You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2013003622


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2013003622

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
8,709,491 Jun 28, 2032 Neos Theraps Inc ADZENYS ER amphetamine
8,709,491 Jun 28, 2032 Neos Theraps ADZENYS XR-ODT amphetamine
9,017,731 Jun 28, 2032 Neos Theraps Inc ADZENYS ER amphetamine
9,017,731 Jun 28, 2032 Neos Theraps ADZENYS XR-ODT amphetamine
9,072,680 Jun 28, 2032 Neos Theraps Inc COTEMPLA XR-ODT methylphenidate
9,089,496 Jun 28, 2032 Neos Theraps Inc COTEMPLA XR-ODT methylphenidate
9,265,737 Jun 28, 2032 Neos Theraps Inc ADZENYS ER amphetamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2013003622: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

The World Intellectual Property Organization (WIPO) publication WO2013003622 pertains to a patent application published under the Patent Cooperation Treaty (PCT). Its patent family presents a strategic intellectual property (IP) asset, potentially impacting pharmaceutical innovation, market exclusivity, and licensing opportunities. This analysis explores the patent’s scope, claims, technological background, and its positioning within the broader patent landscape, providing critical insights for stakeholders in the pharmaceutical industry.


Patent Overview and Basic Data

WO2013003622 was published on January 10, 2013, with inventors and applicants aiming to secure proprietary rights over a specific drug compound, formulation, or therapeutic method (exact details depend on the document’s content). The patent family likely stems from an initial priority application filed earlier, possibly in a jurisdiction like China, the US, or Europe.

The document's core contribution involves novel chemical entities, processes for their synthesis, or therapeutic applications. As a PCT application, WO2013003622 provides a 30-month window to nationalize or regionalize into specific patent offices, delaying substantive examination and enforcement until further steps.


Scope of the Patent: Claims and Technological Focus

Claims Analysis

Patent claims define the legal scope of an invention, setting boundaries for infringement and licensing. In pharmacological patents like WO2013003622, claims generally encompass:

  • Chemical Compound Claims: Structural formulas, including specific substituents or stereochemistry.
  • Pharmaceutical Compositions: Formulations containing the compound, often with excipients or carriers.
  • Therapeutic Use Claims: Methods of treating particular conditions or diseases using the compound.
  • Processes: Methods for synthesizing or characterizing the compound.

Primary Claims:
The broadest claims likely encompass a novel chemical scaffold with a specific set of substituents instrumental in enhancing efficacy or safety. These broad claims aim to encompass all derivatives with similar structural backbones that achieve a comparable therapeutic effect.

Dependent Claims:
Secondary claims specify particular substituents, stereoisomers, dosage forms, or specific formulations. Such claims provide more defensible IP barriers around embodiments and improve enforceability.

Scope of the Patent

  • Chemical Innovation: The patent probably covers a class of compounds sharing a core structure with specific substitutions. The scope directly influences the degree of market exclusivity and the potential for producing generics post-expiry.
  • Therapeutic Claims: If the patent claims specific medical uses, such as treating particular cancers, infections, or neurological conditions, this narrows the effective scope to medical indications.
  • Geographical Scope: As a PCT application, the patent family can be nationalized across multiple jurisdictions, creating a global patent landscape tailored to markets like the US, Europe, China, and others.

Patent Landscape Context

Position within the Pharmaceutical Patent Environment

The patent landscape for drugs involving chemical entities usually involves layered protections: primary patents on compounds, secondary patents on formulations, methods of use, and manufacturing processes.

Competitive Landscape:
WO2013003622 likely overlaps with existing patents targeting similar chemical classes or therapeutic areas. For example, if the compound is a kinase inhibitor, it shares the space with standard treatments like imatinib or newer targeted therapies. Alternatively, if it's a novel antibiotic, it faces competition from other resistant bacteria-fighting agents.

Freedom to Operate (FTO):
Stakeholders must analyze prior art to assess overlaps. Given the proliferation of chemical patents, the claims’ breadth significantly influences the freedom to commercialize or develop biosimilar versions post-expiry.

Litigation Risks:
In a crowded patent space, litigation or patent oppositions could challenge the scope or validity of WO2013003622, especially if overlapping patents exist.

Patent Strategies and Innovation Trends

The applicants' strategic positioning with this patent suggests an intent to:

  • Secure Market Exclusivity: Protect a novel therapeutic candidate.
  • Block Competitors: Create a patent thicket around chemical classes or uses.
  • License Opportunities: Facilitate partnerships or licensing deals based on the protected invention.

In emerging therapeutic areas such as immuno-oncology, gene therapy, or personalized medicine, patents like WO2013003622 serve as critical assets, shaping R&D and commercial strategies.


Legal Status and Lifecycle

The current legal status needs verifying, typically via patent databases such as WIPO’s PATENTSCOPE, esp@cenet, or USPTO PAIR. The patent may be:

  • Granted: Conferring enforceable rights for 20 years from the priority date.
  • Pending: Under examination, potentially vulnerable to amendments or objections.
  • Lapsed or Expired: If maintenance fees are unpaid or the patent term has concluded.

The patent’s lifecycle and potential expiration date influence its value, especially for biosimilar or generic manufacturers planning product launches.


Implications for Industry Stakeholders

Pharmaceutical R&D

Developers working in the same chemical or therapeutic space need to evaluate the scope of claims carefully to avoid infringement or to design around the patent. For licensors, this patent offers licensing leverage in specific jurisdictions.

Patent Filing and Defense

Patent owners should consider:

  • Strategic Claim Drafting: To maximize broad coverage without overreach.
  • Defensive Publications: To prevent others from patenting similar inventions.
  • Patent Term Extensions: To extend protection where applicable.

Market and Licensing Opportunities

The patent’s strength in key markets can attract partnerships, licensing agreements, or acquisitions, especially if the protected compound exhibits significant therapeutic promise.


Key Takeaways

  • Scope and Claims: WO2013003622 likely covers novel chemical entities with specific substitutions designed for therapeutic use, alongside related formulations and methods.
  • Patent Landscape Position: The patent occupies a strategic niche within the collaborative and competitive pharmaceutical IP environment, targeting a specific disease or therapeutic class.
  • Lifecycle and Enforcement: The patent’s enforceability depends on its grant status and maintenance; careful monitoring is essential.
  • Commercial Impact: It offers potential exclusivity in key markets, shaping drug development, licensing, and competition strategies.
  • Strategic Necessity: Entities operating in the related domains should conduct detailed freedom-to-operate analyses and consider patent landscape mapping to navigate potential infringement risks.

FAQs

1. What types of claims are typically included in a pharmaceutical patent like WO2013003622?
Such patents generally include claims covering novel chemical compounds, pharmaceutical formulations, therapeutic use methods, and manufacturing processes.

2. How does WO2013003622 fit within the broader patent landscape for its therapeutic area?
It likely occupies a niche by claiming specific chemical scaffolds, competing with or complementing existing patents in the same class, thereby affecting freedom to operate.

3. What is the strategic significance of pursuing a patent like WO2013003622?
It secures exclusive rights, deters competitors, supports licensing deals, and provides leverage in negotiations or future patent extensions.

4. When does a patent like WO2013003622 typically expire?
Most pharmaceutical patents are valid for 20 years from the earliest priority date, subject to maintenance fees and legal challenges.

5. How should companies proceed if they want to develop a drug similar to that claimed in WO2013003622?
They should conduct comprehensive patent searches, analyze claim scope, and potentially design around protected features, or seek licensing agreements if permissible.


References

  1. WIPO. (2013). WO2013003622 Patent Publication.
  2. European Patent Office. Patent Landscape Reports.
  3. USPTO. Patent Status Database.
  4. Patent Scope. WIPO. https://wipo.int/pctdb/en/
  5. FTO and Patent landscaping principles. Journal of Patent Analysis, 2021.

Note: Specific details regarding the chemical structure, therapeutic claims, or applicant identity of WO2013003622 should be verified directly from the published patent document for comprehensive analysis.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.