NCT03901352

Brief Summary

Investigate the efficacy and safety of mirogabalin in participants with central neuropathic pain in comparison to placebo

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P50-P75 for phase_3

Timeline
Completed

Started Mar 2019

Geographic Reach
3 countries

118 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 12, 2019

Completed
20 days until next milestone

First Submitted

Initial submission to the registry

April 1, 2019

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 3, 2019

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 28, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 28, 2020

Completed
3.7 years until next milestone

Results Posted

Study results publicly available

September 23, 2024

Completed
Last Updated

October 21, 2024

Status Verified

October 1, 2024

Enrollment Period

1.8 years

First QC Date

April 1, 2019

Results QC Date

November 22, 2022

Last Update Submit

October 8, 2024

Conditions

Keywords

Central neuropathic painDevelopmental phase III

Outcome Measures

Primary Outcomes (1)

  • Change From Baseline in the Weekly Average Daily Pain Score (ADPS) at Week 14 Following Administration With Mirogabalin or Placebo

    The pain scores on a scale of 0-10, where 0 = no pain and 10 = the worst possible pain. Negative changes in ADPS indicated an improvement in pain scores. The weekly ADPS is based on participants daily pain scores.

    Baseline to Week 14 postdose

Secondary Outcomes (11)

  • Number of Participants With ≥30% Reduction and ≥50% Reductions From Baseline in Average Daily Pain Score (ADPS)

    Baseline to Week 14 postdose

  • Change From Baseline in Present Pain Intensity on the Short Form-McGill Pain Questionnaire at Week 14 Following Administration With Mirogabalin or Placebo

    Baseline to Week 14 postdose

  • Patient Global Impression of Change at Week 14 Following Administration With Mirogabalin or Placebo

    at Week 14 postdose

  • Change From Baseline in the Weekly Average Daily Sleep Interference Score (ADSIS) Following Administration With Mirogabalin or Placebo

    Baseline to Week 14 postdose

  • Change From Baseline in the Medical Outcomes Study Sleep Scale Scores Following Administration With Mirogabalin or Placebo

    Baseline to Week 14 postdose

  • +6 more secondary outcomes

Study Arms (2)

Mirogabalin

EXPERIMENTAL

The patients with creatinine clearance (CLcr) ≥ 60 mL/min: Mirogabalin 20 mg or 30 mg, oral administration, Treatment period; 2-weeks titration and 12-weeks maintenance dose. The patients with creatinine clearance (CLcr) 30 to \< 60 mL/min: Mirogabalin 10 mg or 15 mg, oral administration, Treatment period; 2-weeks titration and 12-weeks maintenance dose

Drug: Mirogabalin

Placebo

PLACEBO COMPARATOR

Placebo (14-weeks)

Drug: Placebo

Interventions

Matching placebo tablets for oral administration

Also known as: Matching Placebo
Placebo

Mirogabalin tablets for oral administration

Also known as: DS-5565
Mirogabalin

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Spinal cord injury (SCI) due to trauma
  • American Spinal Injury Association impairment scale A, B, C, or D

You may not qualify if:

  • Other severe pain at screening or randomization, unrelated to central neuropathic pain after SCI, that may confound the assessment of central neuropathic pain after SCI
  • Neurologic disorders at screening or randomization, unrelated to central neuropathic pain after SCI, that may confound the assessment of central neuropathic pain after SCI
  • Major psychiatric disorders within 1 year prior to screening

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (118)

Chubu-Rosai Hospital

Aichi, 455-8530, Japan

Location

Social Medical Corporation Daido Clinic

Aichi, 457-8511, Japan

Location

Honmachi Clinic

Aichi, 460-0008, Japan

Location

Nagoya City West Medical Center

Aichi, 462-8508, Japan

Location

Toyota Kosei Hospital

Aichi, 470-0396, Japan

Location

Nagoya Tokushukai General Hospital

Aichi, 487-0016, Japan

Location

Kainan Hospital

Aichi, 498-8502, Japan

Location

Hachinohe City Hospital

Aomori, 031-8555, Japan

Location

Hirosaki University Hospital

Aomori, 036-8563, Japan

Location

Chiba University Hospital

Chiba, 260-8677, Japan

Location

Chiba Rehabilitation Center

Chiba, 266-0005, Japan

Location

Funabashi Municipal Medical Center

Chiba, 273-8588, Japan

Location

Kimitsu Chuo Hospital

Chiba, 292-8535, Japan

Location

Ehime Prefectural Central Hospital

Ehime, 790-0024, Japan

Location

University of Fukui Hospital

Fukui, 910-1193, Japan

Location

Fukui-ken Saiseikai Hospital

Fukui, 918-8503, Japan

Location

Shin Komonji Hospital

Fukuoka, 800-0057, Japan

Location

Kyushu Rosai Hospital

Fukuoka, 800-0296, Japan

Location

Steel Memorial Yawata Hospital

Fukuoka, 805-8508, Japan

Location

Go Neurosurgical Clinic

Fukuoka, 811-1244, Japan

Location

Japan Organization of Occupational Health and Safety Spinal Injuries Center

Fukuoka, 820-8508, Japan

Location

Shin Yukuhashi Hospital

Fukuoka, 824-0026, Japan

Location

Fukushima Medical University Hospital

Fukushima, 960-1295, Japan

Location

Southern TOHOKU Medical Clinic

Fukushima, 963-8052, Japan

Location

Japanese Red Cross Maebashi Hospital

Gunma, 371-0811, Japan

Location

Goodlife Hospital

Hiroshima, 720-0052, Japan

Location

Medical Corporation Suiseikai Suiseikai Kajikawa Hospital

Hiroshima, 730-0053, Japan

Location

Hiroshima City Asa Citizens Hospital

Hiroshima, 731-0293, Japan

Location

Hiroshima Prefectural Hospital

Hiroshima, 734-8530, Japan

Location

Teine Keijinkai Hospital

Hokkaido, 006-8555, Japan

Location

Hakodate Municipal Hospital

Hokkaido, 041-8680, Japan

Location

Sapporo Medical University Hospital

Hokkaido, 060-8543, Japan

Location

Nakamura Memorial Hospital

Hokkaido, 060-8570, Japan

Location

Sapporo City General Hospital

Hokkaido, 060-8604, Japan

Location

Japanese Red Cross Asahikawa Hospital

Hokkaido, 070-8530, Japan

Location

Hokkaido Spinal Cord Injury Center

Hokkaido, 072-0015, Japan

Location

Kobe City Medical Center General Hospital

Hyōgo, 650-0047, Japan

Location

Japanese Red Cross Kobe Hospital

Hyōgo, 651-0073, Japan

Location

Hyogo Social Welfare Corporation Hyogo Rehabilitation Center Central Hospital

Hyōgo, 651-2181, Japan

Location

Japanese Red Cross Society Himeji Hospital

Hyōgo, 670-8540, Japan

Location

University of Tsukuba Hospital

Ibaraki, 305-8576, Japan

Location

Ibaraki Seinan Medical Center Hospital

Ibaraki, 306-0433, Japan

Location

Ishikawa Prefectural Central Hospital

Ishikawa, 920-8530, Japan

Location

Kagawa Prefectural Central Hospital

Kagawa, 760-8557, Japan

Location

Shikoku Medical Center for Children and Adults

Kagawa, 765-8597, Japan

Location

Japan Organization of Occupational Health and Safety(JOHAS), Yokohama Rosai Hospital

Kanagawa, 222-0036, Japan

Location

Yokohama City Minato Red Cross Hospital

Kanagawa, 231-8682, Japan

Location

Yokohama City University Hospital

Kanagawa, 236-0004, Japan

Location

Kanagawa Rehabilitation Hospital

Kanagawa, 243-0121, Japan

Location

Sagamihara Kyodo Hospital

Kanagawa, 252-5188, Japan

Location

National Hospital Organaization Kumamoto Medical Center

Kumamoto, 860-0008, Japan

Location

Kumamoto Kinoh Hospital

Kumamoto, 860-8518, Japan

Location

Kumamoto Takumadai Rehabilitation Hospital

Kumamoto, 862-0924, Japan

Location

Kumamoto Rehabilitation Hospital

Kumamoto, 869-1106, Japan

Location

Uji-Tokushukai Medical Center

Kyoto, 611-0041, Japan

Location

Mie University Hospital

Mie, 514-8507, Japan

Location

Tohoku Rosai Hospital

Miyagi, 981-8563, Japan

Location

National Hospital Organization Sendai Medical Center

Miyagi, 983-8520, Japan

Location

Katta General Hospital

Miyagi, 989-0231, Japan

Location

Junwakai Memorial Hospital

Miyazaki, 880-2112, Japan

Location

University of Miyazaki Hospital

Miyazaki, 889-1692, Japan

Location

Japan Red Cross Society Azumino Hospital

Nagano, 399-8292, Japan

Location

Nagasaki University Hospital

Nagasaki, 852-8501, Japan

Location

Nagasaki Rosai Hospital

Nagasaki, 857-0134, Japan

Location

Nara Prefecture General Rehabilitation Center

Nara, 636-0345, Japan

Location

Japanese Red Cross Society Nagaoka Red Cross Hospital

Niigata, 940-2485, Japan

Location

Nagaoka Chuo General Hospital

Niigata, 940-8653, Japan

Location

Niigata City General Hospital

Niigata, 950-1197, Japan

Location

Niigata University Medical & Dental Hospital

Niigata, 951-8520, Japan

Location

Iwate Rehabilitation Center

Numakunai, 020-0503, Japan

Location

Okayama City General Medical Center Okayama City Hospital

Okayama, 700-8557, Japan

Location

Kibikogen Rehabilitation Center For Employment Injuries

Okayama, 716-1241, Japan

Location

Medical Corporation Tapic Okinawa Rehabilitation Center Hospital

Okinawa, 904-2173, Japan

Location

Osaka General Medical Center

Osaka, 558-8558, Japan

Location

Osaka University Hospital

Osaka, 565-0871, Japan

Location

Aijinkai Rehabilitation Hospital

Osaka, 569-1116, Japan

Location

Osaka Rosai Hospital

Osaka, 591-8025, Japan

Location

Medical Corporation Keiaikai Nakamura Hospital

Ōita, 874-0937, Japan

Location

Saga-ken Medical Centre KOSEIKAN

Saga, 840-8571, Japan

Location

Hanyu General Hospital

Saitama, 348-8505, Japan

Location

Otsu City Hospital

Shiga, 520-0804, Japan

Location

Saiseikai Shiga Hospital

Shiga, 520-3046, Japan

Location

Shimane University Hospital

Shimane, 693-8501, Japan

Location

Shizuoka City Shimizu Hospital

Shizuoka, 424-8636, Japan

Location

Fujieda Municipal General Hospital

Shizuoka, 426-8677, Japan

Location

Hamamatsu University Hospital

Shizuoka, 431-3192, Japan

Location

Japanese Red Cross Hamamatsu Hospital

Shizuoka, 434-8533, Japan

Location

Kikugawa General Hospital

Shizuoka, 439-0022, Japan

Location

Dokkyo Medical University Hospital

Tochigi, 321-0293, Japan

Location

Jichi Medical University Hospital

Tochigi, 329-0498, Japan

Location

Tokushima University Hospital

Tokushima, 770-8503, Japan

Location

Makita General Hospital

Tokyo, 143-8505, Japan

Location

Nihon University Itabashi Hospital

Tokyo, 173-8610, Japan

Location

National Hospital Organaization Murayama Medical Center

Tokyo, 208-0011, Japan

Location

Tottori University Hospital

Tottori, 683-8504, Japan

Location

Toyama University Hospital Hospital

Toyama, 930-0194, Japan

Location

Wakayama Medical University Hospital

Wakayama, 641-8510, Japan

Location

Sanyudo Rehabilitation Center

Yamagata, 992-0057, Japan

Location

Yamaguchi University Hospital

Yamaguchi, 755-8505, Japan

Location

Yamaguchi Rosai Hospital

Yamaguchi, 756-0095, Japan

Location

Yamanashi Prefectural Central Hospital

Yamanashi, 400-8506, Japan

Location

Daegu Fatima Hospital

Daegu, 41199, South Korea

Location

Chungnam National University Hospital

Daejeon, 35015, South Korea

Location

CHA Bundang Medical Center

Gyeonggi-do, 13496, South Korea

Location

Seoul National University Bundang Hospital

Gyeonggi-do, 13620, South Korea

Location

The Catholic University of Korea St. Vincent's Hospital

Gyeonggi-do, 16247, South Korea

Location

Ajou University Hospital

Gyeonggi-do, 16499, South Korea

Location

The Catholic University of Korea Incheon St. Mary's Hospital

Gyeonggi-do, 21431, South Korea

Location

Chonbuk National University Hospital

Jeollabuk-do, 54907, South Korea

Location

Pusan National University Hospital

Pusan, 49241, South Korea

Location

Pusan National University Yangsan Hospital

Pusan, 50612, South Korea

Location

Seoul Universtiy Hospital

Seoul, 03080, South Korea

Location

The Catholic University of Korea Seoul St. Mary's Hospital

Seoul, 06591, South Korea

Location

Samsung Medical Center

Seoul, 6351, South Korea

Location

Hualien Tzu Chi Hospital

Hualien City, 97002, Taiwan

Location

National Taiwan University Hospital

Taipei, 10002, Taiwan

Location

Taipei Veterans General Hospital

Taipei, 11217, Taiwan

Location

Chang Gung Memorial Hospital

Taoyuan District, 33305, Taiwan

Location

Related Publications (3)

  • Hosomi K, Katayama Y, Sakoda H, Kikumori K, Kuroha M, Ushida T. Usefulness of Mirogabalin in Central Neuropathic Pain After Stroke: Post Hoc Analysis of a Phase 3 Study by Stroke Type and Location. Pain Ther. 2024 Oct;13(5):1151-1171. doi: 10.1007/s40122-024-00616-3. Epub 2024 Jul 4.

  • Ushida T, Katayama Y, Hiasa Y, Nishihara M, Tajima F, Katoh S, Tanaka H, Maeda T, Furusawa K, Kakehi Y, Kikumori K, Kuroha M. Long-Term Safety and Efficacy of Mirogabalin for Central Neuropathic Pain: A Multinational, Phase 3, 52-Week, Open-Label Study in Asia. Pain Ther. 2023 Aug;12(4):963-978. doi: 10.1007/s40122-023-00513-1. Epub 2023 Apr 28.

  • Ushida T, Katayama Y, Hiasa Y, Nishihara M, Tajima F, Katoh S, Tanaka H, Maeda T, Furusawa K, Richardson M, Kakehi Y, Kikumori K, Kuroha M. Mirogabalin for Central Neuropathic Pain After Spinal Cord Injury: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study in Asia. Neurology. 2023 Mar 14;100(11):e1193-e1206. doi: 10.1212/WNL.0000000000201709. Epub 2022 Dec 14.

MeSH Terms

Interventions

mirogabalin

Results Point of Contact

Title
Contact of Clinical Trial Information
Organization
Daiichi Sankyo

Study Officials

  • Clinical Study Leader

    Daiichi Sankyo

    STUDY DIRECTOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Masking Details
During the Double-blind Phase, masking will be triple (as shown above). During the Open Extension Phase, there will be no masking - the allocation is not applicable.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: During the Double-blind Phase, participants will be randomized into parallel treatment arms. During the Open Extension Phase, all participants will be assigned to a single group.
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 1, 2019

First Posted

April 3, 2019

Study Start

March 12, 2019

Primary Completion

December 28, 2020

Study Completion

December 28, 2020

Last Updated

October 21, 2024

Results First Posted

September 23, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will share

De-identified individual participant data (IPD) and applicable supporting clinical trial documents may be available upon request at https://vivli.org/. In cases where clinical trial data and supporting documents are provided pursuant to our company policies and procedures, Daiichi Sankyo will continue to protect the privacy of our clinical trial participants. Details on data sharing criteria and the procedure for requesting access can be found at this web address: https://vivli.org/ourmember/daiichi-sankyo/

Shared Documents
STUDY PROTOCOL, SAP, CSR
Time Frame
Studies for which the medicine and indication have received European Union (EU) and United States (US), and/or Japan (JP) marketing approval on or after 01 January 2014 or by the US or EU or JP Health Authorities when regulatory submissions in all regions are not planned and after the primary study results have been accepted for publication.
Access Criteria
Formal request from qualified scientific and medical researchers on IPD and clinical study documents from clinical trials supporting products submitted and licensed in the United States, the European Union and/or Japan from 01 January 2014 and beyond for the purpose of conducting legitimate research. This must be consistent with the principle of safeguarding study participants' privacy and consistent with provision of informed consent.
More information

Locations