EU application 006844
Pertuzumab biosimilar developed by Applicant not yet named by EMA. Reference product Perjeta.
Brands by market: Under evaluation by EMA since December 2025 · Commercial partner or holder: EU application
FDAnot listed
EMAunder review
PMDAnot listed
HCnot listed
CDSCOnot listed
EDEnot listed
Status by market
FDA
United States
Not listed by FDA.
EMA
European Union · Application 006844
European Medicines Agency and European CommissionUnder reviewBrand
Application 006844
Holder or applicant
Applicant not yet named by EMA
Pathway
Centralised (Article 10(4))
Status
Under evaluation by the CHMP since Dec 2025; procedure restarted May 2026
Presentations
see SmPC
Note
Under CHMP evaluation since 2025-12-25; procedure restarted after questions 2026-05-25. Applicant not named in EMA's list.
Source
S019
PMDA
Japan
Not listed by PMDA.
HC
Canada
Not listed by HC.
CDSCO
India
Not listed by CDSCO.
EDE
United Arab Emirates
Not listed by EDE.
Chronology
- EMADec 2025CHMP evaluation started
Sources
S019EMA, applications for new human medicines under evaluation by the CHMP, August 2026 Primary (regulator)
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