C4IP Slams ETHIC Act Targeting Patent Thickets as Destabilizing to Innovation Ecosystem

“Prohibiting the enforcement of validly issued U.S. patents destabilizes the entire innovation ecosystem.” –  C4IP Executive Director Frank Cullen.

ETHIC ActThe Council for Innovation Promotion (C4IP) today issued a statement taking Congress to task for supporting a bill introduced in July that would limit the ability of patent owners to assert more than one patent from the same “Patent Group” in a patent infringement action, with the goal of addressing so-called patent thickets.

Patent thicketing is a controversial term that is criticized by the pro-patent community as being a misnomer. While the common perception is that patent thickets are a way for pharmaceutical companies to extend the life of a patented drug to the detriment of generic entry, C4IP called this narrative “misleading.”

“In reality, many patents can be necessary to capture the full scope of all the inventions in sophisticated and complicated products, especially in highly advanced fields — and, as confirmed by the U.S. Patent and Trademark Office, the number of patents is not correlated to the timing of generic entry,” said today’s statement.

The ETHIC Act would prohibit anyone from asserting more than one patent in the same Patent Group against a particular party. A “Patent Group” is defined in the bill as “2 or more commonly owned patents or applications that—”:

‘(I) are identified on 1 or more disclaimers under section 253 to obviate obviousness-type double patenting of another commonly owned patent; or

‘(II) are subject to 1 or more disclaimers under section 253 to obviate obviousness-type double patenting of another commonly owned patent.

‘(ii) For purposes of clause (i)(I)—

(I) each patent or application that identifies the same patent or application on a disclaimer under section 253 is part of the same Patent Group; and

‘(II) each patent or application that is identified on a disclaimer under section  253 is part of the same Patent Group as the patent or application subject to the disclaimer.’’

The USPTO report C4IP referenced in its statement was published in 2024 and found that “simply quantifying raw numbers of patents and exclusivities is an imprecise way to measure the intellectual property landscape of a drug product because not every patent or exclusivity has the same scope.”

In particular, the report suggested that some of the data most relied upon to support the need for bills like the ETHIC Act may be faulty. The Initiative for Medicines, Access & Knowledge (I-MAK), whose studies have been cited in many congressional hearings, for instance, has been charged with a lack of transparency about the underlying dataset behind its findings that makes its numbers “impossible to confirm.”

The USPTO report did not specifically analyze I-MAK’s or any other source’s data or methodologies. “Rather, the USPTO, with the assistance of the FDA, conducted an analysis of a representative sample of 25 New Drug Applications (NDAs) (representing 13 distinct active ingredients) listed in the FDA’s Orange Book1 between 2005-2018 that were also considered by these data sources using available public data points (e.g., patent numbers and exclusivities listed in the Orange Book, patent filing and issue dates, and drug application approval dates),” said the report. The samples were selected based on a number of factors, including “top grossing products by revenue in 2017, most prescribed branded products in 2017, and other factors….”

Among the report’s conclusions, the USPTO found that “[w]ith respect to multiple patents that cover a single product, multiple patents associated with a single marketed product are not unique to the pharmaceutical industry and are a common practice in many innovative industries, especially for complex products.”

The ETHIC Act was introduced in the Senate on a bipartisan basis by U.S. Senators Peter Welch (D-VT), Josh Hawley (R-MO), and Amy Klobuchar (D-MN). It was also introduced in the House of Representatives in May by Representative Jodey Arrington (R-TX) along with two other Republicans and four Democrats.

According to the Senators’ press release, the bill would “streamline drug patent litigation, encourage fair market competition, and lower prescription drug prices by making it easier for generic and biosimilar companies to enter the market.”

But C4IP said the bill would merely weaken patent rights and threaten innovation. “Prohibiting the enforcement of validly issued U.S. patents destabilizes the entire innovation ecosystem,” said C4IP’s Executive Director Frank Cullen. He added:

“Limiting the innovators’ ability to enforce these patents would strip companies — especially startups — of the tools they need to attract investment, build partnerships, and bring new technologies to market. Weakening patent rights does not foster competition; it chokes off the development of future cures. A sector-specific measure like the ETHIC Act risks setting a dangerous precedent — inviting broader efforts to weaken the patent system and erode protections across all innovative industries.”

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Author: thaneeh.gmail.com

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2 comments so far.

  • [Avatar for John Paul Archuleta]
    John Paul Archuleta
    August 6, 2025 07:50 am

    This bill is another type of political tool of underlying consequences for the best innovation and intellectual property rights for patent owners who have dedicated their lives to innovation of complex situations. Another Wall thrown in front of national security innovation which doesn’t always come from big tech companies to attract small startup companies. Stupid is just the beginning of the bill

  • [Avatar for mike]
    mike
    August 5, 2025 03:24 pm

    This bill is stupid and identifies those in Congress who don’t know patents or patent law. Separate from C4IP’s statement, the bill is DOA because one can file a terminal disclaimer a) without even receiving a double patent rejection and/or b) without agreeing to merits of the rejection, but just for expediency.

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