Truvada
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84
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
HIV/AIDS
Conditions
HIV/AIDS, Substance Use Disorders, Adherence, Medication
Trial Timeline
Oct 1, 2018 → Apr 22, 2020
NCT ID
NCT03842436About Truvada
Truvada is a approved stage product being developed by Gilead Sciences for HIV/AIDS. The current trial status is completed. This product is registered under clinical trial identifier NCT03842436. Target conditions include HIV/AIDS, Substance Use Disorders, Adherence, Medication.
Hype Score Breakdown
Clinical
30
Activity
20
Company
9
Novelty
10
Community
12
Clinical Trials (5)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06631365 | Phase 2 | Recruiting |
| NCT03512418 | Phase 3 | Completed |
| NCT03842436 | Approved | Completed |
| NCT02732730 | Approved | Completed |
| NCT00323687 | Approved | Completed |
Competing Products
11 competing products in HIV/AIDS
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Metformin | Merck | Phase 2/3 | 65 |
| Elvitegravir, Cobicistat, TAF, FTC + Efavirenz, TDF, and 3TC | Gilead Sciences | Pre-clinical | 22 |
| Switch to E/C/FTC/TAF daily | Gilead Sciences | Phase 1/2 | 40 |
| Biktarvy + Symtuza | Gilead Sciences | Phase 3 | 76 |
| bictegravir/emtricitabine/tenofovir alafenamide (BIC/F/TAF) + Standard initiation of antiretroviral therapy (ART) | Gilead Sciences | Approved | 84 |
| ChAdOx1.HTI + MVA.HTI + GS-9620 + Placebo + Placebo Oral Tablet | Gilead Sciences | Phase 2 | 51 |
| Emtricitabine and Tenofovir | Gilead Sciences | Approved | 84 |
| TDF/FTC 300mg/200mg fixed-dose combination tablets + TAF/FTC 25mg/200mg fixed-dose combination tablets | Gilead Sciences | Phase 3 | 76 |
| Maraviroc | Pfizer | Phase 1 | 32 |
| Efavirenz | Bristol Myers Squibb | Pre-clinical | 22 |
| Moxifloxacin + Placebo + Efavirenz | Bristol Myers Squibb | Phase 1 | 32 |