Trials / Recruiting
RecruitingNCT07219927
Real-World Patient Experiences Using Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) in the United States:
Real-World Patient Experiences Using Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) in the United States: A Prospective, Phase 4, Multicenter, Observational Study in Parkinson's Disease
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 120 (estimated)
- Sponsor
- Supernus Pharmaceuticals, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Real-World Participants Experiences Using Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) in the United States: A Prospective, Phase 4, Multicenter, Observational Study in Parkinson's Disease
Detailed description
This observational study includes an Enrollment Day (participants enrolled any time between their prescription for the infusion and ONAPGO initiation); a Baseline Period (prior to ONAPGO initiation which includes in-home education on the use of ONAPGO by the Clinical Nurse Navigator \[CNN\] according to standard practice for patients with PD-prescribed ONAPGO); Dose Initiation, Titration, and Optimization per Prescription Periods; a Maintenance Period; Maintenance CNN standard of care visits; and an End-of-Study (EOS)/Discontinuation Visit.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Observational study | Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) |
Timeline
- Start date
- 2025-03-31
- Primary completion
- 2027-08-01
- Completion
- 2027-08-01
- First posted
- 2025-10-22
- Last updated
- 2025-10-22
Locations
5 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT07219927. Inclusion in this directory is not an endorsement.