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:
2025-12-24 @ 2:54 PM
Ignite Modification Date:
2025-12-24 @ 2:54 PM
NCT ID:
NCT01148459
Eligibility Criteria:
Inclusion Criteria:
All subjects must satisfy ALL the following criteria at study entry:
* A male or female infant or child between and including 6 weeks to 17 months of age, at the time of first vaccination.
* Signed or thumb-printed informed consent obtained from the parent(s)/LAR(s) of the infant or child. Where parents/LARs are illiterate, the consent form will be countersigned by a witness.
* Subjects who the investigator believes that their parents/LARs can and will comply with the requirements of the protocol should be enrolled in the study.
* Subjects who are known to be HIV-infected (documented positive DNA PCR), whether taking HIV antiretroviral treatment (ART) or not.
* Subjects who are born following a normal gestation period.
Exclusion Criteria:
The following criteria should be checked at the time of study entry. If ANY exclusion criterion applies, the subject must not be included in the study:
* Acute disease at the time of enrolment. However, the presence of an illness listed as Grade I or Grade II (WHO pediatric AIDS clinical staging) will not of itself constitute an exclusion criterion. Enrolment should be deferred if axillary temperature is \>=37.5°C.
* Grade III or Grade IV abnormality on screening laboratory blood sample.
* Grade III or IV AIDS at the time of enrolment (WHO pediatric AIDS clinical staging).
* Major congenital defects.
* Planned administration/administration of a vaccine not foreseen by the study protocol prior to or within 7 days of study vaccine.
* Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine 30 days preceding Dose°1 of study vaccine, or planned use during the study period.
* Previous participation in any other malaria vaccine trial.
* Simultaneous participation in another clinical trial including administration of experimental treatment.
* Same sex twins.
* History of allergic reactions (significant IgE-mediated events) or anaphylaxis to previous immunizations.
* History of allergic disease or reactions likely to be exacerbated by any component of the study vaccine.
* Child in care.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
6 Weeks
Maximum Age:
17 Months
Study:
NCT01148459
Study Brief:
Protocol Section:
NCT01148459