EMEA-001220-PIP01-11-M10 - paediatric investigation plan | European Medicines Agency (EMA)
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EMEA-001220-PIP01-11-M10 - paediatric investigation plan
Baricitinib
PIPHuman
Key facts
Invented name
Olumiant
Active Substance
Baricitinib
Therapeutic area
Musculoskeletal and connective tissue disorders
Decision number
P/0117/2024
PIP number
EMEA-001220-PIP01-11-M10
Pharmaceutical form(s)
Oral suspension
Film-coated tablet
Condition(s) / indication(s)
Treatment of chronic idiopathic arthritis (including rheumatoid arthritis, ankylosing spondylarthritis, psoriatic arthritis and juvenile idiopathic arthritis)
Route(s) of administration
Oral use
Contact for public enquiries
Eli Lilly And Company Limited email: EU_PAEDIATRIC@lilly.com phone: +44 1256315000
Decision type
PM: decision on the application for modification of an agreed PIP
Decision date
Decision
P/0117/2024: EMA decision of 12 April 2024 on the acceptance of a modification of an agreed paediatric investigation plan for baricitinib (Olumiant), (EMEA-001220-PIP01-11-M10)