Safety and Efficacy of CIS43LS Anti-malaria mAb in Mali

NCT ID: NCT04329104

Last Updated: 2025-04-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 348 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-02-15
• Study Completion Date: 2023-07-05

Brief Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of VRC MALMAB0100-00-AB (CIS43LS), a human monoclonal antibody, against naturally occurring Plasmodium falciparum (Pf) infection.

Detailed Description

This study will evaluate the safety, tolerability, and efficacy of VRC MALMAB0100-00-AB (CIS43LS), a human monoclonal antibody, against naturally occurring Plasmodium falciparum (Pf) infection.

The first part of the study is an open-label dose-escalation study for safety and tolerability. Participants will be assigned to one of three dose arms. Dosing will begin in the lowest dose arm. Once all participants in that arm reach Day 7 post-infusion, if no safety concerns have arisen, dosing will begin at the subsequent dose level. This process will be repeated until participants complete the third dose arm. Participants will be followed for safety to assess adverse events (AEs) at study visits 1, 3, 7, 14, 21, and 28 days after administration, then monthly through 24 weeks after administration.

After the last subject in the highest dose arm reaches Day 7 safety follow-up, an interim safety evaluation will be performed before enrollment begins for the second part of the study.

The second part of the study is a randomized, double-blind, placebo-controlled trial to assess safety and protective efficacy of CIS43LS and placebo. Participants in the efficacy study will receive the study agent and be followed at study visits 1, 3, 7, 14, 21, and 28 days later, and once every 2 weeks thereafter through 24 weeks. Primary study assessments include physical examinations and blood collection for identification of Pf infection and other research laboratory evaluations.

Conditions

Plasmodium Falciparum Infection; Malaria

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Dose-escalation study: Arm 1: 5 mg/kg of CIS43LS

Participants receive 5 mg/kg of CIS43LS as one time intravenous infusion on Day 0.

Group Type: EXPERIMENTAL

VRC-MALMAB0100-00-AB (CIS43LS)

Intervention Type: BIOLOGICAL

Administered via one-time intravenous infusion

Dose-escalation study: Arm 2: 10 mg/kg of CIS43LS

Participants receive 10 mg/kg of CIS43LS as one time intravenous infusion on Day 0.

Group Type: EXPERIMENTAL

VRC-MALMAB0100-00-AB (CIS43LS)

Intervention Type: BIOLOGICAL

Administered via one-time intravenous infusion

Dose-escalation study: Arm 3: 40 mg/kg of CIS43LS

Participants receive 40 mg/kg of CIS43LS as one time intravenous infusion on Day 0.

Group Type: EXPERIMENTAL

VRC-MALMAB0100-00-AB (CIS43LS)

Intervention Type: BIOLOGICAL

Administered via one-time intravenous infusion

Efficacy study: Arm 1: 10 mg/kg of CIS43LS

Participants receive 10 mg/kg of CIS43LS as one time intravenous infusion on Day 0.

Group Type: EXPERIMENTAL

VRC-MALMAB0100-00-AB (CIS43LS)

Intervention Type: BIOLOGICAL

Administered via one-time intravenous infusion

Efficacy study: Arm 2: 40 mg/kg of CIS43LS

Participants receive 40 mg/kg of CIS43LS as one time intravenous infusion on Day 0.

Group Type: EXPERIMENTAL

VRC-MALMAB0100-00-AB (CIS43LS)

Intervention Type: BIOLOGICAL

Administered via one-time intravenous infusion

Efficacy study: Arm 3: Placebo

Participants receive placebo as one time intravenous infusion on Day 0.

Group Type: PLACEBO_COMPARATOR

Normal saline

Intervention Type: OTHER

Administered via one-time intravenous infusion

Interventions

VRC-MALMAB0100-00-AB (CIS43LS)

Administered via one-time intravenous infusion

Intervention Type: BIOLOGICAL

Normal saline

Administered via one-time intravenous infusion

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Aged ≥18 and ≤55 years.
• Able to provide proof of identity to the satisfaction of the study clinician completing the enrollment process.
• In good general health and without clinically significant medical history.
• Able to provide informed consent.
• Willing to have blood samples and data stored for future research.
• Resides in or near Kalifabougou or Torodo, Mali, and available for the duration of the study.
• Females of childbearing potential must be willing to use reliable contraception from 21 days prior to study day 0 through the final study visit as described below.

• Reliable methods of birth control include 1 of the following: confirmed pharmacologic contraceptives via parenteral delivery or intrauterine or implantable device.
• Nonchildbearing women will be required to report date of last menstrual period, history of surgical sterility (i.e., tubal ligation, hysterectomy) or premature ovarian insufficiency, and will have urine or serum pregnancy test performed per protocol.

Exclusion Criteria

• Pregnancy, as determined by a positive urine or serum beta-human choriogonadotropin (β-hCG) test (if female).
• Currently breastfeeding.
• Behavioral, cognitive, or psychiatric disease that in the opinion of the investigator affects the ability of the subject to understand and comply with the study protocol.
• Study comprehension examination score of <80% correct or per investigator discretion.
• Hemoglobin, white blood cell, absolute neutrophil, or platelet count outside the local laboratory-defined limits of normal. (Subjects may be included at the investigator's discretion for "not clinically significant" values.)
• Alanine transaminase (ALT) or creatinine (Cr) level above the local laboratory-defined upper limit of normal. (Subjects may be included at the investigator's discretion for "not clinically significant" values.)
• Infected with human immunodeficiency virus (HIV), hepatitis C virus (HCV), or hepatitis B virus (HBV).
• Known or documented sickle cell disease by history. (Note: Known sickle cell trait is NOT exclusionary.)
• Clinically significant abnormal electrocardiogram (ECG; corrected QT interval [QTc] >460 or other significant abnormal findings, including unexplained tachycardia or bradycardia).
• Evidence of clinically significant neurologic, cardiac, pulmonary, hepatic, endocrine, rheumatologic, autoimmune, hematological, oncologic, or renal disease by history, physical examination, and/or laboratory studies including urinalysis.
• Receipt of any investigational product within the past 30 days.
• Participation or planned participation in an interventional trial with an investigational product until the last required protocol visit. (Note: Past, current, or planned participation in observational studies is NOT exclusionary.)
• Medical, occupational, or family problems as a result of alcohol or illicit drug use during the past 12 months.
• History of a severe allergic reaction or anaphylaxis.
• Severe asthma (defined as asthma that is unstable or required emergent care, urgent care, hospitalization, or intubation during the past 2 years, or that has required the use of oral or parenteral corticosteroids at any time during the past 2 years).
• Pre-existing autoimmune or antibody-mediated diseases including but not limited to: systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, Sjögren's syndrome, or autoimmune thrombocytopenia.
• Known immunodeficiency syndrome.
• Known asplenia or functional asplenia.
• Use of chronic (≥14 days) oral or IV corticosteroids (excluding topical or nasal) at immunosuppressive doses (i.e., prednisone >10 mg/day) or immunosuppressive drugs within 30 days of day 0.
• Receipt of a live vaccine within the past 4 weeks or a killed vaccine within the past 2 weeks prior to study agent administration.
• Receipt of immunoglobulins and/or blood products within the past 6 months.
• Previous receipt of an investigational malaria vaccine in the last 5 years.
• Known allergies or contraindication against artemether-lumefantrine.
• Other condition(s) that, in the opinion of the investigator, would jeopardize the safety or rights of a subject participating in the trial, interfere with the evaluation of the study objectives, or render the subject unable to comply with the protocol.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Malaria Research and Training Center, Bamako, Mali

OTHER

Sponsor Role: collaborator

University of Washington

OTHER

Sponsor Role: collaborator

Harvard School of Public Health (HSPH)

OTHER

Sponsor Role: collaborator

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kassoum Kayentao, MD, MPH, PhD

Role: PRINCIPAL_INVESTIGATOR

Faculté de Médecine Pharmacie d'Odontostomatologie (FMPOS)

Peter D. Crompton, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

National Institutes of Health (NIH)

Locations

Kalifabougou MRTC Clinic

Kalifabougou, Koulikoro, Mali

Torodo MRTC Clinic

Torodo, Koulikoro, Mali

Countries

Mali

References

Kayentao K, Ongoiba A, Preston AC, Healy SA, Doumbo S, Doumtabe D, Traore A, Traore H, Djiguiba A, Li S, Peterson ME, Telscher S, Idris AH, Kisalu NK, Carlton K, Serebryannyy L, Narpala S, McDermott AB, Gaudinski M, Traore S, Cisse H, Keita M, Skinner J, Hu Z, Zeguime A, Ouattara A, Doucoure M, Dolo A, Djimde A, Traore B, Seder RA, Crompton PD; Mali Malaria mAb Trial Team. Safety and Efficacy of a Monoclonal Antibody against Malaria in Mali. N Engl J Med. 2022 Nov 17;387(20):1833-1842. doi: 10.1056/NEJMoa2206966. Epub 2022 Oct 31.

Reference Type: RESULT

PMID: 36317783 (View on PubMed)

Skinner J, Kayentao K, Ongoiba A, Healy SA, Hu Z, Preston AC, Niangaly A, Schwabl P, Cisse H, Doumbo S, Doumtabe D, Traore A, Li S, Peterson ME, Seilie AM, Chavtur C, Staubus W, Chang M, Kelley K, Traore H, Djiguiba A, Keita M, Ouattara A, Doucoure M, Keita M, Diarra D, Sylla M, Diakite D, Konate M, Traore S, Zeguime A, Dolo A, Neafsey DE, Murphy SC, Traore B, Seder RA, Crompton PD. Anti-sporozoite monoclonal antibody for malaria prevention: secondary efficacy outcome of a phase 2 randomized trial. Nat Med. 2025 Aug;31(8):2682-2690. doi: 10.1038/s41591-025-03739-y. Epub 2025 Jun 3.

Reference Type: DERIVED

PMID: 40461818 (View on PubMed)

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

2020/32/CE/FMOS/FAPH

Identifier Type: -

Identifier Source: org_study_id