Daewoong Pharmaceutical 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 the lungs to lose the function of them. It is known a 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 the 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.