New Parkinson's drug ABBV-951 under Real-World watch in japan
NCT ID NCT05916157
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 250 adults with advanced Parkinson's disease who are prescribed ABBV-951 by their doctors. The goal is to see how safe and effective the drug is in everyday use over 52 weeks. Participants continue their normal care with no extra visits required.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 250 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2023
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult participants who are prescribed ABBV-951 for the treatment of advanced Parkinson's disease (aPD).
- Ages
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15 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosed with advanced Parkinson's disease (aPD). * Prescribed ABBV-951 as physicians' decision according to the approved label for treatment of aPD. * Given informed consent (or by her/his legal representative, if it's a requirement from the participating hospital/clinic) for participating this study. Exclusion Criteria: * Prior treatment with ABBV-951 for PD. * Currently participating in interventional clinical trials.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Dokkyo Medical University Hospital /ID# 269116
Mibu, Tochigi, 321-0293, Japan
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Fujimoto General Hospital /ID# 277287
Miyakonojo-shi, Miyazaki, 885-0055, Japan
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Hakodate Municipal Hospital /ID# 276757
Hakodate-shi, Hokkaido, 041-8680, Japan
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Juntendo University Hospital /ID# 264438
Bunkyo-ku, Tokyo, 113-8431, Japan
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Municipal Toyonaka Hospital /ID# 271277
Toyonaka, 560-0055, Japan
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National Center of Neurology and Psychiatry - Kodaira /ID# 267372
Xiaoping City, Tokyo, 187-8551, Japan
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National Hospital Organization Asahikawa Medical Center /ID# 269115
Asahikawa, Hokkaido, 070-0901, Japan
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National Hospital Organization Utano Hospital /ID# 268350
Kyoto, 616-8255, Japan
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Nitobe Memorial Nakano General Hospital /ID# 275668
Nakano-ku, Tokyo, 164-0011, Japan
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Okatsu Hospital /ID# 262781
Kagoshima, Kagoshima-ken, 890-0067, Japan
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Okayama Neurology Clinic /ID# 269117
Okayama, 702-8005, Japan
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Ryugasaki Saiseikai Hospital /ID# 264435
Ryūgasaki, Ibaraki, 305-0854, Japan
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Saiseikai Matsuyama Hospital /ID# 276259
Matsuyama, Ehime, 791-8026, Japan
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Sendai Nishitaga National Hospital /ID# 268349
Sendai, Miyagi, 982-8555, Japan
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Shiga University of Medical Science Hospital /ID# 265637
Ōtsu, Shiga, 520-2192, Japan
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University Hospital Kyoto Prefectural University of Medicine /ID# 267445
Kyoto, Kyoto, 602-8566, Japan
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University of Tsukuba Hospital /ID# 268353
Tsukuba, Ibaraki, 305-8576, Japan
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Other studies related to the condition(s) this trial covers.
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