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    ReproNovo Announces Clinical Trial Approval Notice for RPN-001 in China

    Für Sie zusammengefasst
    • ReproNovo receives approval for RPN-001 trial in China.
    • Phase 1 trial aims to treat male infertility issues.
    • Expanding global presence with trials in U.S. and China.

    EQS-News: ReproNovo SA / Key word(s): Miscellaneous
    ReproNovo Announces Clinical Trial Approval Notice for RPN-001 in China

    30.09.2025 / 07:00 CET/CEST
    The issuer is solely responsible for the content of this announcement.


    REPRONOVO ANNOUNCES CLINICAL TRIAL APPROVAL NOTICE FOR RPN-001 IN CHINA

    • The approval enables initiation of RPN-001 Phase 1 trial in China
       
    • Key regulatory milestone in the global development of RPN‑001
       

    Lausanne, Switzerland and Copenhagen, Denmark, September 30, 2025 - ReproNovo, a company dedicated to developing innovative treatments for reproductive medicine and women’s health, today announced that China’s National Medical Products Administration (NMPA) has issued a clinical trial approval notice for RPN-001 (leflutrozole). This approval enables the initiation of a Phase 1 trial in China, marking a key regulatory milestone in the global development of RPN‑001 as a potential treatment for male infertility associated with low serum testosterone.

    “Entering China with our first approved clinical study marks a meaningful geographic expansion for ReproNovo,” said Joan-Carles Arce, MD, PhD, Chief Scientific & Medical Officer of ReproNovo. “With this approval, we will soon have active clinical programs in the U.S. and China, two of the world’s largest healthcare markets, which reinforces our commitment to global development in reproductive medicine.”

    RPN-001 is being studied to show improvements in testicular function and promotion of sperm production (spermatogenesis). The latest approval in China aligns with ReproNovo’s global development strategy and follows recent progress in the U.S., where a Phase 2 trial is underway.

    “We are committed to expanding access to innovative therapies where few treatment options currently exist,” said Jean Duvall, Chief Executive Officer of ReproNovo. “With clinical activities now advancing in both the U.S. and China, we are building the foundation for a truly global approach to reproductive medicine and women’s health innovation.”
     

    ABOUT REPRONOVO:
    ReproNovo is a cutting-edge biopharmaceutical company developing innovative solutions to address critical gaps in reproductive medicine and women’s health. Our team is composed of proven experts with deep experience in reproductive medicine, drug development, regulatory affairs and business development who have throughout their careers successfully brought multiple therapies to market. Lead clinical compound, RPN-001 (leflutrozole), is being developed to treat male infertility. RPN-002 (nolasiban) is a first-in-disease and first-in-class molecular entity being developed to manage adenomyosis and increase the probability of embryo implantation in women undergoing assisted reproductive technology (ART) treatments. Both assets are Phase 2 ready. ReproNovo is financed by Jeito Capital, AXA IM Alts, founding investor M Ventures, Ysios Capital and ALSA Ventures. Headquartered in Lausanne, Switzerland, the company has its primary development team in Copenhagen, Denmark and an additional development site in Barcelona, Spain. For more information, visit the Company’s website at www.repronovo.com or follow us on LinkedIn.

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    EQS-News ReproNovo Announces Clinical Trial Approval Notice for RPN-001 in China EQS-News: ReproNovo SA / Key word(s): Miscellaneous ReproNovo Announces Clinical Trial Approval Notice for RPN-001 in China 30.09.2025 / 07:00 CET/CEST The issuer is solely responsible for the content of this announcement. REPRONOVO ANNOUNCES …