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Study identifier: NCT07560943 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Tolerability of AI-Designed Pan-Cancer Neoantigen mRNA Vaccine (PAN-NeoVax) in Advanced Solid Tumors

Condition: Cancer  ·  Sponsor: West China Hospital

PhasePhase 1
Planned participants9
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

This is a phase I, open-label, single-arm, single-center, dose-escalation study to evaluate the safety, tolerability, and preliminary anti-tumor efficacy of PAN-NeoVax, an artificial intelligence (AI)-designed pan-cancer neoantigen mRNA vaccine delivered via lipid nanoparticles (LNP), administered by intratumoral injection in patients with advanced or metastatic solid tumors who have failed second-line therapy. The study employs a classical "3+3" dose-escalation design with three dose levels (25 μg, 50 μg, and 100 μg mRNA). Each subject will receive 5 doses of basic immunization (first 4 doses at weekly intervals, fifth dose at 1 month after the fourth dose).

This description comes directly from the study's public registry record.

Talk to the study team

Xingchen Peng  ·  18980606753  ·  pxx2014@163.com

Always discuss trial participation with your own doctor first.

Locations (2)

West China HospitalChengdu, Sichuan, ChinaNot Yet Recruiting
The West China HospitalChengdu, Sichuan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07560943