DEL_Basilea Pharmaceutica ((DEL_0QNA)), Basilea Pharmaceutica ((CH:BSLN)) announced an update on their ongoing clinical study.
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Study Overview: Basilea Pharmaceutica is conducting a Phase 3 study titled An Interventional Phase 3, Open-label, Two-cohort Study to Investigate the Efficacy and Safety of Fosmanogepix in Adult Patients With Invasive Mold Infections. The study aims to evaluate the efficacy and safety of fosmanogepix for treating invasive mold infections in adults, focusing on reducing all-cause mortality by Day 42. This research is significant due to the increasing threat of multidrug-resistant molds.
Intervention/Treatment: The study tests fosmanogepix, administered either intravenously or orally, as a treatment for invasive mold infections. The drug is compared against standard antifungal therapies in one cohort, while another cohort receives fosmanogepix as a salvage treatment.
Study Design: This is an open-label, randomized, parallel-group study with two cohorts. The primary aim is treatment-focused, with no masking involved, allowing direct comparison between fosmanogepix and standard treatments.
Study Timeline: The study began in July 2025, with an estimated completion timeline of approximately eight months. The primary completion date is crucial for assessing initial results, while the last update was submitted in July 2025, indicating ongoing recruitment and study progress.
Market Implications: This study update could positively impact Basilea Pharmaceutica’s stock performance by showcasing potential advancements in treating invasive mold infections, a growing concern in healthcare. Success in this study could enhance investor confidence and position the company favorably against competitors in the antifungal market.
The study is ongoing, with further details available on the ClinicalTrials portal.