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BCG SSI

Phase 1

Tuberculosis | Monoclonal antibody | Infectious Disease |Sanofi|Last Updated: Jan 24, 2017

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
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Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
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Trial Design
RandomizedDouble-BlindPLACEBO_CONTROLLEDBiomarker
Total Trials1
Total Enrollment70
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT02420444A Study for Safety and Immunogenicity of BCG and AERAS-404 in HIV-Negative, TB-Negative, BCG-Naive AdultsPHASE1 COMPLETED 70Jan 1, 2011Nov 1, 2013Jan 24, 20171 Switzerland
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Study Endpoints
Primary Endpoints
Number of unsolicited, solicited, and serious adverse events (SAEs).
259 days

Includes injection site AEs and systemic AEs.

Secondary Endpoints
Immunogenicity of BCG and a 2- or 3-dose regimen of AERAS-404 measured by intracellular staining assay (ICS).
259 Days
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Study Design & Arms
AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposePREVENTION
Treatment Arms
ArmTypeDescription
BCG SSI prime with PlaceboPLACEBO_COMPARATORAll subjects received BCG Vaccine SSI, 2-8 x 10\^5 CFU (BCG) on Study Day -42. Placebo containing 0,8 mL sterile buffer consisting of 10 mmol Tris and 169 mmol NaCl aqueous solution was administered on Study Days 0, 56, and 231.
BCG SSI prime with Placebo and AERAS-404EXPERIMENTALAll subjects received BCG Vaccine SSI, 2-8 x 10\^5 CFU (BCG) on Study Day -42. Placebo on Study Day 0 followed by AERAS-404 50/500 on Study Days 56 and 231. AERAS-404 50/500 was a fixed dose combination of H4 50 mcg and IC31 500 nmol (KLK equivalent). H4 and IC31 adjuvant were supplied as separate single-dose vials containing frozen product as follows: * H4 antigen: 500 mcg/mL (100 mcg/0.2 mL), in 10 mmol/L Tris-HCl, pH 8.3. * IC31 adjuvant: 1250 nmol/mL (1000 nmol/0.8 mL) KLK equivalent, in 10 mmol/L Tris-HCl and 169 mmol/L NaCl.
BCG SSI prime with AERAS-404EXPERIMENTALAll subjects received BCG Vaccine SSI, 2-8 x 10\^5 CFU (BCG) on Study Day -42. AERAS-404 50/500 on Study Days 0, 56, and 231. AERAS-404 50/500 was a fixed dose combination of H4 50 mcg and IC31 500 nmol (KLK equivalent). H4 and IC31 adjuvant were supplied as separate single-dose vials containing frozen product as follows: * H4 antigen: 500 mcg/mL (100 mcg/0.2 mL), in 10 mmol/L Tris-HCl, pH 8.3. * IC31 adjuvant: 1250 nmol/mL (1000 nmol/0.8 mL) KLK equivalent, in 10 mmol/L Tris-HCl and 169 mmol/L NaCl.
Interventions
NameTypeDescription
BCG SSIBIOLOGICALThe dose volume administered for BCG was 0.1 mL, and the mode of administration was ID injection to the deltoid area.
PlaceboBIOLOGICALThis is the identical buffer solution in which H4:IC31 was formulated. The dose volume administered for Placebo was 0.5mL, and the mode of administration was an IM injection.
AERAS-404BIOLOGICALAERAS-404 vaccine was reconstituted on site by adding 0.2 mL H4 antigen solution to 0.8 mL IC31 adjuvant solution. The dose volume administered for AERAS-404 was 0.5mL, and the mode of administration was an IM injection.
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Eligibility Criteria
Age Range18 Years — 50 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: 1. Had completed the written informed consent process. 2. Was male or female. 3. Was age ≥ 18 years and ≤ 50 years. 4. Agreed to stay in contact with the study site for the duration of the study, provide updated contact information as necessary, and had no current plans to move ...

Countries:Switzerland
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