Source: European Medicines Agency (EU) Revision Year: 2020 Publisher: Genzyme Europe BV, Paasheuvelweg 25, 1105 BP Amsterdam, The Netherlands
Evoltra 1 mg/ml concentrate for solution for infusion.
| Pharmaceutical Form |
|---|
|
Concentrate for solution for infusion. Clear, practically colourless solution with a pH of 4.5 to 7.5 and an osmolarity of 270 to 310 mOsm/l. |
Each ml of concentrate contains 1 mg of clofarabine.
Each 20 ml vial contains 20 mg of clofarabine.
Excipient with known effect: Each 20 ml vial contains 180 mg of sodium chloride.
For the full list of excipients, see section 6.1.
| Active Ingredient | Description | |
|---|---|---|
| Clofarabine |
Clofarabine is a purine nucleoside anti-metabolite. Its antitumour activity is believed to be due to 3 mechanisms. Clofarabine produces DNA polymerase inhibition resulting in termination of DNA chain elongation and/or DNA synthesis/repair and ribonucleotide reductase inhibition with reduction of cellular deoxynucleotide triphosphate (dNTP) pools. Clofarabine also produces disruption of mitochondrial membrane integrity with the release of cytochrome C and other proapoptotic factors leading to programmed cell death even in non-dividing lymphocytes. |
| List of Excipients |
|---|
|
Sodium chloride |
Type I glass vial with bromobutyl rubber stopper, polypropylene flip-off cap and aluminium overseal.
The vials contain 20 ml concentrate for solution for infusion and are packaged in a box.
Each box contains 1, 3, 4, 10 or 20 vials.
Not all pack sizes may be marketed.
Genzyme Europe BV, Paasheuvelweg 25, 1105 BP Amsterdam, The Netherlands
EU/1/06/334/001 3 vials
EU/1/06/334/002 4 vials
EU/1/06/334/003 10 vials
EU/1/06/334/004 20 vials
EU/1/06/334/005 1 vial
Date of first authorisation: 29 May 2006
Date of latest renewal: 14 January 2016
| Drug | Countries | |
|---|---|---|
| EVOLTRA | Austria, Cyprus, Estonia, Spain, Finland, France, Hong Kong, Ireland, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, United Kingdom |
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