Clolar is a prescription medication approved by the Food and Drug Administration (FDA) to treat acute lymphoblastic leukemia (ALL) in children and young adults up to the age of 21. Clolar is indicated in cases where leukemia has relapsed or failed to respond after at least two previous drug regimens. Clolar may also be referred to by its drug name, Clofarabine.
Clolar is an anticancer drug. Clolar is a member of a class of drugs called antimetabolites. Clolar is believed to work by interfering with the DNA synthesis in replicating cells.
How do I take it?
Clolar is administered by intravenous injection on five consecutive days. Treatment may be repeated every two to six weeks.
Clolar comes in the form of a single-dose vial.
The FDA-approved label for Clolar lists common side effects including headache, fever, chills, fatigue, rash, itching, nausea, vomiting, abdominal pain, nosebleeds, pain in extremities, tachycardia (rapid heart rate), hypotension (low blood pressure), and low blood cell counts.
Sepsis, a potentially fatal systemic infection, is both a common and severe side effect of Clolar.
Rare but serious side effects listed for Clolar include life-threatening hemorrhages (bleeds), damage to kidneys, liver, or gastrointestinal system, and tumor lysis syndrome – a potentially fatal metabolic condition caused when many cancer cells die at the same time. Other serious side effects include potentially fatal skin reactions known as Stevens-Johnson syndrome and toxic epidermal necrolysis. Clolar can also cause fetal harm in pregnant women and cytokine release syndrome (CRS), a potentially fatal inflammatory reaction with severe neurological symptoms such as hallucinations and tremors.
For more details about this treatment, visit:
Clolar – RxList
ALL: Relapsed and Refractory – Leukemia & Lymphoma Society