Biosimilar timeline

TECVAYLI biosimilars — when can they launch?

TECVAYLI (TECLISTAMAB-CQYV) · BLA761291 · JANSSEN BIOTECH

Reference exclusivity
2034-10-25
8 years remaining
Original approval
2022-10-25
FDA BLA761291
Originator
JANSSEN BIOTECH
 

Where TECVAYLI sits in the biosimilar timeline

BPCIA 12-year reference product exclusivity for TECVAYLI extends to 2034 (8 years from today). Biosimilars cannot be approved by the FDA before this date. Biosimilar developers begin clinical comparability studies 4-6 years before the cliff.

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 TECVAYLI

EventDateStatus
FDA approval (BLA filed by JANSSEN BIOTECH) 2022-10-25 Past
4-year data exclusivity ends (first biosimilar 351(k) submission permitted) 2026-10-25 Future
12-year reference product exclusivity ends (first biosimilar can be marketed) 2034-10-25 Future

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

Other JANSSEN BIOTECH biologics

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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