A Study to Determine Whether 2 Investigational Malaria Vaccines Are Safe, Protective Against Malaria in Adults

United States Army Medical Research and Development Command (USAMRDC)

Status and phase

Completed

Phase 2

Phase 1

Conditions

Malaria

Treatments

Biological: Group A FMP2.1/AS01B

Biological: Group B FMP2.1/AS02A

Study type

Interventional

Funder types

Other

Other U.S. Federal agency

Industry

Identifiers

NCT00385047

A-13949 (Other Identifier)

WRAIR 1280

MAL-045 (Other Identifier)

#20060900 (Other Identifier)

ETrack Protocol No. 104936 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to determine whether 2 investigational malaria vaccines are safe as well as protective against malaria in adults living in the United States

Full description

35 volunteers aged 18 to 50 years will be enrolled to receive one of 2 investigational malaria vaccines. The vaccines are made of a malaria protein FMP2.1 mixed in 2 different adjuvants (AS01B and AS02A). Five volunteers will get a small (10 µg) dose of FMP2.1/AS01B since this vaccine has not yet been in humans. If it is safe, then 15 volunteers will get 50 µg FMP2.1 in AS02A and 15 will get 50 µg FMP2.1 in AS01B. All vaccines are given IM in the deltoid of the non-dominant arm, every 1 month for 3 months. After vaccination, the subjects will follow up at clinical trials for evaluation of any adverse events.

20 vaccinees (10 from each 50 µg vaccine group) will undergo primary sporozoite challenge 14-30 days after dose 3 via bite of 5 malaria-infected mosquitoes. All subjects will have a blood slide prepared and read to check for asexual P. falciparum parasitemia at least once daily beginning day 5 post challenge. Beginning on day 10 post challenge, subjects will check into a designated hotel, where 24 hour evaluation and care will be available for 10 nights. After this hotel phase, there will be follow-up visits to ensure there are no late developments of malaria in those who have not fallen ill (and thus are considered protected).

Any subject who tests positive for malaria will be treated with chloroquine. Efficacy readouts are complete protection or significant delay in patency defined as >2 days than the median prepatent period for the 6 infectivity controls. These 6 controls receive no vaccine and are enrolled for malaria-challenge only in order to provide comparison group for vaccinated individuals.

Enrollment

41 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

A male or non-pregnant female 18 to 50 years of age (inclusive) at the time of screening
Written informed consent obtained from the participant before screening procedures
Free of clinically significant health problems as established by medical history and clinical examination before entering into the study*
Available to participate for duration of study (approximately five months, not including screening)
If the participant is female, she must be of non-childbearing potential, i.e., either surgically sterilized or one year post-menopausal; or, if of childbearing potential, she must be abstinent or have used adequate contraceptive precautions (e.g., intrauterine contraceptive device; oral contraceptives; diaphragm or condom in combination with contraceptive jelly, cream or foam; Norplant® or Depo-Provera®) during this study, have a negative pregnancy test at the time of each immunization, and must agree to continue such precautions for two months after completion of the immunization series and the malaria challenge.
Prior to entry into this study, participants must score at least 80% correct on a short multiple-choice quiz that assesses their understanding of this study. If they do not score 80% on the initial quiz, the protocol information will be reviewed with them to ensure comprehension and they will have the opportunity to retest. Participants who fail the Comprehension Assessment for the second time will not be enrolled.

Exclusion criteria

Prior receipt of an investigational malaria vaccine
Use of any investigational or non-registered drug or vaccine other than the study vaccine(s) within 30 days preceding the first study immunization or planned use during the study period, or receipt of investigational vaccine containing 3-D MPL and/or QS-21 at any time in the past (Have you received an experimental vaccine with a GSK adjuvant in the past?)
Administration of chronic (defined as more than 14 days) immunosuppressants or other immune-modifying drugs within six months of immunization. (For corticosteroids, this will mean prednisone, or equivalent, greater than or equal to 0.5 mg/kg/day. Inhaled and topical steroids are allowed.)
Chronic use of antibiotics with anti-malarial effects (e.g., tetracyclines for dermatologic patients, sulfa for recurrent urinary tract infections, etc.)
Planned administration of a vaccine not foreseen by the study protocol 30 days prior to or after the first immunization
History of malaria chemoprophylaxis within 60 days prior to immunization
Any history of malaria
Known exposure to malaria within the previous 12 months
Planned travel to malarious areas during the study period
Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection
History of allergic disease or reactions to any vaccine
Chronic or active neurologic disorders including seizures, excluding a single febrile seizure as a child
History of splenectomy
Acute disease at the time of enrollment (Acute disease is defined as the presence of a moderate or severe illness with or without fever. All vaccines can be administered to persons with a minor illness such as diarrhea, mild upper respiratory infection with or without low-grade febrile illness, i.e., oral temperature < 37.5°C/99.5°F).
Acute or chronic, clinically significant pulmonary, cardiovascular, hepatic or renal functional abnormality, as determined by physical examination or laboratory screening tests
Personal medical histories including the following diagnoses: systemic lupus erythematosus, rheumatoid arthritis, mixed connective tissue disease, scleroderma, vasculitis, and multiple sclerosis
Seropositive for hepatitis B surface antigen or hepatitis C antibody
Hepatomegaly, right upper quadrant abdominal pain or tenderness
Elevated serum creatinine, defined in this study as greater than or equal to 1.7 mg/dL in males and 1.4 mg/dL in females
Significant unexplained anemia: hematocrit < 35%
Administration of immunoglobulins and/or any blood products within the three months preceding the first study immunization or planned administration during the study period
Pregnant or lactating female or female who intends to become pregnant during the study
Suspected or known current alcohol abuse as defined by the American Psychiatric Association in DSM IV (Diagnostic and Statistical Manual of Mental Disorders- 4th edition)
Chronic or active illicit and/or intravenous drug use
History of severe anaphylactic reactions to mosquito bites
History of psoriasis (given its interaction with chloroquine)
Any history of anaphylaxis in reaction to immunization
History of allergy to nickel, imidazole or tetracycline group of antibiotics
History of sickle cell disease or sickle cell trait
Any other significant finding that in the opinion of the investigator would increase the risk of having an adverse outcome from participating in this study