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FiREBOLT: LY4337713 in Adults with FAP-Positive Solid Tumors - Clinical Trial
What is the Purpose of this Study?
We are doing this study to find out if an experimental drug called LY4337713 (the study drug) is a safe and effective option for people who have FAP-positive solid tumors. The study drug is a type of radiotherapy that is intended to target and attach only to FAP. The goal of targeted radiotherapy is to provide selective delivery of radiation doses that can destroy tumor cells.
What is the Condition Being Studied?
Cancers with Fibroblast Activation Protein (FAP) Positive Solid Tumors
Who Can Participate in the Study?
Adults ages 18+ who:
- Are diagnosed with one of the following forms of cancer with a solid tumor present: adenocarcinoma of the pancreas, HR-positive & HER2-negative breast cancer, HER2-positive breast cancer, triple-negative breast cancer, platinum-resistant or refractory ovarian cancer, gastric adenocarcinoma, colorectal cancer, squamous cell carcinoma or adenocarcinoma esophageal cancer, or cholangiocarcinoma
- Have clinical or imaging evidence of FAP expression
For more information, contact the study team at dana.a.warren@duke.edu.
Grupo etario
Adultos
What is Involved?
Si elige unirse a este estudio, podrá:
- Get an intravenous (IV) injection of the study drug either every 4 weeks or every 6 weeks, depending on when you are enrolled
- Hacer extracciones de sangre y dar muestras de orina
- Realice tomografías computarizadas o resonancias magnéticas de manera regular.
Study Details
Full Title
A Dose Escalation and Dose Optimization Phase 1a/1b Study to Evaluate Safety,
Tolerability and Dosimetry of Radioligand Therapy with LY4337713 in Adults
with FAP-Positive Solid Tumors (FiREBOLT)
Principal Investigator
Especialista en oncología médica
Protocol Number
IRB:
PRO00118353
NCT:
NCT07213791
Phase
Fase I
ClinicalTrials.gov
View on ClinicalTrials.gov
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