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NCT05829187: MCHUPF

Momordica Charantia and Dihydroartemisinin-piperaquined-primaquine for Uncomplicated Plasmodium Falciparum Malaria Patients in Southwest Sumba Regency

Completed Phase 2 Last updated 16 May 2023
What this trial tests

Phase 2 trial testing Dihydroartemisinin in Uncomplicated Plasmodium Falciparum in 36 participants. Completed in 31 December 2022.

Timeline
1 November 2022
Primary endpoint
31 December 2022
31 December 2022

Quick facts

Lead sponsorSyamsudin Abdillah,Ph.D, Pharm D
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment36
Start date1 November 2022
Primary completion31 December 2022
Estimated completion31 December 2022
Sites1 location across Indonesia

Drugs / interventions tested

Conditions studied

Sponsor

Syamsudin Abdillah,Ph.D, Pharm D — full company profile →

Who can join

Adults 18 to 60, any sex, with Uncomplicated Plasmodium Falciparum. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Currently, the first-line combination of artemisinin, piperaquine and prima-quine is quite effective in controlling malaria, however, the threat of spread of drug-resistant parasites has been reported. A study is conducted to assess the efficacy and safety extract of bitter melon (Momordica charantia/MC) regimens compared to the combination of dihydroartemisinin piperaquine primaquine (DHP+PQ) on the sexual and asexual stage of P. Falciparum uncomplicated in Sumba Barat Daya District, Indonesia

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing