早坂・三嶋国際特許事務所 HAYASAKA & MISHIMA GLOBAL PATENT   大阪市中央区,バイオテクノロジー,医薬,有機化学,無機化学,医療器具,機械,特許

 

Court Decisions/判決例
[17/E] Applicant Bears Burden of Proving That Support-by-Description Requirement Is Met - IP High Court, Nov. 11, 2005
Applicant Bears Burden of Proving That Support-by-Description Requirement Is Met Nippon Synthetic Chemical Industry Co., Ltd v. Director-General of the Patent Office

The Intellectual Property High Court ruled on Nov. 11, 2005 that, in an appeal against a JPO Board's decision, it is the applicant/patentee that bears the burden of proving that the support-by-description requirement stipulated by Section 36(6)(i) of the Patent Law is met. It also ruled that the support-by-description requirement cannot be met in a patent application by submitting, after the filing of the application, experimental data to externally supplement the content of the description, stating that otherwise it would go against the principle of the Patent Law, which grants patents for inventions on condition that they are disclosed to the public.

[15/E] No Extension of Patent Term Available upon Patent for Dosage Form (IP High Court, Oct. 11, 2005)
No Extension of Patent Term Available upon Patent for Dosage Form The Intellectual Property (IP) High Court affirmed the decision by the JPO's trial board rejecting an application for patent term extension of a patent about a dosage form of a medical drug. The patented dosage form at issue is a microcapsule-type composition, which releases an active ingredient, buserelin acetate, over one month or more. A product containing the active ingredient had already been approved by the health authorities as a marketable medical drug for the same indication as that of the patented dosage form. The IP High Court concluded that the later approval of the patented dosage form did not meet the requirement that "the approval was necessary for the patented invention to be put into practice" as provided by Section 67(2), and also by Section 67-3(1)(i) of the Patent Law, stating that the requirement should be construed as requiring that the approval was necessary with regard to its active ingredient and indication (i.e., intended effect).

According to this ruling, it should be noted that once a medical drug has been approved with regard to an active ingredient for an indication, no extension of patent term is available to a patented invention of a new dosage form (composition, specially designed container, etc.) of the same active ingredient used for the same indication.

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[D/E1] Application of the Doctrine of Equivalents by Japan’s Courts
Application of the Doctrine of Equivalents by Japan’s Courts The Supreme Court, H6(O)1083, February 24, 1998.

The doctrine of equivalents is applicable in Japan in finding infringement of a patent. In the captioned case, the Supreme Court set forth for the first time in Japan the requirements for finding infringement under the doctrine of equivalents. To note is that not only the specification but also the prosecution history constitute the basis of finding/denying an infringement under the doctrine of equivalents. Deciding the case, the Court wrote as follows.

    "In assessing, in patent infringement litigation, whether or not the product or process the defendant is making or using falls within the technical scope of the patented invention, the technical scope must be determined based on the claims appended to the specification of the granted application. When a part of what is defined by a patented claim differs from a corresponding part of the product or process, the product or process cannot be said to fall within the technical scope of the patented invention. However, even when there is such a part in what is defined by the patented claim, the product or process may properly be considered as being equivalent to what is defined by the patented claim and falling within the technical scope of the patented invention, if:
  (1) that part is not an essential part of the patented invention,
  (2) replacing the part with the corresponding part of the product or process would still allow the invention to fulfill its objective and exhibiting the same function/effect,
  (3) such replacement could have easily been conceived by a skilled person in the pertaining art at the time the product or process was made or used,
  (4) the product or process is neither the same as, nor what would have easily been conceived by a skilled person from, a technology that was publicly known at the time of filing the application of the invention upon which the patent was granted, and
  (5) no particular circumstance is found, e.g., that the product or process was excluded from the scope of the claim in the prosecution of the application."

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