a strain of the filamentous fungus T. emersonii that had glucoamylase activity.

The court rejected claims that merely defined the enzyme using either open-ended “comprising” language or percent homology language, saying the scope was too open-ended and not supported by the examples. However, the court allowed claims that further narrowed the claim to cover sequences made by a particular strain. The court reasoned that only a very narrow set of sequences could possibly be made from the strain, and thus the limitation was adequately supported by the two examples.

Practice Points

As a practice point, consider multiple ways of defining your invention (e.g., “source” was the winner here, but the possibilities depend on the situation). There are many creative ways to define your invention: the more examples showing the “reasonable, predictable scope” of the active species, the better. Ideally, focus on describing how the function is linked to the structure or other properties (e.g., structural and functional domains of a polypeptide, source, method of preparation, physicochemical properties, etc.).

Sources: lungtin unitalen

Jennifer Che, J.D. is a US Patent Attorney and Vice President and Partner at Eagle IP, a Boutique Patent Firm with offices in Hong Kong, Shenzhen, and Macau.

[email protected]

This article is for general informational purposes only and should not be considered legal advice or a legal opinion on a specific set of facts.

Other Articles

AI is magical but NOT magic! Be specific in your AI patents!

9 January 2025
What is the standard of sufficient disclosure for AI-related patents: A case study in China The rapid growth of AI patent applications present significant challenges to existing patent application and examination practices. One of them is satisfying the requirement for sufficient disclosure. The following case was featured in the 2023 CNIPA Compilation of Key Decisions […]

CNIPA further clarifies how it counts “delays” when calculating Patent Term Adjustment (PTA) in the new Draft Examination Guidelines and how it affects international applicants

12 April 2023
At the end of October 2022, the China National Intellectual Property Administration (CNIPA) released a new draft amendment of the Patent Examination Guidelines1 (hereinafter referred to as the “New Draft”) to the new Chinese Patent Law that came into effect in 2021. We highlight two key amendments below. 1. The starting date for calculating PTA […]

Everything you need to know about Patent Term Adjustment (PTA) in China

7 May 2024
We previously discussed patent term compensation for patent office delay (‘Patent Term Adjustment’ or ‘PTA’) when such new system was introduced in the Fourth Amendment of the Chinese Patent Law (2020), as well as in the different versions of the Draft Examination Guidelines released in 2021 and 2022. In this article, we consolidate everything you need to […]

New Fee Standards Released for Chinese Patent Applications

6 September 2024
Recently, the Chinese government issued four official notices introducing new fee standards and deduction rules for Chinese patent applications.1 These updates address international applications (PCT applications) and the Chinese national phase applications thereof, as well as patent term adjustment/extension (PTA/PTE). Please find our summary below: PCT application fee deduction rules   Application fee & extra […]

Our Past Events

Top crossarrow-right