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

Last Updated: March 12, 2026

Profile for Spain Patent: 2943668


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Spain Patent: 2943668

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Patent ES2943668: Scope, Claims, and Landscape Analysis

Last updated: February 28, 2026

What is the scope of patent ES2943668?

Patent ES2943668 is a Spanish patent filed by PharmaSurg, granted in 2019, concerning a novel formulation for the treatment of infectious diseases, particularly viral infections such as hepatitis C. The patent claims include a combination of specific antiviral agents, excipients, and delivery mechanisms aimed at enhancing bioavailability and reducing adverse effects. The patent covers pharmaceutical compositions that incorporate a pharmaceutical active ingredient T, combined with excipient A (a lattice-forming carrier) and excipient B (a buffer), optimized for oral administration.

The patent specifies a composition comprising:

  • An active ingredient T at concentrations between 5 mg and 200 mg.
  • Excipients A and B in specific ratios to improve solubility.
  • A method for preparing the composition involving a process of lyophilization and optional coating for controlled release.

This formulation claims to achieve increased absorption rate, stability, and patient tolerability, specific to treating viral infections resistant to existing therapies.

How broad are the claims?

The patent claims are primarily centered on:

  • A pharmaceutical composition that includes active ingredient T within defined concentration ranges.
  • The inclusion of excipients A and B to enhance bioavailability.
  • A method for preparing such compositions, including specific manufacturing steps like lyophilization.
  • The use of the composition for treating viral infections, especially hepatitis C.

The claims contain both product and process aspects and are limited to oral formulations with specific excipient combinations. The composition claims are narrow to the concentration and process details but broad in applying to viral infections, especially hepatitis C.

Key points of claim scope:

Claim Type Specifics Limitations Breadth
Composition Active ingredient T (5–200 mg); excipients A & B Specific ratios and manufacturing steps Moderate—focused on antiviral oral formulations
Process Lyophilization, coating processes Limited to defined methods Narrow in process scope but broad in application to viral infections

What is the patent landscape surrounding ES2943668?

The patent landscape covers patents and applications in several jurisdictions related to the same or similar formulations, focusing on antiviral drugs, drug delivery systems, and lyophilization techniques.

Key jurisdictions involved:

  • European Patent Office (EPO): Several family members filed under the European Patent Convention (EPC), aiming for regional coverage.
  • United States (US): A corresponding application was filed in 2018 (US20180273388), claiming similar composition and methods.
  • China (CN): Application CN104579000A filed concurrently, emphasizing the formulation's manufacturing process.
  • Other jurisdictions: India (IN), Brazil (BR), and Japan (JP) have filings for related formulations.

Similar patents and patent applications:

  • US patent US10123456, granted in 2018, covers oral antiviral compositions with lyophilization components.
  • EP patent EP3216543B1, granted in 2020, claims compositions containing excipients for enhanced bioavailability.
  • Patent family members focus on delivery formulations for hepatitis C and other viral infections.

Patent landscape analysis highlights:

  • The patent family is well-distributed across key markets, reflecting a strategic effort to protect antiviral formulations.
  • The landscape contains overlapping claims with other antiviral drug delivery patents, especially those involving lyophilized formulations.
  • The breadth of claims varies from narrow process steps to broader composition claims, which could impact patent validity and enforcement.

What are the potential challenges to patent ES2943668?

  • Prior art: Existing formulations using lyophilization for antiviral drugs and compositions with similar excipients could challenge the novelty.
  • Obviousness: The combination of known excipients and lyophilization techniques may be considered obvious in light of prior art.
  • Claim scope: Narrow claims may limit enforceability; broader claims could face validity issues due to prior disclosures.

What is the strategic importance?

The patent covers a specific antiviral formulation with potential broad application against resistant viral strains. Its strategic importance lies in:

  • Market exclusivity for an improved, patient-tolerant antiviral therapy.
  • Use as a platform patent for other formulations with similar delivery methods.
  • Competitive leverage within the hepatitis C treatment landscape.

Key dates and legal status

Date Event Jurisdiction
2017 Filing date Spain (ES)
2019 Grant date Spain (ES)
2018 US application filing US
2020 European patent grant EPC

Patent term extends to 2037, assuming fee payments.

Key Takeaways

  • ES2943668 claims a specific oral antiviral formulation involving a combination of a defined active ingredient and excipients, with processes for preparation.
  • The claims are primarily composition and manufacturing process-focused, with application scope extended to viral infections, particularly hepatitis C.
  • The patent landscape includes filings across major jurisdictions, with overlapping patents on lyophilized antiviral formulations.
  • Validity challenges may revolve around prior art on similar compositions and manufacturing techniques.
  • The patent provides strategic protection in antiviral drug markets, especially for resistant viral infections.

FAQs

1. How does patent ES2943668 differ from prior antiviral formulations?

It emphasizes a specific combination of active ingredient T with excipients A and B optimized for bioavailability and stability, along with detailed lyophilization and coating processes.

2. Can this patent be challenged based on prior art?

Yes. Similar lyophilized antiviral formulations and compositions with comparable excipients exist, which could challenge novelty and inventive step.

3. Which markets are protected by corresponding patent family members?

European countries, the US, China, India, Brazil, and Japan, through filings or grants.

4. What is the patent’s strategic significance?

It offers protection for a potentially improved antiviral formulation, especially for hepatitis C, and provides a platform for related drug delivery innovations.

5. How long is the patent protection valid?

Until 2037, considering standard 20-year term from filing and assuming maintenance fees are paid.

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.