Niaspan
Pre-clinicalUNKNOWN 1 views this week 0 watching💤 Quiet
Interest: 22/100
22
Development Stage
1
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Atherosclerosis
Conditions
Atherosclerosis
Trial Timeline
Sep 1, 2004 → Feb 1, 2009
NCT ID
NCT00232531About Niaspan
Niaspan is a pre-clinical stage product being developed by Merck for Atherosclerosis. The current trial status is unknown. This product is registered under clinical trial identifier NCT00232531. Target conditions include Atherosclerosis.
What happened to similar drugs?
13 of 20 similar drugs in Atherosclerosis were approved
Approved (13) Terminated (3) Active (6)
Hype Score Breakdown
Clinical
3
Activity
4
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00232531 | Pre-clinical | UNKNOWN |
Competing Products
20 competing products in Atherosclerosis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Orforglipron + Placebo | Eli Lilly | Phase 3 | 47 |
| Olmesartan medoxomil + Placebo | Daiichi Sankyo | Phase 3 | 40 |
| Pactimibe sulfate | Daiichi Sankyo | Phase 2/3 | 30 |
| Pactimibe | Daiichi Sankyo | Phase 2 | 35 |
| Bempedoic acid + Ezetimibe + Rosuvastatin + Atorvastatin | Daiichi Sankyo | Phase 3 | 47 |
| Micronized 17B-estradiol | Johnson & Johnson | Phase 2/3 | 38 |
| Rosuvastatin + placebo + aspirin + placebo | AstraZeneca | Approved | 43 |
| Rosuvastatin + Placebo | AstraZeneca | Approved | 35 |
| rosuvastatin + placebo | AstraZeneca | Phase 1 | 29 |
| Rosuvastatin + Placebo | AstraZeneca | Phase 1 | 29 |
| Rosuvastatin + Atorvastatin | AstraZeneca | Phase 3 | 40 |
| Rosuvastatin + Placebo | AstraZeneca | Phase 3 | 40 |
| Rosuvastatin (5mg,10mg,20mg) + Rosuvastatin 5mg | AstraZeneca | Approved | 39 |
| Vorapaxar + Placebo | Merck | Phase 3 | 40 |
| Vorapaxar + Placebo + Aspirin + Clopidogrel | Merck | Phase 2 | 35 |
| Niacin/simvastatin compared to simvastatin alone at 2 doses | Merck | Approved | 43 |
| lovastatin | Merck | Phase 2/3 | 38 |
| Ezetimibe + Placebo | Merck | Approved | 43 |
| Vorapaxar + Placebo | Merck | Phase 3 | 32 |
| MK0633 | Merck | Phase 2 | 35 |