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

NCT ID: NCT01599897

Last Updated: 2017-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-08-31

Study Completion Date

2014-05-31

Brief Summary

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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.

Detailed Description

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Conditions

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Pulmonary Tuberculosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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2 µg ID93 + 2 µg GLA-SE

Low dose and antigen and low dose of adjuvant.

Group Type EXPERIMENTAL

ID93 + GLA-SE

Intervention Type BIOLOGICAL

ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.

10 µg ID93 + 2 µg GLA-SE

High dose of antigen and low dose of adjuvant.

Group Type EXPERIMENTAL

ID93 + GLA-SE

Intervention Type BIOLOGICAL

ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.

2 µg ID93 + 5 µg GLA-SE

Low dose of antigen and high dose of adjuvant.

Group Type EXPERIMENTAL

ID93 + GLA-SE

Intervention Type BIOLOGICAL

ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.

10 µg ID93 + 5 µg GLA-SE

High dose of antigen and high dose of adjuvant.

Group Type EXPERIMENTAL

ID93 + GLA-SE

Intervention Type BIOLOGICAL

ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.

2 µg ID93 alone

Low dose of antigen alone.

Group Type ACTIVE_COMPARATOR

ID93 alone

Intervention Type BIOLOGICAL

ID93 antigen alone. 3 injections and Days 0, 28, and 56.

10 µg ID93 alone

High dose of antigen alone.

Group Type ACTIVE_COMPARATOR

ID93 alone

Intervention Type BIOLOGICAL

ID93 antigen alone. 3 injections and Days 0, 28, and 56.

Interventions

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ID93 + GLA-SE

ID93 antigen and GLA-SE adjuvant. 3 injections at Days 0, 28, and 56.

Intervention Type BIOLOGICAL

ID93 alone

ID93 antigen alone. 3 injections and Days 0, 28, and 56.

Intervention Type BIOLOGICAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Aeras

OTHER

Sponsor Role collaborator

Paul G. Allen Family Foundation

OTHER

Sponsor Role collaborator

Access to Advanced Health Institute (AAHI)

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Franco Piazza, MD, MPH

Role: STUDY_DIRECTOR

Access to Advanced Health Institute (AAHI)

Anna Marie Beckmann, PhD

Role: STUDY_DIRECTOR

Access to Advanced Health Institute (AAHI)

Locations

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Johnson County Clin-Trials

Lenexa, Kansas, United States

Site Status

Countries

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United States

References

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Coler RN, Day TA, Ellis R, Piazza FM, Beckmann AM, Vergara J, Rolf T, Lu L, Alter G, Hokey D, Jayashankar L, Walker R, Snowden MA, Evans T, Ginsberg A, Reed SG; TBVPX-113 Study Team. The TLR-4 agonist adjuvant, GLA-SE, improves magnitude and quality of immune responses elicited by the ID93 tuberculosis vaccine: first-in-human trial. NPJ Vaccines. 2018 Sep 4;3:34. doi: 10.1038/s41541-018-0057-5. eCollection 2018.

Reference Type DERIVED
PMID: 30210819 (View on PubMed)

Other Identifiers

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IDRI-TBVPX-113

Identifier Type: -

Identifier Source: org_study_id