Trials / Recruiting
RecruitingNCT06511063
Antiviral Clinical Trial for Long Covid-19
Investigating the Feasibility of Repurposing HIV Antivirals in Adults With Long Covid
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- Sponsor
- Icahn School of Medicine at Mount Sinai · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The trial will test if two repurposed HIV antivirals can reduce symptom burden in adult participants with Long Covid compared to placebo. Viral infection and viral reactivation have been documented in Long Covid. Participants will be randomly allocated to receive antivirals, Truvada (tenofovir disoproxil/emtricitabine, TDF/FTC, Group 1) or Selzentry (Group 2), or a placebo (pill) (Group 3), taken daily for 90 days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | tenofovir disoproxil/emtricitabine | Participants will take Truvada (TDF/FTC, tenofovir disoproxil/emtricitabine) for 90 days. |
| DRUG | Selzentry | Participants will take Selzentry for 90 days. |
| DRUG | Placebo | Matching placebo. |
Timeline
- Start date
- 2024-10-01
- Primary completion
- 2026-11-01
- Completion
- 2026-12-01
- First posted
- 2024-07-19
- Last updated
- 2026-03-13
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06511063. Inclusion in this directory is not an endorsement.