DISP-10 for Gastrointestinal Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores a new treatment called DISP-10 for individuals with advanced gastrointestinal cancers, such as esophageal and gastric adenocarcinomas. The goal is to determine the safety and effectiveness of DISP-10, which combines a virus (DV-10) with a special type of immune cell therapy (CAR T cells). The trial consists of two parts to identify the optimal dose and assess its efficacy. Suitable participants include those with specific advanced GI cancers and at least one tumor that can be biopsied. As a Phase 1 trial, this research aims to understand how the treatment functions in people, offering participants the chance to be among the first to receive this innovative therapy.
Do I have to stop taking my current medications for the trial?
The trial information does not specify if you need to stop taking your current medications. However, it does mention that active treatment with antiviral agents is not allowed, so you may need to stop those if applicable.
Is there any evidence suggesting that DISP-10 is likely to be safe for humans?
Research has shown that the DISP-10 treatment, which combines a virus targeting cancer cells and a cell therapy targeting a protein on these cells, is under study for safety in people with advanced gastrointestinal cancers. As a Phase 1 trial, the primary goal is to assess the treatment's safety and tolerability in humans.
In early studies with similar treatments, researchers often identify side effects and determine safe dose levels. While side effects may occur, they are closely monitored. These studies aim to find the right dose that balances effectiveness with safety. Although specific data on DISP-10 side effects is not yet available, similar therapies can sometimes cause reactions like fever or tiredness.
Since this is an early-phase trial, understanding that the treatment's safety is still under exploration is crucial. However, careful monitoring and gradual dose increases aim to ensure participant safety as much as possible.12345Why do researchers think this study treatment might be promising for gastrointestinal cancer?
Unlike the standard treatments for gastrointestinal cancer, which often include surgery, chemotherapy, and radiation, DISP-10 offers a novel approach by combining a new active ingredient, DV-10, with ide-cel, a type of CAR-T cell therapy. Most traditional treatments target cancer cells directly, but DISP-10 works by enhancing the immune system's ability to fight cancer through genetically modified T-cells. Researchers are excited about DISP-10 because it could provide a more personalized and potentially more effective treatment option with fewer side effects than conventional therapies.
What evidence suggests that DISP-10 could be an effective treatment for gastrointestinal cancer?
Research has shown that DISP-10, which participants in this trial will receive, combines DV-10 (a type of virus) and idecabtagene vicleucel (a type of immune therapy). This immune therapy, known as CAR T-cell therapy, boosts the body's natural defenses to target and destroy cancer cells. Studies have found that these therapies can significantly shrink tumors in other types of cancer. Viruses like DV-10 deliver treatment directly into cancer cells, aiding in their destruction. Early evidence from similar treatments suggests they may slow cancer growth and improve patient outcomes. This combination aims to attack cancer cells in different ways, increasing the chances of success.13678
Are You a Good Fit for This Trial?
This trial is for adults (18+) with advanced or metastatic cancers of the esophagus, stomach, gastroesophageal junction, or colon/rectum. Participants must have cancer that can be measured and biopsied, good organ function, and be in generally good physical condition.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Dose-Escalation
Evaluation of safety and tolerability of increasing dose levels of DISP-10 to establish the recommended dose for expansion
Dose-Expansion
Evaluation of safety and efficacy of DISP-10 in participants treated at the recommended dose for expansion
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- DISP-10
Trial Overview
The study is testing DISP-10—a combination of a virus-based therapy (DV-10) and CAR T-cell therapy (ide-cel)—in people with advanced GI cancers. The trial will first find a safe dose, then test how well it works at that dose.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Participants will receive DV-10 in combination with ide-cel. Lymphodepleting chemotherapy (fludarabine and cyclophosphamide) will be administered a few days prior to ide-cel.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Dispatch Biotherapeutics
Lead Sponsor
Bristol-Myers Squibb
Industry Sponsor
Christopher Boerner
Bristol-Myers Squibb
Chief Executive Officer since 2023
PhD in Business Administration from the Haas School of Business, University of California, Berkeley; BA in Economics and History from Washington University in St. Louis
Deepak L. Bhatt
Bristol-Myers Squibb
Chief Medical Officer since 2024
MD from Yale University; MSc in Clinical Epidemiology from the University of Pennsylvania
Citations
A Phase 1 Study to Evaluate the Safety and Efficacy of ...
A Phase 1 Study to Evaluate the Safety and Efficacy of DISP-10 in Participants with Advanced Gastrointestinal Cancers. NOT ENROLLING.
DISP-10 for Gastrointestinal Cancer
This Phase 1 medical study run by Dispatch Biotherapeutics is evaluating whether DISP-10 will have tolerable side effects & efficacy for patients with ...
NCT04426669 | A Study of Metastatic Gastrointestinal ...
A clinical trial to assess the safety and efficacy of genetically-engineered, neoantigen-specific Tumor Infiltrating Lymphocytes (TIL)
Gastrointestinal Cancer: Outcomes and Therapeutic ... - PMC
The contributions to this Special Issue, titled “Gastrointestinal Cancer: Outcomes and Therapeutic Management”, provide valuable perspectives on ...
5.
curetoday.com
curetoday.com/view/expert-insights-into-advances-in-gastrointestinal-cancer-treatmentExpert Insights into Advances in Gastrointestinal Cancer ...
There was a new report that came out about improved cancer outcomes showing more people are living to five years with cancers across the board.
A Phase 1 Study Evaluating DISP-10 in Participants With ...
Part 1 of the study will evaluate the safety and tolerability of increasing dose levels of DISP-10 to establish the recommended dose for expansion (RDE); Part 2 ...
NCT07221357 | A Study to Evaluate the Safety and ...
The purpose of this study is to evaluate the safety and efficacy of pumitamig in combination with chemotherapy versus bevacizumab in combination with ...
Gastrointestinal toxicity of targeted cancer therapies in ... - PMC
In DESTINY-Breast01 pooled safety, nausea occurred in 79%, vomiting 47%, diarrhea 29% (grade ≥3 diarrhea 1.7%). In the gastric-cancer trial ...
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.