A Late Phase II Clinical Trial of KDT-3594 in Patients With Advanced Parkinson's Disease With Levodopa

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This trial is a late phase II, multicenter, randomized, double-blind, placebo-controlled, parallel group trial to evaluate the efficacy, safety, and pharmacokinetics of KDT-3594 administered at escalating doses ranging from 0.25 to 2 mg per day for 17 weeks in patients with advanced PD with levodopa.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients diagnosed with PD according to the Parkinson's disease society brain bank clinical diagnostic criteria of the UK Parkinson's Disease Society

• Patients who are being treated with levodopa or levodopa combination drugs and have any of the following troublesome symptoms or conditions:

• Patients with wearing-off phenomenon

• Patients with ON-/OFF-phenomenon

• Patients with no-on/delayed on phenomenon

• Patients with inadequate response to levodopa

Locations
Other Locations
Japan
Research Site
RECRUITING
Multiple Locations
Contact Information
Primary
Yoshitaka Shimizu
rinsyousiken@pharm.kissei.co.jp
Email only
Time Frame
Start Date: 2024-12
Estimated Completion Date: 2026-04
Participants
Target number of participants: 150
Treatments
Experimental: KDT-3594
KDT-3594 capsules will be orally administered at escalating doses ranging from 0.25 to 2 mg per day for 17 weeks.
Placebo_comparator: Placebo
Placebo capsules will be orally administered at escalating doses ranging from 0.25 to 2 mg per day for 17 weeks.
Related Therapeutic Areas
Sponsors
Leads: Kissei Pharmaceutical Co., Ltd.

This content was sourced from clinicaltrials.gov

Similar Clinical Trials