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Phase 1 ID93 + GLA-SE Vaccine Trial in Healthy Adult Volunteers

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ClinicalTrials.gov Identifier: NCT01599897
Recruitment Status : Completed
First Posted : May 16, 2012
Last Update Posted : September 15, 2017
Sponsor:
Collaborators:
Information provided by (Responsible Party):

Study Description
Brief Summary:
The purpose of this study is to determine the safety, tolerability, and immunogenicity in healthy adult subjects of an investigational vaccine being developed for the prevention of pulmonary tuberculosis. The vaccine, identified as ID93 + GLA-SE, consists of the recombinant four-antigen Mycobacterium tuberculosis recombinant protein ID93 together with the adjuvant GLA-SE.

Condition or disease Intervention/treatment Phase
Pulmonary Tuberculosis Biological: ID93 + GLA-SE Biological: ID93 alone Phase 1

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 60 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: A Phase 1, Randomized, Dose-escalation Study to Evaluate the Safety and Immunogenicity of the ID93 + GLA-SE Vaccine at Two Dose Levels of the ID93 Antigen and the GLA-SE Adjuvant in Healthy Adults
Study Start Date : August 2012
Primary Completion Date : May 2014
Study Completion Date : May 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Tuberculosis
U.S. FDA Resources

Arms and Interventions

Arm Intervention/treatment
Experimental: 2 µg ID93 + 2 µg GLA-SE
Low dose and antigen and low dose of adjuvant.
Biological: ID93 + GLA-SE
ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.
Experimental: 10 µg ID93 + 2 µg GLA-SE
High dose of antigen and low dose of adjuvant.
Biological: ID93 + GLA-SE
ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.
Experimental: 2 µg ID93 + 5 µg GLA-SE
Low dose of antigen and high dose of adjuvant.
Biological: ID93 + GLA-SE
ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.
Experimental: 10 µg ID93 + 5 µg GLA-SE
High dose of antigen and high dose of adjuvant.
Biological: ID93 + GLA-SE
ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.
Active Comparator: 2 µg ID93 alone
Low dose of antigen alone.
Biological: ID93 alone
ID93 antigen alone. 3 injections and Days 0, 28, and 56.
Active Comparator: 10 µg ID93 alone
High dose of antigen alone.
Biological: ID93 alone
ID93 antigen alone. 3 injections and Days 0, 28, and 56.


Outcome Measures

Primary Outcome Measures :
  1. Number of patients experiencing adverse events. [ Time Frame: 420 days ]
    To evaluate the safety and tolerability of 2 or 10 μg of ID93 together with 2 or 5 μg of GLA-SE compared to 2 or 10 µg of ID93 alone following intramuscular administration on Days 0, 28, and 56. The safety assessments will be based on local and systemic reactions, including reported adverse events, changes in laboratory values, and changes in vital signs. The severity and relationship to treatment will be recorded for all adverse events.


Secondary Outcome Measures :
  1. Immunogenicity [ Time Frame: Days 0, 1, 3, 7, 14, 28, 42, 56, 70, 84, 238 ]
    To assess the immunogenicity of ID93 + GLA-SE compared to ID93 alone by evaluating IgG antibody and T-cell responses to ID93 at specified timepoints.


Eligibility Criteria

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Has completed the written informed consent process prior to start of screening evaluations
  • Male or female who is 18 to 45 years of age at the time of randomization
  • Agrees to stay in contact with the study site for the duration of the study, provide updated contact information as necessary, and has no current plans to move from the study area for the duration of the study
  • Agrees to avoid elective surgery for the full duration of the study
  • For female subjects: agrees to avoid pregnancy through Study Day 238. Women physically capable of pregnancy (not sterilized and still menstruating or within 1 year of the last menses if menopausal) in sexual relationships with men must use an acceptable method of avoiding pregnancy during this period. Acceptable methods of avoiding pregnancy include a sterile sexual partner, sexual abstinence (not engaging in sexual intercourse), hormonal contraceptives (oral, injection, transdermal patch, or implant), vaginal ring, intrauterine device (IUD), condoms or the combination of diaphragm with spermicide
  • Has body mass index (BMI) between 19 and 33 (weight/height2) by nomogram at the time of randomization

Exclusion Criteria:

  • Acute illness at the time of randomization
  • Oral temperature greater than 37.5C (99.5F) at the time of randomization
  • Values for any of the following screening laboratory parameters, from blood collected within 15 days prior to randomization, outside the normal ranges per local laboratory parameters: hemoglobin, hematocrit, absolute neutrophil count, absolute lymphocyte count, white blood cell count, electrolytes, ALT, AST, total bilirubin, alkaline phosphatase (ALP), creatinine, BUN, and lipid profile
  • Evidence of systemic or local disease process on screening urinalysis
  • Evidence of significant active infection
  • Positive laboratory test (e.g., QuantiFERON(R)-TB) evidence of Mtb infection at screening
  • History of treatment for active or latent tuberculosis infection
  • History or evidence of active tuberculosis
  • Has received vaccination or immunotherapy with a BCG product at any time prior to randomization
  • Shared a residence within the last year prior to randomization with an individual on anti-tuberculosis treatment or with culture or smear positive tuberculosis
  • History of or evidence of current hypertension
  • History of autoimmune disease or immunosuppression
  • Used immunosuppressive medication within 42 days before randomization (inhaled and topical corticosteroids are permitted)
  • Received immunoglobulin or blood products within 42 days before randomization
  • Received any investigational drug therapy or investigational vaccine within 182 days before randomization, or planned participation in any other investigational study during the study period
  • Received investigational Mtb vaccine at any time prior to randomization
  • Unable to discontinue current chronic prescription drug therapy including hormone replacement such as thyroxin, insulin, and medications that can be hepatotoxic or toxic to the bone marrow (such as statins) etc (estrogen and progesterone replacement and contraceptives, topical medications, and nasal steroids are acceptable)
  • History or laboratory evidence of immunodeficiency state including but not limited to laboratory indication of HIV 1 infection at screening
  • History of allergic disease or reactions (such as an allergic reaction to eggs), including eczema, likely to be exacerbated by any component of the study vaccine
  • History of allergic reaction to kanamycin-related antibiotics
  • Previous medical history that may compromise the safety of the subject in the study, including but not limited to: severe impairment of pulmonary function from tuberculosis infection or other pulmonary disease; chronic illness with signs of cardiac or renal failure; suspected progressive neurological disease; or uncontrolled epilepsy or infantile spasms
  • History of positive tuberculin skin test
  • Evidence of chronic hepatitis (e.g., hepatitis B core antibody or hepatitis C antibody) at screening
  • History of alcohol or drug abuse within the past 2 years or consumes more than 1 (women) or 2 (men) alcoholic beverage(s) per day
  • Tobacco or cannabis smoking 3 or more days per week
  • History of keloid formation
  • Positive urine test for illicit drugs (opiates, cocaine, amphetamines) at screening
  • History or evidence on physical examination of any systemic disease or any acute or chronic illness that, in the opinion of the investigator, may interfere with the evaluation of the safety or immunogenicity of the vaccine, including axillary lymphadenopathy
  • All female subjects: currently pregnant or lactating/nursing; or positive urine pregnancy test during screening or positive urine pregnancy test on the day of study injection
  • Received a tuberculin skin test within 3 months (90 days) prior to the time of randomization
  • Any current medical, psychiatric, occupational, or substance abuse problems that, in the opinion of the investigator, will make it unlikely that the subject will comply with the protocol
Contacts and Locations

Information from the National Library of Medicine

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): NCT01599897


Locations
United States, Kansas
Johnson County Clin-Trials
Lenexa, Kansas, United States, 66219
Sponsors and Collaborators
IDRI
Aeras
Paul G. Allen Family Foundation
Investigators
Study Director: Franco Piazza, MD, MPH IDRI
Study Director: Anna Marie Beckmann, PhD IDRI
More Information

Responsible Party: IDRI
ClinicalTrials.gov Identifier: NCT01599897     History of Changes
Other Study ID Numbers: IDRI-TBVPX-113
First Posted: May 16, 2012    Key Record Dates
Last Update Posted: September 15, 2017
Last Verified: September 2017

Keywords provided by IDRI:
Tuberculosis
TB
Pulmonary
Vaccine

Additional relevant MeSH terms:
Tuberculosis
Tuberculosis, Pulmonary
Mycobacterium Infections
Actinomycetales Infections
Gram-Positive Bacterial Infections
Bacterial Infections
Lung Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Vaccines
Immunologic Factors
Physiological Effects of Drugs