TY - JOUR
T1 - Efficacy and Safety of MT10107 (Coretox) in Poststroke Upper Limb Spasticity Treatment
T2 - A Randomized, Double-Blind, Active Drug-Controlled, Multicenter, Phase III Clinical Trial
AU - Lee, Junekyung
AU - Chun, Min Ho
AU - Ko, Young Jin
AU - Lee, Shi Uk
AU - Kim, Deog Young
AU - Paik, Nam Jong
AU - Kwon, Bum Sun
AU - Park, Yoon Ghil
N1 - Publisher Copyright:
© 2020 American Congress of Rehabilitation Medicine
PY - 2020/9
Y1 - 2020/9
N2 - 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.
AB - 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.
KW - Botulinum toxins
KW - Muscle spasticity
KW - Rehabilitation
KW - Safety
KW - Stroke
KW - Upper extremity
UR - http://www.scopus.com/inward/record.url?scp=85088783625&partnerID=8YFLogxK
U2 - 10.1016/j.apmr.2020.03.025
DO - 10.1016/j.apmr.2020.03.025
M3 - Article
C2 - 32497599
AN - SCOPUS:85088783625
SN - 0003-9993
VL - 101
SP - 1485
EP - 1496
JO - Archives of Physical Medicine and Rehabilitation
JF - Archives of Physical Medicine and Rehabilitation
IS - 9
ER -