A Study to Evaluate the Effectiveness of Two Doses of AP-472 as Adjunctive Therapy to Levodopa in Parkinson's Disease (PD) Participants With Motor Fluctuations (NCT07432958)
Phase 2, Double-blind, Placebo-controlled Study to Evaluate the Effectiveness of Two Doses of AP-472 as Adjunctive Therapy to Levodopa in Parkinson's Disease (PD) Participants With Motor Fluctuations
🩺 Plain-English Summary (8th-Grade Level)
This is a Phase 2 study in people with Parkinson's disease who experience motor fluctuations while taking levodopa. The study will evaluate how effective two different doses of the study drug AP-472 are when added to levodopa treatment, compared with a placebo. The study will last about 12 weeks. Participants will be randomly assigned to receive one of the two doses of AP-472 or a placebo. Neither the participants nor the study staff will know which treatment is given. The study includes a screening period, a 4-week period during which Parkinson's medications must remain stable, and an 8-week treatment period. During the treatment period, limited adjustments to levodopa are allowed if needed.
Who can join: Review the eligibility criteria below.
Location: University of Arkansas for Medical Sciences (Site #208) — Little Rock, Arkansas
Age range: 30 Years to 80 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (30 Sites)
Showing the first 25 of 30 sites.
- University of Arkansas for Medical Sciences (Site #208) — Little Rock, Arkansas
- Profound Research LLC (Site #222) — Carlsbad, California
- Collaborative Neuroscience Network - Los Alamitos- CenExel - PPDS (Site #217) — Los Alamitos, California
- Keck Medicine of USC - USC Healthcare Center 2 (Site #221) — Los Angeles, California
- Parkinson's Research Centers of America (Site #218) — Palo Alto, California
- Rocky Mountain Clinical Research - CenExel - PPDS (Site #215) — Englewood, Colorado
- Parkinson's Disease & Movement Disorders Center of Boca Raton (Site #227) — Boca Raton, Florida
- UM-UHealth at Boca Raton (Site #226) — Boca Raton, Florida
- Velocity Clinical Research - Hallandale Beach (Site #228) — Hallandale, Florida
- University of Miami (Site #220) — Miami, Florida
- Neurology One (Site #205) — Orlando, Florida
- USF Parkinson's Disease and Movement Disorders Center (Site #206) — Tampa, Florida
- Augusta University Medical Center (Site #212) — Augusta, Georgia
- Josephson Wallack Munshower Neurology PC (Site #231) — Indianapolis, Indiana
- The University of Kansas (KU) (Site #216) — Kansas City, Kansas
- Kentucky Neuroscience Institute (Site #213) — Lexington, Kentucky
- Beth Israel Deaconess Medical Center (Site #211) — Boston, Massachusetts
- University of Michigan Health System (UMHS) (Site #202) — Ann Arbor, Michigan
- Quest Research Institute - Alcanza - PPDS (Site #201) — Farmington Hills, Michigan
- University of New Mexico Health Sciences Center (Site #225) — Albuquerque, New Mexico
- Joan and Sanford I. Weill Department of Medicine (Site #224) — New York, New York
- Mount Sinai School of Medicine (Site #209) — New York, New York
- Asheville Neurology Specialists, P.A. (Site #229) — Asheville, North Carolina
- Duke Neurological Disorders Clinic (Site #210) — Durham, North Carolina
- Cleveland Clinic (Site #223) — Cleveland, Ohio
📞 Contact the Study Coordinator
Phone: (615) 427-1935
Email: annie@appellopharma.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.