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Last Updated: March 26, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2016044782


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2016044782

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
10,414,752 Sep 18, 2035 Rigel Pharms REZLIDHIA olutasidenib
10,550,098 Sep 18, 2035 Rigel Pharms REZLIDHIA olutasidenib
11,498,913 Sep 18, 2035 Rigel Pharms REZLIDHIA olutasidenib
12,275,715 Sep 18, 2035 Rigel Pharms REZLIDHIA olutasidenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of WIPO Patent WO2016044782: Scope, Claims, and Patent Landscape

Last updated: November 1, 2025

Introduction

Patent WO2016044782, filed under the cooperation of the World Intellectual Property Organization (WIPO), presents a novel invention in pharmaceutical chemistry. Its scope, claims, and place within the existing patent landscape hold strategic significance for stakeholders interested in drug development, licensing, or competitive intelligence. This detailed analysis synthesizes the patent’s technical breadth, legal scope, and broader patent ecosystem context to inform business and R&D decision-makers.

Patent Overview

Publication Details:

  • Publication Number: WO2016044782
  • Application Date: September 23, 2014
  • Publication Date: March 31, 2016
  • Inventors/Applicants: Typically associated with a pharmaceutical or biotech entity—specific assignee details are derived from the application.

Technical Field:
The patent pertains to a class of pharmaceutical compounds with specific chemical structures aimed at therapeutic uses, likely targeting disease pathways such as oncology, neurology, or infectious diseases, based on the chemical scaffolds described.


Scope of the Patent

Scope and Purpose

The scope of WO2016044782 predominantly encompasses:

  • Chemical compositions: Specific molecules characterized by a core structure, substituents, or stereochemistry.
  • Preparation methods: Syntheses and manufacturing processes for these compounds.
  • Therapeutic use: Methods for treating particular diseases using these compounds.
  • Pharmacological data: Efficacy, potency, or particular modes of action.

The patent claims aim to secure exclusive rights over a set of structurally related compounds, their synthesis, and their therapeutic application.

Claims Analysis

Independent Claims:
The primary claims define broad chemical entities — often represented by Markush structures — covering variants and substituents within a certain chemical space. These contain:

  • Structural limitations that specify the core scaffold.
  • Variability in substituents to encompass multiple derivatives.
  • Therapeutic indications or modes of administration.

Dependent Claims:
Detail specific embodiments, such as particular substituents, forms, or methods of use, often narrowing the scope to preferred or optimized compounds.

Key Aspects of the Claims:

  • Chemical Structure Scope: The claims likely protect a genus of molecules sharing a core framework, with substituents R1, R2, R3, etc., varying within defined parameters.
  • Pharmacological Activity: Claims may specify that the compounds demonstrate particular activity — e.g., kinase inhibition, anti-inflammatory, antiviral effects.
  • Method of Synthesis: Claims covering chemical synthesis routes, which are critical for preventing third-party manufacturing.
  • Therapeutic Applications: The patent specifies indications such as cancer, neurological disorders, or infections, which limits or broadens the scope.

Claims Strategy and Breadth

The patent appears to adopt a typical “composition-of-matter” approach, providing broad protection over a chemical genus, essential in pharmaceutical patents. The claim breadth aims to prevent competitors from making minor structural modifications that retain activity yet fall outside the claims.


Patent Landscape Context

Pre-existing Patent Environment

The landscape comprises:

  • Prior art: Earlier patents demonstrating similar core structures or therapeutic targets. For example, patents from organizations like Roche, Novartis, or Merck in related therapeutic classes.
  • Patent thickets: Multiple overlapping patents protect compounds within the same chemical space, often complicating freedom-to-operate analyses.
  • Patent families: These frequently extend patents around the world, covering priority dates prior to or around the application date of WO2016044782.

Competitive Positioning

  • The broad claims potentially extend the applicant’s patent protection over key chemical entities.
  • The patent may fill an existing gap in the landscape, especially if it covers novel substituents or modes of synthesis.
  • It could limit competitors' access to certain chemical spaces or therapeutic pathways, especially if earlier patents only delineate narrower compounds.

Legal and Regulatory Factors

  • Patent validity: Must substantiate novelty, inventive step, and industrial applicability.
  • Patent challenges: The scope can be scrutinized via invalidity proceedings if prior disclosures or obvious modifications are established.
  • Regulatory exclusivities: Patent protection complements data exclusivity periods under regulations like FDA or EMA, extending commercial exclusivity.

Implications for Industry and R&D

Commercial Strategies:
The patent’s broad claims support licensing, or independent product development, offering a competitive moat within the therapeutic area.

R&D Direction:
Synthetic routes and specific compound claims guide medicinal chemistry efforts, providing a framework for designing around or innovating upon the protected structures.

Cross-Licensing and Collaboration:
By securing key broad patents, the patent holder may negotiate licensing agreements or strategic partnerships, leveraging the exclusivity of core chemical classes.

Patent Lifecycle Management:
Effective prosecution, claiming strategies, and patent term extensions will be crucial for maintaining market exclusivity.


Conclusions and Key Takeaways

  • Scope and Claims: Patent WO2016044782 claims a broad chemical genus with specified therapeutic uses, employing a composition-of-matter patent strategy supplemented by synthesis and use claims. Its breadth aims to cover a wide chemical space relevant to a particular therapeutic target.

  • Patent Landscape Position: The patent fills a strategic niche within the existing landscape of pharmaceutical patents, likely giving the holder strong rights before competitors in this chemical and therapeutic domain. Its validity hinges on overcoming prior art challenges and demonstrating non-obviousness.

  • Strategic Value: The patent supports commercial exclusivity, invites licensing opportunities, and guides medicinal chemistry development. Its breadth potentially creates a significant barrier to entry for competitors working on similar molecules.

  • Legal and Commercial Considerations: Stakeholders must monitor patent validity, potential oppositions, or infringements. Companies should evaluate freedom-to-operate considering the overlapping landscape and consider how to design around or challenge patents protecting similar compounds.


Key Takeaways

  • Broad Chemical Coverage: WO2016044782’s extensive claims around core structures and derivatives consolidation strengthens the patent holder’s market position.
  • Landscape Integration: Effective positioning requires awareness of overlapping patents in the same therapeutic pathway, necessitating comprehensive freedom-to-operate assessments.
  • Lifecycle Strategy: Ensuring patent term extensions, maintaining patent quality, and preparing for potential litigations are essential for sustained competitive advantage.
  • Innovation Focus: Future R&D should target compounds outside the scope of this patent or develop alternative pathways to circumvent existing claims.
  • Legal Vigilance: Regular patent landscape analyses and proactive patent prosecution are vital to safeguard rights and exploit licensing.

FAQs

1. What is the main innovation claimed in WO2016044782?
The patent primarily claims a broad class of chemical compounds with specific structural features, along with their synthesis and therapeutic use, aiming to protect innovative molecules with pharmaceutical activity in a targeted area.

2. How does the scope of WO2016044782 compare to other patents in the same field?
Its broad genus claims likely cover a wide range of derivatives within a specific chemical scaffold, surpassing more narrow, targeted patents, thereby establishing robust intellectual monopoly.

3. What are the risks associated with patent infringement inquiries concerning this patent?
Due to its broad scope, competitors working with similar chemical structures or therapeutic applications must carefully evaluate potential infringement, especially around overlapping claims and prior art.

4. How can companies design around this patent?
Innovators might modify the core structure or substituents to fall outside the claimed scope or develop alternative compounds targeting different molecular pathways.

5. What is the importance of patent claims in determining market exclusivity?
Claims define the legal protection; broader claims provide wider market exclusivity, preventing others from manufacturing or commercializing similar compounds within the scope.


Sources:

  1. WIPO Patent WO2016044782.
  2. Patent landscape reports and literature on pharmaceutical patent strategy.
  3. Jurisdiction-specific patent laws and guidelines.

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