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aMIL

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · FDA-approved active Biologic

aMIL is a personalized neoantigen vaccine that trains the immune system to recognize and attack cancer cells expressing patient-specific tumor mutations.

aMIL is a personalized neoantigen vaccine that trains the immune system to recognize and attack cancer cells expressing patient-specific tumor mutations. Used for Lymphoma (personalized neoantigen therapy).

At a glance

Generic nameaMIL
SponsorSidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Drug classPersonalized neoantigen vaccine
TargetPatient-specific tumor neoantigens
ModalityBiologic
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

aMIL (autologous Mutation-specific Immunotherapy for Lymphoma) is an individualized therapeutic cancer vaccine designed to stimulate T-cell responses against neoantigens derived from somatic mutations in a patient's own tumor. The vaccine is manufactured by sequencing the patient's tumor, identifying non-synonymous mutations, and creating a personalized immunogen that primes cytotoxic T lymphocytes to target cancer cells bearing these unique mutations.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results