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Modification of Prasugrel based on a biological assay + prasugrel / clopidogrel

ApprovedCompleted
1 views this week 0 watching⚡ Active
Interest: 43/100
43
Hype Score

Development Stage

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

Acute Coronary Syndrome

Conditions

Acute Coronary Syndrome

Trial Timeline

Mar 1, 2012 → May 1, 2016

NCT ID
NCT01538446

About Modification of Prasugrel based on a biological assay + prasugrel / clopidogrel

Modification of Prasugrel based on a biological assay + prasugrel / clopidogrel is a approved stage product being developed by Daiichi Sankyo for Acute Coronary Syndrome. The current trial status is completed. This product is registered under clinical trial identifier NCT01538446. Target conditions include Acute Coronary Syndrome.

What happened to similar drugs?

20 of 20 similar drugs in Acute Coronary Syndrome were approved

Approved (20) Terminated (4) Active (0)
✅high-dose rosuvastatin + low-dose rosuvastatin plus ezetimibeYuhanApproved
✅PrasugrelDaiichi SankyoApproved
✅30-day DAPT + Guideline-directed therapyDaiichi SankyoApproved
✅Sitafloxacin + Moxifloxacin HydrochlorideDaiichi SankyoApproved
✅micafungin + posaconazoleAstellas PharmaApproved
✅Selbex + SelbexEisaiApproved
✅Sivelestat sodium hydrate + Sivelestat sodium hydrateOno PharmaceuticalApproved

Hype Score Breakdown

Clinical
20
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT01538446ApprovedCompleted

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