GUCY2C Vaccine for Colorectal and Small Bowel Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new vaccine treatment for individuals with advanced colorectal or small bowel cancer that hasn't responded to standard treatments. The study administers two types of vaccines in a specific sequence to evaluate their safety and potential effectiveness. Participants will receive varying doses to determine the safest and most effective amount. The trial seeks individuals diagnosed with advanced colorectal or small bowel cancer who have not benefited from standard therapies. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.
Do I need to stop my current medications for the trial?
The trial does not specify if you need to stop taking your current medications. However, you cannot use systemic steroids or immunosuppressive drugs, except for certain exceptions like low-dose adrenal replacement or brief courses for non-autoimmune conditions.
Is there any evidence suggesting that this treatment is likely to be safe for humans?
Research has shown that the GUCY2C Prime-Boost Vaccination is under study for safety in people with advanced cancers. In previous studies, two main vaccines were used: Ad5.F35-hGUCY2C-PADRE and Lm-GUCY2C. These studies aim to determine the safest dose levels and monitor any side effects after treatment.
Earlier research reported that the adenoviral vaccine Ad5.F35-hGUCY2C-PADRE was generally safe. Another trial used the Listeria-based vaccine, Lm-GUCY2C, to deliver a cancer antigen, a substance that triggers an immune response. This method has been tested to assess if it can safely help the immune system fight cancer cells.
As a Phase 1 trial, the focus is on finding the right dose and monitoring safety. The study will carefully observe any side effects related to the treatment. Overall, early findings suggest these vaccines are being tested at doses considered safe, but further research is needed to confirm their safety in larger groups.12345Why are researchers excited about this trial's treatments?
Researchers are excited about the GUCY2C Prime-Boost Vaccination because it targets colorectal and small bowel cancer in a novel way. Unlike traditional treatments like chemotherapy and radiation, which can affect healthy cells, this vaccine leverages the body's immune system to specifically attack cancer cells by targeting GUCY2C, a biomarker present on these cancer cells. The treatment involves a two-step vaccine approach: an initial intramuscular injection followed by an intravenous boost, which potentially enhances the immune response. This method could offer a more precise, less toxic alternative to conventional therapies, potentially improving outcomes and quality of life for patients.
What evidence suggests that this trial's treatments could be effective for colorectal and small bowel cancer?
Research has shown that the GUCY2C prime-boost vaccination strategy holds promise for treating colorectal and small bowel cancer. This trial will test different dose levels of the GUCY2C vaccine. Studies have found that this method effectively activates the immune system to attack cancer cells. Specifically, one study demonstrated that a combination of a modified virus and a Listeria-based vaccine safely and successfully triggered an immune response against cancer in previous patients. Evidence indicates that the GUCY2C vaccine can help reduce the spread of tumors that have metastasized. These findings suggest that the vaccine could be useful in treating advanced cancers that have not responded to other treatments.12346
Who Is on the Research Team?
Babar Bashir, M.D., M.S.
Principal Investigator
Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Are You a Good Fit for This Trial?
This trial is for adults with advanced colorectal or small bowel cancer that has gotten worse after standard treatments, who are generally in good health and able to care for themselves. Participants must have working major organs, not be pregnant or breastfeeding, and cannot have certain infections or immune system problems.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive Ad5.F35-hGUCY2C-PADRE vaccine intramuscularly followed by two administrations of Lm-GUCY2C vaccine intravenously, four weeks apart
Follow-up
Participants are monitored for safety and effectiveness after treatment, with evaluations every 3 months until disease progression or new therapy
What Are the Treatments Tested in This Trial?
Interventions
- GUCY2C Prime-Boost Vaccination
Trial Overview
The study tests a two-step vaccine approach: first an Ad5.F35-hGUCY2C-PADRE shot into the muscle, then two doses of Lm-GUCY2C given by IV four weeks apart. The goal is to find the safest dose and see how well the vaccines trigger an immune response against cancer.
How Is the Trial Designed?
4
Treatment groups
Experimental Treatment
Participants receive Ad5.F35-hGUCY2C-PADRE vaccine, administered as a single intramuscular (IM) injection (5 × 10¹² viral particles), followed by Lm-GUCY2C vaccine, administered intravenously at a dose of 3 × 10⁹ colony-forming units (CFU) on two occasions approximately four weeks apart.
Participants receive Ad5.F35-hGUCY2C-PADRE vaccine, administered as a single intramuscular (IM) injection (5 × 10¹² viral particles), followed by Lm-GUCY2C vaccine, administered intravenously at a dose of 1 × 10⁹ colony-forming units (CFU) on two occasions approximately four weeks apart.
Participants receive Ad5.F35-hGUCY2C-PADRE vaccine, administered as a single intramuscular (IM) injection (5 × 10¹² viral particles), followed by Lm-GUCY2C vaccine, administered intravenously at a dose of 3 × 10⁸ colony-forming units (CFU) on two occasions approximately four weeks apart.
Participants receive Ad5.F35-hGUCY2C-PADRE vaccine, administered as a single intramuscular (IM) injection (5 × 10¹² viral particles), followed by Lm-GUCY2C vaccine, administered intravenously at a dose of 1 × 10⁸ colony-forming units (CFU) on two occasions approximately four weeks apart.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Thomas Jefferson University
Lead Sponsor
United States Department of Defense
Collaborator
Citations
Study Details | NCT07417488 | GUCY2C Prime-Boost ...
This phase 1 study is an open-label study of heterologous prime-boost vaccination with Ad5.F35-hGUCY2C-PADRE and recombinant listeria monocytogenes (Lm-GUCY2C) ...
Prime-Boost Immunization Eliminates Metastatic Colorectal ...
Here, we examined a prime-boost strategy comprising GUCY2C-expressing DNA and adenoviral vaccines to enhance antitumor efficacy, identifying a heterologous ...
3.
ctv.veeva.com
ctv.veeva.com/study/gucy2c-prime-boost-vaccination-for-advanced-colorectal-and-small-bowel-adenocarcinomasGUCY2C Prime-Boost Vaccination for Advanced Colorectal ...
This phase 1 study is an open-label study of heterologous prime-boost vaccination with Ad5.F35-hGUCY2C-PADRE and recombinant listeria ...
GUCY2C Vaccine for Colorectal and Small Bowel Cancer
... Boost Vaccination will have tolerable side effects & efficacy for patients with Small Bowel Cancer, Colorectal Cancer and Colorectal Cancer. See
Chimeric adenoviral (Ad5.F35) and listeria vector prime ...
We examined a prime-boost strategy using a chimeric adenoviral vector (Ad5.F35) that resists pre-existing immunity followed by recombinant Listeria ...
Clinical Trial
A Phase I, Single-Center, Dose Escalation Trial of Heterologous Prime-Boost Vaccination with Ad5.F35-hGUCY2C-PADRE and Lm-GUCY2C Vaccines in Adults with ...
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