Isoniazid Plus Antiretroviral Therapy to Prevent Tuberculosis in HIV-infected Persons

HIV Infections Clinical Trial

— HAART-IPT  

Official title:

A Randomized-controlled Trial of Isoniazid Plus Highly Active Antiretroviral Therapy Against Placebo to Prevent Tuberculosis in HIV-infected Persons

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00463086
• Other study ID #: HAARTIPT07
• Status: Completed
• Phase: N/A
• First received: April 19, 2007
• Last updated: July 16, 2012
• Start date: November 2007
• Est. completion date: November 2011

Study information

• Verified date: July 2012
• Source: University of Cape Town
• Contact: n/a
• Is FDA regulated: No
• Health authority: South Africa: Medicines Control Council
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate whether isoniazid can safely (and further) reduce the risk of tuberculosis in HIV infected people receiving HAART.

Description:

The incidence of Tuberculosis (TB) in poor settlements around Cape Town continues to rise despite highly-active-anti-retroviral therapy (HAART) roll-out and DOTS. In Khayelitsha district, where this project will be conducted, TB incidence is about 1600/100000. There is an equally high HIV prevalence, currently 33%. Over 50% of adults presenting with active TB are co-infected with HIV and a third of all patients starting HAART have active TB. Although HAART has been shown to reduce the overall risk of TB by 59-80%, this risk still far exceeds the general risk. In the Khayelitsha HAART cohort, the risk of developing TB whilst on HAART is ~12 per 100 p-y. In the nearby community of Gugulethu, there is a 14% risk of active TB with at least half of the cases occurring within the first 3months on HAART. In a region where RD1-detected prevalence of latent TB infection is at least 80%, there is a real concern that TB will likely undo the benefit of HAART in the long run. Additional measures are therefore required to reduce the risk of TB in those already receiving or starting HAART. Isoniazid preventive therapy (IPT) represents an option but there is insufficient evidence to determine whether IPT can further (and safely) reduce the risk of TB in the HAART era. In a RCT, we propose to evaluate whether IPT can reduce the risk of active TB in patients receiving HAART.

A total minimum sample size of 1204 is required for the study to detect a 35% reduction in the hazard rates for tuberculosis in the intervention group (h1= 0.052) compared to the control group (h0=0.085) at a power of 80% and a Type II error of 0.05. Our maximum targeted sample size when losses to follow-up and subgroup analyses are considered is 1445. Development of TB will be the primary endpoint.

Additional information (on 10 August 2010):

Recruitment and enrolment into the study was completed in October 2009. We have screened over 2000 patients already on ART and those newly starting ART. However, instead of enrolling our desired maximum sample size of 1445, a revised minimum total of 1368 were instead randomized to the study drug. This followed an amendment to the sample size necessitated by new information on the clinical site; primarily higher rates of patients lost to follow-up at the clinical site than previously anticipated. The amendment to our sample size was reported to, and acknowledged by, the Research Ethics Committee of the University of Cape Town. Follow-up of participants will continue until Oct/November 2011.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1368
• Est. completion date: November 2011
• Est. primary completion date: November 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male and female attendees (age =18yo) of the Ubuntu HIV and ARV Clinic identified as eligible for the ARV programme will be invited to participate.

2. Willingness to participate

3. Able to engage in informed consent procedures

Exclusion Criteria:

1. Evidence of active TB or suspicion of active TB as determined by a symptoms screening algorithm.

2. Current TB chemotherapy ( TB treatment completed in the preceding 30 days will not be an exclusion)

3. Current or previous treatment of latent TB infection since HIV infection (any duration)

4. Current treatment with fluoroquinolones or other antibiotics with significant anti-tuberculous activity currently being used to treat TB in South Africa

5. Past reaction/intolerance to INH.

6. Acute hepatitis or existing Grade III-IV peripheral neuropathy.

7. Pregnancy or < 6weeks post-partum period (Due to increased risk of hepatotoxicity).

8. Grade III or higher baseline abnormal liver function. (Note: toxicity grades are all according to ACTG toxicity tables for persons on ART).

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Communicable Diseases
• HIV Infections
• Infection
• Latent Tuberculosis
• Latent Tuberculosis Infection
• Tuberculosis

Intervention

Drug:
• isoniazid
A self-administered daily dose of 5mg/kg of Isoniazid or placebo for 12months(300mg if weight is more than or equal to 50kg and 200mg if weight is less than 50kg)
• Placebo
A self-administered dose of 5mg/kg of placebo (300mg if weight is more than or equal to 50kg and 200mg if weight is less than 50kg)

Locations

Country	Name	City	State
South Africa	Ubuntu Clinic,Site B Khayelitsha	Cape Town	Western Cape

Sponsors (5)

Lead Sponsor	Collaborator
University of Cape Town	Imperial College London, Johns Hopkins University, London School of Hygiene and Tropical Medicine, Medecins Sans Frontieres

Country where clinical trial is conducted

South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of development of TB (microbiologically confirmed TB or highly probable TB) during the 36 month risk period		Patients are assessed for TB one two monthly at each ART re-fill appointment	Yes
Secondary	Rate of drug toxicity (specifically, peripheral neuropathy, hepatitis +/-raised ALT grade III or worse and allergic rashes grade III or worse		during the intervention period (ALT determined at baseline, 1, 2 and 3 months and then 3-monthly. the last safety determination is at 12 months post initiation of the study drug)	Yes
Secondary	Proportions adhering to study drug and HAART at the end of each study year as measured by pharmacy refills		1 month to two monthly, depending on the individual patient's clinic appointment	Yes
Secondary	Rate of development of INH monoresistance during the 36 month risk period.		36 months	Yes
Secondary	Death		36 months	Yes
Secondary	Worsening ART outcomes (virological and immunological failure)		CD4+count and viral load are assessed as per clinic protocol (6 monthly post ART initiation)	Yes