ClinicalTrials.Veeva

Menu

Safety and Immunogenicity of Recombinant Pichia Pastoris AMA1-DiCo Candidate Malaria Vaccine With GLA-SE and Alhydrogel ® as Adjuvant in Healthy Malaria Non-Exposed European and Malaria Exposed African Adults

I

Institut National de la Santé Et de la Recherche Médicale, France

Status and phase

Completed
Phase 1

Conditions

Malaria, Falciparum

Treatments

Biological: Group B2 : Placebo
Biological: Group A1 : 50µg AMA1-DiCo + Alhydrogel
Biological: Group A2 : 50 µg AMA1-DiCo+ GLA-SE

Study type

Interventional

Funder types

Other

Identifiers

NCT02014727
C12-18 AMA-DiCo
2013-001920-20 (EudraCT Number)

Details and patient eligibility

About

The primary objective is to evaluate the safety of 3 doses given at D0, W4, and W26 of 50 µg dosage of AMA1-DiCo adjuvanted either with GLA-SE or Alhydrogel® in healthy European adults not previously exposed to the parasite P.falciparum and in healthy African adults exposed to the parasite. The safety and the tolerability of the vaccine will be assessed on the rate of solicited and unsolicited events/reactions. The safety profile will include local and systemic reactions/events as well as the biological safety, based on a clinically significant change of the baseline value of the main biological criteria.

Full description

The project aims are :

-To evaluate the safety of 50 µg AMA1-DiCo malaria vaccine candidate with GLA-SE and Alhydrogel® as adjuvant, in healthy European adults not previously exposed to the parasite Plasmodium falciparum and in healthy African adults exposed to the parasite.

T-o assess the humoral immune response to the vaccine antigens by measuring the level of IgG in all volunteers.

To assess the cellular immune response by measuring the T cell cytokines IL-5 and IFNγ production following in vitro stimulation with the vaccine antigens in all volunteers.

Design :

This trial is a staggered Phase Ia/Ib, Randomised, Double-blind, Multi-center Centre trial.

Two different adjuvants will be assessed, Alhydrogel® and GLA-SE. One dosage of 50 µg/3 injections of AMA1-DiCo will be evaluated for each adjuvant.

Sixty six (66) healthy volunteers will be included into the 2 following cohorts (A and B):

Cohort A: 30 Non-exposed European Volunteers (France) Cohort B: 36 Malaria Exposed African Volunteers (Burkina Faso)

The non-exposed European volunteers (cohort A) will be randomised in a 1:1 ratio into two groups of 15 volunteers per group.

The malaria exposed African volunteers (cohort B) will be randomised in a 1:1 ratio, into two groups of 18 volunteers per group.

European Volunteers: Cohort A (30):

Group A1 (15): 50µg AMA1-DiCo + Alhydrogel® Group A2 (15): 50 µg AMA1-DiCo+ GLA-SE

African Volunteers Cohort B (36) :

Group B1 (18): 50 µg AMA1-DiCo + GLA-SE Group B2 (18): Placebo (isotonic saline solution)

In order to start recruitment in cohort B (Africa), the safety will be evaluated on the data of all European volunteers until Day 7 after 1st immunisation of the last European volunteer Data will be presented to an Independent Data safety Monitoring Board (DSMB) that will be appointed for this trial

Enrollment

66 patients

Sex

All

Ages

20 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age > 20 and < 45 years healthy female and male
  2. General good health based on history and clinical examination.
  3. Written informed consent obtained before any trial procedure.
  4. Female and male volunteers practicing contraception before and up to four (4) weeks after the third vaccination.
  5. Available to participate in follow-up for the duration of trial.
  6. Reachable by phone during the whole trial period.
  7. Volunteers should be affiliated to a social security regimen

Exclusion criteria

  1. Positive pregnancy test

  2. Active breast feeding

  3. Previous participation in any malaria vaccine trial

  4. History of blood transfusion within the last 6 months

  5. Symptoms, physical signs or laboratory values suggestive of systemic disorders, including renal, hepatic, cardiovascular, pulmonary, skin, immunodeficiency, psychiatric and other conditions, which could interfere with the interpretation of the trial results or compromise the health of the volunteers.

  6. Any clinically significant laboratory abnormalities on screened blood samples outside the normal range, as defined at the clinical trial site.

  7. Enrolment in any other clinical trial during the whole trial period

  8. Intake of chronic medication, especially immunosuppressive agents (steroids, immunomodulating or immunosuppressive drugs) during the thirteen weeks preceding the screening visit or during the trial period except topical steroid use including intranasal.

  9. Any confirmed or suspected immunosuppressive or immunodeficiency condition during the whole trial period

  10. Volunteers unable to be closely followed for social, geographic or psychological reasons.

  11. Previous history of drug or alcohol abuse interfering with normal social function during a period of one year prior to enrolment in the trial.

  12. History of anaphylaxis or Known severe hypersensitivity to any of the vaccine components (adjuvant or antigen or excipient)

  13. Vaccination or gamma globulin: 4 weeks prior and after each vaccination if a vaccination is necessary during this period, the volunteer will be withdrawn from the study.

  14. Positive HIV, HBV (Ag HBS) and HCV tests.

  15. History of malaria or travel in malaria endemic areas within the past twenty-six weeks.

  16. Positive serology for malaria antigen PfAMA-1

  17. Intention to travel to malaria endemic countries during the trial period.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

66 participants in 4 patient groups, including a placebo group

AMA1-DiCo + Alhydrogel
Experimental group
Description:
AMA1-DiCo: 50µg Alhydrogel® : 0.85 mg Al3+ per dose Route : Intramuscular Vaccination schedule : Do, W4, W26
Treatment:
Biological: Group A1 : 50µg AMA1-DiCo + Alhydrogel
AMA1-DiCo+ GLA-SE
Experimental group
Description:
Group A2 (15) : European volunteer : AMA1-DiCo + GLA-SE AMA1-DiCo: 50µg GLA-SE 2.5 µg GLA per dose Route : Intramuscular Vaccination schedule : Do, W4, W26
Treatment:
Biological: Group A2 : 50 µg AMA1-DiCo+ GLA-SE
AMA1-DiCo + GLA-SE
Experimental group
Description:
Group B1 (18) : African volunteer : AMA1-DiCo + GLA-SE AMA1-DiCo: 50µg GLA-SE 2.5 µg GLA per dose Route : Intramuscular Vaccination schedule : Do, W4, W26
Treatment:
Biological: Group A2 : 50 µg AMA1-DiCo+ GLA-SE
Placebo
Placebo Comparator group
Description:
Group B2 (18) : African volunteer : Placebo Placebo : isotonic saline solution Route : Intramuscular Vaccination schedule : Do, W4, W26
Treatment:
Biological: Group B2 : Placebo

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems