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Efficacy and Safety of MT10107 (Coretox) in Poststroke Upper Limb Spasticity Treatment: A Randomized, Double-Blind, Active Drug-Controlled, Multicenter, Phase III Clinical Trial.
Lee, Junekyung; Chun, Min Ho; Ko, Young Jin; Lee, Shi-Uk; Kim, Deog Young; Paik, Nam-Jong; Kwon, Bum Sun; Park, Yoon Ghil.
Afiliación
  • Lee J; Department of Rehabilitation Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul.
  • Chun MH; Department of Rehabilitation Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul. Electronic address: mhchun@amc.seoul.kr.
  • Ko YJ; Department of Rehabilitation Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul.
  • Lee SU; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Boramae Medical Center, Seoul.
  • Kim DY; Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul.
  • Paik NJ; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam.
  • Kwon BS; Department of Rehabilitation Medicine, Dongguk University Ilsan Hospital, Goyang.
  • Park YG; Department of Rehabilitation Medicine, Gangnam Severance Hospital Yonsei University College of Medicine, Seoul, Republic of Korea.
Arch Phys Med Rehabil ; 101(9): 1485-1496, 2020 09.
Article en En | MEDLINE | ID: mdl-32497599
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Toxinas Botulínicas Tipo A / Accidente Cerebrovascular / Espasticidad Muscular / Fármacos Neuromusculares Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Arch Phys Med Rehabil Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Toxinas Botulínicas Tipo A / Accidente Cerebrovascular / Espasticidad Muscular / Fármacos Neuromusculares Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Arch Phys Med Rehabil Año: 2020 Tipo del documento: Article
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