Cegfila is a medicine used in cancer patients to help with neutropenia (low levels of neutrophils, a type of white blood cell), which is a common side effect of cancer chemotherapy and can leave patients vulnerable to infections. It is given specifically to reduce the duration of neutropenia and prevent febrile neutropenia (when neutropenia is accompanied by fever due to an infection). Cegfila is not intended for use in patients with the blood cancer chronic myeloid leukaemia or with myelodysplastic syndromes (conditions in which large numbers of abnormal blood cells are produced, which can develop into leukaemia). Cegfila is a ‘biosimilar medicine’. This means that Cegfila is highly similar to another biological medicine (the ‘reference medicine’) that is already authorised in the EU. The reference medicine for Cegfila is Neulasta. Cegfila contains the active substance pegfilgrastim.
Therapeutic Indication
Reduction in the duration of neutropenia and the incidence of febrile neutropenia in adult patients treated with cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes).
Therapeutic Area (MeSH)
N/AATC Code
L03AA13
ATC Item
N/A
Pharmacotherapeutic Group
Immunostimulants
Active Substance (Summary)
INN / Common Names
| Substance | CAS | Monograph |
|---|---|---|
| pegfilgrastim | N/A | pegfilgrastim |
EMA Name
Cegfila (previously Pegfilgrastim Mundipharma)
Medicine Name
Cegfila (previously Pegfilgrastim Mundipharma)
Aliases
N/ANo risk management plan link.
