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MediciNova

MediciNova is a biopharmaceutical company developing small-molecule therapeutics licensed from Japanese originators for serious diseases with unmet medical need, and is dual-listed on Nasdaq and the Tokyo Stock Exchange. Its lead compound MN-166 (ibudilast) is an oral anti-inflammatory and neuroprotective agent in clinical development for amyotrophic lateral sclerosis (the Phase 2b/3 COMBAT-ALS registration trial enrolled 234 patients, with top-line data expected by year-end 2026), progressive multiple sclerosis, chemotherapy-induced peripheral neuropathy, degenerative cervical myelopathy, glioblastoma and prevention of acute respiratory distress syndrome; an expanded-access program in ALS is supported by a $22 million NIH grant. The second compound, MN-001 (tipelukast), is an orally bioavailable small molecule in development for fibrotic and metabolic disorders including nonalcoholic fatty liver disease and hypertriglyceridemia. Management has framed 2026 as a data-driven year led by readouts from these two programs rather than by financing.

Company Info

Sector:Biopharmaceuticals / CNS, Neuroinflammatory and Metabolic Disease
Headquarters:La Jolla, California, USA
Founded:2000

Upcoming Milestones & Key Dates

Q4 2026
Clinical Readout

Top-line data from the COMBAT-ALS Phase 2b/3 trial of MN-166 (ibudilast) in ALS

H2 2026
Clinical Readout

Top-line data from the MN-001 (tipelukast) metabolic program

Clinical Development Pipeline

MN-166 (ibudilast)

Target: Oral anti-inflammatory and neuroprotective phosphodiesterase inhibitor
Amyotrophic lateral sclerosis — Phase 2b/3 COMBAT-ALS registration trial, 234 patients enrolled
Preclinical
Phase 1
Phase 2
Phase 3
Approved

MN-166 (ibudilast)

Target: Oral anti-inflammatory and neuroprotective agent
Progressive multiple sclerosis, chemotherapy-induced peripheral neuropathy, degenerative cervical myelopathy and glioblastoma
Preclinical
Phase 1
Phase 2
Phase 3
Approved

MN-166 (ibudilast)

Target: Oral anti-inflammatory and neuroprotective agent, supported by a $22 million NIH grant
ALS expanded-access program (SEANOBI study)
Preclinical
Phase 1
Phase 2
Phase 3
Approved

MN-001 (tipelukast)

Target: Orally bioavailable small-molecule leukotriene and phosphodiesterase inhibitor
Nonalcoholic fatty liver disease and hypertriglyceridemia
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Recent News

No recent news updates available for this company.

Leadership Team

Yuichi Iwaki

Co-Founder, President and Chief Executive Officer

Careers & Job Openings

No active job listings. Check back later.