CClinicalTrials.gg
Status unknownNCT03557021Updated Jun 14, 2018

Impact of HIV Drug Resistance Testing, and Subsequent Change to an Individualized Therapy in Tanzania

An interventional study of HIV Drug resistance testing in HIV Drug Resistance, sponsored by Medical Mission Institute, Germany. Status unknown at 3 sites in Tanzania. Open to participants aged 1 Month to 99 Years. Per ClinicalTrials.gov, last updated 2018-06-14.

Sponsored by Medical Mission Institute, Germany · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jun 2018), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
1,250
Allocation
Randomized
Ages
1 Month to 99 Years
Sex
All
01

Study summary

The current therapy regimens in Sub-Saharan countries, consisting of standardized first and second line drug combinations, yield a high rate of treatment failure, even within the first 12 months of therapy (23). These and other facts hint at the need for HIV resistance testing to improve treatment outcomes in resource-limited settings, but no prospective clinical data about this intervention exists. The proposed study aims to evaluate the impact of HIV drug resistance testing, and subsequent change to an individualized (second-line) therapy based on the resistance profile, in Tanzanian patients (children, adolescents and adults) with virological failure of their first-line and second-line therapy. Additionally, prevalence, patterns and clinical impact of HIVDR will be assessed, as well as the effect of enhanced adherence counselling.

The results of this study will help doctors to take evidence-based diagnostic and therapeutic decisions at an individual level, and will inform policy-makers in their decisions about future treatment and management concepts for HIV/AIDS.

Read the detailed description

HIV/AIDS is one of the main health challenges of our time, with a global burden of disease higher than any other infectious disease. The widespread use of antiretroviral drugs has changed its face from a fatal fate to a chronic disease. However, there are still many differences in the standard of care globally. Drug resistance testing is routinely performed in high income countries, but is often not available in resource limited settings. Instead, treatment consists of standardized therapy regimes, chosen from a limited amount of antiretroviral drugs. This may contribute to the high rates of virological failure seen in patients, and especially children and adolescents, on therapy. Virological failure persisting despite intensified enhanced adherence-counselling result in poor treatment success in HIV infected adults, children and adolescents on treatment and therefore early deaths. If therapy failure occurs, and HIV drug resistance is the likely reason, physician in Tanzania need to blindly choose a second-line therapy regimen, without knowledge of the exact resistance profile. However, multiple studies have discovered high rates of HIV drug resistance in patients with first line treatment failure, and even in therapy-naïve patients. To obtain information about presence of resistance mutations HIV genotypic resistance testing is required. This test is used to detect HIV genomic mutations that confer resistance to specific types of antiretroviral drugs as an aid in monitoring and treating HIV-infection. The test identifies mutation on the protease and reverse transcriptase gene, which are responsible for very crucial steps in the viral replication process. Results from this test can identify the medication for whom the virus is still susceptible and for whom it is already resistant. With this, it can be avoid switching to second-line regimen without the knowledge of the presence or absence of antiretroviral drug resistance. An individualized therapy can follow making sure that medication works best and the clinical outcome can increase.

While the positive impact of HIV resistance testing on treatment outcomes in high-income countries is well established, no prospective data has been published about the effect in resource-limited settings. This absence of data poses a hole in clinical knowledge, because the results from high-income countries are not readily transferable to low-income settings.

The proposed study aims to evaluate the impact of HIV drug resistance testing, and subsequent change to an individualized (second-line) therapy based on the resistance profile, compared to standardized second-line therapy. The study is designed as a randomised controlled trial. The study participants, Tanzanian patients (children, adolescents and adults) with virological failure of their first-line therapy, will be recruited at several study sites. All patients will first receive enhanced adherence counselling. The patients that still show virological failure three months after the counselling will be eligible for resistance testing. The regimen will be switched to individualized (second-line) ART or standardized second-line ART, and clinical, immunological and virological outcome parameters will be collected in a 6 month and 12 month follow up visit (Group I,II,III IV). In addition to the outcome of individualized therapy, the proposed study would yield insights about the prevalence and patterns of HIV drug resistance in patients with failure of their first-line therapy, and also about the effectiveness of enhanced adherence counselling.

For ethical reasons also 250 seconnd line treatment failure patients (Group V) with fast clinical progress will be included and transfered directly to the individualized therapy arm. With that we hope to bring them back to a working treatment.

The main diagnostic method of this study, HIV genomic sequencing, will be implemented and performed at the National Institute for Medical Research in Mwanza, Tanzania. This will contribute directly to the HIV-related diagnostic capacities of Tanzanian laboratories.

02

Conditions studied

  • HIV Drug Resistance
03

In context

Lead sponsor

Medical Mission Institute, Germany is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Month to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Confirmed HIV positive patients on first-line ART
  2. Virological treatment failure with > 1000 copies/ ml

Exclusion criteria

Exclusion Criteria:

  1. No consent given
  2. HIV patients with psychiatric disorders
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,250 participants (estimated)

Study arms

  • Experimental
    Individualized therapy arm

    HIV Treatment failure patients will undergo an HIV Drug resistance testing and the followed therapy will be adjusted with in this setting available medications to the outcome of the resistance profile

    Diagnostic Test: HIV Drug resistance testing

  • Active comparator
    standard therapy arm

    HIV Treatment failure patients will undergo an HIV Drug resistance testing and the national defined standard therapy will be applied as second line treatment.

    Diagnostic Test: HIV Drug resistance testing

Interventions

  • Diagnostic testHIV Drug resistance testing

    HIV Drug resistance testing by HIV pro DNA sanger sequencing

06

What researchers measure

Primary outcomes

  1. Viral Load

    Viral load will be measured by plasma HIV viral load measurement (copies per ml) after switching first-line treatment failure patients to individualized therapy compared to standard second line therapy.

    Time frame: 12 month

Secondary outcomes

  1. Incidence of HIV related adverse events at 6 month

    HIV related adverse events at 6 month will be determined according to CTC AE list version 4

    Time frame: 6 month

  2. Incidence of HIV related adverse events at at 12 month

    HIV related adverse events at 6 month will be determined according to CTC AE list version 4

    Time frame: 12 month

  3. Prevalence of HIV Drug resistance mutations

    The prevalence of HIV drug resistance mutations will be determined in patients with virological failure of first-line antiretroviral therapy

    Time frame: study start

  4. Pattern of HIV Drug resistance mutations

    The patterns of HIV drug resistance mutations will be determined in patients with virological failure of first-line antiretroviral therapy

    Time frame: study start

  5. Viral load at 3th month

    Viral load will be measured by plasma HIV viral load measurement (copies per ml) after enhanced conselling.

    Time frame: 3 month

07

Study locations

2 of 3 sites recruiting
  • PASADA
    Dar es Salaam, Tanzania
    Recruiting
  • Baylor Hospital
    Mwanza, Tanzania
    Not yet recruiting
  • Bugando Medical Center
    Mwanza, Tanzania
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 14, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03557021
Lead sponsor
Medical Mission Institute, Germany
Collaborators
National Institute for Medical Research, Tanzania
Responsible party
Dr. Christa Kasang (Research Coordinator, Medical Mission Institute, Germany) — Principal investigator
First posted
Jun 14, 2018
Start date
Jul 1, 2017
Primary completion
Sep 30, 2019 (estimated)
Completion
Sep 30, 2020 (estimated)
Last update
Jun 14, 2018

Study contacts

Christa Kasang, PhD
Contact
christa.kasang@medmissio.de
+4993180485 ext. 18
Daniel Magesa, MD
Contact
djnmagesa@yahoo.com
+255754307750
John Changalucha, MD
study chair · National Institute of Medical research Mwanza

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion