HNC364 – Phase I Clinical Trial

Frontage Clinical Services prioritizes the safety and well-being of our study participants, our employees, and visitors to our clinic. As such, we have incorporated additional policies and procedures, as recommended by the CDC.

Participate in a Phase I Clinical Trial

  • Compensation between $12,000 to $15,650 for your time and participation.
This is a Phase 1 research study to compare a investigational injectable medication (HNC364) with an approved oral medication called AZILECT. The goal is to see how the new drug works in the body, and to check its safety and how well it is tolerated.

Eligibility Criteria

  • Be a Healthy Adult
  • Be 18 to 55 years old
  • Have a BMI between 18 to 32.0 kg/m2
  • Be a Non-Smokers, Non-Vapers and not used other Tabacco Products
  • Have a Good Venous Access

Study Requirements:

If you are chosen for the investigational Injection Group (HNC364):
  • You will receive 4 study drug injections in the shoulder, once every 4 weeks.
  • Total study length: about 5–6 months
  • Clinic stay: 4 overnight stays (one per dose)
  • Additional 4 outpatient visits between doses
  • Requirement: 4 separate one night stay in the clinic and 4 follow-up visits in between doses
  • Compensation: up to $12,000 upon completion
If you are chosen for the Tablet Group (AZILECT):
  • You will take a pill once daily for 25 days
  • Total study length: about 2 months
  • Clinic stay: about 25 consecutive overnights
  • 1 follow-up visit after discharge
  • Requirement: 26 overnight stays (27days) and one follow-up visit
  • Compensation: up to $15,650 upon completion

Application for Clinical Research Study

HNC364 – Phase I Clinical Trial

Your information will be used solely for research recruitment purposes by our research team and will not be shared externally. All submissions are stored securely in accordance with HIPAA and Good Clinical Practice (GCP) standards.

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