CLINICAL TRIALS PROFILE FOR KAE609
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Clinical Trials for KAE609
| Trial ID | Title | Status | Sponsor | Phase | Summary |
|---|---|---|---|---|---|
| NCT01524341 ↗ | Efficacy, Safety, Tolerability and Pharmacokinetics of KAE609 in Adult Patients With Acute, Uncomplicated Plasmodium Falciparum or Vivax Malaria Mono-infection | Completed | Novartis Pharmaceuticals | Phase 2 | This study will assess efficacy, safety , tolerability and PK in uncomplicated adult malaria patients with P. vivax or P. falciparum infection after 3 day dosing with KAE609 at 30 mg/day |
| NCT01836458 ↗ | A Study to Find the Minimum Inhibitory Concentration of KAE609 in Adult Male Patients With P. Falciparum Monoinfection | Completed | Novartis Pharmaceuticals | Phase 2 | This study aims to determine the Minimum Inhibitory Concentration of KAE609 in adult male patients with acute, uncomplicated malaria due to P.falciparum monoinfection after single dosing with KAE609 |
| NCT01860989 ↗ | A Study to Assess Efficacy, Safety of KAE609 in Adult Patients With Acute Malaria Mono-infection | Completed | Novartis Pharmaceuticals | Phase 2 | This study will assess efficacy, safety , tolerability and PK in uncomplicated adult malaria patients with acute P. falciparum infection after single dose with KAE609 at 75 mg, 150mg, 225mg and 300mg/day |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for KAE609
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Clinical Trial Locations for KAE609
Clinical Trial Progress for KAE609
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Clinical Trial Sponsors for KAE609
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