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 @ 1:28 PM
Ignite Modification Date:
2025-12-24 @ 1:28 PM
NCT ID:
NCT02509195
Eligibility Criteria:
Inclusion Criteria:
1. HIV-1 infected males or females
2. Has voluntarily signed informed consent after having enough time to consider the study information.
3. Is willing to comply with the protocol requirements
4. Documentation that the subject is negative for the HLA-B\*5701 allele, either on historical sample or if none available, at screening.
5. Aged 60 years and over (approximately 70% of the study participants will be ≥65 year of age), willing to switch therapy as per study protocol with no previous use of dolutegravir
6. Plasma HIV RNA \< 50 copies/mL at screening (single re-test allowed) and on at least one other occasion over the last 6-8 months
7. Has a CD4 cell count at screening \>50 cells/mm3
8. Currently receiving a stable antiretroviral regimen with no antiretroviral drug switches for at least 3 months prior to planned study baseline.
9. No previous clinically-significant resistance documented on HIV-1 genotypic resistance to NRTIs and INIs
10. Subjects in good health upon medical history, physical exam, and laboratory testing and with a clinically managed cardiovascular disease in the opinion of the Investigator
11. Body mass over 40 kg and body mass index (BMI) above or equal to 18 and below 35
12. Male subjects who are heterosexually active must be willing to use appropriate and consistent dual method contraception during heterosexual intercourse with women of child bearing potential, from screening through to one month post completion of the study. The following combined contraceptive methods are acceptable (please see appendix 3):
1. Double barrier method:
* Male Condom combined with a Female Diaphragm with or without a vaginal spermicide\* (foam, gel, film, cream, or suppository)
* Male Condom combined with a Cervical cap\*\* (with spermicide)
2. Male Condom + one of the following:
* Combined Oral Contraceptive Pill
* Combined Contraceptive Patch
* Combined Vaginal Ring
* The Progesterone Only Pill
* Intra-uterine Device (Copper IUD or the IUS)
* Injectable progestogen (Depo provera®)
* The progestogen-only Subdermal Implant
Footnotes:
1. \*Cervical caps in women who have given birth is less effective than other methods of contraception.
2. \*\*Spermicide should be used with caution as this can potentially increase the rate of HIV-1 transmission.
3. \*\*\*It is advised not to use a male and female condom together due to risk of breakage or damage caused by latex friction.
If a female partner has had a total hysterectomy (surgical removal of the womb) or bilateral tubal ligation/clip (surgical sterilization), then she cannot get pregnant and the above section does not apply. If the male subject has had a vasectomy at least 1 month prior to starting the study, he does not need to use any other birth control.
Exclusion Criteria:
1. History or presence of allergy to the study drugs or their components
2. Infected with HIV-2
3. Using any concomitant therapy disallowed as per SPC for the study drugs. The SPC of a drug is updated regularly. The most recent version can be found on http://www.medicines.org.uk/emc/
4. Known acute viral hepatitis including, but not limited to, A, B, or C
5. Known chronic hepatitis B and/or C
6. Tests newly positive for active Hepatitis B (HBsAg positive), or active Hepatitis C (PCR positive) at screening visit
7. Any investigational drug within 30 days prior to the trial drug administration
8. Alanine aminotransferase (ALT) ≥5 times the upper limit of normal (ULN), OR ALT ≥3xULN and bilirubin ≥1.5xULN (with \>35% direct bilirubin)
9. Subjects with moderate to severe hepatic impairment (Class B or greater) as determined by Child-Pugh classification
10. Moderate or severe renal impairment (creatinine clearance \< 50ml/min)
11. Screening blood result with any grade 3/4 toxicity according to Division of AIDS (DAIDS) grading scale, except: asymptomatic grade 3 glucose, amylase or lipid elevation or asymptomatic grade 4 triglyceride elevation (re-test allowed).
12. Any condition (including drug/alcohol abuse) or laboratory results which, in the investigator's opinion, interfere with the assessments or completion of the trial.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
60 Years
Study:
NCT02509195
Study Brief:
Protocol Section:
NCT02509195