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BioElectron Announces Positive Results from Phase 2A ALS Trial

BioElectron
Posted on: 27 Sep 18

MOUNTAIN VIEW, Calif., Sept. 24, 2018 /PRNewswire/ -- BioElectron Technology Corporation (BioElectron), a clinical-stage platform biotechnology company, today announced positive results from its recently completed phase 2a clinical trial of EPI-589 in patients with Amyotrophic Lateral Sclerosis (ALS).

The phase 2a trial (NCT02460679) was designed to assess EPI-589's safety, tolerability, and pharmacology in a cohort of ALS patients already receiving medications for ALS. In addition, the trial sought to identify signals of central nervous system and blood-based biomarkers consistent with ALS, drug target, and mechanism of action.

The study achieved its primary safety and tolerability endpoint without drug-related serious adverse events or dose-limiting toxicities. Drug treatment was also associated with a statistically significant improvement in cerebrospinal fluid (CSF) and plasma-based biomarkers known to be associated with neuroinflammation and ALS disease progression. A series of clinical assessments further suggested the drug treatment was associated with a slowing of disease progression on the validated ALS Functional Rating Scale, in addition to associated improvements in grip strength and swallowing.

"These data demonstrating drug safety, tolerability, and disease biomarker effect all provide a strong rationale for the continued development of EPI-589 for ALS," said BioElectron CEO Dr. Matthew Klein. "Furthermore, the biochemical evidence of EPI-589's effect on biomarkers of neuroinflammation and disease progression support the development of EPI-589 for other neurological disorders characterized by neuroinflammation."

The clinical trial was conducted at three leading ALS sites in the United States: California Pacific Medical Center (CPMC) in San Francisco; Cedars-Sinai Medical Center in Los Angeles; and Providence Portland Medical Center in Portland. A total of 21 subjects were enrolled in the trial for a 30-day run-in period to establish baseline biomarker and clinical status. The subjects were treated for 90 days with EPI-589 and followed for an additional three months after withdrawal of therapy.

"The results of this trial are very encouraging for the ALS community," said Robert Miller, MD, study principal investigator and director of the Forbes Norris ALS/MDA Center at CPMC. "A safe and effective orally administered medication would be a significant addition to the treatment of ALS patients."

EPI-589 is BioElectron's second compound in active clinical development. EPI-589 is a novel, orally administered, small molecule being developed for adult neurodegenerative diseases in collaboration with Sumitomo Dainippon Pharma Co., Ltd, who holds licensing rights for the compound in Japan and North America. EPI-589 targets oxidoreductase enzymes known to be critical to the regulation of inflammation and programmed cell death. Accordingly, it is being developed for CNS diseases characterized by inflammation. BioElectron's lead clinical compound, EPI-743, is in late-stage clinical development for the treatment of mitochondrial disease.

The results of this study have been accepted for poster presentation at the International Symposium on ALS and Motor Neuron Disease in Scotland in December, 2018. Planning is underway of a subsequent trial of longer duration with a placebo-control group to establish clinical benefit.

About BioElectron
Located in Mountain View, CA, BioElectron is a clinical-stage platform biotechnology company utilizing its expertise in the chemistry of energy regulation (redox chemistry) to develop first-in-class therapeutics for genetic and acquired diseases of energy. The Company has been a leader in the development of drugs for the treatment of inherited mitochondrial disease. Through reverse engineering the amplified clinical and biochemical signals of energy dysregulation in mitochondrial disease patients, the Company has identified a number of enzyme targets essential to the regulation of inflammation, oxidative stress, and ferroptosis in biological systems. BioElectron can uniquely drug these enzyme targets to develop therapeutic solutions beyond the reach of current drug development approaches.

For additional information on BioElectron, please visit www.bioelectron.com or contact pr@bioelectron.com.

Editor's Details

Mike Wood
PharmiWeb.com
www.pharmiweb.com
editor@pharmiweb.com

Last updated on: 27/09/2018

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