The BENeFiTS Trial in Beta Thalassemia Intermedia

The study will first evaluate 3 doses of the investigational drug which are considered safe with chronic use in a combination therapeutic used widely for a different disease in Europe and Canada. The doses to be studied are human equivalent doses of doses that are active in nonhuman primates in inducing high level fetal globin messenger ribonucleic acid (mRNA), protein, and proportions of red blood cells expressing fetal globin protein (F-cells). Additive effects are observed with hydroxyurea in sickle cell patients' cells in vitro.

The study will first evaluate the study therapeutic in male and female patients who are 18 years and older. After a screening period to obtain baseline medical and laboratory data, the study drug will be taken by mouth once per day, every other day. The first dose will be taken in a clinical unit, and thereafter will be taken at home for 12 weeks. Laboratory tests, physical exams, and tolerability will be assessed 6 times over 4 months, including for one month after completion of dosing.

The cohorts will be enrolled sequentially. Each new cohort will begin after the prior lower dose cohort has received 2 weeks of treatment without serious adverse events related to the study drug. The dose that increases fetal globin assays to the highest degree will be evaluated in a larger group of subjects with beta thalassemia intermedia and a groups with sickle cell disease. Other regimens or test doses may be added as needed to identify an active dose and regimen. The study drug is expected to be safe when added to most other medications used to treat thalassemia.

Inclusion criteria

• Beta thalassemia intermedia (BTI) or (NTDT, Non-Transfusion Dependent Thalassemia) with at least one documented beta thalassemia mutation, including HbE beta thalassemia or an established diagnosis of sickle cell disease
• >18 years of age at time of consent
• Average of 2 total hemoglobin (Hgb) levels between 6.0 and 10.0 g/dL in the preceding 6 months
• Able and willing to give consent and comply with all study procedures
• If female and of childbearing potential, must have a documented negative pregnancy test prior to entry and agree to use one or more locally medically accepted methods of contraception

Exclusion criteria

• Red blood cell (RBC) transfusion within 2 months prior to administration of study medication
• Participating in a chronic transfusion program
• Pulmonary hypertension requiring oxygen therapy
• Use of erythropoiesis stimulating agents within 90 days of first dose
• Transaminases > 3 times upper limit of institution normal (ULN)
• Total and direct bilirubin > 3 times institution ULN unless due solely to hemolysis
• Known infection with HIV or hepatitis C (untreated)
• Fever > 38.5°C in the week prior to first administration of study medication
• History of osteoporosis or osteomalacia with a fragility fracture
• Received other investigational systemic therapy within 30 days prior to first dose
• Narrow angle glaucoma
• Currently pregnant or breast feeding a child
• Known current drug or alcohol abuse
• Taking monoamine oxidase inhibitors
• Other co-morbidity that substantially increases subject risk for the study per Investigator discretion