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Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(5-6):345-52. doi: 10.3109/21678421.2015.1026826. Epub 2015 Apr 2.

A multi-center screening trial of rasagiline in patients with amyotrophic lateral sclerosis: Possible mitochondrial biomarker target engagement.

Author information

1
a University of Kansas Medical Center , Kansas.
2
b California Pacific Medical Center , San Francisco , California.
3
c Phoenix Neurological Associates , Phoenix , Arizona , Kansas City , Kansas.
4
d University of Minnesota , Minneapolis , Minnesota.
5
e The Methodist Hospital , Houston , Texas.
6
f McGill University , Montreal , Quebec.
7
g University of Tennessee , Memphis , Tennessee.
8
h University of Nebraska , Omaha , Nebraska.
9
i University of Iowa Health Care , Iowa City , Iowa.
10
j University of Pennsylvania , Philadelphia , Pennsylvania.

Abstract

Rasagiline, a monoamine oxidase B inhibitor, slowed disease progression in the SOD1 mouse, and in a case series of patients with amyotrophic lateral sclerosis (ALS). Here we determine whether rasagiline is safe and effective in ALS compared to historical placebo controls, and whether it alters mitochondrial biomarkers. We performed a prospective open-label, multicenter screening trial of 36 ALS patients treated with 2 mg oral rasagiline daily for 12 months. Outcomes included the slope of deterioration of the revised ALS Functional Rating Scale (ALSFRS-R), adverse event monitoring, time to treatment failure, and exploratory biomarkers. Participants experienced no serious drug-related adverse events, and the most common adverse event was nausea (11.1%). Rasagiline did not improve the rate of decline in the ALSFRS-R; however, differences in symptom duration compared to historical placebo controls differentially affected ALSFRS-R slope estimates. Rasagiline changed biomarkers over 12 months, such that the mitochondrial membrane potential increased (JC-1 red/green fluorescent ratio 1.92, p = 0.0001) and apoptosis markers decreased (Bcl-2/Bax ratio 0.24, p < 0.0001). In conclusion, engagement of exploratory biomarkers and questions about comparability of baseline characteristics lead us to recommend a further placebo-controlled trial.

KEYWORDS:

Biomarker; apoptosis; clinical trials; mitochondria; rasagiline

PMID:
25832828
PMCID:
PMC4610861
DOI:
10.3109/21678421.2015.1026826
[Indexed for MEDLINE]
Free PMC Article

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