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A study of the plasma concentration-time profile and antimalarial activity of plasma samples collected from healthy Vietnamese volunteers after the administration of artesunate-amodiaquine alone and with methylene blue.

Pharmacokinetics and ex vivo antimalarial activity of methylene blue combined with artesunate and amodiaquine in healthy Vietnamese volunteers.

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001298808
Enrollment
16
Registered
2012-12-17
Start date
2012-12-21
Completion date
2013-02-21
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Artemisinin combination therapies (ACT) such as artesunate-amodiaquine (ASAQ) are currently recommended worldwide for first-line treatment of uncomplicated Plasmodium falciparum malaria. However, recent reports of reduced susceptibility of artemisinins and ACTs in western Cambodia, western Thailand and south Vietnam is very worrisome and highlights the urgent need to identify alternative drug combination options for effective and affordable treatment. To extend the efficacy life of ACTs, a triple drug combination strategy may be worthy of consideration. We propose to determine whether methylene blue (MB), an old and affordable antimalarial drug, can be combined with ASAQ to extend the efficacy life of the ACT by studying the tolerability, pharmacokinetics and ex vivo antimalarial activity of ASAQ alone and with MB in healthy Vietnamese volunteers. If MB combined with ASAQ is well tolerated and does not adversely alter the pharmacokinetics of ASAQ in healthy volunteers, and enhanced blood stage ex vivo antimalarial activity can be demonstrated in volunteers' plasma containing ASAQ plus MB, then further studies a warranted to appraise the clinical value of the triple drug combination of AS+AQ+MB.

Interventions

In a randomized, open label, 2-way cross-over design, 16 healthy Vietnamese volunteers will be administered a single oral dose of either 2 tablets of artesunate-amodiaquine (ASAQ Winthrop-Registered Trademark) from Sanofi-Aventis; 100 mg AS and 270 mg AQ per tablet) or 2 tablets of ASAQ Winthrop plus 5 tablets of methylene blue (MB Urolene Blue-Registered Trademark) from Star Pharmaceuticals; 65 mg per tablet). The wash-out period between treatments will be 8 weeks.

Sponsors

Australian Army Malaria Institute
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
Male
Age
17 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

(i) Males: 17-40 years (ii) Normal clinical parameters: medical history, physical examination (iii) Normal haematological and biochemical indices, and electrocardiogram (iv) Normal glucose-6-phosphate dehydrogenase (G6PD) (v) Able to understand and willing to provide written informed consent

Exclusion criteria

(i) A history of serious past medical diseases (ii) A history of drug or alcohol abuse (iii) Use of regular medications including prescribed and natural therapies (iv) Use of serotonergic psychiatric medications

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 28, 2026