Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trial

Research output: Contribution to journalJournal articleResearchpeer-review

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Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy : MOTOR trial. / Madsen, Karen L.; Buch, Astrid E.; Cohen, Bruce H.; Falk, Marni J.; Goldsberry, Angela; Goldstein, Amy; Karaa, Amel; Koenig, Mary K.; Muraresku, Colleen C.; Meyer, Colin; O'Grady, Megan; Scaglia, Fernando; Shieh, Perry B.; Vockley, Jerry; Zolkipli-Cunningham, Zarazuela; Haller, Ronald G.; Vissing, John.

In: Neurology, Vol. 94, No. 7, 2020, p. e687-e698.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Madsen, KL, Buch, AE, Cohen, BH, Falk, MJ, Goldsberry, A, Goldstein, A, Karaa, A, Koenig, MK, Muraresku, CC, Meyer, C, O'Grady, M, Scaglia, F, Shieh, PB, Vockley, J, Zolkipli-Cunningham, Z, Haller, RG & Vissing, J 2020, 'Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trial', Neurology, vol. 94, no. 7, pp. e687-e698. https://doi.org/10.1212/WNL.0000000000008861

APA

Madsen, K. L., Buch, A. E., Cohen, B. H., Falk, M. J., Goldsberry, A., Goldstein, A., Karaa, A., Koenig, M. K., Muraresku, C. C., Meyer, C., O'Grady, M., Scaglia, F., Shieh, P. B., Vockley, J., Zolkipli-Cunningham, Z., Haller, R. G., & Vissing, J. (2020). Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trial. Neurology, 94(7), e687-e698. https://doi.org/10.1212/WNL.0000000000008861

Vancouver

Madsen KL, Buch AE, Cohen BH, Falk MJ, Goldsberry A, Goldstein A et al. Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trial. Neurology. 2020;94(7):e687-e698. https://doi.org/10.1212/WNL.0000000000008861

Author

Madsen, Karen L. ; Buch, Astrid E. ; Cohen, Bruce H. ; Falk, Marni J. ; Goldsberry, Angela ; Goldstein, Amy ; Karaa, Amel ; Koenig, Mary K. ; Muraresku, Colleen C. ; Meyer, Colin ; O'Grady, Megan ; Scaglia, Fernando ; Shieh, Perry B. ; Vockley, Jerry ; Zolkipli-Cunningham, Zarazuela ; Haller, Ronald G. ; Vissing, John. / Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy : MOTOR trial. In: Neurology. 2020 ; Vol. 94, No. 7. pp. e687-e698.

Bibtex

@article{274dc78736cb4fc18c4d8ad2d79383d0,
title = "Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trial",
abstract = "OBJECTIVE: To investigate the safety and efficacy of escalating doses of the semi-synthetic triterpenoid omaveloxolone in patients with mitochondrial myopathy. METHODS: In cohorts of 8-13, 53 participants were randomized double-blind to 12 weeks of treatment with omaveloxolone 5, 10, 20, 40, 80, or 160 mg, or placebo. Outcome measures were change in peak cycling exercise workload (primary), in 6-minute walk test (6MWT) distance (secondary), and in submaximal exercise heart rate and plasma lactate (exploratory). RESULTS: No differences in peak workload or 6MWT were observed at week 12 with omaveloxolone treatment vs placebo for all omaveloxolone dose groups. In contrast, omaveloxolone 160 mg reduced heart rate at week 12 by 12.0 ± 4.6 bpm (SE) during submaximal exercise vs placebo, p = 0.01, and by 8.7 ± 3.5 bpm (SE) vs baseline, p = 0.02. Similarly, blood lactate was 1.4 ± 0.7 mM (SE) lower vs placebo, p = 0.04, and 1.6 ± 0.5 mM (SE) lower vs baseline at week 12, p = 0.003, with omaveloxolone 160 mg treatment. Adverse events were generally mild and infrequent. CONCLUSIONS: Omaveloxolone 160 mg was well-tolerated, and did not lead to change in the primary outcome measure, but improved exploratory endpoints lowering heart rate and lactate production during submaximal exercise, consistent with improved mitochondrial function and submaximal exercise tolerance. Therefore, omaveloxolone potentially benefits patients with mitochondrial myopathy, which encourages further investigations of omaveloxolone in this patient group. CLINICALTRIALSGOV IDENTIFIER: NCT02255422. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that, for patients with mitochondrial myopathy, omaveloxolone compared to placebo did not significantly change peak exercise workload.",
author = "Madsen, {Karen L.} and Buch, {Astrid E.} and Cohen, {Bruce H.} and Falk, {Marni J.} and Angela Goldsberry and Amy Goldstein and Amel Karaa and Koenig, {Mary K.} and Muraresku, {Colleen C.} and Colin Meyer and Megan O'Grady and Fernando Scaglia and Shieh, {Perry B.} and Jerry Vockley and Zarazuela Zolkipli-Cunningham and Haller, {Ronald G.} and John Vissing",
year = "2020",
doi = "10.1212/WNL.0000000000008861",
language = "English",
volume = "94",
pages = "e687--e698",
journal = "Neurology",
issn = "0028-3878",
publisher = "Lippincott Williams & Wilkins",
number = "7",

}

RIS

TY - JOUR

T1 - Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy

T2 - MOTOR trial

AU - Madsen, Karen L.

AU - Buch, Astrid E.

AU - Cohen, Bruce H.

AU - Falk, Marni J.

AU - Goldsberry, Angela

AU - Goldstein, Amy

AU - Karaa, Amel

AU - Koenig, Mary K.

AU - Muraresku, Colleen C.

AU - Meyer, Colin

AU - O'Grady, Megan

AU - Scaglia, Fernando

AU - Shieh, Perry B.

AU - Vockley, Jerry

AU - Zolkipli-Cunningham, Zarazuela

AU - Haller, Ronald G.

AU - Vissing, John

PY - 2020

Y1 - 2020

N2 - OBJECTIVE: To investigate the safety and efficacy of escalating doses of the semi-synthetic triterpenoid omaveloxolone in patients with mitochondrial myopathy. METHODS: In cohorts of 8-13, 53 participants were randomized double-blind to 12 weeks of treatment with omaveloxolone 5, 10, 20, 40, 80, or 160 mg, or placebo. Outcome measures were change in peak cycling exercise workload (primary), in 6-minute walk test (6MWT) distance (secondary), and in submaximal exercise heart rate and plasma lactate (exploratory). RESULTS: No differences in peak workload or 6MWT were observed at week 12 with omaveloxolone treatment vs placebo for all omaveloxolone dose groups. In contrast, omaveloxolone 160 mg reduced heart rate at week 12 by 12.0 ± 4.6 bpm (SE) during submaximal exercise vs placebo, p = 0.01, and by 8.7 ± 3.5 bpm (SE) vs baseline, p = 0.02. Similarly, blood lactate was 1.4 ± 0.7 mM (SE) lower vs placebo, p = 0.04, and 1.6 ± 0.5 mM (SE) lower vs baseline at week 12, p = 0.003, with omaveloxolone 160 mg treatment. Adverse events were generally mild and infrequent. CONCLUSIONS: Omaveloxolone 160 mg was well-tolerated, and did not lead to change in the primary outcome measure, but improved exploratory endpoints lowering heart rate and lactate production during submaximal exercise, consistent with improved mitochondrial function and submaximal exercise tolerance. Therefore, omaveloxolone potentially benefits patients with mitochondrial myopathy, which encourages further investigations of omaveloxolone in this patient group. CLINICALTRIALSGOV IDENTIFIER: NCT02255422. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that, for patients with mitochondrial myopathy, omaveloxolone compared to placebo did not significantly change peak exercise workload.

AB - OBJECTIVE: To investigate the safety and efficacy of escalating doses of the semi-synthetic triterpenoid omaveloxolone in patients with mitochondrial myopathy. METHODS: In cohorts of 8-13, 53 participants were randomized double-blind to 12 weeks of treatment with omaveloxolone 5, 10, 20, 40, 80, or 160 mg, or placebo. Outcome measures were change in peak cycling exercise workload (primary), in 6-minute walk test (6MWT) distance (secondary), and in submaximal exercise heart rate and plasma lactate (exploratory). RESULTS: No differences in peak workload or 6MWT were observed at week 12 with omaveloxolone treatment vs placebo for all omaveloxolone dose groups. In contrast, omaveloxolone 160 mg reduced heart rate at week 12 by 12.0 ± 4.6 bpm (SE) during submaximal exercise vs placebo, p = 0.01, and by 8.7 ± 3.5 bpm (SE) vs baseline, p = 0.02. Similarly, blood lactate was 1.4 ± 0.7 mM (SE) lower vs placebo, p = 0.04, and 1.6 ± 0.5 mM (SE) lower vs baseline at week 12, p = 0.003, with omaveloxolone 160 mg treatment. Adverse events were generally mild and infrequent. CONCLUSIONS: Omaveloxolone 160 mg was well-tolerated, and did not lead to change in the primary outcome measure, but improved exploratory endpoints lowering heart rate and lactate production during submaximal exercise, consistent with improved mitochondrial function and submaximal exercise tolerance. Therefore, omaveloxolone potentially benefits patients with mitochondrial myopathy, which encourages further investigations of omaveloxolone in this patient group. CLINICALTRIALSGOV IDENTIFIER: NCT02255422. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that, for patients with mitochondrial myopathy, omaveloxolone compared to placebo did not significantly change peak exercise workload.

U2 - 10.1212/WNL.0000000000008861

DO - 10.1212/WNL.0000000000008861

M3 - Journal article

C2 - 31896620

AN - SCOPUS:85082780142

VL - 94

SP - e687-e698

JO - Neurology

JF - Neurology

SN - 0028-3878

IS - 7

ER -

ID: 255840187