Biotech中国Court CasesInvalidationPharma
2018年11月23日

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.

其他文章

China Announcing More Proposed Amendments to the Examination Guidelines in 2022

2022年11月17日
It’s been a year and a half since the new Chinese Patent Law came into effect (1 June 2021). Although various versions of draft Examination Guidelines have been released, thus far no official finalized versions have been confirmed. On October 31, 2022, yet another new list of proposed amendments was published1, this time consolidating the […]

China’s Newest Examination Guidelines: Post-Filing Supplemental Data for Compounds (Part I)

2021年4月28日
Post-filing data in China has been a constant issue for many patent practitioners around the world. Examiners seem to require it often, and yet the rules regarding when it is acceptable have seemed much stricter than other jurisdictions worldwide. In fact, we tried to summarize the latest state of the law in an earlier blog […]

Introducing the New USPTO Cancer Moonshot Expedited Examination Pilot Program

2023年1月10日
Starting from February 1, 2023, the USPTO will begin the new Cancer Moonshot Expedited Examination Pilot Program that advances out-of-turn applications that are directed to oncology or smoking cessation. This new program will replace the Cancer Immunotherapy Pilot Program that has been in place since 2016, and covers more technologies than only cancer immunotherapies. Applications […]

China Releases Draft Implementation Guidelines for the Drug Administration Law

2022年6月2日
The latest draft implementation guidelines for China’s Drug Administration Law (“Guidelines”) are out and open for comment. Previously, the new implementation measures for early dispute resolution mechanisms for drug patents (“Patent Linkage Measures”) came into effect on July 4, 2021. The Guidelines indicate that the final approval of generic chemical drug applications for marketing approval […]

我们的过去活动

Top crossarrow-right