Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:58 PM
Ignite Modification Date:
2025-12-24 @ 9:58 PM
NCT ID:
NCT04064632
Eligibility Criteria:
Inclusion Criteria:
1. Written signed and dated informed consent to participate in the study must be given by the subject, in accordance with the International Conference of Harmonisation (ICH) Good Clinical Practice (GCP) Guideline E627 and applicable regulations, before completing any procedure related to the study.
2. HIV-1 documented infection
3. Male and female subjects \> 18 years of age.
4. Males, or non-pregnant, non-lactating females of childbearing potential, as demonstrated by a negative pregnancy test, who agree to comply with any applicable contraceptive requirements of the protocol. Women of child-bearing potential with a negative pregnancy test at Screening and Day 1 should agree to use one of the following methods: Complete abstinence from penile-vaginal intercourse from 2 weeks prior to administration of IMP, throughout the study, and for at least 2 weeks after; Double barrier method (male condom/spermicide, male condom/diaphragm, diaphragm/spermicide) IUD and male condom Male partner sterilization confirmed and male condom Approved hormonal contraception and male condom Any other method with published data showing that the expected failure rate is \<1% per year and use male condo Any contraception method must be used for at least 2 weeks after discontinuation of IMP.
5. Being on a stable therapy for at least 6 months.
6. SBR must be based on any 2NRTI plus a third NNRTI, PI or INI agent. Any possible registered drug is allowed among NRTI (e.g. tenofovir, lamivudine, emtricitabine and abacavir), PI (e.g. lopinavir, atazanavir, darunavir), NNRTI (efavirenz, nevirapine, rilpivirine) or INI (raltegravir, elvitegravir, dolutegravir).
7. Having a fully suppressed HIV replication as documented by 2 prior HIV-RNA tests (at least two months apart) below the detection limit (50 copies/ml).
8. Subjects and investigator must agree that participation in this study is in the best interest of the subject.
Exclusion Criteria:
1. Patients co-infected with HBV
2. Pregnancy or breast feeding.
3. Positive anamnesis for allergy to NNRTI
4. A positive historical genotypic test showing resistance-inducing mutation either toward NNRTIs or PIs
5. History or other evidence of severe illness (malignancy or OI) requiring active treatment and/or any other conditions which would make the patient, in the opinion of the investigator, unsuitable for the study.
6. Anticipated need for Hepatitis C virus (HCV) therapy during the study period
7. Treatment with any of the following agents within 28 days of Screening: radiation therapy; cytotoxic chemotherapeutic agents; any immunomodulators that alter immune responses
8. All conditions and medicinal products listed in contraindications of DRV/c and rilpivirine
9. Subjects with current or prior (previous year) history of alcohol or other substance abuse.
10. Patients who have previously been screened for or enrolled into this study and subsequently withdrawn.
11. Patients having been given investigational drugs within 12 weeks prior to screening.
12. Inability or unwillingness to provide informed consent.
13. Life expectancy \< 18 months
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04064632
Study Brief:
Protocol Section:
NCT04064632