Daewoong Pharmaceutical Begins the First Administration of the Bersiporocin, a New Treatment for Idiopathic Pulmonary Fibrosis
The world’s first-in-class candidate substance against idiopathic pulmonary fibrosis, ‘Bersiposocin‘ (DWN12088), which is under the development of Daewoong Pharmaceutical, has entered its Phase II clinical administration.
Daewoong Pharmaceutical has announced that the first patient has been administrated in Phase II on the 6th. The Bersiporocin’s multinational Phase II has been performed by approx. 30 institutions in Korea and US. A total of 102 patients are evaluated for the safety of Bersiporocin and the efficacy of changes in the improvement rate of FVC(forced vital capacity) after administering the Bersiporocin or placebo for 24 weeks. They are aiming to complete the administration to the subjects and check the results by 2024.
Daewoong Pharmaceutical is planning to prove Bersiporocin’s excellent antifibrotic efficacy and pulmonary function improvement results with the oncoming multinational Phase II clinical administration, which has been confirmed from the last non-clinical test. If Daewoong Pharmaceutical succeeds in Bersiporocin’s Proof of Concept, it will be probable for the extended adaptability against various rare fibrosis diseases as well as the export of technology.
The main disease which Bersiporocin is effective against is idiopathic pulmonary fibrosis, which is a lung disease caused by overly formed fibrous tissue hardening the lungs, resulting in the lungs to lose their function. It is a known rare and complicated disease with a 5-year survival rate of less than 40% after diagnosis, as it is challenging to treat. The current treatment for idiopathic pulmonary fibrosis in the market by multinational pharmaceutical companies cannot completely stop the process of the disease and has a high rate of giving up on the administration due to side effects, so the medical demand for such treatment is still high.
“We are working hard to develop a new treatment for patients with idiopathic pulmonary fibrosis.” said the chair of the Trial steering committee, Toby Maher, M.D., Ph.D., Professor of Clinical Medicine, Keck School of Medicine, USC Los Angeles. “The Phase II clinical trial of Daewoong Pharmaceutical’s Bersiposocin represents an important step in developing treatments that address the shortcomings of existing anti fibrotic therapies.”
According to the global market research institution Research And Markets, the global market of idiopathic pulmonary fibrosis treatment is growing by 7% each year, and anticipated to reach approx. 6.1 billion dollars (approx. 8 trillion won) by 2030. Daewoong Pharmaceutical will continue to make efforts on developing highly-demanded treatment for the fibroid lung patients, as well as extending the target to other progressive rare fibrosis diseases of the lung, skin, kidney, liver, and heart.
Companies In This Post
- Eloxx Pharmaceuticals Announces Final Data Assessment from Phase 2 Combination Clinical Trial of ELX-02 in Class 1 Cystic Fibrosis Patients Read more
- Verge Genomics Announces Positive Safety and Tolerability Data from the Phase 1 Clinical Trial of VRG50635, a Potential Best-in-Class Therapeutic for All Forms of ALS Read more
- DEM BioPharma Appoints Wendy Young, Ph.D., to Scientific Advisory Board Read more
- Confo Therapeutics Enters into Research Collaboration for GPCR-Targeting Antibody Discovery with AbCellera Read more
- Vyriad Announces Expansion of T-Cell Lymphoma Trial at Mayo Clinic Read more