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Kenny Walter is an editor with HCPLive. Prior to joining MJH Life Sciences in 2019, he worked as a digital reporter covering nanotechnology, life sciences, material science and more with R&D Magazine. He graduated with a degree in journalism from Temple University in 2008 and began his career as a local reporter for a chain of weekly newspapers based on the Jersey shore. When not working, he enjoys going to the beach and enjoying the shore in the summer and watching North Carolina Tar Heel basketball in the winter.
Data supporting BI 1015550 as a IPF therapy will be presented at the upcoming ATS meeting.
The US Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for BI 1015550, a novel investigational therapy for the treatment of patients with idiopathic pulmonary fibrosis (IPF).
The oral, phosphodiesterase 4B (PDE4B) inhibitor is being developed by Boehringer Ingelheim Pharmaceuticals as a potential drug to address both pulmonary fibrosis and inflammation associated with progressive fibrosing interstitial lunch diseases (ILDs).
BI 1015550 was investigated as both a monotherapy and a combination therapy with background antifibrotic therapies to assess the effectiveness of slowing the rate of lung function decline in patients with IPF.
The FDA designation was based on the results of a phase 2 randomized, double-blind, placebo-controlled trial involving 147 patients with IPF. While the full results of the study are going to be presented at the American Thoracic Society (ATS) 2022 meeting on May 16, the FDA designation is based on the data collected to date.
"The accelerated development of BI 1015550 is part of Boehringer Ingelheim's next wave of potential innovative treatments for interstitial lung diseases aimed at preserving lung function and improving the lives of patients," said Thomas Seck, MD, senior vice president, Medicine and Regulatory Affairs, Boehringer Ingelheim Pharmaceuticals, in a statement. "BI 1015550 represents the first molecule in the class of PDE4B inhibitors that is being studied for IPF and other progressive fibrosing ILDs. We have built on our heritage in pulmonary fibrosis and are acting on the breakthrough designation and clinical data with the goal that this potential novel medicine can reach patients as soon as possible."