Active, not recruitingPhase 1NCT06541665
Phase I Study Evaluating Tolerability, Safety, Pharmacokinetics, and Efficacy of Combined ONO-4059 and R-MPV Therapy for PCNSL
Studying Primary central nervous system lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Ono Pharmaceutical Co. Ltd
- Principal Investigator
- Project LeaderOno Pharmaceutical Co. Ltd
- Intervention
- ONO-4059(drug)
- Enrollment
- 20 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2028
Study locations (30)
- Aichi Cancer Center, Nagoya, Aichi-ken, Japan
- Nagoya City University Hospital, Nagoya, Aichi-ken, Japan
- Akita University Hospital, Akita, Akita, Japan
- Juntendo University Urayasu Hospital, Urayasu-shi, Chiba, Japan
- Fukuoka University Hospital, Fukuoka, Fukuoka, Japan
- Kyushu University Hospital, Fukuoka, Fukuoka, Japan
- Hospital of the University of Occupational and Environmental Health,Japan, Kitakyushu-shi, Fukuoka, Japan
- Kurume University Hospital, Kurume-shi, Fukuoka, Japan
- Fukushima Medical University Hospital, Fukushima, Fukushima, Japan
- Gifu University Hospital (Tokai National Higher Education and Research System), Gifu, Gifu, Japan
- Gunma University Hospital, Maebashi, Gunma, Japan
- Sapporo Medical University Hospital, Sapporo, Hokkaido, Japan
- Kobe City Medical Center General Hospital, Kobe, Hyōgo, Japan
- Hyogo Medical University Hospital, Nishinomiya-shi, Hyōgo, Japan
- University of Tsukuba Hospital, Tsukuba, Ibaraki, Japan
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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