A Phase I Study to Evaluate Safety and Immunogenicity of AERAS 404 Administered in Adults

Aeras

Status and phase: Completed; Phase 1

Conditions: Tuberculosis

Treatments: Biological: AERAS-404; Biological: Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT02074956

C-006-404 (Other Identifier)

C 006 404

Details and patient eligibility

About

This Phase I study will be conducted as a randomized, double-blind, dose-escalation study in five groups of healthy adult male and female subjects who are BCG-vaccinated, HIV-negative, and have no evidence of tuberculosis infection. Since BCG-vaccinated individuals are the target population for which AERAS 404 might be indicated, AERAS 404 will be administered to individuals already vaccinated with BCG

Full description

Sixty subjects will be sequentially enrolled into one of five study groups (i.e., Group 1, Group 2, Group 3, Group 4, or Group 5) with 10 subjects per group in Groups 1-4 and 20 subjects in Group 5. Within each study group, subjects will be randomized to a treatment assignment of either AERAS-404 or placebo control at a ratio of 4:1 (Groups 1-4) or two different dose amounts of AERAS-404 or placebo control at a ratio of 9:9:2 (Group 5) administered by intramuscular injection on Study Day 0 and Study Day 56. The principal investigator will determine an appropriate interval between the vaccinations such that the entire group is not dosed at the same time. All subjects will receive the same treatment on Study Day 0 as they receive on Study Day 56. All subjects will be followed for safety and immunogenicity evaluations for 182 days. A total of eleven clinic visits are planned (excluding screening) for all subjects

Enrollment: 60 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Has completed written informed consent
2. Is male or female
3. Is age 18 through 45 years on Study Day 0
4. Had BCG vaccination at least 5 years ago, documented through medical history or presence of scar
5. Has general good health, confirmed by medical history and physical examination
6. Has a Body Mass Index (BMI) between 19 and 33
7. Agrees to complete a follow-up period of 182 days as required by the protocol
8. Females: Agrees to avoid pregnancy from 28 days prior to Study Day 0 through the follow-up period of 182 days. Women physically capable of pregnancy (not sterilized and still menstruating or within 1 year of the last menses) must agree to avoid pregnancy using an acceptable method
9. Agrees to avoid elective surgery for the duration of the study
10. Agrees to stay in contact with the investigative site for the study duration
11. Completed simultaneous enrollment in Aeras Vaccine Development Registry protocol

Exclusion criteria

1. Acute illness on Study Day 0
2. Axillary temperature >=37.5 degrees Celsius on Study Day 0
3. Evidence of significant active infection
4. Used immunosuppressive medication within 42 days before Study Day 0
5. Received immunoglobulin or blood products within 42 days before Study Day 0
6. Received any investigational drug therapy or investigational vaccine within 182 days before Study Day 0
7. Received inactivated influenza vaccine or inactivated tick-borne encephalitis vaccine within 14 days before entry into the study, or any other standard vaccine within 42 days before Study Day 0
8. Current chronic drug therapy including hormone replacement such as thyroxin, insulin
9. History or laboratory evidence of past, present or future possible immunodeficiency state which include any laboratory indication of HIV infection
10. History of allergic disease or reactions, including eczema
11. Previous medical history that may compromise safety of the subject in the study
12. Evidence of new acute illness that may compromise the safety of subject in the study
13. Evidence of chronic hepatitis
14. Inability to discontinue daily medications except contraceptives during study period
15. History of alcohol or drug abuse within past 2 years
16. Tobacco or cannabis smoking three or more days per week
17. Positive urine test for illicit drugs
18. History or evidence of any systemic disease on physical examination
19. History or evidence of active tuberculosis
20. Shared a residence within the last year with a individual on anti-tuberculosis treatment or with culture or smear positive tuberculosis
21. All females: Positive urine pregnancy test during screening
22. Abnormal (per local laboratory parameters) chemistry and hematology parameters
23. QuantiFERON®-TB Gold evidence of Mtb infection
24. Received a tuberculin skin test within 3 months (90 days) prior to Study Day 0

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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60 participants in 5 patient groups

Cohort 1 AERAS-404

Experimental group

Description:

H4 Antigen at 5 ug IC31 Adjuvant 500 nmol 2 doses at Study days 0 and 56

Treatment:

Biological: Placebo

Biological: AERAS-404

Cohort 2 AERAS-404

Experimental group

Description:

H4 Antigen at 15 ug IC31 Adjuvant 500 nmol 2 doses at Study days 0 and 56

Treatment:

Biological: Placebo

Biological: AERAS-404

Cohort 3 AERAS-404

Experimental group

Description:

H4 Antigen at 50 ug IC31 Adjuvant 500 nmol 2 doses at Study days 0 and 56

Treatment:

Biological: Placebo

Biological: AERAS-404

Cohort 4 AERAS-404

Experimental group

Description:

H4 Antigen at 150 ug IC31 Adjuvant 500 nmol 2 doses at Study days 0 and 56

Treatment:

Biological: Placebo

Biological: AERAS-404

Cohort 5 AERAS-404

Experimental group

Description:

H4 Antigen at 5 ug or 15 ug IC31 Adjuvant 100 nmol Placebo - sterile buffer 2 doses at Study days 0 and 56

Treatment:

Biological: Placebo

Biological: AERAS-404