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Cancer Vaccine

Vaccine Nous-209 for Lynch Syndrome

Phase 1 & 2
Recruiting
Led By Eduardo Vilar-Sanchez
Research Sponsored by National Cancer Institute (NCI)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Participants must have a clinical diagnosis of Lynch syndrome (LS) as defined by specific genetic and clinical criteria
Participants must have no evidence of active or recurrent invasive cancer for 6 months prior to screening
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at 12 months
Awards & highlights

Study Summary

This trial is testing a vaccine for Lynch syndrome, which is an inherited disorder that causes a higher than normal chance of developing colorectal cancer and certain other types of cancer.

Who is the study for?
This trial is for Lynch syndrome patients without active cancer for 6 months, who can undergo colonoscopy with biopsies yearly. They must be past any cancer treatment by at least 6 months, avoid certain meds, use contraception, and adhere to the study protocol including vaccine cycles and blood sample collection.Check my eligibility
What is being tested?
The Nous-209 vaccine's safety and immune response are being tested in this phase Ib/II trial. It involves biospecimen collection, endoscopic biopsy, two types of vaccines (GAd-209-FSP and MVA-209-FSP), and questionnaire administration to see if it affects polyp or tumor development in the colon.See study design
What are the potential side effects?
Specific side effects aren't listed but may include typical vaccine reactions like discomfort at injection site, fever or fatigue. Participants will be monitored for any high-grade adverse events especially since those with severe reactions from previous cohorts are excluded.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have been diagnosed with Lynch syndrome based on genetic tests and clinical criteria.
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I have been cancer-free for at least 6 months.
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Doctors can reach my lower colon and rectum with an endoscope.
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I have finished all initial tests and received a full cycle of the vaccine for my group.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and at 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Rate of immunogenicity following revaccination (Cohort II)
Rate of immunogenicity following vaccination (Cohort I)
Rates of grade 2/3 adverse events and symptom reactivity following revaccination (Cohort II)
+1 more
Secondary outcome measures
Change in cell free deoxyribonucleic acid (cfDNA) detectability and mutation profile in the peripheral blood
Changes in T cell immune profile and T cell receptor (TCR) repertoire in the peripheral blood
Changes in TCR repertoire within histologically normal colorectal mucosal
+6 more

Trial Design

3Treatment groups
Experimental Treatment
Group I: Part II Arm B (MVA-209-FSPs)Experimental Treatment4 Interventions
Patients receive MVA-209-FSPs IM at week 52. Patients undergo endoscopy with biopsy as well as blood sample collection on the trial.
Group II: Part II Arm A (GAd20-209-FSPs, MVA-209-FSPs)Experimental Treatment5 Interventions
Patients receive GAd20-209-FSPs IM at week 52 and MVA-209-FSPs IM at week 60. Patients undergo endoscopy with biopsy as well as blood sample collection on the trial.
Group III: Part I (GAd20-209-FSPs, MVA-209-FSPs)Experimental Treatment5 Interventions
Patients receive GAd20-209-FSPs IM on day 1 and MVA-209-FSPs IM at week 8. Patients undergo endoscopy with biopsy during screening and follow up as well as blood sample collection on the trial.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Biospecimen Collection
2004
Completed Phase 2
~1720

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Lynch Syndrome treatments often focus on enhancing the immune system's ability to recognize and destroy cancer cells. The Nous-209 vaccine, for example, uses synthetic copies of neoantigens produced by cancer cells due to DNA mismatch repair deficiencies. By stimulating an immune response against these neoantigens, the vaccine helps the body identify and eliminate cancerous cells more effectively. This targeted approach is significant for Lynch Syndrome patients as it offers a potential method to prevent cancer development by leveraging the body's natural immune defenses.
Emerging and mechanism-based therapies for recurrent or metastatic Merkel cell carcinoma.[Molecule based diagnosis].Relevance of the immune system in human urological malignancies: prospective for future clinical treatments.

Find a Location

Who is running the clinical trial?

National Cancer Institute (NCI)Lead Sponsor
13,729 Previous Clinical Trials
40,965,854 Total Patients Enrolled
18 Trials studying Lynch Syndrome
53,006 Patients Enrolled for Lynch Syndrome
Eduardo Vilar-SanchezPrincipal InvestigatorM.D. Anderson Cancer Center
2 Previous Clinical Trials
161 Total Patients Enrolled
1 Trials studying Lynch Syndrome
81 Patients Enrolled for Lynch Syndrome

Media Library

Nous-209 (Cancer Vaccine) Clinical Trial Eligibility Overview. Trial Name: NCT05078866 — Phase 1 & 2
Lynch Syndrome Research Study Groups: Part II Arm A (GAd20-209-FSPs, MVA-209-FSPs), Part I (GAd20-209-FSPs, MVA-209-FSPs), Part II Arm B (MVA-209-FSPs)
Lynch Syndrome Clinical Trial 2023: Nous-209 Highlights & Side Effects. Trial Name: NCT05078866 — Phase 1 & 2
Nous-209 (Cancer Vaccine) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05078866 — Phase 1 & 2
~24 spots leftby Jul 2025