Human Acellular Vessel (HAV)
Phase 2/3Active 0 watching 0 views this week⚡ Active
57
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Trauma
Conditions
Trauma, Vascular System Injury
Trial Timeline
Sep 1, 2018 → Sep 1, 2027
NCT ID
NCT03005418About Human Acellular Vessel (HAV)
Human Acellular Vessel (HAV) is a phase 2/3 stage product being developed by Humacyte for Trauma. The current trial status is active. This product is registered under clinical trial identifier NCT03005418. Target conditions include Trauma, Vascular System Injury.
Hype Score Breakdown
Clinical
22
Activity
15
Company
2
Novelty
7
Community
8
Clinical Trials (4)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03005418 | Phase 2/3 | Active |
| NCT03183245 | Phase 3 | Completed |
| NCT02887859 | Phase 2 | Completed |
| NCT02644941 | Phase 3 | Completed |
Competing Products
20 competing products in Trauma
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Duloxetine + Sugar pill | Eli Lilly | Phase 2 | 52 |
| Neurosteroid enantiomer | Oragenics | Phase 2 | 44 |
| Transdermal Patch + Loxoprofen sodium + Placebo (for loxoprofen sodium) + Placebo (for transdermal patch) | Daiichi Sankyo | Phase 3 | 77 |
| Celecoxib | Astellas Pharma | Pre-clinical | 23 |
| Mupirocin Calcium Cream, 2% + Bactroban® Cream + Cream vehicle of test product | Sun Pharmaceutical | Phase 1 | 33 |
| Duloxetine hydrochloride | Eli Lilly | Phase 3 | 77 |
| Galcanezumab-Gnlm | Eli Lilly | Approved | 85 |
| SYN117 (nepicastat) + Placebo comparator | Johnson & Johnson | Phase 2 | 52 |
| Nepicastat + Placebo | Johnson & Johnson | Phase 2 | 52 |
| JNJ-17299425 | Johnson & Johnson | Phase 2 | 52 |
| Placebo + sertraline | Johnson & Johnson | Approved | 85 |
| Quetiapine Fumarate + quetiapine fumarate placebo | AstraZeneca | Phase 3 | 77 |
| Adjunctive asenapine | Merck | Approved | 85 |
| Rizatriptan + Placebo | Merck | Pre-clinical | 23 |
| Alendronate | Merck | Approved | 85 |
| Iloperidone + Placebo | Novartis | Phase 2 | 52 |
| AMG 334 | Novartis | Phase 2 | 52 |
| Rivastigmine | Novartis | Phase 3 | 77 |
| Rivastigmine | Novartis | Approved | 85 |
| Balovaptan + Placebo | Roche | Phase 2 | 52 |