Dose-escalation Safety and Immunogenicity Study to Compare MTBVAC to BCG in Newborns With a Safety Arm in Adults (MTBVAC-Ph1b)
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|ClinicalTrials.gov Identifier: NCT02729571|
Recruitment Status : Completed
First Posted : April 6, 2016
Last Update Posted : May 1, 2018
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|Condition or disease||Intervention/treatment||Phase|
|Tuberculosis||Biological: MTBVAC Biological: BCG||Phase 1 Phase 2|
Eighteen (18) adult participants will be recruited and randomized equally into 1 of 2 study groups (n=9 per group): MTBVAC highest dose group (approx. 5x10E05 CFU/0.1mL) or BCG SSI standard human dose (approx. 5x10E05 CFU/0.1mL).
Safety assessments will be conducted at D0, D7, D14, D28, D56, D90, and D180 post study vaccination. A diary card will be used to collect solicited local, regional, and systemic adverse event data from D0 through D14. Reactogenicity data will be collected at each study visit. Non-serious adverse events will be collected through D28. Serious adverse events will be collected during the entire study period.
Thirty-six (36) infant participants will be recruited, randomized and allocated into 4 groups of 9 participants: BCG (single dose level 2.5 x 10E05 CFU/0.05 mL); or MTBVAC at three different dose levels (lowest 2.5x10E03 CFU/0.05mL, middle 2.5x10E04 CFU/0.05mL, highest 2.5x10E05 CFU/0.05mL).
Vaccination of neonates will be staggered by cohorts on a 3 verum : 1 control basis to allow gradual evaluation of safety and reactogenicity, as follows:
Cohort 1: 9 who receive the lowest MTBVAC dose level and 3 BCG control; Cohort 2: 9 who receive the highest MTBVAC dose level and 3 BCG control; Cohort 3: 9 who receive the highest MTBVAC dose level and 3 BCG control.
All AEs and biochemical and haematological parameters (safety data) collected up until Day 28 after vaccination of the last subject of each cohort will be reviewed by DSMB to authorize progression to the next group. Safety assessments will be conducted at D0, D7, D14, D28, D70, D90, D180 and D360 post study vaccination. A diary card will be used to collect solicited local, regional, and systemic adverse event data from D0 through D14. Reactogenicity data will be collected at each study visit. Non-serious adverse events will be collected through D28. Serious adverse events will be collected during the entire study period. Unscheduled follow-up face-to-face visits will be performed as needed for safety and adverse event management.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||54 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Randomized, Double-blind, Dose-escalation Clinical Trial of the Safety, Reactogenicity and Immunogenicity of MTBVAC Compared to BCG Vaccine SSI, in Newborns Living in a Tuberculosis Endemic Region With a Safety Arm in Adults|
|Study Start Date :||September 2015|
|Actual Primary Completion Date :||September 2016|
|Actual Study Completion Date :||March 2018|
Experimental: MTBVAC Group 1
Intervention: MTBVAC live vaccine (low dose)
Live-attenuated tuberculosis vaccine
Experimental: MTBVAC Group 2
Intervention: MTBVAC live vaccine (middle dose)
Live-attenuated tuberculosis vaccine
Experimental: MTBVAC Group 3
Intervention: MTBVAC live vaccine (high dose)
Live-attenuated tuberculosis vaccine
Active Comparator: BCG Control Group
Intervention: commercially available BCG live vaccine
Commercially available live-attenuated tuberculosis vaccine
- Safety and reactogenicity in infants and adults: includes injection site and systemic and regional adverse events, solicited and unsolicited. A diary card will be for solicited local, regional, and systemic adverse event data. [ Time Frame: Six (6) months post-study vaccination ]
- Primary immunogenicity analysis (in infants only): Measure of frequencies and co-expression patterns of CD4 and CD8 T cells expressing specific cytokines in whole blood. [ Time Frame: Six (6) months post-study vaccination ]
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
|Ages Eligible for Study:||1 Day to 50 Years (Child, Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||Yes|
- Male or female, age 18 to 50 years
- Written informed consent, including permission for access to medical records and an HIV test.
- Available for study follow up and display a willingness and capacity to comply to study procedures.
- In good general health, as assessed by medical history and a focused physical examination.
- HIV test (rapid test, ELISA, or PCR) negative
- Quantiferon®-TB Gold (Cellestis) test for latent TB infection negative within 3 weeks of enrolment
- BCG vaccination at birth as confirmed by history or the presence of a BCG scar
- In the case of female participants, a negative urine or serum pregnancy test at enrolment, not lactating, and willingness to use an acceptable method of contraception to avoid pregnancy for the duration of the study
- Male or female neonates within 96 hours of birth.
- Written informed parental consent, including permission to access medical records and results of antenatal HIV tests.
- Infant participants and their caregivers available for study follow-up and display the willingness and capacity to comply with study procedures.
- Neonates must be in good general health as assessed by antenatal history, delivery records, and focused physical examination.
- Birth weight more than or equal to 2500 grams.
- Apgar score at 5 minutes more than or equal to 7.
- A maternal HIV test result (rapid test, ELISA or PCR) taken during pregnancy must be available, documented and negative.
- Estimated gestational age more than or equal to 38 weeks
Adult stage Exclusion criteria
- A history or evidence of an acute or chronic medical or surgical condition likely to affect the safety, reactogenicity, or immunogenicity of the investigational vaccine
- Skin condition, bruising or birth mark at the intended injection site.
- History or evidence of previous or current active TB disease
- History of a household contact with active TB disease who has received less than 2 months treatment
Infant Stage Exclusion criteria:
- Infant must not have received routine BCG vaccination prior to enrolment.
- Antenatal, intrapartum, or postnatal medical or surgical condition that may affect the safety, reactogenicity, or immunogenicity of the investigational vaccine.
- Maternal HIV test (rapid test, ELISA or PCR) not performed antenatally, HIV test results not available, or HIV test result known positive.
- Maternal or other household contact with newly diagnosed or incompletely treated active TB disease.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02729571
|South African Tuberculosis Vaccine Initiative, Brewelskloof Hospital|
|Worcester, Western Cape, South Africa, 6850|
|Principal Investigator:||Michele Tameris, MD||South African Tuberculosis Vaccine Initiative|
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
|Responsible Party:||Biofabri, S.L|
|Other Study ID Numbers:||
|First Posted:||April 6, 2016 Key Record Dates|
|Last Update Posted:||May 1, 2018|
|Last Verified:||April 2018|
|Individual Participant Data (IPD) Sharing Statement:|
|Plan to Share IPD:||Undecided|
Gram-Positive Bacterial Infections
Bacterial Infections and Mycoses