drugset / Trial / NCT06783114
A Clinical Study on Recombinant Botulinum Toxin Type A (YY001) for Injection in The Treatment of Upper Limb Spasticity in Adults
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This is a randomized, double-blind, multi-center phase II/III study to evaluate the efficacy and safety of Recombinant Botulinum Toxin Type A (YY001) for injection in the treatment of upper limb spasticity in adults
Timeline
- Start
- 2024-09-14
- Primary completion
- 2026-09-30
- Completion
- 2026-09-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Botulinum toxin type A | Protein / enzyme biologic | 200 iu | Intramuscular |
| Subject | YY001 | Protein / enzyme biologic | 200 iu | Intramuscular |
| Subject | YY001 | Protein / enzyme biologic | 400 iu | Intramuscular |
Indications
No indication recorded.