A Proof of Concept Study to Investigate the Effect of IPT803 Adjunct Treatment in Patients with Parkinson’s Disease


The purpose of this study is to learn more about the effects of treatment with IPT803 on Parkinson’s disease symptoms and how it impacts your daily life.


  • Participants in this study will be randomly assigned to one of two groups (also called cohorts)
  • Cohort 1 and Cohort 2 involve different procedures that can be explained by the study team
  • The study will involve 5 study visits within 16 weeks. Study length and individual visits depend on cohort assignment and will be explained by the study team.
  • Compensation is provided

For additional study details please reach out to Kyle Rizer: 


  •  35 years old and older
  • Diagnosed with Parkinson's disease


18 to 65
65 and over



Monetary compensation


Can be done from home



Parkinson disease, Parkinson's disease, Parkinson's disease - resources

Principal Investigator

Wissam Deeb, MD

Sponsoring Group

Department of Neurology

Contact Information



Be an Informed Participant

Before deciding to participate in a research study, take time to learn about clinical research, how it's conducted and your rights as a research participant. Following are some helpful resources from independent sources. Always remember that a clinical research study is research, not treatment.

Know Who to Contact

  • Eligibility: For questions about a specific study and who is eligible to participate, call or email the contact person listed for that study.
  • Your Rights: For questions about your rights as a research participant, contact the UF Institutional Review Boards at 352-273-9600.
  • Feedback: For general questions or feedback about study listings, email the UF Clinical and Translational Science Institute at CTSI-Studies-L@lists.ufl.edu.

Other Resources

  • HealthStreet: Health-focused services, classes and events, and opportunities to participate in research.
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