A vaccine custom-built for one patient from their own tumor's mutations — the central product of this field.

Unlike preventive vaccines, a personalized (or “individualized”) neoantigen vaccine is manufactured per patient: sequence the tumor and healthy tissue, identify mutations, predict the best neoantigens, and produce a vaccine — often as mRNA or synthetic peptides — encoding those targets.
The aim is to train the patient's immune system to attack cells bearing their specific neoantigens. High-profile programs (e.g. mRNA-based vaccines in melanoma) have driven much of the field's recent commercial momentum.
The economics and turnaround time hinge on the prediction step and manufacturing — the better the targets are chosen, the fewer doses are wasted on neoantigens that don't elicit a response.
Not yet as approved products — they remain investigational, in clinical trials. The most advanced programs (such as mRNA-based individualized vaccines in melanoma and other tumors) are in Phase 2/3 trials, with the earliest approvals expected in the latter half of the decade.
They overlap but aren't identical. "Neoantigen vaccine" describes what the vaccine targets (a tumor's mutation-derived antigens); "mRNA vaccine" describes how it's delivered (as messenger RNA). Many leading personalized neoantigen vaccines use the mRNA platform, but neoantigens can also be delivered as peptides, DNA, or viral vectors.
A patient's tumor and healthy tissue are sequenced and compared to find tumor-specific mutations; AI ranks which mutated peptides are most likely to be presented and immunogenic for that patient's HLA type; and a vaccine encoding the top targets is manufactured per patient — typically in a matter of weeks.