Nuvectis Pharma Says Paroxysmal Nocturnal Hemoglobinuria Drug Approved by Chinese Regulator

MT Newswires Live07-23

Nuvectis Pharma (NVCT) said Thursday that ciprocopan, also known as NXP100, has received marketing approval from the National Medicinal Products Administration of China for the treatment of patients with Paroxysmal Nocturnal Hemoglobinuria who had previously been untreated with Complement inhibitors.

China-based Haisco developed the drug and handles its development, regulatory approvals, and commercialization in the country, while Nuvectis holds exclusive rights to develop and commercialize ciprocopan outside of Greater China, India, and certain Southeast Asian countries, Nuvectis said.

The approval was based on a late-stage study by Haisco that demonstrated ciprocopan's superiority over eculizumab in patients with Paroxysmal Nocturnal Hemoglobinuria who had previously not been treated with Complement inhibitors, the statement said.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Comments

We need your insight to fill this gap
Leave a comment