Biosimilar timeline

ZARXIO biosimilars — when can they launch?

ZARXIO (Filgrastim-sndz) · BLA125553 · SANDOZ INC

Reference exclusivity
2027-03-06
1 year remaining
Original approval
2015-03-06
FDA BLA125553
Originator
SANDOZ INC
Marketed by M.D. Anderson Cancer Center

Where ZARXIO sits in the biosimilar timeline

BPCIA 12-year reference product exclusivity for ZARXIO expires in 2027 (1 year 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 ZARXIO

EventDateStatus
FDA approval (BLA filed by SANDOZ INC) 2015-03-06 Past
4-year data exclusivity ends (first biosimilar 351(k) submission permitted) 2019-03-06 Past
12-year reference product exclusivity ends (first biosimilar can be marketed) 2027-03-06 Future

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

Other SANDOZ INC biologics

  • ADALIMUMAB — exclusivity to 2030-10-30
  • ZIEXTENZO — exclusivity to 2031-11-04
  • CIMERLI — exclusivity to 2034-08-02
  • TYRUKO — exclusivity to 2035-08-24
  • WYOST — exclusivity to 2036-03-05

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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