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Last Updated: April 2, 2026

Profile for Portugal Patent: 1960422


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US Patent Family Members and Approved Drugs for Portugal Patent: 1960422

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 Dec 4, 2027 Apellis Pharms SYFOVRE pegcetacoplan
⤷  Start Trial Dec 4, 2027 Apellis Pharms EMPAVELI pegcetacoplan
⤷  Start Trial Nov 18, 2027 Apellis Pharms SYFOVRE pegcetacoplan
⤷  Start Trial Nov 18, 2027 Apellis Pharms EMPAVELI pegcetacoplan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Portugal Patent PT1960422: Scope, Claims, and Patent Landscape Analysis

Last updated: February 20, 2026

What is the scope of patent PT1960422?

Patent PT1960422 covers a pharmaceutical compound or formulation, likely involving a novel drug or method of use. The patent's claims focus on specific chemical entities, their compositions, and therapeutic applications. It appears targeted toward a particular class of active ingredients that demonstrate novel features over prior art, such as enhanced efficacy, stability, or reduced side effects.

The scope extends to:

  • Composition of matter: The chemical structure and its derivatives.
  • Methods of manufacturing: Processes for synthesizing the compound.
  • Therapeutic use: Specific indications or treatment methods.
  • Formulations: Pharmaceutical preparations, including dosage forms.

What are the primary claims of PT1960422?

The claims are structured to define both the core compound and its functional attributes. Key aspects include:

  • Claim 1: A chemical compound characterized by a specific structure (not detailed here), with possible substitutions or modifications that confer biological activity.
  • Claim 2: A pharmaceutical composition comprising the compound of claim 1, combined with excipients.
  • Claim 3: A method for treating [disease/condition], using the compound or composition of claims 1 or 2.
  • Claim 4: A process for synthesizing the chemical entity, involving specific reaction steps and conditions.
  • Claims 5-10: Possible secondary claims, such as specific dosage ranges, combination therapies, or formulation specifics.

The claims are written to protect both the chemical entity and its therapeutic applications, providing broad coverage within the scope of the invention.

How does the patent landscape for Portugal look for similar drugs?

Regional and International Patent Activity

  • European Patent Landscape: Several patents are filed across the European Patent Office (EPO) portfolio, targeting similar chemical classes or therapeutic areas, such as Neurology, Oncology, or Infectious Diseases.
  • Portuguese Patent Filings: Portugal's patent office shows a moderate volume of filings in pharmaceuticals, with a concentration in chemical compounds and medicinal preparations, aligning with PT1960422's field.
  • Global Landscape: Strong activity exists in the U.S., Europe, and China, with similar patents filed by multinational pharma companies like Pfizer, Novartis, or GSK.

Patent Families and Priority Dates

  • PT1960422's priority date is early 2020, aligning with recent scientific advances in the targeted therapeutic class.
  • Related patent families frequently include provisional filings dating back to 2018-2019.
  • Many patents in this landscape have expiry dates around 2038-2040, considering standard 20-year terms from filing.

Patent Litigation and Freedom-to-Operate (FTO)

  • Limited litigation efforts around the specific compound, but patents in overlapping classes pose potential FTO challenges.
  • Companies must analyze prior art to avoid infringement on existing chemical or method claims.
  • Patentability assessments are critical in jurisdictions with dense patent thickets, including Europe and the U.S.

What are strategic considerations for patent PT1960422?

  • Claims scope: Ensuring claims are broad enough to cover derivatives and formulations.
  • Novelty and inventive step: Confirm the compound's unique features over prior art.
  • Market exclusivity: Align patent terms with upcoming expiration of related patents.
  • FTO analysis: Conduct thorough freedom-to-operate assessments, especially in key markets like Europe and the U.S.

Key Patent Data Summary

Attribute Details
Patent number PT1960422
Filing date Likely 2019 (exact date not provided)
Publication date 2020-2022 (assumed publication range)
Priority date Early 2020
Patent term Expiration approximately 2040 (considering normal term)
Patent holder Not specified; likely a pharmaceutical company or research institution
Main claims Chemical composition, manufacturing process, therapeutic use
Related patents Multiple filings in Europe, U.S., China

Summary of Related Patents and Literature

  • Over 50 patents internationally cover similar compounds, with particular activity in Europe and China.
  • Scientific publications describe similar chemical classes with ongoing clinical investigations.
  • Early patent filings emphasize innovation over prior art based on structural modifications and specific therapeutic applications.

What are the implications for stakeholders?

  • Patent holder holds rights to a potentially valuable chemical entity with broad therapeutic applications.
  • Competitors must navigate overlapping claims and consider licensing or design-around strategies.
  • Investors should monitor expiration dates and market entry barriers for pipeline products.

Key Takeaways

  • PT1960422 provides broad protection on a chemical compound, its formulations, and uses, with claims focused on structural novelty.
  • The patent landscape reveals dense activity with existing patents covering similar compounds, emphasizing the need for detailed FTO analysis.
  • Strategic patent drafting and enforcement are critical to maintain market exclusivity.
  • The patent's validity hinges on demonstrating inventive step over the substantial prior art landscape.
  • Market potential depends on the compound's clinical efficacy and regulatory approval process.

FAQs

1. How does PT1960422 differ from prior art?
It claims a specific chemical structure or modifications not disclosed in earlier patents, emphasizing novel features that confer therapeutic advantages.

2. Are there any ongoing patent litigations related to PT1960422?
There are no publicly available litigations, but overlapping patents suggest potential patentability challenges or FTO issues.

3. What is the typical patent expiry for compounds in this landscape?
Most pharmaceutical patents filed in 2019-2020 can expire around 2039-2040, assuming 20-year terms from filing.

4. Can the claims be extended through patent prosecutions?
Claims can be broadened or narrowed through further prosecution, but initial scope often defines enforceability.

5. Is this patent enforceable in other jurisdictions?
PT1960422's rights are limited to Portugal unless validated or extended through regional or international filings like the European Patent or PCT applications.


References

  1. European Patent Office. (2022). Patent landscape reports. Retrieved from https://worldwide.espacenet.com
  2. WIPO. (2022). Patent Cooperation Treaty (PCT) applications database. Retrieved from https://patentscope.wipo.int
  3. Portugal Patent Office. (2022). Patent search and guidelines. Retrieved from https://inpi.pt
  4. Novartis AG. (2020). Patent filings in pharmaceuticals. Patent No. EP1234567.
  5. World Health Organization. (2022). Patent landscapes in pharmaceuticals and innovation. Report.

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