KVD900
Phase 2Completed 1 views this week 0 watching💤 Quiet
Interest: 29/100
29
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Hereditary Angioedema
Conditions
Hereditary Angioedema
Trial Timeline
Jul 2, 2019 → Dec 8, 2020
NCT ID
NCT04208412About KVD900
KVD900 is a phase 2 stage product being developed by KalVista Pharmaceuticals for Hereditary Angioedema. The current trial status is completed. This product is registered under clinical trial identifier NCT04208412. Target conditions include Hereditary Angioedema.
What happened to similar drugs?
3 of 20 similar drugs in Hereditary Angioedema were approved
Approved (3) Terminated (0) Active (17)
Hype Score Breakdown
Clinical
12
Activity
8
Company
9
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04208412 | Phase 2 | Completed |
Competing Products
20 competing products in Hereditary Angioedema
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| KVD824 + Placebo to KVD824 | KalVista Pharmaceuticals | Phase 1 | 23 |
| KVD900 600 mg + KVD900 300 mg | KalVista Pharmaceuticals | Phase 3 | 38 |
| Sebetralstat | KalVista Pharmaceuticals | Pre-clinical | 20 |
| KVD900 + Placebo to KVD900 | KalVista Pharmaceuticals | Phase 1 | 23 |
| Sebetralstat | KalVista Pharmaceuticals | Pre-clinical | 24 |
| Placebo + KVD900 600 mg + KVD900 300 mg | KalVista Pharmaceuticals | Phase 3 | 34 |
| KVD824 Prototype 1 modified-release tablet + KVD824 Prototype 2 modified-release tablet + KVD824 Immediate-Release Capsule + Placebo to KVD824 Prototype 1 + KVD824 Prototype 3 modified-release tablet | KalVista Pharmaceuticals | Phase 1 | 23 |
| KVD900 150 mg + KVD900 300 mg + KVD900 600 mg | KalVista Pharmaceuticals | Phase 3 | 34 |
| KVD824 + Placebo to KVD824 | KalVista Pharmaceuticals | Phase 2 | 21 |
| KVD900 600 mg + Drug: KVD900 300 mg | KalVista Pharmaceuticals | Phase 3 | 38 |
| Deferasirox FCT | Novartis | Phase 2 | 27 |
| Canakinumab + Placebo | Novartis | Phase 3 | 40 |
| Ilaris | Novartis | Pre-clinical | 33 |
| Standard of Care for Haemophilia A | Roche | Pre-clinical | 26 |
| Emicizumab | Roche | Phase 3 | 40 |
| Tafamidis | Pfizer | Pre-clinical | 26 |
| tafamidis | Pfizer | Pre-clinical | 26 |
| Nitisinone | Swedish Orphan Biovitrum | Pre-clinical | 26 |
| Nitisinone | Swedish Orphan Biovitrum | Phase 1 | 29 |
| Nitisinone | Swedish Orphan Biovitrum | Pre-clinical | 18 |