San Diego, CANow Enrolling

Port-Wine Birthmarks Clinical Trial in San Diego, CA

Access cutting-edge port-wine birthmarks treatment through this clinical trial at a research site in San Diego. Study-provided care at no cost to qualified participants.

Expert Care

Access port-wine birthmarks specialists in San Diego at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related port-wine birthmarks treatment provided free

About This Port-Wine Birthmarks Study in San Diego

This is a multi-center, randomized, double-blind, vehicle-controlled, and sequential group Phase 2 study. Eligible subjects aged 18 to 65 years old with PWB of face and/or neck area (except subjects for Stage One) will receive Hemoporfin PDT or vehicle PDT in 8-week cycles at fixed drug dose (5 mg/kg) and different light fluence.

Sponsor: Shanghai Fudan-Zhangjiang Bio-Pharmaceutical Co., Ltd.

Apply for This San Diego Location

Check if you qualify for this port-wine birthmarks clinical trial in San Diego, CA

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Your information is protected and will only be shared with the research team.

Port-Wine Birthmarks Treatment Options in San Diego, CA

If you're searching for port-wine birthmarks treatment options in San Diego, CA, this clinical trial may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our San Diego research site is actively enrolling participants for this clinical trial. You'll receive care from experienced port-wine birthmarks specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Why Consider a Clinical Trial for Port-Wine Birthmarks?

  • Access to new treatments before they're widely available
  • Receive care from leading port-wine birthmarks specialists in San Diego
  • Contribute to medical research that could help future patients
  • Study-related care is typically provided at no cost
  • Close monitoring by a dedicated research team
  • Possible compensation for time and travel