Biosimilar timeline

BRINEURA biosimilars — when can they launch?

BRINEURA (CERLIPONASE ALFA) · BLA761052 · BIOMARIN PHARM

Reference exclusivity
2029-04-27
3 years remaining
Original approval
2017-04-27
FDA BLA761052
Originator
BIOMARIN PHARM
Marketed by BioMarin

Where BRINEURA sits in the biosimilar timeline

BPCIA 12-year reference product exclusivity for BRINEURA expires in 2029 (3 years from today). Biosimilar developers are typically preparing 351(k) applications 36-48 months ahead of this date. Expect first biosimilar filings to surface in this window.

Under the US Biologics Price Competition and Innovation Act (BPCIA), a reference biologic is protected from biosimilar competition for 12 years from FDA approval (with 4 years of data exclusivity preventing 351(k) submissions). Biosimilars enter via the abbreviated 351(k) pathway, which requires comparability — not exact identity — to the reference product.

Key dates for BRINEURA

EventDateStatus
FDA approval (BLA filed by BIOMARIN PHARM) 2017-04-27 Past
4-year data exclusivity ends (first biosimilar 351(k) submission permitted) 2021-04-27 Past
12-year reference product exclusivity ends (first biosimilar can be marketed) 2029-04-27 Future

Note: composition-of-matter and method-of-use patent expiries (separate from BPCIA exclusivity) may set the actual launch window. See BRINEURA on Drug Landscape for the full patent picture.

Other BIOMARIN PHARM biologics

  • VIMIZIM — exclusivity to 2026-02-14
  • PALYNZIQ — exclusivity to 2030-05-24

Sources

Not legal advice. BPCIA exclusivity may interact with composition-of-matter patents and patent term extensions — see the full drug profile for the consolidated picture.

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