ProMetic Life Sciences announced today that its orally-active drug candidate, PBI-4050, has been issued a Promising Innovative Medicine designation by the UK MHRA as add-on treatment to nintedanib in patients with idiopathic pulmonary fibrosis.
|
[11-December-2017] |
LAVAL, QC, Dec. 11, 2017 /PRNewswire/ - ProMetic Life Sciences Inc. announced today that its orally-active drug candidate, PBI-4050, has been issued a Promising Innovative Medicine (PIM) designation by the United Kingdom (UK) Medicines and Healthcare Products Regulatory Agency (MHRA) as add-on treatment to nintedanib in patients with idiopathic pulmonary fibrosis (IPF). “We are proud to have received a second PIM designation in the UK for PBI-4050, following the designation previously received for Alström syndrome,” said Pierre Laurin, President and Chief Executive Officer of Prometic. “We believe PBI-4050 has the capabilities to address various unmet medical conditions such as IPF and Alström syndrome, for which there are severe limitations with the existing standards of care. We look forward to continuing to collaborate with the MHRA with the goal of advancing both the PBI-4050 IPF and Alström syndrome clinical programs as quickly as possible.” A PIM designation is an early indication that a medicinal product is a promising candidate for the Early Access to Medicines Scheme (EAMS), intended for the treatment, diagnosis or prevention of a life-threatening or seriously debilitating condition with unmet medical need. The PIM designation is a prerequisite to proceed to the EAMS scientific opinion assessment phase, the second and final step in the EAMS process. The EAMS provides an opportunity for important drugs to be used in UK clinical practice in parallel with the later stages of the regulatory process. It is anticipated that medicines with a positive EAMS opinion could be made available to patients 12 - 18 months before receiving marketing authorization. More about Idiopathic Pulmonary Fibrosis (IPF) Idiopathic pulmonary fibrosis (IPF) is a chronic, devastating, and ultimately fatal disease characterized by a progressive decline in lung function. It is a specific type of interstitial lung disease in which the small air sacs of the lung, the “alveoli,” gradually become replaced by fibrotic (scar) tissue and is the cause of worsening dyspnea (shortness of breath). IPF is usually associated with a poor prognosis. The term “idiopathic” is used because the cause of pulmonary fibrosis is still unknown. IPF usually occurs in adult individuals of between 50 and 70 years of age, particularly those with a history of cigarette smoking, and affects men more often than women. IPF affects about 130,000 people in the United States, with about 48,000 new cases diagnosed annually. Approximately 40,000 people with IPF die each year, a similar number of deaths to those due to breast cancer. The 5-year mortality rate for patients with IPF is estimated to range from 50% to 70%. More about PBI-4050 PBI-4050 is an orally-active lead drug candidate with excellent safety and efficacy profiles confirmed in several in vivo experiments targeting fibrosis. Fibrosis is a very complex process by which continuing inflammation causes vital organs to lose their function as normal tissue is replaced by fibrotic scar tissue. The proof-of-concept data confirms the anti-fibrotic activity of PBI-4050 in several key organs including the kidneys, the heart, the lungs and the liver. It is also effective in improving glucose control in preclinical models of diabetes. Open label Phase II studies in idiopathic pulmonary fibrosis, Alström syndrome and type 2 diabetes have provided preliminary evidence that the results seen in preclinical models translate into the corresponding human diseases. About Prometic Life Sciences Inc. Forward Looking Statements
SOURCE ProMetic Life Sciences Inc. | ||
Company Codes: OTC-QX:PFSCF, Toronto:PLI |