EMEA-002075-PIP01-16-M03 - paediatric investigation plan | European Medicines Agency (EMA)
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EMEA-002075-PIP01-16-M03 - paediatric investigation plan
Lefamulin
PIPHuman
Key facts
Invented name
Xenleta
Active Substance
Lefamulin
Therapeutic area
Infectious diseases
Decision number
P/0535/2022
PIP number
EMEA-002075-PIP01-16-M03
Pharmaceutical form(s)
Concentrate for solution for infusion
Age-appropriate oral solid dosage form
Coated tablet
Condition(s) / indication(s)
Treatment of community-acquired pneumonia
Route(s) of administration
Intravenous use
Oral use
Contact for public enquiries
Nabriva Therapeutics DAC
email: officeUS@nabriva.com tel: +1 6102091499
Decision type
PM: decision on the application for modification of an agreed PIP
Decision date
Decision
P/0535/2022 : EMA decision of 30 December 2022 on the acceptance of a modification of an agreed paediatric investigation plan for lefamulin (Xenleta) (EMEA-002075-PIP01-16-M03)