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Pebrilzo (pertuzumab)

Biosimilar
Region
🇪🇺 EU
Active substance
pertuzumab
Company
Biosimilar Collaborations Ireland Limited
Status
Opinion
Therapeutic area
Breast Neoplasms
Designations
Biosimilar
Application
EMEA/H/C/006844
ATC
L01FD02
Official record
www.ema.europa.eu

Indication

Treatment of breast cancer in adults

Regulatory milestones

No milestones recorded in the last year.

Same substance in other markets

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.