Healthy Subjects
Conditions
Keywords
Mefloquine, Malaria, (+) Mefloquine, Pharmacokinetics
Brief summary
Mefloquine is a quinolinemethanol antimalarial that is effective as therapy and prophylaxis for all species of malaria infecting humans, including multi-drug resistant Plasmodium falciparum. The marketed anti-malaria drug consists of two enantiomers of mefloquine. Mefloquine's clinical utility has been impaired by its association with neuropsychiatric side effects. The pharmacological basis of mefloquine's side effects is not known but two of the most reported hypotheses relate to its action on (i) the adenosine receptor and (ii) its effect on the cholinesterase enzyme. For both of these mechanisms, there is a significant stereoselective activity of the two enantiomers. In vitro studies show that the (-) isomer is 50-100 fold more potent towards adenosine receptors compared with the (+) isomer. In addition, (-)-mefloquine has considerably more anti-cholinesterase activity. It has therefore been hypothesised that (+)-mefloquine may have a better central nervous system (CNS) safety profile compared with either the racemate or (-)-mefloquine. This study is a randomized, ascending dose, double-blind, active and placebo-controlled, parallel group study in healthy male and female volunteers designed to investigate this hypothesis and to describe the comparative pharmacokinetics of the racemate and the single enantiomer.
Interventions
DRUGAD 452 (+) mefloquine
Single dose delivered as over-encapsulated tablet at ascending doses
DRUGRacemic Mefloquine
Single dose delivered as over-encapsulated tablet at ascending dose
DRUGPlacebo
Over-encapsulated placebo to maintain blinding
Sponsors
Medicines for Malaria Venture
Treague Ltd
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
* A BMI of between 19 and 28 * Negative urine drugs of abuse and breath alcohol test * Willing to use double barrier contraception for 13 weeks after administration of study drug
Exclusion criteria
* Pregnant or lactating females * Existence of any surgical or medical condition which, in the judgement of the Principal Investigator, might interfere with the absorption and disposition of the drug or with the aim of the study including clinically significant lactose intolerance * Receipt of prescription medication within 21 days of the first study day or over the counter medication (with the exception of multi-vitamins or paracetamol) within 1 week before the planned dosing date without prior approval * Definite or suspected personal or family history of adverse drug reaction or hypersensitivity to drugs with a chemical structure similar to AD 452 * Participation in a clinical study within the previous 12 weeks * A history of sensitivity to antimalarial or related compounds * Definite or suspected personal or family history of adverse drug reaction or hypersensitivity to drugs with a chemical structure similar to AD 452 * Active depression or a recent history of depression or generalised anxiety disorder * Any personal history of psychosis or schizophrenia or other major psychiatric disorders or convulsions * Previous exposure to racemic mefloquine
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The dose-concentration-effect relationship of AD 452 [(+)-mefloquine] for safety and toleration in comparison with that of racemic mefloquine across a range of potentially therapeutic doses and concentrations. | Following single dose |
Secondary
| Measure | Time frame |
|---|---|
| The comparative pharmacokinetics of AD 452 [(+)mefloquine] and racemic mefloquine | Single dose |
Countries
United Kingdom
Outcome results
None listed