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Safety and efficacy...
Safety and efficacy of arimoclomol in patients with early amyotrophic lateral sclerosis (ORARIALS-01) : a randomised, double-blind, placebo-controlled, multicentre, phase 3 trial
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- Benatar, Michael (author)
- Department of Neurology, University of Miami Miller School of Medicine, FL, Miami, United States
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- Hansen, Thomas (author)
- Orphazyme, Copenhagen, Denmark
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- Rom, Dror (author)
- Prosoft Clinical, PA, Chesterbrook, United States
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- Geist, Marie A (author)
- Orphazyme, Copenhagen, Denmark
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- Blaettler, Thomas (author)
- Orphazyme, Copenhagen, Denmark
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- Camu, William (author)
- Department of Neurology University of Montpellier, CHU Montpellier, INM INSERM, Montpellier, France
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- Kuzma-Kozakiewicz, Magdalena (author)
- Department of Neurology, Medical University of Warsaw, Warsaw, Poland
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- van den Berg, Leonard H (author)
- Department of Neurology, University Medical Center Utrecht, Utrecht, Netherlands
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- Morales, Raul Juntas (author)
- Department of Neurology, Vall d'Hebron University Hospital, Barcelona, Spain
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- Chio, Adriano (author)
- Rita Levi Montalcini Department of Neuroscience, University of Torino, Torino, Italy
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- Andersen, Peter M., 1962- (author)
- Umeå universitet,Neurovetenskaper
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- Pradat, Pierre-Francois (author)
- APHP, Department of Neurology, Hôpital Pitié-Salpêtrière, Paris, France
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- Lange, Dale (author)
- Department of Neurology, Hospital for Special Surgery, NY, New York, United States
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- Van Damme, Philip (author)
- Department of Neurology, University Hospital Leuven, KU Leuven, Leuven, Belgium
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- Mora, Gabriele (author)
- Istituti Clinici Scientifici Maugeri, IRCCS Milano, Milan, Italy
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- Grudniak, Mariusz (author)
- Research and Development Department, Polish Stem Cell Bank, Warsaw, Poland
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- Elliott, Matthew (author)
- University of Virginia Medical Center, VA, Charlottesville, United States
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- Petri, Susanne (author)
- Department of Neurology, Hannover Medical School, Hannover, Germany
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- Olney, Nicholas (author)
- Providence Portland Medical Center, Providence Brain and Spine Institute, OR, Portland, United States
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- Ladha, Shafeeq (author)
- Department of Neurology, Barrow Neurological Institute, AZ, Phoenix, United States
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- Goyal, Namita A (author)
- Department of Neurology, University of California Irvine, CA, Irvine, United States
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- Meyer, Thomas (author)
- Department of Neurology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany
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- Hanna, Michael G (author)
- University College London, National Hospital for Neurology and Neurosurgery, London, United Kingdom
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- Quinn, Colin (author)
- Department of Neurology, Perelman School of Medicine, University of Pennsylvania, PA, Philadelphia, United States
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- Genge, Angela (author)
- Department of Neurology, Montreal Neurological Institute, QC, Montreal, Canada
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- Zinman, Lorne (author)
- Sunnybrook Health Sciences Centre, ON, Toronto, Canada
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- Jabari, Duaa (author)
- Department of Neurology, The University of Kansas Medical Center, KS, Kansas City, United States
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- Shoesmith, Christen (author)
- Department of Clinical Neurological Sciences, London Health Sciences Centre, Western University, ON, London, Canada
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- Ludolph, Albert C (author)
- Department of Neurology, University of Ulm, Ulm, Germany
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- Neuwirth, Christoph (author)
- Neuromuscular Disease Unit/ALS Clinic, Kantonspital St Gallen, St Gallen, Switzerland
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- Nations, Sharon (author)
- University of Texas Southwestern, TX, Dallas, United States
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- Shefner, Jeremy M (author)
- Department of Neurology, Barrow Neurological Institute, AZ, Phoenix, United States
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- Turner, Martin R (author)
- Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom
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- Wuu, Joanne (author)
- Department of Neurology, University of Miami Miller School of Medicine, FL, Miami, United States
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- Bennett, Richard (author)
- Orphazyme, Copenhagen, Denmark
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- Dang, Hoang (author)
- Orphazyme, Copenhagen, Denmark
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- Sundgreen, Claus (author)
- Orphazyme, Copenhagen, Denmark
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- Granit, Volkan (author)
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(creator_code:org_t)
- Elsevier, 2024
- 2024
- English.
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In: Lancet Neurology. - : Elsevier. - 1474-4422 .- 1474-4465. ; 23:7, s. 687-699
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
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- Background: Amyotrophic lateral sclerosis is a progressive neurodegenerative disorder leading to muscle weakness and respiratory failure. Arimoclomol, a heat-shock protein-70 (HSP70) co-inducer, is neuroprotective in animal models of amyotrophic lateral sclerosis, with multiple mechanisms of action, including clearance of protein aggregates, a pathological hallmark of sporadic and familial amyotrophic lateral sclerosis. We aimed to evaluate the safety and efficacy of arimoclomol in patients with amyotrophic lateral sclerosis.Methods: ORARIALS-01 was a multinational, randomised, double-blind, placebo-controlled, parallel-group trial done at 29 centres in 12 countries in Europe and North America. Patients were eligible if they were aged 18 years or older and met El Escorial criteria for clinically possible, probable, probable laboratory-supported, definite, or familial amyotrophic lateral sclerosis; had an ALS Functional Rating Scale-Revised score of 35 or more; and had slow vital capacity at 70% or more of the value predicted on the basis of the participant's age, height, and sex. Patients were randomly assigned (2:1) in blocks of 6, stratified by use of a stable dose of riluzole or no riluzole use, to receive oral arimoclomol citrate 1200 mg/day (400 mg three times per day) or placebo. The Randomisation sequence was computer generated centrally. Investigators, study personnel, and study participants were masked to treatment allocation. The primary outcome was the Combined Assessment of Function and Survival (CAFS) rank score over 76 weeks of treatment. The primary outcome and safety were analysed in the modified intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT03491462, and is completed.Findings: Between July 31, 2018, and July 17, 2019, 287 patients were screened, 245 of whom were enrolled in the trial and randomly assigned. The modified intention-to-treat population comprised 239 patients (160 in the arimoclomol group and 79 in the placebo group): 151 (63%) were male and 88 (37%) were female; mean age was 57·6 years (SD 10·9). CAFS score over 76 weeks did not differ between groups (mean 0·51 [SD 0·29] in the arimoclomol group vs 0·49 [0·28] in the placebo group; p=0·62). Cliff's delta comparing the two groups was 0·039 (95% CI –0·116 to 0·194). Proportions of participants who died were similar between the treatment groups: 29 (18%) of 160 patients in the arimoclomol group and 18 (23%) of 79 patients in the placebo group. Most deaths were due to disease progression. The most common adverse events were gastrointestinal. Adverse events were more often deemed treatment-related in the arimoclomol group (104 [65%]) than in the placebo group (41 [52%]) and more often led to treatment discontinuation in the arimoclomol group (26 [16%]) than in the placebo group (four [5%]).Interpretation: Arimoclomol did not improve efficacy outcomes compared with placebo. Although available biomarker data are insufficient to preclude future strategies that target the HSP response, safety data suggest that a higher dose of arimoclomol would not have been tolerated.Funding: Orphazyme.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Neurologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Neurology (hsv//eng)
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Benatar, Michael
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Hansen, Thomas
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Rom, Dror
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Geist, Marie A
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Camu, William
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Elliott, Matthew
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Petri, Susanne
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Olney, Nicholas
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Ladha, Shafeeq
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Goyal, Namita A
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Meyer, Thomas
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Hanna, Michael G
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Quinn, Colin
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Genge, Angela
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Bennett, Richard
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Dang, Hoang
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Moglia, Cristina
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Canosa, Antonio
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Fuda, Giuseppe
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Querin, Giorgia
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Coudoin, Sylvie
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Holzberg, Shara
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Serrien, Anouk
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