Botulinum toxin type A + Placebo
Phase 3Completed 0 views this week 0 watching💤 Quiet
Interest: 37/100
37
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 24
Phase 35
ApprovedIndication / Disease
Cerebral Palsy
Conditions
Cerebral Palsy, Muscle Spasticity, Children
Trial Timeline
Jul 1, 2011 → Jun 1, 2014
NCT ID
NCT01249417About Botulinum toxin type A + Placebo
Botulinum toxin type A + Placebo is a phase 3 stage product being developed by Ipsen for Cerebral Palsy. The current trial status is completed. This product is registered under clinical trial identifier NCT01249417. Target conditions include Cerebral Palsy, Muscle Spasticity, Children.
What happened to similar drugs?
5 of 16 similar drugs in Cerebral Palsy were approved
Approved (5) Terminated (1) Active (11)
Hype Score Breakdown
Clinical
17
Activity
8
Company
12
Novelty
0
Community
0
Clinical Trials (14)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03569098 | Phase 2 | Completed |
| NCT03598777 | Phase 2 | Terminated |
| NCT02493946 | Phase 3 | Completed |
| NCT02353871 | Phase 3 | Completed |
| NCT02321436 | Approved | Completed |
| NCT01753310 | Phase 3 | Completed |
| NCT01249417 | Phase 3 | Completed |
| NCT01357980 | Phase 2 | Completed |
| NCT01249404 | Phase 3 | Completed |
| NCT00578097 | Phase 2 | Terminated |
| NCT00257660 | Phase 3 | Completed |
| NCT00447876 | Phase 2/3 | Completed |
| NCT00216411 | Approved | Completed |
| NCT00234546 | Approved | Completed |
Competing Products
20 competing products in Cerebral Palsy
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| mouse nerve growth factor | Sun Pharmaceutical | Approved | 39 |
| Edaravone Dexborneol + Placebo | Sun Pharmaceutical | Phase 2 | 31 |
| Oral Glycopyrrolate Liquid | Shionogi | Phase 3 | 40 |
| recombinant human erythropoietin alfa + 0.9% NaCl | Johnson & Johnson | Phase 2/3 | 38 |
| UDI-001 | Rohto Pharmaceutical | Phase 1/2 | 32 |
| NXY-059 | AstraZeneca | Phase 3 | 40 |
| NXY-059 | AstraZeneca | Phase 2 | 35 |
| Rosuvastatin | AstraZeneca | Approved | 39 |
| NXY-059 | AstraZeneca | Phase 3 | 40 |
| Comparator: Placebo + Comparator: MK0724 | Merck | Phase 2 | 27 |
| Vorapaxar 2.5 mg + Vorapaxar 1 mg + Placebo + Aspirin 75-150 mg | Merck | Phase 2 | 35 |
| Recombinant Factor VIIa + Biological/Vaccine: Placebo | Novo Nordisk | Phase 3 | 47 |
| Recombinant Activated Factor VII (rFVIIa) + Placebo | Novo Nordisk | Phase 3 | 44 |
| Ponezumab | Pfizer | Phase 2 | 35 |
| PF-05230907 | Pfizer | Phase 1 | 21 |
| Azithromycin + Pyrimethamine + Leucovorin calcium | Pfizer | Phase 1 | 29 |
| clopidogrel (SR25990C) | Sanofi | Approved | 43 |
| Intrarectal quinine | Sanofi | Phase 3 | 36 |
| Piracetam | UCB | Approved | 35 |
| Placebo + ALN-APP | Alnylam Pharmaceuticals | Phase 2 | 39 |