A Monoclonal Antibody for Malaria Prevention.

dc.contributor.author

Gaudinski, Martin R

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Berkowitz, Nina M

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Idris, Azza H

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Coates, Emily E

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Holman, LaSonji A

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Mendoza, Floreliz

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Gordon, Ingelise J

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Plummer, Sarah H

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Trofymenko, Olga

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Hu, Zonghui

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Campos Chagas, Andrezza

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O'Connell, Sarah

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Basappa, Manjula

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Douek, Naomi

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Narpala, Sandeep R

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Barry, Christopher R

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Widge, Alicia T

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Hicks, Renunda

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Awan, Seemal F

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Wu, Richard L

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Hickman, Somia

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Wycuff, Diane

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Stein, Judy A

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Case, Christopher

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Evans, Brian P

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Carlton, Kevin

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Gall, Jason G

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Vazquez, Sandra

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Flach, Britta

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Chen, Grace L

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Francica, Joseph R

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Flynn, Barbara J

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Kisalu, Neville K

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Capparelli, Edmund V

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McDermott, Adrian

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Mascola, John R

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Ledgerwood, Julie E

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Seder, Robert A

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VRC 612 Study Team

dc.date.accessioned

2024-11-19T23:15:55Z

dc.date.available

2024-11-19T23:15:55Z

dc.date.issued

2021-08

dc.description.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. To assess the protective efficacy of CIS43LS, some participants underwent controlled human malaria infection in which they were exposed to mosquitoes carrying P. falciparum sporozoites 4 to 36 weeks after administration of CIS43LS.

Results

A total of 25 participants received CIS43LS at a dose of 5 mg per kilogram of body weight, 20 mg per kilogram, or 40 mg per kilogram, and 4 of the 25 participants received a second dose (20 mg per kilogram regardless of initial dose). No safety concerns were identified. We observed dose-dependent increases in CIS43LS serum concentrations, with a half-life of 56 days. None of the 9 participants who received CIS43LS, as compared with 5 of 6 control participants who did not receive CIS43LS, had parasitemia according to polymerase-chain-reaction testing through 21 days after controlled human malaria infection. Two participants who received 40 mg per kilogram of CIS43LS and underwent controlled human malaria infection approximately 36 weeks later had no parasitemia, with serum concentrations of CIS43LS of 46 and 57 μg per milliliter at the time of controlled human malaria infection.

Conclusions

Among adults who had never had malaria infection or vaccination, administration of the long-acting monoclonal antibody CIS43LS prevented malaria after controlled infection. (Funded by the National Institute of Allergy and Infectious Diseases; VRC 612 ClinicalTrials.gov number, NCT04206332.).
dc.identifier.issn

0028-4793

dc.identifier.issn

1533-4406

dc.identifier.uri

https://hdl.handle.net/10161/31660

dc.language

eng

dc.publisher

Massachusetts Medical Society

dc.relation.ispartof

The New England journal of medicine

dc.relation.isversionof

10.1056/nejmoa2034031

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.subject

VRC 612 Study Team

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Humans

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Plasmodium falciparum

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Malaria, Falciparum

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Antibodies, Monoclonal

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Antibodies, Protozoan

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Antimalarials

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Infusions, Intravenous

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Injections, Subcutaneous

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Dose-Response Relationship, Drug

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Adult

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Middle Aged

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Antibodies, Monoclonal, Humanized

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Healthy Volunteers

dc.title

A Monoclonal Antibody for Malaria Prevention.

dc.type

Journal article

pubs.begin-page

803

pubs.end-page

814

pubs.issue

9

pubs.organisational-group

Duke

pubs.organisational-group

Pratt School of Engineering

pubs.organisational-group

Student

pubs.organisational-group

Biomedical Engineering

pubs.publication-status

Published

pubs.volume

385

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