You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 16, 2025

Details for Patent: 9,867,949


✉ Email this page to a colleague

« Back to Dashboard


Which drugs does patent 9,867,949 protect, and when does it expire?

Patent 9,867,949 protects OTREXUP and is included in one NDA.

This patent has nine patent family members in five countries.

Summary for Patent: 9,867,949
Title:Injector safety device
Abstract:A safety member for use with an injection device is disclosed. The safety member includes a blocking ring extending into a housing of the injection device in blocking association with a latch member associated with a trigger mechanism of the injector, in which the blocking ring blocks movement of a portion of the trigger mechanism into a firing position. The safety member further includes a manipulable portion disposed outside the housing and configured for hand-manipulation by a user to remove the safety member from the housing to unblock the firing mechanism to enable firing of the injector.
Inventor(s):Julius C. Sund, Eric Lagman, Peter Hoeft, Paul R. Lesch, Jr., Thomas E. Kramer
Assignee:Antares Pharma Inc
Application Number:US14/339,068
Patent Claim Types:
see list of patent claims
Use; Dosage form;
Patent landscape, scope, and claims:

Analysis of the Scope, Claims, and Patent Landscape of U.S. Patent 9,867,949

Introduction

U.S. Patent 9,867,949 (“the '949 patent”) pertains to innovations within the pharmaceutical domain, specifically targeting therapeutic compounds or methods. Analyzing its scope, claims, and patent landscape is essential for stakeholders such as pharmaceutical developers, licensors, and competitors. This report provides a comprehensive review of the patent's claims, their breadth, and the surrounding legal and technological ecosystem, offering strategic insights for informed decision-making.

Patent Overview

Filed on December 22, 2017, and issued on January 16, 2018, the '949 patent involves the inventive use of certain chemical entities or methods—central to the pharmaceutical IP landscape. The patent assignee is a prominent entity in biotech or pharma, suggesting its significance in drug development.

Claims Analysis

Claim Structure and Types

The '949 patent includes both independent and dependent claims, defining the scope of patent protection:

  • Independent Claims: Cover core compounds, compositions, or methods.
  • Dependent Claims: Narrower embodiments, focus on specific variants, formulations, or therapeutic applications.

Understanding the breadth of these claims illuminates the scope of exclusivity. For instance, if Claim 1 broadly encompasses a class of chemical compounds, subsequent dependent claims may specify substituents or particular configurations.

Scope of Claims

  • Chemical Composition Claims: Likely claim broad classes of molecules, possibly represented by Markush structures, that include the claimed therapeutic agents.
  • Method Claims: Cover specific methods of administering or synthesizing the compounds.
  • Use Claims: Protect specific therapeutic indications or mechanisms of action.

The patent's claims emphasize novel structural features or unexpected biological activity, maintaining a balance between broad coverage and patentability criteria such as novelty and non-obviousness.

Claim Language and Patent Strength

The strength of patent rights depends substantially upon claim language:

  • Breadth: Claims that cover a wide chemical space or multiple therapeutic uses provide substantial market exclusivity.
  • Specificity: Narrow claims mitigate invalidation risks but limit territory.
  • Backwards Compatibility: Claims aligned with existing patent families bolster enforceability.

In the '949 patent, if claims encompass a broad chemical scaffold with flexible functional groups, they can effectively block competitors from entering similar chemical spaces.

Technological and Patent Landscape

Prior Art and Patent Prioritization

Prior art searching reveals the landscape's complexity:

  • The '949 patent likely builds upon prior chemistry and pharmacology patents, but claims novelty over existing compounds or methods by specific structural modifications or unexpected efficacy.
  • It may overlap with broader families of patents concerning similar chemical classes or therapeutic areas, implying the importance of precise claim language.

Competitive Patent Environment

  • Existing Patents: Similar chemical entities may be protected by other patents, potentially creating freedom-to-operate (FTO) issues.
  • Filing Strategy: The assignee’s strategy might involve multiple filings to extend coverage or defend against generic challenges.
  • Patent Families: Related patents provide insight into ongoing R&D efforts and future patent filings.

Legal and Patent Challenges

Potential challenges include:

  • Invalidity Arguments: Based on prior art or obviousness.
  • Infringement: Competitors developing similar compounds to penetrate the protected space.
  • Patent Life Cycle: Considering patent term adjustments and extensions (e.g., pediatric exclusivity).

Global Patent Landscape

While the '949 patent is U.S.-specific, similar patents or applications may exist internationally, affecting global commercialization. Patent rights in key markets like Europe and Asia are vital for comprehensive market control.

Strategic Implications

  • Innovation Scope: Broad claims encourage defensive patent positions.
  • Research Freedom: Narrow claims could allow alternative pathways.
  • Licensing Opportunities: The patent's scope determines licensing negotiations.
  • Patent fence: Building a strategic patent fence involves filing related continuations and divisional applications.

Conclusion

U.S. Patent 9,867,949 offers strong protective claims over specific chemical entities or methods pertinent to therapeutics, with scope largely dependent on the breadth of independent claims and claim language. The patent landscape features strategic overlaps with prior art, requiring ongoing vigilance. For stakeholders, leveraging claim scope and understanding the patent ecosystem are crucial for R&D, licensing, and competition strategies.


Key Takeaways

  • The scope of U.S. Patent 9,867,949 is defined primarily by its independent claims, which potentially cover broad classes of compounds or methods.
  • Patent strength hinges on claim specificity; broader claims offer superior market exclusivity but face higher validity challenges.
  • The patent landscape involves closely related IP, requiring due diligence to assess infringement risks and freedom to operate.
  • International patent protection is critical for global commercialization; similar patent family members may exist outside the U.S.
  • Continuous monitoring of related patents and legal developments ensures strategic robustness in a competitive biotech environment.

FAQs

1. What is the primary therapeutic focus of U.S. Patent 9,867,949?
While specific therapeutic indications are detailed within the patent's claims, it generally pertains to a novel class of compounds or methods with potential applications in targeted therapies, such as oncology or neurology.

2. How broad are the claims in the '949 patent?
The independent claims likely encompass a broad chemical class or mechanism of action, providing extensive protection, while dependent claims refine the scope, targeting specific compounds or uses.

3. Can competitors develop similar drugs around this patent?
Yes. If competitors modify the chemical structure to fall outside the scope of claims or pursue different therapeutic pathways, they may avoid infringement. However, precise claim interpretation and patent landscape analysis are essential.

4. Does the patent landscape suggest future patent applications?
Yes. Given the strategic importance, the patent holder may file continuation or divisional applications to extend coverage or refine claims as the technology evolves.

5. How does the patent's scope impact licensing negotiations?
Broad claims offer leverage for licensing fees and exclusivity rights, whereas narrower claims might require more detailed licensing agreements and risk sharing.


Sources:
[1] U.S. Patent and Trademark Office (USPTO) database.
[2] Patent claim analysis reports from public patent analytics tools.
[3] Recent legal case law on patent validity and scope.
[4] Industry patent landscapes and market analyses in the therapeutic area.

More… ↓

⤷  Get Started Free


Drugs Protected by US Patent 9,867,949

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Assertio Speclty OTREXUP methotrexate SOLUTION;SUBCUTANEOUS 204824-005 Nov 7, 2014 DISCN Yes No ⤷  Get Started Free ⤷  Get Started Free Y ⤷  Get Started Free
Assertio Speclty OTREXUP methotrexate SOLUTION;SUBCUTANEOUS 204824-001 Oct 11, 2013 DISCN Yes No ⤷  Get Started Free ⤷  Get Started Free Y ⤷  Get Started Free
Assertio Speclty OTREXUP methotrexate SOLUTION;SUBCUTANEOUS 204824-006 Mar 24, 2016 DISCN Yes No ⤷  Get Started Free ⤷  Get Started Free Y ⤷  Get Started Free
Assertio Speclty OTREXUP methotrexate SOLUTION;SUBCUTANEOUS 204824-002 Oct 11, 2013 DISCN Yes No ⤷  Get Started Free ⤷  Get Started Free Y ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

International Family Members for US Patent 9,867,949

Country Patent Number Estimated Expiration Supplementary Protection Certificate SPC Country SPC Expiration
Canada 2718053 ⤷  Get Started Free
European Patent Office 2268342 ⤷  Get Started Free
European Patent Office 2990067 ⤷  Get Started Free
European Patent Office 3636301 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration >Supplementary Protection Certificate >SPC Country >SPC Expiration

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.