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Making Ivacaftor Easier for the Body to Absorb

A patent describing a specific way to turn a drug molecule into an amorphous solid to help the body absorb it more effectively.

Granted 2013ActiveExpires 2032Owned by Vertex Pharmaceuticals IncInvented by Yushi Feng, William Rowe, Yuchuan Gong + 6 more

Original patent title: “Solid forms of N-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide

Plain-English explanation by SahiLast reviewed · June 15, 2026

A patent describing a specific way to turn a drug molecule into an amorphous solid to help the body absorb it more effectively. Granted to Vertex Pharmaceuticals Inc in 2013 with 26 claims and 50 forward citations.

Key facts

Patent numberUS 8410274
StatusActive
FieldBiotech & Medicine
AssigneeVertex Pharmaceuticals Inc
InventorsYushi Feng, William Rowe, Yuchuan Gong and 6 others
Filed2012
Granted2013
Claims26
Times cited50
LitigationNone on record
Value · $307K$983KSubstantial

Coverage

What does this patent actually cover?

This patent describes how to create a solid dispersion of a drug molecule, specifically the compound known as Ivacaftor. In its natural state, this molecule is crystalline, which makes it hard for the human body to dissolve and absorb. By creating an amorphous solid dispersion—where the drug is mixed into a polymer matrix like HPMCAS—the molecules are locked in a disordered state that dissolves much faster in the gut. The patent specifically claimsclaimsThe numbered statements at the end of a patent that legally define what the inventor owns.Read more → combinations of this drug with polymers and surfactants, often prepared through a process called spray drying.

The gap

What does this patent NOT cover?

  • Does not cover the chemical structure of the drug molecule itself.
  • Does not cover crystalline forms of the drug.
  • Does not cover methods of treating specific diseases like cystic fibrosis.
  • Does not cover drug delivery methods that do not use solid dispersions.

These exclusions are unique to PatentBrief — derived from the actual claim language, not patent-office boilerplate.

What made this novel

The innovation lies in preventing the drug from reverting to its stable, poorly soluble crystalline form by trapping it within a polymer matrix, effectively 'freezing' it in a high-energy, easily dissolvable state.

Solid forms of N-[2,4-bis(1,1-…(Primary claim)biotechpharmaceutical

Schematic visualization of the patent's claim structure. Hand-drawn diagrams in progress for each landmark patent.

Where you've seen this

Real-world examples

01

Kalydeco (ivacaftor) tablets

02

Orkambi (lumacaftor/ivacaftor) tablets

03

Symdeko (tezacaftor/ivacaftor) tablets

04

Trikafta (elexacaftor/tezacaftor/ivacaftor) tablets

Why it matters

The bigger picture

This technology is essential for the commercial viability of Ivacaftor, a breakthrough treatment for cystic fibrosis. By solving the solubility problem, Vertex Pharmaceuticals enabled the drug to reach the bloodstream in therapeutic concentrations, forming the basis for the Kalydeco medication.

Filed

January 26, 2012

Granted

April 2, 2013

Market context

Who's building on this

Companies in this space

Vertex Pharmaceuticals remains the primary entity utilizing this specific formulation technology for their cystic fibrosis portfolio. Other pharmaceutical companies use similar amorphous solid dispersion techniques to improve the bioavailability of various poorly soluble drug candidates.

Market impact

This patent helped secure the market position of Vertex Pharmaceuticals in the cystic fibrosis space. It enabled the development of highly effective oral medications that transformed cystic fibrosis from a condition managed by symptoms to one treated by addressing the underlying protein defect.

Claim 1 — Plain English

What this patent covers

This patent describes how to create a solid dispersion of a drug molecule, specifically the compound known as Ivacaftor. In its natural state, this molecule is crystalline, which makes it hard for the human body to dissolve and absorb. By creating an amorphous solid dispersion—where the drug is mixed into a polymer matrix like HPMCAS—the molecules are locked in a disordered state that dissolves much faster in the gut. The patent specifically claims combinations of this drug with polymers and surfactants, often prepared through a process called spray drying.

The clever bit

The innovation lies in preventing the drug from reverting to its stable, poorly soluble crystalline form by trapping it within a polymer matrix, effectively 'freezing' it in a high-energy, easily dissolvable state.

What it does not cover

  • Does not cover the chemical structure of the drug molecule itself.
  • Does not cover crystalline forms of the drug.
  • Does not cover methods of treating specific diseases like cystic fibrosis.
  • Does not cover drug delivery methods that do not use solid dispersions.

Patent timeline

Filing

Application submitted to the patent office

Publication

Application published, typically 18 months after filing

Grant

Patent officially issued

PatentBrief Score

Impact Score

Moderate

Citation count

34/40

Moderately cited

Claim breadth

17/20

Very broad protection

Recency

5/20

Granted 10–20 years ago

Assignee scale

0/20

Independent or smaller assigneeassigneeThe entity that owns the patent — usually the inventor's employer or a company.Read more →

PatentBrief Impact Score — based on citation count, claim breadth, recency, and assignee scale. Not a legal assessment.

Heuristic Value Estimate

What this patent might be worth

Substantial

$307K$983K

Midpoint $614K · 5.6 yr remaining · industry ×3.0

Adjust inputs →

Heuristic only — blends forward/backward citation counts, claim scope, time remaining, litigation history, and CPC-derived industry baseline. Real valuations need a professional appraisal.

The original legal language

Original claims

26 claims as filed with the patent office.

Concepts involved

ClaimPrior artNon-obviousnessNoveltySpecificationAssigneePatent term

Citations

Patent lineage

Cites earlier patents

132

earlier patents this invention cites as foundations

View prior art →

Cited by later patents

50

later patents that build on this invention

View patents →

Cite this patent

Feng, Y., Rowe, W., Gong, Y., Connelly, P. R., Hurter, P., Costache, A., Trudeau, M., Young, C. R., & Krawiec, M. (2013). Making Ivacaftor Easier for the Body to Absorb (U.S. Patent No. 8,410,274). U.S. Patent and Trademark Office. https://patentbrief.org/patent/us/8410274/kalydeco-ivacaftor

Auto-generated from the patent record. Double-check author order and the issue date against the official USPTO document before submitting.

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Common Questions

Frequently Asked Questions

What does Making Ivacaftor Easier for the Body to Absorb cover?

A patent describing a specific way to turn a drug molecule into an amorphous solid to help the body absorb it more effectively.

Who owns patent US 8410274?

Vertex Pharmaceuticals Inc owns this patent, granted in 2013.

When does this patent expire?

This patent is expected to expire on April 2, 2033, when the invention enters the public domain.

What is patent US 8410274 cited by?

This patent has been cited by 50 later patents that build on its ideas.

What problem does this patent solve?

This technology is essential for the commercial viability of Ivacaftor, a breakthrough treatment for cystic fibrosis. By solving the solubility problem, Vertex Pharmaceuticals enabled the drug to reach the bloodstream in therapeutic concentrations, forming the basis for the Kalydeco medication.

What does this patent NOT cover?

Does not cover the chemical structure of the drug molecule itself.

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Last reviewed: June 15, 2026 · PatentBrief is not a law firm and this is not legal advice.