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RecruitingNCT06195293

Anti-cancer Neoantigen Polypeptide Vaccine to Treat Solid Tumors

Anti-cancer Neoantigen Polypeptide Vaccine to Treat Advanced Solid Tumors: Phase I Clinical Trial

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Second Affiliated Hospital of Guangzhou Medical University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The WES and RAN-seq will be performed to identify and verify neoantigens and appropriate polypeptide sequences will be verified, manufactured and protected for vaccine production by multiple in vitro and in vivo studies. Clinical studies will be performed to test anti-cancer function of the polypeptide vaccine for immunotherapy of human cancer patients. In this phase I study, the safety, tolerance, and preliminary efficacy of the polypeptide vaccine immunotherapy on human cancers will firstly be evaluated.

Detailed description

1. Choose appropriate patients with advanced solid cancers, with written consent for this study; 2. Perform biopsy to get fresh sample for DNA/RNA-seqencings and bioinformatics analysis; 3. Produce appropriate polypeptide vaccine for human use and deliver the vaccine into selected patients via local injections, and follow up closely to collect related results as required; 4. To enhance the killing capability, cotreatment the patients with PD1/PDL1/CTLA4 antibodies may be applied; 5. Evaluate the clinical results as needed.

Conditions

Interventions

TypeNameDescription
BIOLOGICALNeoantigen Polypeptide VaccineDeliver neoantigen polypeptide vaccine into patients for anti-ancer therapy.

Timeline

Start date
2024-06-04
Primary completion
2029-12-30
Completion
2037-12-30
First posted
2024-01-08
Last updated
2024-06-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06195293. Inclusion in this directory is not an endorsement.