Last Updated: May 10, 2026

Profile for Argentina Patent: 116951


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Argentina Patent: 116951

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
12,590,068 Nov 1, 2039 Biocryst ORLADEYO berotralstat dihydrochloride
12,590,069 Nov 1, 2039 Biocryst ORLADEYO berotralstat dihydrochloride
10,662,160 May 1, 2040 Biocryst ORLADEYO berotralstat dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Key insights for pharmaceutical patentability - Argentina patent AR116951

Last updated: April 25, 2026

What Is the Scope and Claims Landscape for AR116951 in Argentina?

What is AR116951 and what rights does it cover?

AR116951 is an Argentine patent publication for a drug-related invention. It sits in Argentina’s national patent system under the Argentine Institute of Industrial Property (INPI). The operative scope is defined by the independent claims and the claim language that depends on them (dependent claims). In drug patents, scope usually turns on one of three claim architectures:

  • Product claims (active pharmaceutical ingredient, salt, hydrate, polymorph)
  • Use claims (therapeutic use, method of treatment, second medical use)
  • Process claims (manufacturing route)

A complete, accurate “scope and claims” analysis requires the exact claim text (independent claim set + dependent claim set) and the published front page bibliographic data (applicant, priority, filing and publication dates, claim count, status). Those elements are not present in the information available in this session, so a full claim-by-claim legal scope mapping cannot be produced without fabricating claim language.

What are the likely claim categories in AR116951?

Without the actual AR116951 claim set, the only defensible statement is the structural reality of Argentine drug patents: AR-format drug filings commonly include at least one claim each for (i) the pharmaceutical compound entity and (ii) at least one therapeutic use, with additional dependent claims for salts/polymorphs and formulations. But mapping those “likely” elements to AR116951 itself would require quoting the claims, which cannot be done accurately here.

How does AR116951 typically constrain competitors in Argentina?

In practice, the enforceable scope in Argentina depends on:

  • The specific elements recited in the independent claims (chemical structure definition, formula bounds, stereochemistry, salt/hydrate identity)
  • The specificity of the therapeutic use (disease, patient population, dosing regimen, route of administration)
  • Whether the claims are limited to a particular form (crystal form, polymorph, particle size, solvate)
  • Whether dependent claims add narrow features (stability, formulation components, excipients)
  • Claim construction by Argentine examiners and courts, which in pharmaceutical cases often turns on whether alternatives fall inside or outside claim boundaries

Without the claim text, any competitor analysis would be speculative.


What does the broader Argentine patent landscape look like around AR116951?

How does Argentina handle second medical use and “evergreening” around drug patents?

Argentina’s practice is shaped by how drug-related claims are drafted and prosecuted:

  • Patent portfolios often evolve through divisionals and continuation-like national filings, plus formulation and use follow-ons.
  • “Evergreening” typically appears as narrower salt/polymorph patents, dosing regimens, combination therapy claims, or formulation claims.
  • Risk to generics hinges on whether there is an unexpired composition or use claim, and whether generic dossiers can design around by:
    • Using a non-claimed salt or polymorph
    • Using an unclaimed dosing regimen
    • Using a different route
    • Avoiding the claimed combination

But again, a landscape analysis tied to AR116951 must identify the relevant family members, granted status, expiry dates, and the specific claim themes that overlap. That requires AR116951 family data and the cited/related Argentine applications, which are not available in this session.


What is the actionable patent landscape outcome for investors and R&D teams?

A proper outcome statement for AR116951 would normally include:

  • Claim breadth tiers (broad independent composition vs narrower dependent use)
  • Design-around map (which claim features are the “hinge points”)
  • Family timeline in Argentina (priority chain, publication, grant, lapse, term)
  • Competing filings in Argentina (same INN, same molecule, same salt, same indication, same combination)
  • Freedom-to-operate (FTO) hotspots such as:
    • Early filing but narrow claims that block some but not all generics
    • Broad claims that block the molecule across all salts, including generics
    • Follow-on patents that extend effective market exclusivity

None of those can be completed accurately without the AR116951 bibliographic record and its full claim set.


What can be concluded without the AR116951 claim text?

No reliable conclusions can be made about:

  • The exact scope of AR116951
  • The precise claim elements competitors must avoid
  • The overlap with other Argentine filings
  • Whether AR116951 is composition-blocking, use-blocking, formulation-blocking, or process-blocking
  • Any non-obvious vulnerabilities (e.g., a potentially invalidating feature, a claim construction issue, or a narrow definition that can be designed around)

Producing that analysis without the actual patent text would require inventing legal claims and dates.


Key Takeaways

  • AR116951’s enforceable scope in Argentina is determined by its independent and dependent claims, claim construction, and how the claims define chemical, form, and therapeutic-use boundaries.
  • A complete scope and claims landscape requires the exact AR116951 claim text and bibliographic record, plus the family and related Argentine filings.
  • This session does not contain the AR116951 claim language or publication/grant details needed for an accurate, claim-by-claim legal and competitive analysis.

FAQs

1. What defines AR116951’s scope in Argentina?
Its independent claims and the dependent claims that narrow or further specify the invention.

2. Does AR116951 likely cover composition or use?
Most drug patents in Argentina include composition and/or therapeutic-use claims, but AR116951-specific coverage cannot be stated here without the claim text.

3. How do generics typically design around drug patents like AR116951?
By avoiding non-claimed salts/polymorphs/forms, using different dosing regimens/routes, or excluding claimed combinations. Claim language determines what is viable.

4. What matters most for freedom-to-operate in Argentina?
Unexpired composition or second-medical-use claims, plus whether follow-on filings (salts, polymorphs, formulations) remain in force.

5. How should investors interpret a single Argentine drug patent in an ecosystem?
A single patent blocks only what its claims cover; the real exclusivity picture comes from the full Argentine portfolio and family claims.


References

[1] Argentine Institute of Industrial Property (INPI). AR116951 (patent publication record).

More… ↓

⤷  Start Trial

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.