Riliprubart Prefilled Pen (PFP)
Phase 3Recruiting 0 views this week 0 watching⚡ Active
Interest: 47/100
47
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Polyneuropathy, Inflammatory Demyelinating, Chronic
Conditions
Polyneuropathy, Inflammatory Demyelinating, Chronic
Trial Timeline
Apr 1, 2025 → Oct 3, 2029
NCT ID
NCT06859099About Riliprubart Prefilled Pen (PFP)
Riliprubart Prefilled Pen (PFP) is a phase 3 stage product being developed by Sanofi for Polyneuropathy, Inflammatory Demyelinating, Chronic. The current trial status is recruiting. This product is registered under clinical trial identifier NCT06859099. Target conditions include Polyneuropathy, Inflammatory Demyelinating, Chronic.
What happened to similar drugs?
5 of 17 similar drugs in Polyneuropathy, Inflammatory Demyelinating, Chronic were approved
Approved (5) Terminated (0) Active (12)
Hype Score Breakdown
Clinical
17
Activity
15
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT06859099 | Phase 3 | Recruiting |
Competing Products
20 competing products in Polyneuropathy, Inflammatory Demyelinating, Chronic
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Qutenza + Pregabalin | Astellas Pharma | Approved | 43 |
| Ranirestat + Placebo | Eisai | Phase 2/3 | 38 |
| KITE-363 + Fludarabine + Cyclophosphamide | Gilead Sciences | Phase 1 | 36 |
| Fx-1006A + Placebo | Pfizer | Phase 2/3 | 38 |
| tafamidis meglumine | Pfizer | Approved | 43 |
| Fx-1006A | Pfizer | Phase 2 | 35 |
| Vyndaqel | Pfizer | Pre-clinical | 26 |
| tafamidis | Pfizer | Phase 3 | 40 |
| Imipramine + Pregabalin + Imipramine, pregabalin + Placebo | Pfizer | Approved | 39 |
| Fx-1006A | Pfizer | Phase 2/3 | 38 |
| riliprubart + Placebo + riliprubart + Placebo + IVIg + Placebo | Sanofi | Phase 3 | 47 |
| Intravenous Immunoglobulin | CSL | Pre-clinical | 26 |
| IgPro10 | CSL | Approved | 50 |
| Immune Globulin Subcutaneous (Human) | CSL | Pre-clinical | 26 |
| IgPro20 | CSL | Phase 3 | 40 |
| Hizentra | CSL | Pre-clinical | 33 |
| 10% liquid formulation of human immunoglobulin | CSL | Phase 3 | 40 |
| IgPro20 (low dose) + Placebo + IgPro10 + IgPro20 (high dose) | CSL | Phase 3 | 40 |
| levetiracetam | UCB | Phase 2 | 35 |
| Rozanolixizumab | UCB | Pre-clinical | 26 |