Lenrispodun as Adjunctive Therapy in the Treatment of Patients With Motor Fluctuations Due to Parkinson's Disease

Completed · Phase 2 · Has a placebo group

Conditions studied: Parkinson Disease

In brief

This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group, fixed-dose study in patients with a diagnosis of Parkinson's Disease consistent with the UK Parkinson's Disease Society (UKPDS) Brain Bank diagnostic criteria, who are experiencing wearing off symptoms and levodopa-induced dyskinesia.

Key facts

Study ID

NCT05766813

Run by

Intra-Cellular Therapies, Inc.

People needed

79

Starts

2023-03-13

Expected to finish

2025-11-04

Last updated by the study team

2026-07-24

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female between 40 years of age and older
• Body mass index of 19.0-40.0 kg/m2;
• Diagnosis of PD that is consistent with the UK Parkinson's Disease Society (UKPDS) Brain Bank diagnostic criteria;
• Hoehn and Yahr Scale stage classification of 2 or 3 when in the ON state;
• Have a clinically meaningful response to levodopa (levodopa + DDCI combination) based on Investigator assessment, and meet the following:
• Have been on a stable and optimal dose of levodopa (levodopa + DDCI combination: minimum dose of levodopa equivalent to 100 mg three times daily) for at least 4 weeks prior to Screening, and are expected to continue the same dose regimen throughout the Double-blind Treatment Period;
• If taking other anti-parkinsonian medications (MAO-B [monoamine oxidase B] inhibitor, COMT [catechol-O-methyltransferase] inhibitor, dopamine agonist) in addition to levodopa, have been on a stable dose for at least 4 weeks prior to Screening and are expected to continue the same dose regimen throughout the Double-blind Treatment Period;
• Have wearing-off symptoms and levodopa-induced dyskinesia as per Investigator judgment; 8. Properly complete and return a self-reported home diary for motor function status (Hauser Diary) during the Screening Period, which confirms 3 days (ie, 3 consecutive, 24-hour periods) immediately prior to Baseline, each with at least 2½ hours of OFF time during waking hours.
• Has a caregiver to assist with study participation, if determined by the Investigator to be necessary.

You may not qualify if…

• Medical history indicating parkinsonism other than idiopathic PD, including but not limited to, progressive supranuclear gaze palsy, multiple system atrophy, drug-induced parkinsonism, essential tremor, primary dystonia;
• Has late-stage PD, severe peak-dose dyskinesia, clinically significant end-dose or biphasic dyskinesia, and/or unpredictable or widely swinging fluctuations in their symptoms as assessed by the Investigator;
• Exhibits clinical signs of dementia as indicated by the Mini-Mental State Examination, 2nd Edition: Standard Version (MMSE-2:SV) score of ≤ 24;
• Use of moderate or strong CYP3A4 inhibitors within 5 half-lives of Baseline or CYP3A4 inducers within 2 weeks of Baseline;
• Daily use of nonsteroidal anti-inflammatory drugs (NSAIDs), with the exception of acetylsalicylic acid (ASA);
• Use of MAO-A inhibitors, phosphodiesterase type 5 (PDE5) inhibitors, or alpha blockers including tamsulosin, within 5 half-lives of Baseline;

Where it is running

• Clinical Site — Phoenix, Arizona, United States
• Clinical Site — Scottsdale, Arizona, United States
• Clinical Site — Irvine, California, United States
• Clinical Site — Loma Linda, California, United States
• Clinical Site — Altamonte Springs, Florida, United States
• Clinical Site — Boca Raton, Florida, United States
• Clinical Site — Coral Springs, Florida, United States
• Clinical Site — Doral, Florida, United States
• Clinical Site — Hallandale, Florida, United States
• Clinical Site — Maitland, Florida, United States
• Clinical Site — Miami, Florida, United States
• Clinical Site — Ocala, Florida, United States
• Clinical Site — Orlando, Florida, United States
• Clinical Site — Orlando, Florida, United States
• Clinical Site — Port Orange, Florida, United States
• Clinical Site — Tampa, Florida, United States
• Clinical Site — Augusta, Georgia, United States
• Clinical Site — Decatur, Georgia, United States
• Clinical Site — Kansas City, Kansas, United States
• Clinical Site — Farmington Hills, Michigan, United States
• Clinical Site — Golden Valley, Minnesota, United States
• Clinical Site — Albany, New York, United States
• Clinical Site — Rock Hill, South Carolina, United States
• Clinical Site — Franklin, Tennessee, United States
• Clinical Site — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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