RZ358 Sequential Group Cohort 1 + RZ358 Sequential Group Cohort 2 + RZ358 Sequential Group Cohort 3 + RZ358 Sequential Group Cohort 4
Phase 2Completed 0 views this week 0 watching💤 Quiet
Interest: 25/100
25
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Congenital Hyperinsulinism
Conditions
Congenital Hyperinsulinism
Trial Timeline
Feb 24, 2020 → Aug 19, 2022
NCT ID
NCT04538989About RZ358 Sequential Group Cohort 1 + RZ358 Sequential Group Cohort 2 + RZ358 Sequential Group Cohort 3 + RZ358 Sequential Group Cohort 4
RZ358 Sequential Group Cohort 1 + RZ358 Sequential Group Cohort 2 + RZ358 Sequential Group Cohort 3 + RZ358 Sequential Group Cohort 4 is a phase 2 stage product being developed by Rezolute for Congenital Hyperinsulinism. The current trial status is completed. This product is registered under clinical trial identifier NCT04538989. Target conditions include Congenital Hyperinsulinism.
What happened to similar drugs?
4 of 20 similar drugs in Congenital Hyperinsulinism were approved
Approved (4) Terminated (0) Active (16)
Hype Score Breakdown
Clinical
12
Activity
8
Company
5
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT04538989 | Phase 2 | Completed |
Competing Products
20 competing products in Congenital Hyperinsulinism
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Tideglusib | AMO Pharma | Pre-clinical | 20 |
| Tideglusib + Placebo | AMO Pharma | Phase 2/3 | 28 |
| Tideglusib | AMO Pharma | Phase 2/3 | 35 |
| EDIT-101 | Editas Medicine | Phase 1/2 | 18 |
| Tildacerfont/Placebo | Spruce Biosciences | Phase 2 | 17 |
| SPR001 | Spruce Biosciences | Phase 2 | 25 |
| SPR001 | Spruce Biosciences | Phase 2 | 25 |
| Tildacerfont/Placebo | Spruce Biosciences | Phase 2 | 17 |
| Tildacerfont | Spruce Biosciences | Phase 2 | 17 |
| KW-3357 | Kyowa Kirin | Phase 1 | 29 |
| Pasireotide 0.6Mg Solution for Injection + Saline Solution | Novartis | Phase 2 | 27 |
| Sandostatine LP | Novartis | Phase 2 | 35 |
| mycophenolate mofetil | Roche | Phase 1 | 29 |
| turoctocog alfa + turoctocog alfa | Novo Nordisk | Phase 3 | 40 |
| catridecacog + recombinant factor XIII | Novo Nordisk | Phase 1 | 29 |
| activated recombinant human factor VII | Novo Nordisk | Phase 2 | 35 |
| turoctocog alfa pegol | Novo Nordisk | Phase 3 | 40 |
| recombinant factor XIII | Novo Nordisk | Pre-clinical | 26 |
| activated recombinant human factor VII, long acting + activated recombinant human factor VII, long acting | Novo Nordisk | Phase 1 | 29 |
| Advate® + turoctocog alfa | Novo Nordisk | Phase 1 | 29 |