X-PACT Immunolight (Breast Cancer, Head & Neck Cancer, Melanoma, and Sarcoma) - Clinical Trial
Email to Participate
elizabeth.sachs@duke.edu
What is the Purpose of this Study?
We are doing this study to find out if an experimental drug and device system called X-PACT is a safe and effective treatment for various forms of cancer.
What is the Condition Being Studied?
Sarcoma, Breast Cancer, Melanoma, and Head & Neck Cancer
Who Can Participate in the Study?
Adults ages 18+ who:
- Have soft tissue sarcoma, melanoma, breast cancer, or head and neck cancer
- Still have cancer after treatment with the standard therapies
- Do not have any other treatment options left
For more information about who can join this study, please contact the study team at elizabeth.sachs@duke.edu
Age Group
Adults
What is Involved?
If you join this study, you will:
- Be injected with the study treatment (X-PACT) five times
- Give tumor tissue
- Have physical exams, blood draws, and urine tests
- Have a heart scan (ECG)
- Have imaging scans (X-Rays, MRI and/or CT)
Please visit https://www.immunolight.com/patients to learn more about the study treatment.
Study Details
Full Title
Phase 1 Study of X-PACT (X-ray Psoralen Activated Cancer Therapy) for Intra-tumoral Injection in Patients with Advanced Head and Neck Cancer, Breast Cancer, Soft Tissue Sarcoma or Melanoma
Principal Investigator
Orthopaedic Surgical Oncologist
Protocol Number
IRB:
PRO00105022
NCT:
NCT04389281
Phase
Phase
I
ClinicalTrials.gov
View on ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate
Email elizabeth.sachs@duke.edu