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ABSTRACT: Background
Additional interventions are needed to reduce the morbidity and mortality caused by malaria.Methods
We conducted a two-part, phase 1 clinical trial to assess the safety and pharmacokinetics of CIS43LS, an antimalarial monoclonal antibody with an extended half-life, and its efficacy against infection with Plasmodium falciparum. Part A of the trial assessed the safety, initial side-effect profile, and pharmacokinetics of CIS43LS in healthy adults who had never had malaria. Participants received CIS43LS subcutaneously or intravenously at one of three escalating dose levels. A subgroup of participants from Part A continued to Part B, and some received a second CIS43LS infusion. Additional participants were enrolled in Part B and received CIS43LS intravenously.
SUBMITTER: Gaudinski MR
PROVIDER: S-EPMC8579034 | biostudies-literature | 2021 Aug
REPOSITORIES: biostudies-literature