Raltegravir
ApprovedCompleted 0 views this week 0 watching⚡ Active
Interest: 43/100
43
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
HIV Prevention
Conditions
HIV Prevention, HIV Infections
Trial Timeline
Jul 1, 2010 → Jul 1, 2012
NCT ID
NCT01087840About Raltegravir
Raltegravir is a approved stage product being developed by Merck for HIV Prevention. The current trial status is completed. This product is registered under clinical trial identifier NCT01087840. Target conditions include HIV Prevention, HIV Infections.
What happened to similar drugs?
8 of 20 similar drugs in HIV Prevention were approved
Approved (8) Terminated (0) Active (12)
Hype Score Breakdown
Clinical
20
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00377065 | Pre-clinical | Completed |
| NCT03732625 | Approved | UNKNOWN |
| NCT03667547 | Approved | Completed |
| NCT03374358 | Approved | Completed |
| NCT02097108 | Phase 2 | Completed |
| NCT01978743 | Pre-clinical | Completed |
| NCT01767701 | Phase 2 | Completed |
| NCT01453933 | Approved | UNKNOWN |
| NCT01620736 | Phase 2 | Withdrawn |
| NCT01453192 | Phase 3 | Completed |
| NCT01448486 | Approved | Terminated |
| NCT01327482 | Pre-clinical | Completed |
| NCT01325051 | Phase 1 | Completed |
| NCT01042652 | Pre-clinical | UNKNOWN |
| NCT01164605 | Pre-clinical | UNKNOWN |
| NCT01087840 | Approved | Completed |
| NCT01027182 | Phase 1 | Completed |
| NCT00939874 | Approved | Completed |
| NCT00807443 | Phase 2 | Completed |
| NCT00887653 | Phase 3 | Completed |
Competing Products
20 competing products in HIV Prevention
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mRNA-1944 | Moderna | Phase 1 | 0 |
| Gam-COVID-Vac | Dr. Reddy's Laboratories | Phase 2/3 | 31 |
| edoxaban + enoxaparin sodium | Daiichi Sankyo | Phase 3 | 40 |
| Mifepristone | Eli Lilly | Phase 2 | 35 |
| EXANTA | AstraZeneca | Phase 2 | 27 |
| Risk of low dose aspirin discontinuation | AstraZeneca | Pre-clinical | 26 |
| DAPA/MET XR + DAPA + MET XR | AstraZeneca | Phase 3 | 40 |
| Esomeprazole + Placebo | AstraZeneca | Phase 3 | 40 |
| PCV15 | Merck | Pre-clinical | 18 |
| RotaTeq (V260) + IPV | Merck | Phase 3 | 40 |
| V501 | Merck | Phase 3 | 40 |
| Zostavax | Merck | Phase 3 | 40 |
| V920 Consistency Lot A + V920 Consistency Lot B + V920 Consistency Lot C + V920 High-dose Lot + Placebo to V920 | Merck | Phase 3 | 40 |
| Letermovir + Placebo | Merck | Phase 3 | 40 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 43 |
| Enteric-coated mycophenolate sodium | Novartis | Phase 3 | 40 |
| Meningococcal C conjugate vaccine | Novartis | Approved | 43 |
| rMenB+OMV NZ | Novartis | Phase 3 | 40 |
| Enteric-Coated Mycophenolate Sodium | Novartis | Phase 3 | 40 |
| Inclisiran sodium 300 mg (equivalent to 284 mg inclisiran) in 1.5 mL + Placebo in 1.5ml | Novartis | Phase 3 | 44 |