MediciNova completes enrollment of 200 patients in ALS study
The SEANOBI-ALS trial for MN-166 (ibudilast) reached full enrollment, advancing potential new treatment for ALS.
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Biopharmaceutical company focused on neurology, respiratory, and liver diseases
medicinova.comLast updated
In short: MediciNova advanced its clinical pipeline for ALS, MS, and oncology while achieving key enrollment milestones and reporting fiscal losses.
The SEANOBI-ALS trial for MN-166 (ibudilast) reached full enrollment, advancing potential new treatment for ALS.
MN-001 Phase 2 trial completed, MN-166 patent allowed, ALS enrollment at 50%.
The patent covers use with anti-PD-1 antibodies for glioblastoma treatment, expiring in 2042.
The drug targets neuroinflammatory pathways to slow disease progression and preserve motor function.
MediciNova has achieved the target enrolment of 200 patients in the SEANOBI-ALS clinical study, evaluating MN-166 (ibudilast) for amyotrophic lateral sclerosis (ALS). The SEANOBI...
LA JOLLA, Calif., Nov. 11, 2024 (GLOBE NEWSWIRE) -- MediciNova, Inc., a biopharmaceutical company traded on the NASDAQ Global Market (NASDAQ: MNOV) and the Standard...
MN-166 presents market opportunities through its multi-indication strategy, including ALS, MS, and more, supported by pivotal trials, regulatory incentives like Orphan Drug and Fast Track...
MediciNova Inc. MNOV) on Thursday reported a loss of $2.6 million in its first quarter.
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