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Oligonucleotide Ligation Assay (OLA) Resistance Study (OLA)

Primary Purpose

HIV Positive

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Pre-ART Oligonucleotide Assay (OLA)
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Positive focused on measuring Transmitted Drug Resistance

Eligibility Criteria

2 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Confirmed HIV infection
  2. >2 years of age
  3. Qualifying for 1st-line ART based on Kenyan Guidelines
  4. Plan to reside in area for >1 year
  5. Adult patient or parent of minor agrees to study and provides informed consent

Exclusion Criteria:

  1. Received ART previously from Hope Center
  2. Ongoing ART
  3. Plan to start 2nd-line ART

Sites / Locations

  • Coptic Hospital
  • Coptic Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Pre-ART Oligonucleotide Assay (OLA)

No OLA (Standard of Care [SOC])

Arm Description

Pre-ART OLA will be tested for resistance at 5 pol codons conferring high-level resistance to NNRTI and 3TC (K103N, V106M, Y181C, G190A and M184V)

The participants will receive standard of care as per Kenya guidelines but will be offered OLA resistance testing after 12 months

Outcomes

Primary Outcome Measures

The Overall Difference in Rates of Virologic Failure With OLA-guided ART vs. Standard of Care
The primary endpoint will be a comparison of the rates of viral non-suppression >400 copies/mL between study arms at 12 months

Secondary Outcome Measures

The Difference in Virologic Failure Among the Subgroup of ARV-naïve Participants With Transmitted Drug-resistance (TDR) Associated With Use of OLA-guided ART vs. SOC
The Difference in Virologic Failure Among the Subgroup of Participants Referred to Hope Center With Previous or Ongoing ARV Use Associated With Use of OLA-guided ART vs. SOC
Prevalence of TDR by Consensus Sequencing and OLA
Proportion of Subgroup With TDR With Virologic Failure by Randomization Arm
Prevalence of TDR Increase in the Coptic Clinic
Estimates of Medical Resource Utilization During the One-year Trial Period
An Assessment the Short-term Cost-effectiveness of OLA-guided Testing
An Assessment of the Potential Long-term Cost-effectiveness of OLA-guided Testing Over a Patient's Lifetime
Determination of Whether Low-level ARV Resistance (<5%) Detected by PYRO But Not by OLA is Associated With Virologic Failure

Full Information

First Posted
July 9, 2013
Last Updated
October 18, 2021
Sponsor
University of Washington
Collaborators
Seattle Children's Hospital, University of Nairobi
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1. Study Identification

Unique Protocol Identification Number
NCT01898754
Brief Title
Oligonucleotide Ligation Assay (OLA) Resistance Study
Acronym
OLA
Official Title
Drug-resistance Testing in Kenya to Improve ART Suppression of HIV Replication
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
May 2013 (Actual)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
February 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Seattle Children's Hospital, University of Nairobi

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators propose to gauge improvements in the rate of durable suppression of viral replication by ART when OLA is used to guide clinical decisions at the PEPFAR Coptic Hope Center in Kenya, and to determine the cost-effectiveness of implementing this strategy at Coptic Hope Center.
Detailed Description
Durable suppression of HIV replication is critical to (1) improving the health of infected individuals, (2) to reducing HIV transmission to sexual partners and from mothers to their infants, and (3) to maintaining the effectiveness of the current 1st-line non-nucleoside reverse transcriptase inhibitors (NNRTI)- based ART. Across multiple trials, individuals with NNRTI-resistance, even at low-concentrations, have substantially greater virologic failure when treated with NVP- vs PI-ART. A cost-effective strategy is needed to detect and manage ARV-resistant HIV infections. A simple low-cost innovative assay the investigators developed and successfully transferred to Asian and African countries (oligonucleotide ligation assay (OLA)) can detect NNRTI+lamivudine (3TC) resistant HIV using reagents that costs <$7.00/person. Furthermore, detection of NNRTI-resistance by OLA is highly (P<0.001) associated with virologic failure of nevirapine (NVP)-ART in two retrospective studies; one of Thai women who had been previously randomized to single-dose NVP and the second of ARV-naïve Kenyan adults. The investigators hypothesize that implementation of OLA into routine care will allow Kenyan clinicians to appropriately target protease inhibitor (PI)-based ART and improve rates of durable suppression of viral replication, and thus improve CD4 cell gains and individuals' health, reduce the transmission of ARV-resistant HIV within the community, and maintain the utility of NNRTI-ART. In addition, the investigators hypothesize that programmatically OLA-guided ART will be more cost-efficient compared to the current strategy of empiric use of NNRTI-ART as initial treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Positive
Keywords
Transmitted Drug Resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
991 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pre-ART Oligonucleotide Assay (OLA)
Arm Type
Experimental
Arm Description
Pre-ART OLA will be tested for resistance at 5 pol codons conferring high-level resistance to NNRTI and 3TC (K103N, V106M, Y181C, G190A and M184V)
Arm Title
No OLA (Standard of Care [SOC])
Arm Type
No Intervention
Arm Description
The participants will receive standard of care as per Kenya guidelines but will be offered OLA resistance testing after 12 months
Intervention Type
Other
Intervention Name(s)
Pre-ART Oligonucleotide Assay (OLA)
Other Intervention Name(s)
Pre-ART OLA
Intervention Description
Block randomization (1:1) to pre-ART OLA testing or OLA testing after 12mo on ART
Primary Outcome Measure Information:
Title
The Overall Difference in Rates of Virologic Failure With OLA-guided ART vs. Standard of Care
Description
The primary endpoint will be a comparison of the rates of viral non-suppression >400 copies/mL between study arms at 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
The Difference in Virologic Failure Among the Subgroup of ARV-naïve Participants With Transmitted Drug-resistance (TDR) Associated With Use of OLA-guided ART vs. SOC
Time Frame
15 months
Title
The Difference in Virologic Failure Among the Subgroup of Participants Referred to Hope Center With Previous or Ongoing ARV Use Associated With Use of OLA-guided ART vs. SOC
Time Frame
15 months
Title
Prevalence of TDR by Consensus Sequencing and OLA
Time Frame
15 months
Title
Proportion of Subgroup With TDR With Virologic Failure by Randomization Arm
Time Frame
15 months
Title
Prevalence of TDR Increase in the Coptic Clinic
Time Frame
15 months
Title
Estimates of Medical Resource Utilization During the One-year Trial Period
Time Frame
15 months
Title
An Assessment the Short-term Cost-effectiveness of OLA-guided Testing
Time Frame
15 months
Title
An Assessment of the Potential Long-term Cost-effectiveness of OLA-guided Testing Over a Patient's Lifetime
Time Frame
15 months
Title
Determination of Whether Low-level ARV Resistance (<5%) Detected by PYRO But Not by OLA is Associated With Virologic Failure
Time Frame
15 months
Other Pre-specified Outcome Measures:
Title
Descriptions of Technology Transfer of OLA to the Hope Center Laboratory, Including Intra- and Inter-assay the Reproducibility, and Discussion of Obstacles and Possible Solutions
Time Frame
15 months
Title
A Comparison of OLA Results Obtained Using DBS in Kenya to Retesting of Same Specimens With Input of Viral Templates Measured in Seattle
Time Frame
15 months
Title
A Comparison of Rates of Resistance Detected Across Codons by OLA vs. Consensus Sequencing in Seattle
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed HIV infection >2 years of age Qualifying for 1st-line ART based on Kenyan Guidelines Plan to reside in area for >1 year Adult patient or parent of minor agrees to study and provides informed consent Exclusion Criteria: Received ART previously from Hope Center Ongoing ART Plan to start 2nd-line ART
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa Frenkel, MD
Organizational Affiliation
University of Washington, Seattle Children's Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael H Chung, MD, MPH
Organizational Affiliation
Department of Global Health, University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Coptic Hospital
City
Maseno
Country
Kenya
Facility Name
Coptic Hospital
City
Nairobi
Country
Kenya

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31818716
Citation
Chung MH, McGrath CJ, Beck IA, Levine M, Milne RS, So I, Andersen N, Dross S, Coombs RW, Chohan B, Yatich N, Kiptinness C, Sakr SR, Kiarie JN, Frenkel LM. Evaluation of the management of pretreatment HIV drug resistance by oligonucleotide ligation assay: a randomised controlled trial. Lancet HIV. 2020 Feb;7(2):e104-e112. doi: 10.1016/S2352-3018(19)30337-6. Epub 2019 Dec 7.
Results Reference
derived
PubMed Identifier
29040633
Citation
Silverman RA, Beck IA, Kiptinness C, Levine M, Milne R, McGrath CJ, Bii S, Richardson BA, John-Stewart G, Chohan B, Sakr SR, Kiarie JN, Frenkel LM, Chung MH. Prevalence of Pre-antiretroviral-Treatment Drug Resistance by Gender, Age, and Other Factors in HIV-Infected Individuals Initiating Therapy in Kenya, 2013-2014. J Infect Dis. 2017 Dec 19;216(12):1569-1578. doi: 10.1093/infdis/jix544.
Results Reference
derived

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Oligonucleotide Ligation Assay (OLA) Resistance Study

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