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ARTICLE · 22 JULY 2026

Connecting The Dots: China’s Evolving Standard For Numerical Sub-Range Amendments

China's patent authority has issued a landmark decision clarifying how numerical ranges and subsequently added experimental data are evaluated when claiming priority in pharmaceutical patents. The ruling establishes that while new efficacy data can support priority claims for explicitly disclosed ratios, numerical values that merely fall within a disclosed range—but were never specifically mentioned—constitute new subject matter and lose priority protection.

ChinaIntellectual Property

Managing global pharmaceutical or chemical portfolios requires navigating China’s notoriously rigid standards on the "same subject matter" requirement for priority and claim amendments. A recent invalidation decision (No. 588094) issued by the China National Intellectual Property Administration (CNIPA) concerning a pharmaceutical patent provides clarity on how numerical ranges and later added experimental data are evaluated in priority claims.1 More specifically, how much literal support is needed for a claim directed towards a “new” numerical sub-range supported by later added working examples?

The Core Dispute: Priority Over specific Ratios and "Added" Data

The patent at issue protected a pharmaceutical composition comprising Edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one) and natural borneol (for treating cerebrovascular diseases), specifically claiming weight ratios from 4:1 to 1:1.2 The challenged patent claimed priority to an earlier application that broadly disclosed weight

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