Moonshot Antibodies for Stage IV Cancers
This study is testing a new treatment called Moonshot antibodies for people with Stage IV soft tissue cancer, including breast, colon, lung, and other cancers. The goal is to see how safe Moonshot antibodies are and if they can help your body fight cancer. These antibodies are special because they are made in a lab using cells from your own tumor, so they are designed specifically for your cancer. First, doctors will take blood and tumor samples to create these unique antibodies. Then, you will receive the Moonshot antibodies through infusions. The main thing researchers are looking for is how often serious side effects happen over 6 months.
- Study design
- This is a Phase I, open-label study, meaning both you and your doctors will know what treatment you are receiving. Up to 16 people will participate across several study locations.
- What's involved
- You will provide blood and tumor samples, which may involve a biopsy if enough tissue isn't already available. After antibodies are made, you will receive them through a series of infusions.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your safety will be monitored from your first dose of treatment through an evaluation at 6 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Clinical Trial to Treat Stage IV Cancer Patients
At a glance
Conditions
NCT06674538
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Penn State Cancer Institute
Hershey, Pennsylvaniano site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- David Krag, MD · STUDY_CHAIR · Moonshot Antibodies
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Safety: Frequency of Grade III or greater adverse eventsFrom first dose of treatment through endpoint evaluation at 6 months
Frequency of Grade III or greater adverse events