Enroll In A Study

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

Participate in a Phase I Clinical Trial

This is a Phase 1 drug–drug interaction (DDI) study designed to understand how TP-3654 behaves in the body when taken together with another medication called phenytoin. Phenytoin is known to affect how the body processes certain medications. The purpose of this study is to evaluate how phenytoin may influence the levels of TP-3654 in the bloodstream, as well as to assess the safety and tolerability of this combination in healthy adults. Nuvisertib (TP-3654) is being developed as a potential treatment for certain cancers.

Compensation up to $11,035 for your time and participation.

Eligibility Criteria

To participate, you must:

• Be a Healthy Adult
• Be 18 to 65 years old
• Have a BMI between 18.5 to 32 kg/m²
• Be a Non-Smokers, Non-Vapers and not used other Tabacco Products
• Have a Good Venous Access

Study Requirements:

• 21 overnight (22 days) stays at the research unit followed by 1 follow up phone call.
• Total: up to $11,035 upon completion

✨ Frontage Clinical Services is Looking for Asian Volunteers! ✨

Be part of our upcoming clinical studies and help advance medical science.

Why Join?
✔ Contribute to important medical research
✔ Support the development of future treatments
✔ Play a key role in improving healthcare for all communities

📢 We welcome volunteers from all backgrounds to join our clinical research community. We’re especially interested in increasing participation from Asian communities to help make research more inclusive and representative.

Participate in a Phase I Clinical Trial

• Compensation is $4,225 for your time and travel.

Eligibility Criteria

To participate, :

• You must be a Healthy Adult
• You must be 18 to 65 years old
• You must have a BMI between 27 to 38kg/m²
• You must have had stable weight (no major weight change) over the last 3 months 
• You can smoke more than 5 but no more than 10 cigarettes per day and be willing to refrain from smoking for the entire duration of the study.

Study Requirements:

• Healthy adult ages 18–65 with overweight or obesity may qualify. One screening visit, 4-night clinic stay plus 9 outpatient visits. Compensation $4,225.

• Males who have undergone a vasectomy
• Females who have had a surgical sterilization procedure such as tubal ligation, hysterectomy, oophorectomy.

• New to the clinic
• Paid Compensation
• Healthy Male and Female participants
• Must be 18 years old and older
• Willing to participate in overnight studies

Frontage Clinical Services is looking for volunteers to participate in clinical research studies!

Be compensated for referring a friend!

Ask us about our Referral Program

How does it work?

• Refer a friend/family member who has never
  contacted Frontage Clinical Services before to call
  us about participating in one of our research
  studies.
• Your referral must give your name and telephone
  number to our recruitment staff during the initiation of the profile creation!
• If your friend/family member completes a study
  with us, you will receive a bonus for each referral.
• It’s that simple!