Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:34 AM
Ignite Modification Date:
2025-12-25 @ 2:34 AM
NCT ID:
NCT01366534
Eligibility Criteria:
Inclusion Criteria:
* Subjects who the investigator believes can and will comply with the requirements of the protocol.
* A male or non-pregnant female 18 to 50 years of age at the time of first vaccination.
* Written informed consent obtained from the subject before screening procedures.
* Free of obvious health problems as established by medical history and clinical examination before entering into the study.
* Available to participate for the duration of the study.
* Female subjects of non-childbearing potential.
* Female subjects of childbearing potential may be enrolled in the study, if the subject:
* has practiced adequate Food and Drug Administration (FDA)-approved contraception for 30 days prior to vaccination, and
* has a negative pregnancy test on the day of vaccination, and
* has agreed to continue adequate FDA-approved contraception during the entire treatment period and for 2 months after completion of the vaccination series and/or malaria challenge.
* Pass a comprehension assessment test.
Exclusion Criteria:
* Use of any investigational or non-registered product within 30 days preceding the first dose of study vaccine, or planned use of any investigational or non-registered product other than the study vaccines during the study period.
* Planned administration/ administration of a vaccine not foreseen by the study protocol within 7 days of the first dose of vaccines.
* Prior receipt of an investigational malaria or adenovirus vaccine.
* Chronic use of antibiotics with antimalarial effects.
* History of malaria chemoprophylaxis within 60 days prior to vaccination.
* Any history of malaria.
* Planned travel to malaria endemic areas during the study period.
* History of allergic disease or reactions likely to be exacerbated by any component of the vaccine(s) including latex.
* History of allergic disease or reactions likely to be exacerbated by chloroquine.
* History of psoriasis and porphyria, which may be exacerbated after chloroquine treatment.
* Current use of medications known to cause drug reactions to chloroquine, such as antacids and kaolin.
* Any history of anaphylaxis in reaction to any previous vaccination.
* History of severe reactions to mosquito bites.
* Administration of immunoglobulins and/or any blood products within the three months preceding the first dose of study vaccine or planned administration during the study period.
* Chronic administration of immunosuppressants or other immune modifying drugs within six months prior to first vaccine dose.
* Any confirmed or suspected immunosuppressive or immunodeficient condition, including immunodeficiency virus (HIV) infection.
* Family history of congenital or hereditary immunodeficiency.
* History of splenectomy.
* Major congenital defects or serious chronic illness.
* History of any neurological disorders or seizures.
* Acute disease and/or fever at the time of enrollment.
* Acute disease is defined as the presence of a moderate or severe illness with or without fever. Subjects with a minor illness without fever may be enrolled at the discretion of the investigator.
* Acute or chronic, clinically significant pulmonary, cardiovascular, hepatic or renal functional abnormality, as determined by physical examination or laboratory screening tests.
* Any abnormal baseline laboratory screening tests.
* Evidence of increased cardiovascular disease risk, "moderate" or "high", according to the NHANES I criteria.
* An abnormal baseline screening electrocardiogram (EKG).
* Hepatomegaly, right upper quadrant abdominal pain or tenderness.
* Personal history of autoimmune disease.
* Seropositive for hepatitis B surface antigen or Hepatitis C virus (antibodies to HCV).
* Pregnant or lactating female.
* Female who intends to become pregnant during the study or planning to discontinue contraceptive measures.
* Suspected or known current alcohol abuse.
* Chronic or active intravenous drug use.
* History of blood donation within 56 days preceding enrolment.
* 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.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT01366534
Study Brief:
Protocol Section:
NCT01366534