Last updated: 12/14/2021 11:40:06
A Pharmacokinetics, Safety and Efficacy Study of Tafenoquine (TQ) in Pediatric Subjects with Plasmodium vivax (P. vivax) Malaria
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: An Open Label, Non-comparative, Multicenter Study to Assess the Pharmacokinetics, Safety and Efficacy of Tafenoquine (SB-252263, WR238605) in the Treatment of Pediatric Subjects with Plasmodium vivax Malaria
Trial description: This is a prospective, open-label, multicenter, non-comparative, single arm study of pediatric subjects with Plasmodium vivax (P. vivax) malaria, aged 6 months to <16 years of age. A total of 60 subjects will be enrolled. Potential subjects who are slide-positive for P. vivax will be started by the site on chloroquine (CQ) per local/national guidelines. Sites will have up to 48 hours to obtain consent. Once full consent is provided, all subjects will be screened and, if eligible, receive Tafenoquine (TQ), given as a single dose on Day 1. All study medication should be taken with food. After the treatment period, subjects will attend up to 7 follow-up visits through Day 120 (Days 3, 8, 15, 29, 60, 90 and 120). The main cohort will consist of subjects aged >=2 years to <16 years with no restriction on gender. Subjects will be dosed according to four weight bands. Within the total of 60 enrolled pediatric subjects, a second cohort of up to 6 infants aged >=6 months to <2 years (weighing >=5 kilogram [kg]) will be recruited following completion of a planned first interim analysis. An interim analysis will be conducted once sufficient data from 16 subjects is available to assess pharmacokinetic (PK) and safety parameters. If needed, a second interim analysis will be conducted after a total of 32 subjects have enrolled. The primary objective of this PK bridging study is to adequately characterize the systemic TQ exposure in the pediatric population in order to identify appropriate doses that achieve a similar exposure to that of the TQ adult dose of 300 milligram (mg).
Primary purpose:
Treatment
Trial design:
Single Group Assignment
Masking:
None (Open Label)
Allocation:
Not applicable
Primary outcomes:
Area under the curve from time 0 extrapolated to infinite time (AUC [0-infinity]) of TQ
Timeframe: Up to Day 120
Secondary outcomes:
Number of participants with gastrointestinal adverse events as measure of safety and tolerability
Timeframe: Up to Day 120
Safety as assessed by clinically relevant drop in hemoglobin (Hb)
Timeframe: Up to Day 120
Safety as assessed by incidence and severity of adverse events (AEs)
Timeframe: Up to 120 days
Safety as assessed by abnormal laboratory observations
Timeframe: Up to Day 8
Number of participants recurrence-free at four months post-dosing to assess efficacy
Timeframe: Up to 120 days
AUC (0-infinity) of TQ by weight band In infants aged >=6 months to <2 years (weighing >=5 kg)
Timeframe: Up to Day 120
Interventions:
Drug: Tafenoquine
Drug: Chloroquine
Enrollment:
60
Observational study model:
Not applicable
Primary completion date:
2019-15-12
Time perspective:
Not applicable
Clinical publications:
Ivan D. Velez, Tran T. Hien, Justin A. Green, Ana Martin, Hema Sharma, Victoria M. Rousell, John J. Breton, Terry B. Ernest, Katie Rolfe, Maxine Taylor, Khadda Mohamed, Sion W. Jones, Nguyên Hoang Chau, Nhu Thi Hoa, Stephan Duparc, Lionel K. Tan, Navin Goyal. Tafenoquine plus chloroquine for the treatment and relapse prevention of Plasmodium vivax malaria in children. Lancet Child Adolesc Health. 2021;
DOI: https://doi.org/10.1016/S2352-4642(21)00328-X.
Medical condition
Malaria, Vivax
Product
tafenoquine
Collaborators
Medicines for Malaria Venture
Study date(s)
February 2017 to February 2020
Type
Interventional
Phase
2
Participation criteria
Sex
Female & Male
Age
6 months - 15 years
Accepts healthy volunteers
No
- Subject is >=2 years to <16 years of age at the time of signing of the assent and/or informed consent. An additional cohort of subjects aged >=6 months to <2 years may be recruited following the first interim analysis.
- The subject has a positive malarial smear for P. vivax.
- The subject has a mixed malaria infection (identified by a malarial smear or rapid diagnostic test).
- The subject has a condition that may affect absorption of study medication, such as severe vomiting (no food or inability to take food during the previous 8 hours).
Inclusion and exclusion criteria
Inclusion criteria:
- Subject is >=2 years to <16 years of age at the time of signing of the assent and/or informed consent. An additional cohort of subjects aged >=6 months to <2 years may be recruited following the first interim analysis.
- The subject has a positive malarial smear for P. vivax.
- The subject has a history of fever within 48 hours prior to enrollment.
- The subject has a glucose 6-phosphate dehydrogenase (G6PD) value (measured by a quantitative spectrophotometric phenotype assay) >=70% of the site median value for G6PD normal adult males.
- The subject has a screening Hb value >=8 gram per decilitre (g/dL).
- The subject has a body weight >=5 kg.
- Males and females are eligible to enter the study. A female is eligible to enter and participate in this study if she is non-pregnant, non-lactating and if she is of: Non-childbearing potential (i.e., premenstrual); or Child-bearing potential, has a negative 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 medication: Complete abstinence from intercourse for 2 weeks prior to administration of study medication, throughout the study and for a period of 90 days after stopping study medication; Use of combined oral contraceptive consisting of spermicide with either condom or diaphragm; Use of intrauterine device with a documented failure rate of <1% per year; Use of depo provera injection; Male partner who is sterile prior to the female subject's entry into the study and is the sole sexual partner for that female.
- The subject and/or the subject’s parent(s)/legal guardian(s) agree to G6PD genotyping in the context of a subsequent hemolytic anemia AE.
- The subject and parent(s)/legal guardian(s) are willing and able to comply with the study protocol.
- In accordance with regional/local laws and regulations, the parent(s)/legal guardian(s) has given written informed, dated consent; and the subject has given written assent, if applicable, to participate in the study.
Exclusion criteria:
- The subject has a mixed malaria infection (identified by a malarial smear or rapid diagnostic test).
- The subject has a condition that may affect absorption of study medication, such as severe vomiting (no food or inability to take food during the previous 8 hours).
- The subject has a liver alanine aminotransferase (ALT) >2 time the upper limit of normal (ULN).
- The subject has a clinically significant concurrent illness (for example; pneumonia, meningitis, septicaemia, coagulopathy, severe hemorrhage), pre-existing condition (e.g., renal disease, malignancy, malnutrition, known pre-existing human immunodeficiency virus [HIV]), febrile convulsions prior to consent, or clinical signs and symptoms of severe cardiovascular disease (for example; congenital heart disease).
- The subject has a history of porphyria, psoriasis, or epilepsy.
- The subject has taken anti-malarials (for example; artemisinin-based combination therapies, mefloquine, primaquine, or any other 4- or 8-aminoquinoline) or drugs with antimalarial activity within 30 days prior to study entry.
- The subject has received treatment with any investigational drug within 30 days of study entry, or within 5 half-lives, whichever is longer.
- The subject has taken or will likely require during the study the use of: histamine-2 blockers, antacids, anti-diabetic drugs of the biguanide class (i.e., phenformin, buformin), anti-arrhythmic agents dofetilide, procainamide, pilsicainide.
- The subject has a serum creatinine above the ULN and is currently taking metformin.
- The subject has a history of allergy or intolerance to chloroquine, mefloquine, tafenoquine, primaquine, or to any other 4- or 8-aminoquinoline.
- The subject has previously enrolled in this study.
- The subject has severe P. vivax malaria as defined by world health organization (WHO) criteria
Trial location(s)
Study documents
Protocol
Available language(s): English
Statistical analysis plan
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Completed
Actual primary completion date
2019-15-12
Actual study completion date
2020-17-02
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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