DURHAM, N.C., Nov. 2, 2016 /PRNewswire/ -- Three posters presented bySpyryx Biosciences at the North American Cystic Fibrosis Conference provided data that demonstrates the safety, stability and efficacy of SPX-101 in animal models and supports further clinical development.
Patients with cystic fibrosis (CF) have
"We are excited to share these positive results with the community of researchers and physicians who are all dedicated to finding breakthrough treatments for cystic fibrosis," said John Taylor, President and CEO of Spyryx Biosciences. "We believe that SPX-101 represents the first therapeutic opportunity to leverage a natural, biological mechanism that is important to the maintenance of normal mucus clearance, with the potential to provide meaningful clinical benefit to all CF patients, regardless of mutation."
The posters that were presented summarized Spyryx's findings in relation to SPX-101, including:
Spyryx has demonstrated effective delivery of SPX-101 by nebulization, which results in a dose dependent improvement in survival and mucus clearance in animal models of CF. In these models, operating through a novel mechanism of action that promotes the intracellular internalization of epithelial sodium channels, SPX-101 reestablishes the pathway that naturally controls the concentration of these channels and facilitates appropriate fluid levels on the airway surface to restore mucociliary clearance.
Spyryx presented findings related to the scale-up and compound characterization of SPX-101, including no observed changes in the stability of SPX-101 with regards to pH and that it retained purity over 6 months in long-term and accelerated storage conditions. In order to achieve toxicology coverage in an inhalation exposure study, SPX-101 was produced under cGMP conditions with impressive yields at multi-kilogram batch scale.
In GLP toxicology studies in two species, daily inhalation of SPX-101 at delivered doses up to 19.6 mg/kg/day for 28 days, no SPX-101 related systemic or local respiratory tract toxicity or adverse clinical signs were observed. No SPX-101 related effects on body weights, food consumption, urinalysis, blood chemistry, or circulating electrolytes were observed. Importantly, SPX-101 did not increase serum potassium levels in these studies, demonstrating the potential of inhaled SPX-101 to improve outcomes for CF patients with a favorable safety profile. Given the doses administered, these findings provide adequate safety margins for the proposed clinical development plan.
"These studies provide important data demonstrating low toxicity and supporting the proposed clinical doses, with no dose-limiting toxicity in the lung or systemically, and with no significant systemic bioavailability," said Alistair Wheeler, MD, Chief Medical Officer at Spyryx. "We believe these non-clinical data, combined with the exciting results from the single-ascending dose portion of our Phase 1 safety study, and the pending data from the multiple-ascending dose portion of the Phase 1, supports our intention to move forward with early entry into the clinic in our Phase 2 clinical development plan."
About Cystic Fibrosis Cystic fibrosis (CF) is an autosomal recessive genetic disorder affecting approximately 75,000 individuals worldwide and is caused by mutations in the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The condition affects multiple organ systems including the lungs and respiratory tract, pancreas, intestine, liver and kidneys. However, the highest medical need is in the lungs, where complications from CF-related lung disease accounts for 80% of all CF deaths.
CF lung disease is hallmarked by dehydration of the fluid volume on the airway surface, resulting in reduced clearance of mucus, the lung's principle mechanism for cleaning itself. This mucus becomes thick and sticky, progressively accumulating into obstructions that are chronically colonized by viruses and bacteria, leading to frequent lung infections, inflammation and loss of lung function. The long-term result is permanent tissue damage and scarring (fibrosis) that frequently requires lung transplantation and often leads to early death. No cure for cystic fibrosis is known, although several treatments have been approved to address the underlying cause of the disease in some patients. Even with these therapies, the median age of survival for CF patients is only approximately 37 years of age.
About Spyryx Biosciences Spyryx Biosciences is a privately held, clinical-stage biopharmaceutical company developing innovative therapeutics to address severe lung diseases. Spyryx's lead clinical candidate, SPX-101, is a novel treatment for cystic fibrosis that is currently completing a Phase 1 safety study. The product has demonstrated a robust ability to restore mucociliary clearance in animal models of the disease and has the potential to improve lung function in cystic fibrosis patients independent of their genotype. The Spyryx leadership team and scientific staff have extensive experience in the development of respiratory medicines and work closely with a broad group of clinical and scientific experts in the pulmonary field. Spyryx is funded by a first tier syndicate of life science investors, including Canaan Partners, 5AM Ventures and Hatteras Venture Partners. Further information regarding Spyryx Biosciences is available at www.spyryxbio.com.
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SOURCE Spyryx Biosciences
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