Covid19 Clinical Trial
Official title:
Repeat BCG Vaccinations for the Treatment of Established Type 1 Diabetes
Verified date | May 2024 |
Source | Massachusetts General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to see if repeat bacillus Calmette-Guérin (BCG) vaccinations can confer a beneficial immune and metabolic effect on Type 1 diabetes. Published Phase I data on repeat BCG vaccinations in long term diabetics showed specific death of some of the disease causing bad white blood cells and also showed a short and small pancreas effect of restored insulin secretion. In this Phase II study, the investigators will attempt to vaccinate more frequently to see if these desirable effects can be more sustained. Eligible volunteers will either be vaccinated with BCG in a repeat fashion over a period of four years, or receive a placebo treatment. The investigators hypothesize that each BCG vaccination will eliminate more and more of the disease causing white blood cells that could offer relief to the pancreas for increased survival and restoration of insulin secretion from the pancreas. An additional adaptive trial for COVID-19 is also being conducted on these randomized double blinded type 1 diabetic subjects receiving BCG or placebo injections. An expanded study arm has been approved for repeat dosing of BCG in adult Type I diabetes.
Status | Active, not recruiting |
Enrollment | 150 |
Est. completion date | July 2031 |
Est. primary completion date | July 2029 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Type 1 diabetes treated continuously with insulin from time of diagnosis - Age 18-65 - HIV antibody negative - Normal CBC - HCG negative (females) - Anti-GAD Positive (except for subjects with c-peptide <10pmol/L) - Fasting or stimulated c-peptide between 5-200 pmol/L - Participation in protocol #2001P001379, "Autoimmunity: In Vitro Pathogenesis and Early Detection" Exclusion Criteria: - History of chronic infectious disease such as HIV or hepatitis - History of tuberculosis, TB risk factors, positive interferon-gamma release assay (IGRA, also known as the T-SPOT.TB test), or BCG vaccination - Current treatment with glucocorticoids (other than intermittent nasal or eye steroids), or disease or condition likely to require steroid therapy - Other conditions or treatments associated with increased risk of infections such as patients with a previous history of severe burns, or treatment with immunosuppressive medications of any type (e.g. imuran, methotrexate, cyclosporine, etanercept, infliximab) for any reason - Current treatment with aspirin > 160 mg/day or chronic, daily NSAIDs - Current treatment with antibiotics - History of keloid formation - Average HbA1c over the past 5 years (or since diagnosis if duration is less than 5 years) <6.5 or > 8.5% - History or evidence of chronic kidney disease (serum creatinine > 1.5mg/dL) - History of proliferative diabetic retinopathy that has not been treated with laser therapy - History of neuropathy, foot ulcers, amputations, or kidney disease - Pregnant or not using acceptable birth control - Living with someone who is immunosuppressed and/or at high risk for infectious diseases (for example HIV+ or taking immunosuppressive medications for any reason) |
Country | Name | City | State |
---|---|---|---|
United States | Immunobiology Labs CNY 149 | Charlestown | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Exploratory: A Change in the above primary and secondary endpoints with Latent Autoimmune diabetes of adults (LADA; [a.k.a. Type 1.5 diabetes]; AOO>21 years) | A change in values as compared to self for participants with AOO>21 years of age. | 4 weeks and 1, 2, 3, 4, and 5 years after initial BCG/placebo injection | |
Other | COVID-19 and BCG Adaptive Study: Number of Type 1 Diabetics with COVID-19 symptomatic infections | Number of symptomatic COVID-19 infections determined through PCR and antibody testing and symptoms collected through surveys and visits. | 15 months beginning January 2020 | |
Other | COVID-19 and BCG Adaptive Study: Impact of COVID-19 (severity, duration of symptoms, absence from work) | A different severity of symptoms, duration of symptoms or absence from work for COVID-19 positive patients in the BCG or Placebo group. | 15 months beginning January 2020 | |
Other | COVID-19 and BCG Adaptive Study: Reported Rates of Infectious Diseases | Rate of reported infectious disease adverse events categorized through MedDRA codes between the BCG and Placebo groups. | 15 months beginning January 2020 | |
Primary | Change in HbA1c values in juvenile onset type 1 diabetics | A change in the hemoglobin A1c (HbA1c) measurement compared to self | 1, 2, 3, 4, and 5 years after initial BCG/placebo injection | |
Secondary | Insulin use in juvenile onset type 1 diabetics (AOO<21 years) | A change in insulin (IDAA1c) use as reported at study visits compared to self in juvenile onset type 1 diabetes. | 4 weeks and 1, 2, 3, 4, and 5 years after initial BCG/placebo injection | |
Secondary | Endogenous insulin levels in the blood in juvenile onset type 1 diabetics (AOO<21 years) | A change in c-peptide and proinsulin levels (as an analog for endogenous insulin) in the blood compared to self. | 4 weeks and 1, 2, 3, 4, and 5 years after initial BCG/placebo injection | |
Secondary | Autoimmunity in juvenile onset type 1 diabetes (AOO<21 years) | A change in autoantibodies and autoreactive T cells to monitor the drug mechanism for autoimmune changes. | 4 weeks and 1, 2, 3, 4, and 5 years after initial BCG/placebo injection |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05047692 -
Safety and Immunogenicity Study of AdCLD-CoV19-1: A COVID-19 Preventive Vaccine in Healthy Volunteers
|
Phase 1 | |
Recruiting |
NCT04395768 -
International ALLIANCE Study of Therapies to Prevent Progression of COVID-19
|
Phase 2 | |
Terminated |
NCT04555096 -
A Trial of GC4419 in Patients With Critical Illness Due to COVID-19
|
Phase 2 | |
Completed |
NCT04508777 -
COVID SAFE: COVID-19 Screening Assessment for Exposure
|
||
Completed |
NCT04506268 -
COVID-19 SAFE Enrollment
|
N/A | |
Completed |
NCT04961541 -
Evaluation of the Safety and Immunogenicity of Influenza and COVID-19 Combination Vaccine
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT04546737 -
Study of Morphological, Spectral and Metabolic Manifestations of Neurological Complications in Covid-19 Patients
|
N/A | |
Completed |
NCT04494646 -
BARCONA: A Study of Effects of Bardoxolone Methyl in Participants With SARS-Corona Virus-2 (COVID-19)
|
Phase 2 | |
Terminated |
NCT04542993 -
Can SARS-CoV-2 Viral Load and COVID-19 Disease Severity be Reduced by Resveratrol-assisted Zinc Therapy
|
Phase 2 | |
Completed |
NCT04532294 -
Safety, Tolerability, Pharmacokinetics, and Immunogenicity of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2/COVID-19) Neutralizing Antibody in Healthy Participants
|
Phase 1 | |
Terminated |
NCT04581915 -
PHRU CoV01 A Trial of Triazavirin (TZV) for the Treatment of Mild-moderate COVID-19
|
Phase 2/Phase 3 | |
Not yet recruiting |
NCT04543006 -
Persistence of Neutralizing Antibodies 6 and 12 Months After a Covid-19
|
N/A | |
Completed |
NCT04387292 -
Ocular Sequelae of Patients Hospitalized for Respiratory Failure During the COVID-19 Epidemic
|
N/A | |
Completed |
NCT04507867 -
Effect of a NSS to Reduce Complications in Patients With Covid-19 and Comorbidities in Stage III
|
N/A | |
Completed |
NCT04537663 -
Prevention Of Respiratory Tract Infection And Covid-19 Through BCG Vaccination In Vulnerable Older Adults
|
Phase 4 | |
Not yet recruiting |
NCT04527211 -
Effectiveness and Safety of Ivermectin for the Prevention of Covid-19 Infection in Colombian Health Personnel
|
Phase 3 | |
Completed |
NCT04979858 -
Reducing Spread of COVID-19 in a University Community Setting: Role of a Low-Cost Reusable Form-Fitting Fabric Mask
|
N/A | |
Not yet recruiting |
NCT05038449 -
Study to Evaluate the Efficacy and Safety of Colchicine Tablets in Patients With COVID-19
|
N/A | |
Completed |
NCT04610502 -
Efficacy and Safety of Two Hyperimmune Equine Anti Sars-CoV-2 Serum in COVID-19 Patients
|
Phase 2 | |
Active, not recruiting |
NCT06042855 -
ACTIV-6: COVID-19 Study of Repurposed Medications - Arm G (Metformin)
|
Phase 3 |