Endari (L-glutamine oral powder) — CareFirst (Caremark)
To reduce the acute complications of sickle cell disease in adult and pediatric patients age ≥ 5 years
Initial criteria
- Prescription must be by or in consultation with a hematologist or specialist in sickle cell disease
- Member age ≥ 5 years
- Indicated for reducing acute complications of sickle cell disease
- Member has sickle hemoglobin C (HbSC) or sickle β+-thalassemia (HbSβ+) genotype OR
- Member has homozygous hemoglobin S (HbSS) or sickle β0-thalassemia (HbSβ0) genotype AND any of the following:
- 1. Has experienced an inadequate response or intolerance to hydroxyurea
- 2. Has a contraindication to hydroxyurea
- 3. Will be using Endari with concurrent hydroxyurea therapy
Reauthorization criteria
- Member has experienced a reduction in acute complications of sickle cell disease (e.g., reduction in painful vaso-occlusive episodes, acute chest syndrome episodes, fever, occurrences of priapism, splenic sequestration) since initiating Endari therapy
Approval duration
12 months