US Patent
US10058504 — Methods for the preparation of injectable depot compositions
Formulation · Assigned to Laboratorios Farmaceuticos Rovi SA · Expires 2031-05-31 · 5y remaining
Vulnerability score
44/100
Strong — defensible against typical IPR challenges
What this patent protects
This patent protects methods for preparing injectable depot compositions that can release therapeutic levels of a drug, such as Risperdal, for at least 14 days.
USPTO Abstract
Injectable depot compositions, comprising a biocompatible polymer which is a polymer or copolymer based on lactic acid and/or lactic acid plus glycolic acid having a monomer ratio of lactic to glycolic acid in the range from 48:52 to 100:0, a water-miscible solvent having a dipole moment of about 3.7-4.5 D and a dielectric constant of between 30 and 50, and a drug, were found suitable for forming in-situ biodegradable implants which can evoke therapeutic drug plasma levels from the first day and for at least 14 days.
Drugs covered by this patent
- Risperdal (risperidone) · Johnson & Johnson (Janssen)
Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.
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