Jyong Biotech Presents Topline Results at Urological Association of Asia Congress.
PorAinvest
viernes, 22 de agosto de 2025, 9:41 am ET1 min de lectura
MENS--
The Phase III clinical trials of BOTRESO® included two pivotal studies and two open-label extension studies. The pivotal studies, which lasted 12 weeks, evaluated the clinical efficacy of BOTRESO® compared to placebo. The open-label extension studies, where all participants received BOTRESO®, assessed the long-term safety of the drug over 52 weeks. The results showed no significant difference between groups in the U.S. subgroup, but there was a statistically significant improvement in lower urinary tract symptoms in the Asian (Taiwan) subgroup and the pooled Taiwan-U.S. population [1].
The 52-week extension studies demonstrated consistent long-term improvement with no serious adverse events. This positions BOTRESO® favorably against current treatments like α-blockers and 5-α-reductase inhibitors, which carry cardiovascular and prostate cancer risks [1].
For MCS-8 (PCP), the Phase II trial met its primary efficacy endpoint, showing lower rates of positive prostate biopsies and high-grade prostate cancer compared to placebo over 104 weeks. No treatment-related serious adverse events were observed, providing sufficient evidence to advance MCS-8 to Phase III evaluation [1].
The global BPH market is projected to reach $9.8 billion by 2026, up from $4.1 billion in 2020. Jyong Biotech maintains global patent coverage and is pursuing international partnerships for market entry [1].
References:
[1] https://www.globenewswire.com/news-release/2025/08/22/3137831/0/en/Jyong-Biotech-Ltd-Participated-in-the-22nd-Urological-Association-of-Asia-Congress-to-Display-the-Clinical-Data-for-its-Phase-III-Studies-of-BOTRESO-and-Phase-II-Study-of-MCS-8-PCP.html
Jyong Biotech has announced participation in the 22nd Urological Association of Asia Congress and exhibited topline results from clinical studies of its proprietary drug candidates BOTRESO® for benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS), and MCS‑8 (PCP) for the potential prevention of prostate cancer. The Phase III clinical trials of BOTRESO® consisted of two pivotal studies and two open-label extension studies.
Jyong Biotech Ltd. (Nasdaq: MENS) recently participated in the 22nd Urological Association of Asia Congress, where it showcased topline results from its clinical studies for two key drug candidates: BOTRESO® for benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS), and MCS-8 (PCP) for potential prevention of prostate cancer [1].The Phase III clinical trials of BOTRESO® included two pivotal studies and two open-label extension studies. The pivotal studies, which lasted 12 weeks, evaluated the clinical efficacy of BOTRESO® compared to placebo. The open-label extension studies, where all participants received BOTRESO®, assessed the long-term safety of the drug over 52 weeks. The results showed no significant difference between groups in the U.S. subgroup, but there was a statistically significant improvement in lower urinary tract symptoms in the Asian (Taiwan) subgroup and the pooled Taiwan-U.S. population [1].
The 52-week extension studies demonstrated consistent long-term improvement with no serious adverse events. This positions BOTRESO® favorably against current treatments like α-blockers and 5-α-reductase inhibitors, which carry cardiovascular and prostate cancer risks [1].
For MCS-8 (PCP), the Phase II trial met its primary efficacy endpoint, showing lower rates of positive prostate biopsies and high-grade prostate cancer compared to placebo over 104 weeks. No treatment-related serious adverse events were observed, providing sufficient evidence to advance MCS-8 to Phase III evaluation [1].
The global BPH market is projected to reach $9.8 billion by 2026, up from $4.1 billion in 2020. Jyong Biotech maintains global patent coverage and is pursuing international partnerships for market entry [1].
References:
[1] https://www.globenewswire.com/news-release/2025/08/22/3137831/0/en/Jyong-Biotech-Ltd-Participated-in-the-22nd-Urological-Association-of-Asia-Congress-to-Display-the-Clinical-Data-for-its-Phase-III-Studies-of-BOTRESO-and-Phase-II-Study-of-MCS-8-PCP.html
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