CFARA is the Generic version of CLOLAR®  (CLOFARABINE)

Clolar (clofarabine) Injection contains clofarabine, a purine nucleoside metabolic inhibitor. Clolar (1 mg/mL) is supplied in a 20 mL, single-dose vial. The 20 mL vial contains 20 mg clofarabine formulated in 20 mL unbuffered normal saline (comprised of Water for Injection, USP, and Sodium Chloride, USP).

CFARA-CLOFARABINE is FDA-approved for treating relapsed or refractory acute lymphoblastic leukaemia (ALL) in children after at least two other types of treatment have failed. It is not known if it extends life expectancy. Some investigations of effectiveness in cases of acute myeloid leukaemia (AML) and juvenile myelomonocytic leukaemia (JMML) have been carried out. Ongoing trials are assessing its efficacy, if any, for managing other cancers.



CLOFARABINE 20mg/20ml 
PACK :Single Injection

cfara (clofarabine) Injection is indicated for the treatment of pediatric patients 1 to 21 years old with relapsed or refractory acute lymphoblastic leukemia after at least two prior regimens. This indication is based upon response rate. There are no trials verifying an improvement in disease-related symptoms or increased survival with cfara

Dosing and Administration

Administer the recommended pediatric dose of 52 mg/m² as an intravenous infusion over 2 hours daily for 5 consecutive days.


cfara (clofarabine) should be filtered through a sterile 0.2 micron syringe filter and then diluted with 5% Dextrose Injection, USP, or 0.9% Sodium Chloride Injection, USP, prior to intravenous (IV) infusion to a final concentration between 0.15 mg/mL and 0.4 mg/mL. Use within 24 hours of preparation. Store diluted Clolar at room temperature (15-30°C).


What are the possible side effects of cfara (clofarabine)?

  • The most common side effects with cfara -Clofarabine (seen in more than 1 patient in 10) were febrile neutropenia (low white blood cell counts with fever), anxiety, headache, flushing (reddening of the face), vomiting, diarrhoea, nausea (feeling sick), palmar-plantar erythrodysaesthesia syndrome (rash and numbness on the palms and soles), pruritus (itching), pyrexia (fever), mucosal inflammation (inflammation of the moist body surfaces, such as the lining of the mouth) and fatigue (tiredness). For the full list of all side effects reported with Evoltra, see the package leaflet.Cfara – Clofabine must not be given to patients with severe kidney or liver disease. Breast-feeding should be stopped before, during and after treatment with Cfara. For the full list of restrictions, see the package leaflet Below ,

For more information on Cfara™ (Clofarabine ) Generic  prescribing information please click here

Price of  Cfara in India , Cost of Clofarabine in India

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The above information is only for Medical profession only, please don’t try to self-medicate any of the medicine information Provided in this site, as all Medicine have life-threatening side-effect if not taken under proper medical guidance.  

Cfara (Clofarabine) is to be taken strictly under Medical  Supervision Only