A Clinical Study of ONO-1110 in Patients With Fibromyalgia
- Registration Number
- NCT06752590
- Lead Sponsor
- Ono Pharmaceutical Co. Ltd
- Brief Summary
To Evaluate the Efficacy and Safety of ONO-1110 in Patients with Fibromyalgia
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 160
- Japanese (both sexes)
- Outpatient
- Patients who are considered capable of understanding the study procedures and completing the pain diary and questionnaires appropriately by the investigator (sub-investigator)
- Patients who meet the American College of Rheumatology Fibromyalgia Criteria
- Patients with inflammatory arthritis, infectious arthritis, or autoimmune disease
- Patients with pain other than FM that may affect assessments in this study
- Patients with a past history of or concurrent neurologic diseases that may affect assessments in this study
- Patients with a past history of or concurrent malignant tumor within 3 years
- Patients who are pregnant, nursing, or possibly pregnant, or intending to become pregnant during the study period.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description ONO-1110 ONO-1110 ONO-1110 tablets once a day Placebo Placebo Placebo tablets once daily
- Primary Outcome Measures
Name Time Method Change in weekly mean of average pain score from baseline to Week 8 of the treatment period Up to 16 weeks Adverse events Up to 16 weeks
- Secondary Outcome Measures
Name Time Method Change in weekly mean of average pain score from baseline in each week Up to 16 weeks 30%- and 50%-responder rates based on the weekly mean of average pain score Up to 16 weeks proportions of participants whose weekly mean of average pain score has decreased by 30% and 50% from baseline, respectively
Change in weekly mean of worst pain score from baseline to each week Up to 16 weeks 30%- and 50%-responder rates based on the weekly mean of worst pain score Up to 16 weeks proportions of participants whose weekly mean of worst pain score has decreased by 30% and 50% from baseline, respectively
Change in WPI and SSS score of 2016 Revised FM Diagnostic Criteria by ACR from baseline Up to 16 weeks Change in Japanese version of the Revised Fibromyalgia Impact Questionnaire (JFIQR) score from baseline Up to 16 weeks Change in Patient Global Impression of Change (PGIC) score from baseline Up to 16 weeks Change in Hospital Anxiety and Depression Scale (HADS) score from baseline Up to 16 weeks Change in Medical Outcomes Study Sleep Scale (MOS-Sleep Scale) score from baseline Up to 16 weeks Plasma ONO-1110 concentrations Up to 16 weeks
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (20)
Kimura Clinic
🇯🇵Nagoya, Aichi, Japan
Ginza Neurological Clinic
🇯🇵Tokyo, Japan
National Hospital Organization Shimoshizu National Hospital
🇯🇵Yotsukaidō, Chiba, Japan
Sapporo City General Hospital
🇯🇵Sapporo, Hokkaido, Japan
Shirasawa Orthopedic Clinic
🇯🇵Morioka, Iwate, Japan
Miyashita Rheumatology Clinic
🇯🇵Ōmura, Nagasaki, Japan
Medical Corporation Fujigaki Clinic
🇯🇵Ōita, Oita, Japan
Ai Sakura Clinic
🇯🇵Fukuoka, Japan
Morimoto Clinic
🇯🇵Osaka, Japan
Shizuoka Rehab Pain Clinic
🇯🇵Shizuoka, Japan
Fukuwa Clinic
🇯🇵Tokyo, Japan
Sanno Hospital
🇯🇵Tokyo, Japan
Tokyo-Eki Center-Building Clinic
🇯🇵Tokyo, Japan
Kokorotoitami Clinic
🇯🇵Kawasaki, Kanagawa, Japan
Japanese Red Cross Okayama Hospital
🇯🇵Okayama, Japan
Hayaishi Hospital
🇯🇵Osaka, Japan
Himenotomomi Clinic
🇯🇵Tokyo, Japan
Juntendo University Nerima Hospital
🇯🇵Tokyo, Japan
Nihonbashi Medical
🇯🇵Tokyo, Japan
Juntendo Tokyo Koto Geriatric Medical Center
🇯🇵Tokyo, Japan