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Kissei Pharmaceutical’s Promising Phase III Study on Endometriosis Treatment

Kissei Pharmaceutical’s Promising Phase III Study on Endometriosis Treatment

Kissei Pharmaceutical Co ((KSPHF)) announced an update on their ongoing clinical study.

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Study Overview: Kissei Pharmaceutical Co. is conducting a Phase III confirmatory study titled ‘Phase III Confirmatory Study of KLH-2109 in Patients With Endometriosis.’ The study aims to verify the non-inferiority of KLH-2109 compared to leuprorelin acetate in treating endometriosis-related pelvic pain. This research is significant as it explores a potential new treatment option for endometriosis, a condition affecting many women worldwide.

Intervention/Treatment: The study tests two interventions: KLH-2109, an experimental oral drug, and leuprorelin acetate, an active comparator administered subcutaneously. KLH-2109 is intended to offer a new oral treatment option for endometriosis.

Study Design: This interventional study employs a randomized, parallel assignment model with quadruple masking, meaning that participants, care providers, investigators, and outcomes assessors are blinded to the treatment allocations. The primary purpose is treatment-focused, aiming to assess the efficacy of KLH-2109.

Study Timeline: The study began on June 3, 2025, with the latest update submitted on June 11, 2025. These dates are crucial as they mark the study’s initiation and the most recent information update, indicating active recruitment and progress.

Market Implications: The successful development of KLH-2109 could positively impact Kissei Pharmaceutical’s stock performance by introducing a new treatment option in the endometriosis market. This could enhance investor sentiment, especially if KLH-2109 proves to be a viable alternative to existing treatments like leuprorelin acetate. The study’s outcome may also influence competitive dynamics within the pharmaceutical industry, particularly among companies focusing on women’s health.

The study is ongoing, with further details available on the ClinicalTrials portal.

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