Clinical Trial to Evaluate the Efficacy and Safety of Codivir® in Addition to Standard Antiretroviral Treatment for HIV Infection in Antiretroviral-naïve Participants

PHASE2RecruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

July 20, 2023

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2024

Conditions
HIVHIV Infection
Interventions
OTHER

ICF

Application of Informed Consent Form.

BEHAVIORAL

Eligibility Assessment

Assessment of inclusion, exclusion and discontinuation criteria.

OTHER

Demographic data

Collection of demographic data.

DIAGNOSTIC_TEST

Weight, height and BMI

Weight and height measurement and body mass index calculation.

OTHER

Vital Signs

HR, BP and FR and T°, in addition to oximetry.

DIAGNOSTIC_TEST

Medical evaluation

Medical history and physical examination at screening. In other consultations, the medical evaluation is focused on viral load, CD4+ and new complaints.

DIAGNOSTIC_TEST

Safety exam

Blood collection for safety laboratory exams. Blood count, Na, K, U, C, amylase, total cholesterol and fractions, triglycerides, coagulation tests (TTTP, TT, platelets), TGO, TGP, AP, GGT, glycated hemoglobin, total bilirubin and fractions, creatine kinase and CKmB and urine I.

DIAGNOSTIC_TEST

Pregnancy test

β-HCG in urine in non-sterile women

DIAGNOSTIC_TEST

Serology

HBV (HBsAg, Anti-HBc) and HCV (anti-HCV-Ab).

OTHER

Randomization

Assignment to the Standard Antiretroviral Treatment + Codivir® group or the Standard Antiretroviral Treatment only group

DIAGNOSTIC_TEST

Apoptosis markers

Caspases and Annexin V.

DIAGNOSTIC_TEST

Cell activation markers

PBMCs will be isolated by density gradient centrifugation. The cells will then be tested for CD4+, CD8+, CD38 and HLA DR

DIAGNOSTIC_TEST

Inflammation markers

ultrasensitive CRP, D-dimer.

DIAGNOSTIC_TEST

Proviral DNA:

Total HIV DNA will be measured to estimate the size of the viral reservoir throughout the preparation.

DIAGNOSTIC_TEST

HIV-specific antibodies

Anti-HIV-1 specific antibody titers in plasma.

DIAGNOSTIC_TEST

HIV viral load (RNA)

Performed on plasma.

BEHAVIORAL

Codivir® Training

The participant is trained to self-inject Codivir®

DRUG

Dispensing Codivir®

the participant receives Codivir®

OTHER

Codivir® Accounting

The Codivir® used since the last visit is accounted for

OTHER

Concomitant medication

Record of concomitant medications used.

OTHER

Adverse events

Collection and recording of adverse events.

DRUG

Antiretrovirals

"Tenofovir - inhibits HIV-1 reverse transcriptase activity by competing with the natural substrate, deoxyadenosine 5'-triphosphate and, upon incorporation into DNA, causes DNA chain termination.~* Lamivudine - potent selective inhibitor of HIV-1 and HIV-2 replication in vitro.~* Darunavir - prevents the formation of mature infective viral particles, indicated for the treatment of the human immunodeficiency virus (HIV), which causes AIDS.~* Ritonavir: antiretroviral protease inhibitor, widely used in combination with other protease inhibitors in the therapy and prevention of HIV infection, which causes the syndrome acquired immunodeficiency (AIDS).~* Single solid formulation (in 1 tablet) 1x/day with:~* Tenofovir (TDF) 300 mg~* Lamivudine (3TC) 300 mg~* Darunavir (DRV) 800 mg, 1x/day~* Ritonavir (RTV) 100 mg, 1x/day"

Trial Locations (1)

04037-030

RECRUITING

RDSS Research Center, São Paulo

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Galilee CBR

INDUSTRY

lead

Code Pharma

INDUSTRY