RecruitingPhase not listed

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

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

  • Procedures mentioned: Infusions

Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.

Show the study's own words
  • "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"
Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

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

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Official eligibility criteria

Inclusion Criteria: Participant has received a prescription for ONAPGO™ according to the standard of care. Participant has opted into receiving support services from the Clinical Nurse Navigator (CNN), a registered nurse specially trained to work with persons with Parkinson's disease, as noted on the Prescription Enrollment Form. The HCP/Investigator determines the participant is an appropriate study participant. Participant is able and willing to provide informed consent (or informed assent form \[IAF\], as applicable) and signs the consent form on the Enrollment Day. Exclusion Criteria: Did not receive a prescription for ONAPGO™. Prescribed ONAPGO™, but the HCP/Investigator determines the participant should not participate in this observational study. Concomitant use of ONAPGO™ with 5-HT3 antagonists, including antiemetics (e.g., ondansetron, granisetron, dolasetron, palonosetron) or alosetron. Known hypersensitivity to apomorphine or to excipients of ONAPGO™, including sulfite (e.g., sodium metabisulfite).

Study sites (5)

CA

  • Parkinson's Disease and Movement Disorders Center - Orange County (South) · Aliso Viejo, CA 92656Mindy Bixby, D.O. · Study contactMindy Bixby, D.O. · Principal investigatorMore trials in Aliso Viejo
  • Parkinson's Disease and Movement Disorders Center - Orange County (North) · Irvine, CA 92618Sandeep Thakkar, D.O. · Study contactSandeep Thakkar, D.O. · Principal investigatorMore trials in Irvine
  • Parkinson's Research Centers of America - Palo Alto · Palo Alto, CA 94301Salima Brillman, MD · Study contactSalima Brillman, MD · Principal investigatorMore trials in Palo Alto

FL

  • Parkinson's Disease & Movement Disorders Center of Boca Raton · Boca Raton, FL 33486Stuart Isaacson, MD · Study contactStuart Isaacson, MD · Principal investigatorMore trials in Boca Raton

NY

  • Parkinson's Disease and Movement Disorders Center - Long Island · Commack, NY 11725David Kreitzman, M.D. · Study contactDavid Kreitzman, M.D. · Principal investigatorMore trials in Commack