SB-252263 (Tafenoquine, TQ) is an 8-aminoquinoline (8-AQ) antimalarial drug being developed
by GlaxoSmithKline (GSK), the U. S. Army Medical Research and Materiel Command (USAMRMC) and
Medicines for Malaria Venture (MMV). TQ is currently being developed for the radical cure
of acute P. vivax malaria in combination with standard doses of CQ, which is 1500 mg over 3
days.
The current gold standard for radical cure of P. vivax malaria in many areas of the world is
chloroquine (CQ) for clearance of the acute parasitemia immediately followed by primaquine
(PQ) to clear the liver stages of the parasite and prevent disease relapse. The 8-AQ class
of drugs, including PQ, is hemolytic in subjects with glucose-6-phosphate dehydrogenase
(G6PD) deficiency. The current study will identify a dose of TQ within the target
efficacious dose range that has a hemolytic effect similar to or less than PQ 15 mg OD x 14
days (i. e. ≤ 25-30% hemoglobin decline in WHO class III G6PD-deficient subjects).
Inclusion Criteria:
- A subject will be eligible for inclusion in this study only if all of the following
criteria apply:
- The subject is between 18 and 45 years of age, inclusive
- A female is eligible to enter and participate in this study if she is non-pregnant,
non-lactating and if she is of:
- Non-child bearing potential defined as:
- Is post-menopausal (12 months of spontaneous amenorrhea or 6 months of spontaneous
amenorrhea with serum FSH >40mIU/mL)
- Is pre-menopausal and has had a hysterectomy or a bilateral oophorectomy (removal of
the ovaries) or a bilateral tubal ligation with medical report verification.
- Child-bearing potential, has a negative urine pregnancy test at screening, and agrees
to comply with one of the following during the treatment stage of the study and for a
period of 90 days after stopping study drug:
- Use of oral contraceptive, either combined or progestogen alone, in combination with
a barrier method (e. g., condom or diaphragm)
- Use of an intrauterine device with a documented failure rate of less than 1% per year
- Double barrier method consisting of spermicide with either condom or diaphragm.
- Male partner who is sterile prior to the female subject's entry into the study and is
the sole sexual partner for that female
- Complete abstinence from intercourse for 2 weeks prior to administration of study
drug, throughout the study and for a period of 90 days after stopping study drug.
- A signed and dated informed consent is obtained from the subject or the subject's
legal representative prior to screening.
- The subject is able to understand and comply with protocol requirements, instructions
and protocol-stated restrictions and is likely to complete the study as planned.
- WHO class III G6PD-deficiency or G6PD-normal status must be documented by enzyme
activity and cytochemical staining. G6PD genotype must confirm WHO class III G6PD
deficiency or G6PD-normal status prior to TQ dosing in all parts of the study (i. e.,
P. vivax infected subjects may commence CQ therapy whilst the cytochemical staining,
enzyme activity and G6PD genotype are being determined).
Supplemental Inclusion Criteria for Part A: Healthy volunteers Inclusion criteria 1-7
above AND
- Subject is female
- For G6PD-deficient subjects (WHO class III variant), subject must be heterozygous
with 40-60% normal RBCs by cytochemical staining method. For G6PD-normal subjects,
subject must have >90% normal RBCs by cytochemical staining method.
Supplemental Inclusion Criteria for Part B: P. vivax patients Inclusion criteria 1-7 above
AND
- Subject is female
- Positive blood smear for P. vivax with parasite density >500 and <200,000/µl
- For G6PD-deficient subjects (WHO class III variant), subject must be heterozygous
with 40-60% normal RBC by cytochemical staining method. For G6PD-normal subjects,
subject must have >90% normal RBCs by cytochemical staining method.
Supplemental Inclusion Criteria for Part C: P. vivax patients Inclusion criteria 1-7 above
AND
- Positive blood smear for P. vivax with parasite density >500 and <200,000/µl
- For G6PD-deficient subjects (WHO class III variant), subject is a homozygous female
or a hemizygous male. For G6PD-normal subjects, subject must have >90% normal RBCs by
cytochemical staining method
Exclusion Criteria:
- A subject will not be eligible for inclusion in this study if any of the following
criteria apply:
- Clinically significant illness (intercurrent illness e. g. pneumonia, pre-existing
condition e. g. renal disease, malignancy or conditions that may affect absorption of
study medication e. g. severe diarrhea or any signs of malnutrition as defined
clinically, and clinical signs and symptoms of vascular disease (e. g. cardiac, CNS,
diabetes, hyperlipidemia, etc.).
- Any clinically relevant biological or physical abnormality found or reported at
screening which, in the opinion of the investigator, is clinically significant and
would preclude safe participation in this study. These abnormalities may be
identified on the screening history and physical or laboratory examination, 12-lead
electrocardiogram (ECG).
- Mixed malaria infections by Giemsa smear.
- Female subjects who are pregnant, lactating or unwilling/unable to comply with
recognized contraceptive methods during the treatment stage of the study and for a
period of 90 days after stopping study drug.
- Symptoms of severe vomiting (no food or inability to take food during the previous 8
hours).
- History of hemoglobinopathy (e. g. sickle-cell disease, hereditary spherocytosis,
thalassemias, hemoglobin M, etc.); or current or past history of methemoglobinemia or
methemoglobin percentage above 3%.
- History of porphyria
- History of psoriasis
- History of allergy to tafenoquine, chloroquine, primaquine, mefloquine or any other
4- or 8-aminoquinolines.
- Subject has taken other anti-malarials (e. g., mefloquine, primaquine, chloroquine)
within the past 60 days by history.
- Treatment with an investigational drug within 30 days or 5 half-lives (whichever is
longer) preceding the first dose of study medication.
- Donation of blood in excess of 500mL within 56 days prior to dosing study drug.
- History of regular alcohol consumption exceeding 7 drinks/week for women or 14
drinks/week for men (one drink = five ounces of wine or 12 ounces of beer or 1. 5
ounces of hard liquor) within 6 months of screening.
- History of illicit drug abuse within 6 months of the study.
- Heparin sensitivity (if heparin is used to maintain intravenous catheter patency).
- QTc interval >450 msec at screening Supplemental Exclusion Criteria for Part A:
Healthy volunteers Exclusion criteria 1-16 above AND
- Baseline Hgb <12 g/dL (or Hct <36%). Value to be verified by conducting two
measurements (single blood draw).
- Use of prescription or non-prescription drugs, vitamins, herbal and dietary
supplements within 7 days or 5 half-lives (whichever is longer) prior to the first
dose of study medication, or use of St. John's Wort within 28 days prior to the first
dose of study medication. Unless in the opinion of the investigator and sponsor the
medication will not interfere with study procedures or compromise safety. By
exception, the subject may take paracetamol or acetaminophen (≤2 grams/day) up to 48
hours prior to the first dose of study medication.
Supplemental Exclusion Criteria for Parts B and C: P. vivax patients
Exclusion criteria 1-16 above AND Laboratory criteria for exclusion are:
- platelets <50,000/µL
- WBC <2000/µL
- Calculated creatinine clearance (CrCl) <50ml/min by Cockcroft-Gault formula:
- Men: CrCl = (140 - age) x weight(kg)/(72 x SCr*)
- Woman: CrCl = [(140 - age) x weight(kg)/(72 x SCr*)] x 0. 85
*SCr= serum creatinine
- ALT or AST >2 times upper limit of the reference range
- Total bilirubin level >1. 5 times upper limit of the reference range at screening.
- Screening Hgb <11 g/dL (or Hct <33%). Value to be verified by conducting two
measurements (single blood draw).
Subjects who have taken or will likely require the use of medications from the prohibited
medication list which include the following classes:
- Histamine-2 blockers and antacids
- Drugs with hemolytic potential
- Drugs known to prolong the QTc interval
