Lemborexant 5 mg + Control (placebo) group

Phase 2Recruiting
1 views this week 0 watching Active
Interest: 42/100
42
Hype Score

Development Stage

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

Delirium - Postoperative

Conditions

Delirium - Postoperative, Cardiac Surgery, Cardiac Surgery Subjects, Orexin Antagonist, Feasibility Studies, Sleep, In-hospital Mortality

Trial Timeline

May 1, 2025 → Apr 30, 2027

About Lemborexant 5 mg + Control (placebo) group

Lemborexant 5 mg + Control (placebo) group is a phase 2 stage product being developed by Eisai for Delirium - Postoperative. The current trial status is recruiting. This product is registered under clinical trial identifier NCT06648681. Target conditions include Delirium - Postoperative, Cardiac Surgery, Cardiac Surgery Subjects.

What happened to similar drugs?

5 of 13 similar drugs in Delirium - Postoperative were approved

Approved (5) Terminated (3) Active (6)
Rivastigmine + PlaceboNovartisApproved
Rivastigmine PatchNovartisApproved
ParecoxibPfizerApproved
Cyclopofol + PropofolHaisco Pharmaceutical GroupApproved
Dexmedetomidine Hydrochloride GroupBrain BiotechApproved
🔄Suvorexant + PlaceboMerckPhase 3

Hype Score Breakdown

Clinical
12
Activity
15
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT06648681Phase 2Recruiting

Competing Products

17 competing products in Delirium - Postoperative

See all competitors
ProductCompanyStageHype Score
Suvorexant + PlaceboMerckPhase 3
40
Suvorexant 20 mg + PlaceboMerckPhase 2
35
Rivastigmine + PlaceboNovartisApproved
35
Rivastigmine prevention of deliriumNovartisPhase 3
40
Rivastigmine transdermal patch + placebo patchNovartisPhase 3
40
Rivastigmine PatchNovartisApproved
43
Dexmedetomidine + PlaceboPfizerPhase 3
32
ParecoxibPfizerApproved
39
Dexmedetomidine + PlaceboPfizerPhase 3
32
PregabalinPfizerPhase 3
40
Dexmedetomidine + MidazolamPfizerPhase 3
47
Propofol + DexmedetomidinePfizerPre-clinical
26
Dexmedetomidine + Saline placeboPfizerPhase 2/3
38
Cyclopofol + PropofolHaisco Pharmaceutical GroupApproved
39
Dexmedetomidine + Sodium chloride 0.9%BaxterPhase 3
37
Dexmedetomidine Hydrochloride GroupBrain BiotechApproved
40
Dexmedetomidine sublingual filmBioXcel TherapeuticsPhase 2
17