Efficacy and Safety of MT10107 (Coretox) in Poststroke Upper Limb Spasticity Treatment: A Randomized, Double-Blind, Active Drug-Controlled, Multicenter, Phase III Clinical Trial.

Archives of physical medicine and rehabilitation 2020 Vol.101(9) p. 1485-1496

Lee J, Chun MH, Ko YJ, Lee SU, Kim DY, Paik NJ, Kwon BS, Park YG

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Abstract

[OBJECTIVE] To compare the efficacy and safety of MT10107 (Coretox) with those of onabotulinum toxin A (Botox) in patients with poststroke upper limb spasticity DESIGN: Prospective, randomized, double-blind, active drug-controlled, multicenter, phase III clinical trial.

[SETTING] Seven university hospitals in the Republic of Korea.

[PARTICIPANTS] Patients (N=220) with poststroke upper limb spasticity.

[INTERVENTIONS] All participants received a single injection of either MT10107 (Coretox group) or onabotulinum toxin A (Botox group).

[MAIN OUTCOME MEASURES] The primary outcome was change in wrist flexor spasticity from baseline to week 4, which was assessed using the modified Ashworth scale (MAS). The secondary outcomes were MAS scores for wrist, elbow, and finger flexors; percentage of treatment responders (response rate); Disability Assessment Scale (DAS) score, and global assessment of treatment. Safety was evaluated based on adverse events, vital signs, physical examination findings, and laboratory test results. The efficacy and safety were evaluated at 4, 8, and 12 weeks postintervention.

[RESULTS] The primary outcome was found to be -1.32±0.69 and -1.40±0.69 for the Coretox and Botox groups, respectively. MT10107 showed a non-inferior efficacy compared with onabotulinum toxin A, as the 95% confidence interval for between-group differences was -0.10 to 0.27 and the upper limit was less than the non-inferiority margin of 0.45. Regarding the secondary outcomes, MAS scores for all muscles and DAS scores showed a significant improvement at all time points in both groups, with no significant between-group difference. No significant between-group differences were observed regarding response rate, global assessment of treatment, and safety measures.

[CONCLUSIONS] MT10107 showed no significant difference in efficacy and safety compared with onabotulinum toxin A in poststroke upper limb spasticity treatment.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
시술 botox 보툴리눔독소 주사 dict 3

MeSH Terms

Aged; Botulinum Toxins, Type A; Disability Evaluation; Double-Blind Method; Female; Humans; Male; Middle Aged; Muscle Spasticity; Neuromuscular Agents; Prospective Studies; Republic of Korea; Stroke; Stroke Rehabilitation; Upper Extremity

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