Regulatory Filings • Jul 8, 2020
Regulatory Filings
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Photocure's partner Asieris Received China NMPA's Approval to Start a Global Phase III Clinical Trial for APL-1702 (Cevira)
Shanghai China, July 8, 2020 - Asieris Pharmaceuticals (Asieris), a China-based
biotech company with global aspirations to discover, develop and commercialize
innovative drugs for the treatment of genitourinary tumors and related diseases,
announced today it has received Clinical Trial Approval (CTA) from China's
National Medical Products Administration (NMPA) for the global, multi-centered
Phase III clinical trial of its photodynamic drug-device combination product,
APL-1702 (Cevira[®]), which is being developed for the non-surgical treatment of
high-grade cervical dysplasia (HSIL).
In addition to China, Asieris has concurrently initiated this global pivotal
trial in the United States, Germany, Romania, Hungary, Russia, Ukraine and other
European countries. Data from this trial will support the market approval
applications in China, the United States, the European Union, and other
countries.
Please read the full release here (http://www.asieris.cn/index.php/content/199).
About Photocure
Photocure: The Bladder Cancer Company delivers transformative solutions to
improve the lives of bladder cancer patients. Our unique technology, making
cancer cells glow bright pink, has led to better health outcomes for patients
worldwide. Photocure is headquartered in Oslo, Norway and listed on the Oslo
Stock Exchange (OSE: PHO). For more information, please visit us at
www.photocure.com, www.hexvix.com, www.cysview.com
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