Orforglipron + Placebo
Phase 3RecruitingInterest: 47/100
47
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Atherosclerosis Cardiovascular Disease
Conditions
Atherosclerosis Cardiovascular Disease, Chronic Kidney Disease
Trial Timeline
Dec 1, 2025 → Aug 1, 2031
NCT ID
NCT07241390About Orforglipron + Placebo
Orforglipron + Placebo is a phase 3 stage product being developed by Eli Lilly for Atherosclerosis Cardiovascular Disease. The current trial status is recruiting. This product is registered under clinical trial identifier NCT07241390. Target conditions include Atherosclerosis Cardiovascular Disease, Chronic Kidney Disease.
What happened to similar drugs?
13 of 20 similar drugs in Atherosclerosis Cardiovascular Disease were approved
Approved (13) Terminated (3) Active (6)
Hype Score Breakdown
Clinical
17
Activity
15
Company
15
Novelty
0
Community
0
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT07241390 | Phase 3 | Recruiting |
| NCT07223593 | Phase 3 | Recruiting |
| NCT07202884 | Phase 3 | Recruiting |
| NCT07153471 | Phase 3 | Recruiting |
| NCT06972472 | Phase 3 | Recruiting |
| NCT06972459 | Phase 3 | Recruiting |
| NCT06993792 | Phase 3 | Recruiting |
| NCT06952530 | Phase 3 | Recruiting |
| NCT06948435 | Phase 3 | Recruiting |
| NCT06948422 | Phase 3 | Recruiting |
| NCT06824051 | Phase 1 | Completed |
| NCT06672939 | Phase 3 | Recruiting |
| NCT06672549 | Phase 3 | Recruiting |
| NCT06649045 | Phase 3 | Active |
| NCT06584916 | Phase 3 | Completed |
| NCT06109311 | Phase 3 | Completed |
| NCT05971940 | Phase 3 | Completed |
| NCT05931380 | Phase 3 | Completed |
| NCT05869903 | Phase 3 | Active |
| NCT05872620 | Phase 3 | Completed |
Competing Products
20 competing products in Atherosclerosis Cardiovascular Disease
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| 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 |
| Niaspan | Merck | Pre-clinical | 22 |
| MK0633 | Merck | Phase 2 | 35 |