MK-8583

Phase 1Completed
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33
Hype Score

Development Stage

Pre-clinical
2
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

HIV-1 Infection

Conditions

HIV-1 Infection

Trial Timeline

Oct 7, 2018 → Mar 11, 2019

About MK-8583

MK-8583 is a phase 1 stage product being developed by Merck for HIV-1 Infection. The current trial status is completed. This product is registered under clinical trial identifier NCT03552536. Target conditions include HIV-1 Infection.

Hype Score Breakdown

Clinical
10
Activity
5
Company
10
Novelty
3
Community
2

Clinical Trials (1)

NCT IDPhaseStatus
NCT03552536Phase 1Completed

Competing Products

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ProductCompanyStageHype Score
DOR/ISLMerckPhase 2
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SHR2150;Placebo + SHR2150;Placebo + SHR2150;Placebo + SHR2150;Placebo + SHR2150;PlaceboJiangsu Hengrui MedicinePhase 1
33
Darunavir + Etravirine + Emtricitabine/tenofovir disoproxil fumarate + Raltegravir + Second line ART regimens - based on a boosted protease inhibitor (bPI) plus two nucleoside analogues (NRTIs) + Study provided drugs according to patient resistance profile (DRV, ETR, RTV, FTC/TDF) + any in country available drug as applicable & availableAbbVieApproved
85
lopinavir/ritonavir + lamivudineAbbViePre-clinical
23
CVC 150 mg + CVC 300 mgAbbViePhase 2
52
Doravirine, Tenofovir, Lamivudine - Blinded + Doravirine, Tenofovir, Lamivudine - Open-Label + ATRIPLA^TM + Placebo to ATRIPLA™ + Placebo to Doravirine, Tenofovir, LamivudineMerckPhase 2
52
DOR/ISL + BIC/FTC/TAF + Placebo to BIC/FTC/TAF + Placebo to DOR/ISLMerckPhase 3
77
VorinostatMerckPhase 1/2
41
IslatravirMerckPhase 1
33
Doravirine, Tenofovir, Lamivudine + Baseline regimen of ritonavir- or cobicistat-boosted protease inhibitor + Baseline regimen of cobicistat-boosted elvitegravir + Baseline regimen of a non-nucleoside reverse transcriptase inhibitor + Baseline regimen of two nucleoside reverse transcriptase inhibitorsMerckPhase 3
77
raltegravir and etravirineMerckPhase 2
52
Treatment A: Doravirine 100 mg film coated tablet + Treatment B: Doravirine 150 mg tablet (40% drug loaded granule) + Treatment C: Doravirine 150 mg tablet (30% drug loaded granule) + Treatment D: Doravirine 150 mg tablet (50% drug loaded granule) + Treatment E: Doravirine 100 mg tablet (30% drug loaded granule)MerckPhase 1
33
ISL + ULO + BIC/FTC/TAFMerckPhase 2
52
UlonivirineMerckPhase 1
33
Islatravir + Placebo to Islatravir + Doravirine + Placebo to Doravirine + Lamivudine + Placebo to Lamivudine + Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate + Placebo to Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate + Doravirine/IslatravirMerckPhase 2
52
MK0518 (Raltegravir) + famotidine + omeprazoleMerckPhase 1
33
DoravirineMerckPhase 1
33
MK-8510MerckPhase 1
33
18F-RaltegravirMerckPhase 1
33
Pegylated Interferon alpha 2bMerckPhase 2
52