A Randomized Double Blind Placebo Controlled Trial of Rifapentine and Isoniazid for Prevention of Tuberculosis in People With Diabetes

Who is this study for? People with diabetes
What treatments are being studied? Isoniazid+Rifapentine
Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Diabetes mellitus (DM) increases susceptibility to Tuberculosis (TB) and worsens TB patient outcomes. The number of patients with combined TB and DM now outnumbers that of combined TB and HIV and it has been estimated that 15-30% of TB disease may be attributable to diabetes globally. This may be expected to rise substantially as DM prevalence increases. Treatment of Latent TB Infection (LTBI) in this population will likely have a significant clinical benefit. Similar to HIV-infected individuals, those with DM might benefit from therapy to prevent the development of TB disease. Current international guidelines do not recommend LTBI management in people with DM, but this is because no studies have examined the risk-benefit ratio of such an intervention. To date, no RCTs have been conducted to investigate the efficacy and safety of preventive treatment of LTBI in DM patients. Based on evidence on effectiveness, safety, and treatment completion rates, 3HP has been selected as the regimen of choice for this study of African people living with DM. People living with DM will be randomized to 3HP or placebo to determine the efficacy of 3HP in the prevention of TB disease in this population. PROTID's preventive treatment of LTBI among people with DM will generate the first solid evidence to support or refute the use of preventive treatment against TB in people with DM.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Enrolled in diabetes care with a history of DM and current use of anti-diabetic medication ('known DM'); OR in the absence of anti-diabetic medication an HbA1c of =6.5% (48 mmol/mol) or a fasting venous plasma glucose of =7.0 mmol (126 mg/dl). For those with no previously known DM a repeat test above the diagnostic cut-point is required to confirm the diagnosis ('new DM')

• Adult (18 years or older)

• Diagnosed with LTBI, defined as a positive IGRA test or TST reactivity =10 mm

• Voluntarily signed Informed Consent Form

• If sexually active, willing to use an effective contraceptive method for the duration of preventive therapy.

Locations
Other Locations
Uganda
Makerere University
RECRUITING
Kampala
Martyrs Hospital Lubaga
RECRUITING
Kampala
United Republic of Tanzania
Mbeya zonal referral hospital
RECRUITING
Mbeya
Kilimanjaro Christian Medical Center
RECRUITING
Moshi
Contact Information
Primary
Issa Sabi, MD, MMed, PhD
isabi@nimr-mmrc.org
+255 25 250 3364
Backup
Nyanda E Ntinginya, MD., MSc., PhD.
nelias@nimr-mmrc.org
+255 25 250 3364
Time Frame
Start Date: 2022-06-17
Estimated Completion Date: 2025-12
Participants
Target number of participants: 3000
Treatments
Experimental: Isoniazid and Rifapentine (INH-RPT)
Participants in intervention arm will receive an oral combination of rifapentine (RPT, 900 mg) and isoniazid (INH, 900 mg), once-weekly for 12 weeks.
Placebo_comparator: Control
Participants in the control arm will receive placebo once weekly for 12 weeks.
Related Therapeutic Areas
Sponsors
Leads: Dr. Nyanda Elias Ntinginya
Collaborators: Makerere University, St George's, University of London, United Kingdom, Uganda Martyrs Hospital Lubaga, Uganda, Kilimanjaro Christian Medical University College (KCMUCo), Tanzania, Otago University, New Zealand, Stichting Katholieke Universiteit- Radboudumc (RUMC), Netherlands, King's College London

This content was sourced from clinicaltrials.gov