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Effect of Biktarvy & Symtuza on microRNAs in HIV and Correlation With Weight Gain

Primary Purpose

HIV Infections, Obesity

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Biktarvy
Symtuza
Sponsored by
East Carolina University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for HIV Infections focused on measuring microRNA, miRNA, ARV, Antiretroviral medications

Eligibility Criteria

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

Inclusion Criteria:

  1. Subjects age >/=18 years
  2. HIV infection with HIV RNA >/= 1000 copies/ml of plasma
  3. Treatment naïve
  4. Have access to a smartphone with internet access
  5. Willing to provide written informed consent.

Exclusion Criteria:

  1. Morbid obesity (BMI>/=40) or cachexia (BMI=/<20)
  2. Known or suspected active substance abuse that in the opinion of the investigator would impact study participation
  3. On medications associated with weight loss or gain, including insulin, glucagon-like peptide(GLP)-1 analogs, anti-depressants, antipsychotics, corticosteroids, orlistat
  4. Bedbound due to other chronic conditions
  5. Pregnant females
  6. Prisoners
  7. Unwilling or unable to comply with protocol requirements.
  8. On medication known to interact significantly with any of the components of Symtuza or Biktarvy.

Sites / Locations

  • Adult Specialty Care Clinic-East Carolina UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Biktarvy

Symtuza

Arm Description

15 subjects will get Biktarvy (single-tablet regimen of bictegravir/emtricitabine/tenofovir alafenamide) once daily.

15 subjects will get Symtuza (single-tablet regimen of darunavir/cobicistat/emtricitabine/tenofovir alafenamide) once daily.

Outcomes

Primary Outcome Measures

miRNA(microRNA) profiles of the two groups
we will monitor microRNAs of the two groups
Change from baseline in Body mass index-BMI(kg/m^2) of the participants
Weight(in kilograms or kg) and height(in meters or m) will be combined to report BMI in kg/m^2
Change from baseline in body weight(in kilograms or kg) of the participants
we will monitor change in body weight & BMI

Secondary Outcome Measures

Calorie intake of subjects in the two groups.
we will monitor calorie intake of subjects in two grouos

Full Information

First Posted
May 25, 2022
Last Updated
May 15, 2023
Sponsor
East Carolina University
Collaborators
Janssen Scientific Affairs, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT05463783
Brief Title
Effect of Biktarvy & Symtuza on microRNAs in HIV and Correlation With Weight Gain
Official Title
Effect of Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide and Bictegravir/Emtricitabine/Tenofovir Alafenamide on the Circulatory microRNA Profile in Treatment naïve HIV Patients, and Its Correlation With Change in Body Weight
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 14, 2023 (Actual)
Primary Completion Date
March 2025 (Anticipated)
Study Completion Date
March 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
East Carolina University
Collaborators
Janssen Scientific Affairs, LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to understand why certain HIV medication regimens (called anti-retroviral or ARV medications) cause more weight gain than others. In this research, the investigators will compare micro-RNA profiles of people who take Symtuza(darunavir(D)/cobicistat(C)/emtricitabine(F)/tenofovir alafenamide (TAF))[D/C/F/TAF] with those who take Biktarvy(bictegravir(B)/emtricitabine(F)/tenofovir alafenamide (TAF))[B/F/TAF] and try to correlate this with the change in body weight and BMI over a course of 48 weeks. The investigators will also attempt to monitor the calorie intake of the participants in the two groups and correlate it with treatment-induced weight gain. Micro-RNAs are small molecules that are produced naturally in the human body, and which are responsible for modifying the expressions of genes. They have the potential to be used in diagnostic and therapeutic medicine and their putative role has been explored in many diseases across many clinical trials. By doing this research, the investigators hope to learn more about their role in HIV disease and its correlation with treatment-induced weight gain.
Detailed Description
With advances in HIV treatment, the life expectancy of persons with HIV (PWH) has improved and complications associated with antiretroviral (ARV) medications have become more apparent. Among them, weight gain and obesity, because of their associated complications, is one of the more concerning ones. Certain drug regimens are more adipogenic than others, but not a lot is known about molecular mechanisms responsible for these differences. Micro RNAs (miRNAs) are small non-coding RNAs that control gene expression and regulate a wide array of biological processes. In recent years miRNAs have been studied in a number of diseases for diagnostic and even therapeutic purposes. There are studies showing differences in miRNA profiles in obese vs non-obese non-HIV population, as well as certain miRNAs as biomarkers of response to weight-loss diets. In PWH, there are studies that looked at the effect of HIV infection on the miRNA profile and how a particular miRNA profile is predictive of ARV resistance. But there are no studies that specifically looked at how ARV medications alter the miRNA profile and how (in terms of miRNA profiles) one combination is more adipogenic than the other.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Obesity
Keywords
microRNA, miRNA, ARV, Antiretroviral medications

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Interventional, open-label, parallel-group, randomized trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Biktarvy
Arm Type
Experimental
Arm Description
15 subjects will get Biktarvy (single-tablet regimen of bictegravir/emtricitabine/tenofovir alafenamide) once daily.
Arm Title
Symtuza
Arm Type
Experimental
Arm Description
15 subjects will get Symtuza (single-tablet regimen of darunavir/cobicistat/emtricitabine/tenofovir alafenamide) once daily.
Intervention Type
Drug
Intervention Name(s)
Biktarvy
Other Intervention Name(s)
bictegravir/emtricitabine/tenofovir alafenamide
Intervention Description
microRNA profiles of subjects on Biktarvy, will be compared with those who are on Symtuza, at various time points.
Intervention Type
Drug
Intervention Name(s)
Symtuza
Other Intervention Name(s)
darunavir/cobicistat/emtricitabine/tenofovir alafenamide
Intervention Description
microRNA profiles of subjects on Symtuza, will be compared with those who are on Biktarvy, at various time points.
Primary Outcome Measure Information:
Title
miRNA(microRNA) profiles of the two groups
Description
we will monitor microRNAs of the two groups
Time Frame
48 weeks
Title
Change from baseline in Body mass index-BMI(kg/m^2) of the participants
Description
Weight(in kilograms or kg) and height(in meters or m) will be combined to report BMI in kg/m^2
Time Frame
48 weeks
Title
Change from baseline in body weight(in kilograms or kg) of the participants
Description
we will monitor change in body weight & BMI
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
Calorie intake of subjects in the two groups.
Description
we will monitor calorie intake of subjects in two grouos
Time Frame
48 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects age >/=18 years HIV infection with HIV RNA >/= 1000 copies/ml of plasma Treatment naïve Have access to a smartphone with internet access Willing to provide written informed consent. Exclusion Criteria: Morbid obesity (BMI>/=40) or cachexia (BMI=/<20) Known or suspected active substance abuse that in the opinion of the investigator would impact study participation On medications associated with weight loss or gain, including insulin, glucagon-like peptide(GLP)-1 analogs, anti-depressants, antipsychotics, corticosteroids, orlistat Bedbound due to other chronic conditions Pregnant females Prisoners Unwilling or unable to comply with protocol requirements. On medication known to interact significantly with any of the components of Symtuza or Biktarvy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Paul Cook, MD
Phone
252-744-4500
Email
cookp@ecu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Smit Rajput, MD
Phone
252-744-2574
Email
rajputs20@ecu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Cook, MD
Organizational Affiliation
East Carolina University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Adult Specialty Care Clinic-East Carolina University
City
Greenville
State/Province
North Carolina
ZIP/Postal Code
27834
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jamie Wigent, RN
Phone
252-414-2655
Email
wigentj17@ecu.edu
First Name & Middle Initial & Last Name & Degree
Allison Geigel, RN
Phone
252-414-2655
Email
geigela20@ecu.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Effect of Biktarvy & Symtuza on microRNAs in HIV and Correlation With Weight Gain

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