A Phase 1 interventional study of GLA-AF and Hepatitis B Virus Vaccine (Recombinant) in Schistosomiasis, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Completed at 1 site in Brazil. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-02-02.
Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Phase 1, Interventional, and Prevention
The study will be conducted as a randomized, controlled, double blind Phase 1b dose-escalating clinical trial in up to 60 healthy adult males and non-pregnant females living in the S. mansoni-endemic area of Americaninhas, Brazil. The primary objective of this trial is to assess the safety and reactogenicity of ascending doses of Sm-TSP-2/Alhydrogel(R) (10mcg, 30mcg, or 100mcg) vaccine with or without AP 10-701 given as three doses administered on Days 1, 57, and 113.
The study will be conducted as a randomized, controlled, double blind Phase 1b dose-escalating clinical trial in up to 60 healthy adult males and non-pregnant females living in the S. mansoni-endemic area of Americaninhas, Brazil. The study will recruit up to 60 healthy adult males and non-pregnant females to test two formulations of Sm-TSP-2 vaccine (adjuvanted with Alhydrogel(R) only, or with Alhydrogel(R) plus AP 10-701), each at 3 different doses of antigen: 10mcg, 30mcg, and 100mcg. The study will use a dose-escalation cohort design, in which escalation to the next dose cohort will be determined based on evaluation of pre-defined escalation criteria requiring 7 day safety data to be examined after all subjects in the current cohort have received their first dose of vaccine. Cohorts will be enrolled sequentially. For each Cohort (1-3), an initial 5 subjects (2 Sm-TSP-2/Alhydrogel(R), 2 Sm-TSP-2/Alhydrogel(R)/AP 10-701, and 1 Euvax B Hepatitis B vaccine) will be enrolled, randomized, vaccinated, and have completed Visit 02 (Day 2), before enrolling the rest of the cohort. As with dose-escalation decisions, evidence of significant reactogenicity will require further review prior to proceeding. The primary objective of this trial is to assess the safety and reactogenicity of ascending doses of Sm-TSP-2/Alhydrogel(R) (10mcg, 30mcg, or 100mcg) vaccine with or without AP 10-701 given as three doses administered on Days 1, 57, and 113. The secondary objectives used to evaluate the immunogenicity are: (1) to assess the IgG antibody response to Sm-TSP-2 using an indirect enzyme-linked immunosorbent assay (ELISA) at Day 127, (2) to assess the IgG antibody response to Sm-TSP-2 using an indirect ELISA at 14 days after dose one and two and Days 203, 293, and 478 (3, 6, and 12 months after the third dose) of Sm-TSP-2/Alhydrogel(R) (10mcg, 30mcg, or 100mcg) with or without AP 10-701, and (3) to assess the duration of the IgG antibody response to Sm-TSP-2 using an indirect ELISA following receipt of three doses of Sm-TSP-2/Alhydrogel(R) (10mcg, 30mcg, or 100mcg) with or without AP 10-701.
Are in good health, as determined by vital signs (oral temperature, pulse, and blood pressure), medical history, and brief physical examination at screening.
-Existing medical diagnoses or conditions (except those in the Subject Exclusion Criteria) must be deemed as stable chronic medical conditions. A stable chronic medical condition is defined as no change in prescription medication, dose, or frequency of medication in the last 3 months (90 days) and health outcomes of the specific disease are considered to be within acceptable limits in the last 6 months (180 days). Any change due to change of health care provider, or that is done for financial reasons, as long as in the same class of medication, will not be considered a violation of this inclusion criterion. Any change in prescription medication due to improvement of a disease outcome, as determined by the site principal investigator or appropriate sub-investigator, will not be considered a violation of this inclusion criterion. Subjects may be on chronic or as needed medications if, in the opinion of the site principal investigator or appropriate sub-investigator, they pose no additional risk to subject safety or assessment of reactogenicity and immunogenicity. Topical, nasal, and inhaled medications (with the exception of corticosteroids as outlined in the Subjects Exclusion Criteria), vitamins, and contraceptives are permitted.
Vital signs (oral temperature, pulse, and blood pressure) are all within normal protocol-defined ranges.
-The normal protocol-defined ranges for vital signs include (a) oral temperature less than 38.0 degrees celsius, (b) pulse 50 to 100 bpm, inclusive, (c) systolic blood pressure 85 to 150 mmHg, inclusive, and (d) diastolic blood pressure 55 to 90 mmHg, inclusive. Pulse rate \<50 is acceptable for 2nd and 3rd vaccinations if the subject is otherwise healthy with documented sinus bradycardia at baseline.
Laboratory tests (alanine aminotransferase, creatinine, white blood cell count, hemoglobin, and platelets) are all within protocol-defined reference ranges.
-The protocol-defined ranges for laboratory tests include (a) alanine aminotransferase (ALT) of less than 1.25-times the upper reference limit, (b) creatinine less than 1.25 times the upper reference limit (c) white blood cells (WBC) between 3.3 x10\^3/uL and 10.4 x10\^3/uL, inclusive, (d) hemoglobin 11.4 g/dL or greater for females or 12.1 g/dL or greater for males, (e) platelets greater than 130 x10\^3/uL. Laboratory test results for 2nd and 3rd vaccinations may be at Grade 1 if considered unrelated to study product.
Female subjects of childbearing potential must agree to practice highly effective contraception for a minimum of 30 days prior to study product exposure and for 30 days after last vaccination.
Exclusion Criteria:
Is immunosuppressed as a result of an underlying illness or treatment.
-Causes for immunosuppression may include, but are not limited to, poorly-controlled diabetes mellitus, cirrhosis, renal insufficiency, active neoplastic disease or a history of any hematologic malignancy, connective tissue disease, organ transplant.
Has an acute or chronic medical condition that, in the opinion of the investigator, would render participation in this study unsafe or would interfere with the evaluation of responses.
-This includes, but is not limited to: known liver disease, renal disease, neurological disorders, visual field defects, cardiac disorders, pulmonary disorders, diabetes mellitus, and transplant recipients.
Is participating or plans to participate in another clinical trial with an interventional agent during the duration of the study.
-This may include other licensed or unlicensed vaccines, drugs, biologics, devices, blood products, or medications.
10mcg Sm-TSP-2/Alhydrogel® (n=8)
Biological: Sm-TSP-2/Alhydrogel
10mcg Sm-TSP-2/Alhydrogel®/+ AP 10-701 (n=8)
Biological: GLA-AF · Biological: Sm-TSP-2/Alhydrogel
30mcg Sm-TSP-2/Alhydrogel® (n=8)
Biological: Sm-TSP-2/Alhydrogel
30mcg Sm-TSP-2/Alhydrogel®/+ AP 10-701 (n=8)
Biological: GLA-AF · Biological: Sm-TSP-2/Alhydrogel
100mcg Sm-TSP-2/Alhydrogel® (n=8)
Biological: Sm-TSP-2/Alhydrogel
100mcg Sm-TSP-2/Alhydrogel®/+ AP 10-701 (n=8)
Biological: GLA-AF · Biological: Sm-TSP-2/Alhydrogel
Euvax B Hepatitis B vaccine (n=12)
Biological: Hepatitis B Virus Vaccine (Recombinant)
Previously referred to as Gluco-pyranosylphospho-lipid A aqueous formulation (GLA-AF). It is a toll-like receptor-4 agonist
A non-infectious subunit viral vaccine derived from hepatitis B surface antigen (HBsAg) produced in yeast cells.
Sm-TSP-2/Alhydrogel
The occurrence of new-onset chronic medical conditions (including AESI)
Time frame: From Day 1 to Day 478
The occurrence of solicited injection site reactogenicity
Time frame: From Day 1 to Day 7
The occurrence of solicited injection site reactogenicity
Time frame: From Day 113 to Day 120
The occurrence of solicited injection site reactogenicity
Time frame: From Day 57 to Day 64
The occurrence of solicited systemic reactogenicity
Time frame: From Day 1 to Day 7
The occurrence of solicited systemic reactogenicity
Time frame: From Day 113 to Day 120
The occurrence of solicited systemic reactogenicity
Time frame: From Day 57 to Day 64
The occurrence of study vaccine-related SAEs
Time frame: From Day 1 to Day 478
The occurrence of vaccine-related clinical safety laboratory adverse events
Time frame: Day 113
The occurrence of vaccine-related clinical safety laboratory adverse events
Time frame: Day 120
The occurrence of vaccine-related clinical safety laboratory adverse events
Time frame: Day 57
The occurrence of vaccine-related clinical safety laboratory adverse events
Time frame: Day 64
The occurrence of vaccine-related clinical safety laboratory adverse events
Time frame: Day 8
The anti-Sm-TSP-2 IgG antibody response using an indirect ELISA
Time frame: Day 15
The anti-Sm-TSP-2 IgG antibody response using an indirect ELISA
Time frame: Day 203
The anti-Sm-TSP-2 IgG antibody response using an indirect ELISA
Time frame: Day 293
The anti-Sm-TSP-2 IgG antibody response using an indirect ELISA
Time frame: Day 478
The anti-Sm-TSP-2 IgG antibody response using an indirect ELISA
Time frame: Day 71
The anti-Sm-TSP-2 IgG level using an indirect ELISA
Time frame: Day 127
This study is completed, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.
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National Institute of Allergy and Infectious Diseases (NIAID)