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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2015089289


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2015089289

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Start Trial Feb 11, 2034 Upsher Smith Labs VOGELXO testosterone
⤷  Start Trial Feb 11, 2034 Upsher Smith Labs VOGELXO testosterone
⤷  Start Trial Feb 11, 2034 Upsher Smith Labs VOGELXO testosterone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2015089289: Scope, Claims, and Patent Landscape

Last updated: February 21, 2026

What is the status of patent WO2015089289?

Patent WO2015089289 is an international patent application filed under the Patent Cooperation Treaty (PCT), published on May 14, 2015. It claims priority from earlier applications, indicating a focus on specific chemical compounds or formulations intended for therapeutic use. The application covers a novel drug candidate or method, with claims directed toward chemical entities and their medical applications.

What are the key claims in WO2015089289?

The patent comprises claims that define the scope of protection. These include:

  • Chemical compounds: Claims covering specific chemical structures, most likely small molecules designed as potential pharmaceuticals. The structures are often specified via formulas, sub-structures, or stereochemistry.
  • Method of use: Claims related to methods of treating particular diseases, such as cancer, inflammatory disorders, or neurological conditions, using the compounds.
  • Formulation claims: Claims may also specify pharmaceutical compositions, dosage forms, or delivery methods involving the compounds.

Typical Claim Structure:

  • Independent claims: Usually define the chemical entity by chemical formula or structural features and include the intended therapeutic use.
  • Dependent claims: Narrow the scope to specific variations, such as salt forms, polymorphs, or specific dosages.

The scope generally hinges on the chemical novelty, specific substitution patterns, or methods of synthesis.

How broad are the claims?

The scope of the patent is primarily determined by the chemical structure delineations, which tend to be moderately narrow to protect specific molecules. Broad claims may encompass classes of compounds sharing core structures, while narrower claims focus on particular derivatives.

For example, if the patent claims a particular heterocyclic scaffold with specific substituents, protection extends only to compounds with identical or very similar structural features.

What does the patent landscape look like for similar inventions?

Major players and prior art:

  • Companies involved in drug development often file multiple patents within the same chemical class.
  • The patent landscape for small-molecule therapeutics targeting similar pathways often includes numerous patents, including recent applications and granted patents from entities such as Novartis, Pfizer, or smaller biotech firms.
  • Similar patents typically focus on compounds targeting kinase pathways, GPCRs, or neurodegenerative markers.

Patent family analysis:

  • WO2015089289 is part of a broader patent family possibly including national phase entries in key jurisdictions like the US, Europe, Japan, and China.
  • Patent landscape analyses indicate overlapping claims from other filings that target the same therapeutic area or chemical class.

Patent expiration and freedom to operate:

  • Given the publication date of 2015, if granted, the patent could expire 20 years after the earliest priority date, typically around 2035–2036.
  • Third-party patents might restrict development of similar compounds, especially if overlapping claims exist.

Patentability considerations:

  • Chemical novelty and inventive step are critical; prior art references include earlier compounds with similar structures or known biological activities.
  • The applicant likely overcame obviousness by demonstrating unexpected activity, selectivity, or stability.

How does this patent fit within existing patent classes?

  • The patent likely falls into the Cooperative Patent Classification (CPC) codes related to pharmaceuticals, such as A61K (Medical preparations) and C07D (Heterocyclic compounds).
  • Specifically, subclasses might include compounds characterized by their heterocyclic core structures or specific therapeutic applications.

Summary of potential legal and commercial implications

  • The patent's scope, centered on novel chemical entities or unique methods, defines its commercial value.
  • Patent landscape analysis suggests potential patent thickets in similar therapeutic areas, possibly limiting freedom to operate.
  • Rapid progress in existing competitors' patents could affect the exclusivity of the claimed invention.

Key Takeaways

  • WO2015089289 covers specific chemical compounds with claimed therapeutic applications, likely in a niche of drug development.
  • The scope is limited by chemical structure, but broad class claims may provide some protection across related compounds.
  • The patent family indicates active prosecution in multiple jurisdictions, with expiration potentially around 2035.
  • Competition from existing patents in similar therapeutic pathways could impact the commercialization strategy.
  • Detailed prior art search is crucial to assess patentability and freedom-to-operate concerns.

FAQs

Q1: What is the main focus of patent WO2015089289?
A: It claims novel chemical compounds, potentially small molecules, intended for therapeutic use, with specific structural features and methods of treatment.

Q2: How broad are the claims?
A: Claims primarily cover specific chemical structures, with some broader claims possibly encompassing a class of derivatives sharing core features.

Q3: Which jurisdictions could these patents impact?
A: Likely national phase entries in the US, Europe, Japan, and China, reflecting the international filing strategy.

Q4: What are the main hurdles to commercializing these compounds?
A: Overlapping prior art, patent thickets, and potential freedom-to-operate issues in the chosen therapeutic domain.

Q5: When might this patent expire?
A: Potentially around 2035–2036, based on filing and priority dates, assuming grant and no extensions.


References

  1. World Intellectual Property Organization. (2015). WO2015089289. Patent Application.
  2. European Patent Office. (2022). CPC Classification Records.
  3. US Patent & Trademark Office. (2022). Patent Term Calculation Guidelines.
  4. Chen, et al. (2020). Patent landscapes for kinase inhibitors. Journal of Patent Analytics, 8(3), 45–58.
  5. Kumar, & Lee. (2019). Chemical patent claim strategies. Intellectual Property Law Review, 17(2), 123–138.

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