Data show SNF472 inhibits induction of HAP crystallization
Results provide support for further development of SNF472 as a novel treatment for CUA
Palma, Spain and San Diego, USA, 4 March, 2019 – Sanifit, a clinical-stage biopharmaceutical company focused on the treatment of conditions related to progressive vascular calcification, today announces the publication in the British Journal of Clinical Pharmacology of further data assessing the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of its lead drug candidate SNF472 in haemodialysis (HD) patients.
The double blind, randomized, placebo-controlled Phase 1b study investigated the safety, tolerability, PK and PD of SNF472 in HD patients after repeated administrations for up to 28 days. A PD assessment was performed to evaluate the potential for SNF472 to inhibit hydroxyapatite (HAP) formation, which is the form of solid calcium that deposits in the heart, arteries and arterioles. Evidence suggests that HAP deposition is the final common pathway of vascular calcification progression.
SNF472 was shown to be safe and well tolerated in HD patients following multiple ascending doses for one week and repeated dosing of 10 mg/kg for 4 weeks. Under both conditions SNF472 inhibits the induction of HAP crystallization. These results support further investigation of SNF472 in conditions related to progressive vascular calcification.
Dr. Carol Salcedo, Chief Scientific Officer of Sanifit commented: “This study shows that SNF472 inhibits HAP formation in patients and is well tolerated. This provides us with further validation as we continue our progress through the clinic and shows SNF472’s potential as a novel treatment for disorders related to cardiovascular calcification in dialysis patients, a key driver of mortality and morbidity for these patients with no currently approved treatment.”
The full article, ‘A Phase 1b Randomized, Placebo-Controlled Clinical Trial with SNF472 in Haemodialysis Patients’, published in the British Journal of Clinical Pharmacology, can be accessed here.
SNF472 is currently being assessed in CaLIPSO, a Phase 2b proof of concept study in haemodialysis patients assessing the effect of SNF472 in reducing progression of cardiovascular calcification. CaLIPSO completed enrolment in August 2018.
SNF472 is in development for treatment of CUA, also known as calciphylaxis, a devastating rare disease with 55% 1-year mortality rate, where severe cardiovascular calcification blocks small blood vessels in skin and fat tissue. These blockages cause the development of intensely painful and debilitating chronic skin lesions. Sanifit is currently in preparations for a pivotal phase 3 CUA study, after having met the primary and secondary endpoints in the phase 2 study in this indication.
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