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Continuation Drafter
Reference

Continuation practice, from the authorities

Twenty-eight decisions and rules that govern United States continuation practice. Each one is quoted from its primary source, and every quotation is checked against a cached copy of that source by a script rather than by eye.

Written for licensed patent practitioners. These pages report what an authority held and how it bears on drafting. They do not assess anyone's claims.

Currency. Every record was verified against its primary source on or after 2026-08-15. That is a fidelity check: it means the quotations, locators and attribution are accurate to the source. It does not mean the authority has been re-checked for later decisions narrowing or reversing it. Confirm an authority still stands before relying on it.

Tier A: the term and double-patenting spine

Allergan protects less than practitioners hoped

Ex parte Baurin

The USPTO's own reviewing panel read Allergan v. MSN narrowly, reinstated the double-patenting rejections its Board had reversed, and told examiners the Allergan exception will rarely if ever come up during original examination.

The term the Office gave you can be the term that kills the claim

In re Cellect

The Federal Circuit held that patent term adjustment is added before the double-patenting comparison is run, so a continuation that earned extra term for Office delay can be invalidated by an earlier-expiring relative it is obvious over.

A parent cannot be invalidated by its own children

Allergan v. MSN

The Federal Circuit reversed a district court that had read In re Cellect to invalidate the first patent in a family over two of its own later-filed continuations, holding that the first-filed, first-issued patent sets the family's maximum period of exclusivity.

Extension survives, adjustment does not

Novartis v. Ezra

The Federal Circuit held that obviousness-type double patenting does not cut off a validly obtained patent term extension under Section 156, so long as the patent was already valid at its pre-extension expiration date.

The cure is permanent, and it was nearly made more expensive

Terminal disclaimer mechanics

A terminal disclaimer ties a patent's expiration and its ownership to another patent, it cannot be undone once the patent issues, and the 2024 rule that would have also forfeited enforceability whenever the other patent lost a claim to prior art was withdrawn in December 2024 and never took effect.

All 5 in Tier A

Tier B: written description and priority for continuation claims

The more you claim, the more you must enable

Amgen v. Sanofi

A unanimous Supreme Court held that a specification claiming an entire functionally defined class of antibodies must enable a skilled person to make and use the whole class, and that disclosing 26 working examples plus a screening protocol left scientists to random trial and error rather than enabling them.

Disclosing every possibility describes none of them

Univ. Minnesota v. Gilead

The Federal Circuit affirmed that earlier applications reciting a compendium of possible chemical substituents did not describe the subgenus claimed years later, so the patent lost its priority date and was anticipated by an intervening publication.

A narrower range inside a disclosed range is usually described

RAI Strategic v. Philip Morris

The Federal Circuit reversed a written-description finding and held that a claimed subrange narrower than any range the specification spells out is still described, where the technology is predictable, the limitation is simple, and nothing shows the subrange is a different invention.

The competitor's product became the prior art

Seagen v. Daiichi Sankyo

The Federal Circuit reversed a jury verdict and held a continuation invalid, because the 2004 parent disclosed an enormous genus of peptide units without reasonably specific support for the 81-member subgenus claimed in 2019, so the patent lost its priority date and the competitor's publicly disclosed product anticipated it.

The specification did not change. The claims did.

Biogen v. Mylan

The Federal Circuit affirmed that claims to a specific therapeutically effective dose were invalid for lack of written description, because the 2007 disclosure they claimed priority from was a drug-discovery document that mentioned the dose exactly once, inside a range, and the new claims were written in 2011 once clinical results were in.

The parent's own publication became the reference

Indivior v. Dr. Reddy's

The Federal Circuit affirmed that ranges added by amendment to a fifth continuation lacked written-description support in the 2009 parent, so the claims lost that filing date and were anticipated by the publication of the parent application itself.

Silence is not a description of absence

Novartis v. Accord

The Federal Circuit granted rehearing, vacated its own earlier affirmance, and held that a specification saying nothing about loading doses did not describe a claim limitation requiring their absence, because disclosure rather than silence is what written description needs.

The preamble is not free text

In re Xencor

The Federal Circuit held that the limiting preamble of a Jepson claim must itself be supported by written description, so reciting the prior art in a preamble puts that recitation inside the support burden rather than outside it.

You did not invent what you did not disclose

Enanta v. Pfizer

The Federal Circuit held that a provisional disclosing C2-C12-alkyl does not provide written-description support for C1-alkyl, even where the applicant says the C2 was an obvious typographical error, so the later patent lost its priority date.

All 9 in Tier B

Tier C: effective filing date and the AIA transition

All 4 in Tier C

Tier D: timing, laches, and the new carrying costs

Six years of unexplained delay moves the burden

Hyatt v. Hirshfeld

The Federal Circuit held that where the Patent Office shows unreasonable and unexplained prosecution delay exceeding six years, the burden shifts to the applicant to prove the absence of prejudice, and defined prejudice as intervening investment in the claimed technology.

An infringed patent can still be unenforceable

Personalized Media v. Apple

The Federal Circuit affirmed that a patent a jury had found infringed was unenforceable for prosecution laches, because the patentee's delay was unreasonable and inexcusable under the totality of the circumstances and the accused infringer was prejudiced by it.

Delay alone did not carry it

Google v. Sonos

The Federal Circuit reversed a judgment that had held long-pending patents both invalid for lack of written description and unenforceable for prosecution laches, restating that laches requires unreasonable and inexcusable delay plus prejudice attributable to it.

Late continuations now carry a surcharge

The continuing-application fee

From 19 January 2025 a nonprovisional application whose actual filing date is more than six years after its earliest benefit date owes an additional fee, at one rate between six and nine years and a higher rate beyond nine, payable when the benefit claim that triggers it is presented.

One year, not two, before you must explain the delay

Unintentional-delay petitions

From 13 August 2026 the USPTO requires an additional explanation of the circumstances surrounding a delay whenever a petition based on unintentional delay is filed more than one year after the action was due, down from two years, and the higher petition fee threshold moved to match.

An already-expired patent is worth nothing, including provisionally

In re Forest

The Federal Circuit held that provisional rights under Section 154(d) arise only where the patent would issue with exclusionary rights, so an application whose patent would issue after the term had already run produced no rights at all and the appeal had no jurisdictional basis.

All 6 in Tier D

Tier E: adjacent practice areas

All 4 in Tier E