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F/TAF (High Dose Tablet) + F/TAF (Low Dose Tablet) + F/TAF (Lowest Dose Tablet) + F/TAF (High Dose TOS) + F/TAF (Low Dose TOS) + F/TAF (Lowest Dose TOS) + E/C/F/TAF + E/C/F/TAF (Low Dose) + Cobicistat (High Dose) + Cobicistat (Low Dose) + Cobicistat (TOS) + B/F/TAF (High Dose) + B/F/TAF (Low Dose) + B/F/TAF (High Dose TOS) + B/F/TAF (Low Dose TOS) + B/F/TAF (Lowest Dose TOS) + 3rd ARV Agent + Nucleos(t)ide reverse transcriptase inhibitors (NRTI) + ATV + DRV + Lopinavir Boosted with ritonavir (LPV/r)

ApprovedRecruiting
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84
Hype Score

Development Stage

✓
Pre-clinical
✓
Phase 1
✓
Phase 2
✓
Phase 3
5
Approved
Indication / Disease

HIV-1-infection

Conditions

HIV-1-infection

Trial Timeline

Aug 27, 2024 → Mar 1, 2034

NCT ID
NCT06337032

About F/TAF (High Dose Tablet) + F/TAF (Low Dose Tablet) + F/TAF (Lowest Dose Tablet) + F/TAF (High Dose TOS) + F/TAF (Low Dose TOS) + F/TAF (Lowest Dose TOS) + E/C/F/TAF + E/C/F/TAF (Low Dose) + Cobicistat (High Dose) + Cobicistat (Low Dose) + Cobicistat (TOS) + B/F/TAF (High Dose) + B/F/TAF (Low Dose) + B/F/TAF (High Dose TOS) + B/F/TAF (Low Dose TOS) + B/F/TAF (Lowest Dose TOS) + 3rd ARV Agent + Nucleos(t)ide reverse transcriptase inhibitors (NRTI) + ATV + DRV + Lopinavir Boosted with ritonavir (LPV/r)

F/TAF (High Dose Tablet) + F/TAF (Low Dose Tablet) + F/TAF (Lowest Dose Tablet) + F/TAF (High Dose TOS) + F/TAF (Low Dose TOS) + F/TAF (Lowest Dose TOS) + E/C/F/TAF + E/C/F/TAF (Low Dose) + Cobicistat (High Dose) + Cobicistat (Low Dose) + Cobicistat (TOS) + B/F/TAF (High Dose) + B/F/TAF (Low Dose) + B/F/TAF (High Dose TOS) + B/F/TAF (Low Dose TOS) + B/F/TAF (Lowest Dose TOS) + 3rd ARV Agent + Nucleos(t)ide reverse transcriptase inhibitors (NRTI) + ATV + DRV + Lopinavir Boosted with ritonavir (LPV/r) is a approved stage product being developed by Gilead Sciences for HIV-1-infection. The current trial status is recruiting. This product is registered under clinical trial identifier NCT06337032. Target conditions include HIV-1-infection.

Hype Score Breakdown

Clinical
30
Activity
20
Company
9
Novelty
10
Community
12

Clinical Trials (1)

NCT IDPhaseStatus
NCT06337032ApprovedRecruiting

Competing Products

20 competing products in HIV-1-infection

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ProductCompanyStageHype Score
CVC 150 mg + CVC 300 mgAbbViePhase 2
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18F-RaltegravirMerckPhase 1
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ISL/LEN + Antiretroviral CombinationsMerckPhase 3
77
Delstrigo + KOCITAFMerckPhase 3
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ISL/LEN + B/F/TAF + PTM B/F/TAF + PTM ISL/LENMerckPhase 3
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B/F/TAF + Atripla + B/F/TAF Placebo + Atripla PlaceboGilead SciencesApproved
84
GS-3242 + BVY + Standard of CareGilead SciencesPhase 1
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B/F/TAFGilead SciencesApproved
84
Genvoya + Epclusa + BiktarvyGilead SciencesApproved
84
GS-1720 + GS-4182 + Bictegravir/emtricitabine/tenofovir alafenamide + GS-1720/GS-4182 FDC + Placebo to Match BVY + Placebo to Match GS1720/GS-4182 FDCGilead SciencesPhase 2/3
64
Dapivirine + TruvadaGilead SciencesPhase 2
51
Bictegravir/emtricitabine/tenofovir alafenamideGilead SciencesPre-clinical
22
GS-9131 + BIC + TAF + ARV regimen + DRV + RTVGilead SciencesPhase 2
51
Bavtavirine + B/F/TAF + Standard of Care (Substudy 01) + GS-1720 + Standard of Care (Substudy 02) + GS-6212 + Standard of Care (Substudy 03)Gilead SciencesPhase 1
32
TruvadaGilead SciencesPhase 2
51
B/F/TAFGilead SciencesPhase 1
32
Switch to B/F/TAF + Continue current regimenGilead SciencesApproved
84
B/F/TAF + F/TAF + DTG + DTG Placebo + F/TAF Placebo + B/F/TAF PlaceboGilead SciencesPhase 3
76
GS-1720 + GS-4182 + Placebo to Match BVY + Bictegravir/emtricitabine/tenofovir alafenamide + GS-1720/GS-4182 FDC + Placebo to Match GS1720/GS-4182 FDCGilead SciencesPhase 2/3
64
Vesatolimod + VRC07523LS + CAP256V2LSGilead SciencesPhase 2
51

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