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DRUG CLASS:

MAGE-A3 inhibitor

1m
Nanovaccines in Cancer Immunotherapy: Lymph Node-Targeted Strategies and Mechanistic Insights. (PubMed, Curr Pharm Des)
Nanovaccine platforms can potentially overcome some constraints of conventional vaccines by enhancing lymph node targeting, antigen stability, and immunogenicity. Further research in this field could further advance targeted cancer immunotherapy.
Journal
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STING (stimulator of interferon response cGAMP interactor 1)
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BNT111 • intismeran autogene (mRNA-4157)
2ms
Biomimetic and personalized nanovaccines in cancer immunotherapy: Design innovations, translational challenges, and future directions. (PubMed, J Adv Res)
This review synthesizes recent advances in biomimetic and personalized nanovaccine design, highlighting clinical progress in lipid nanoparticle (LNP)-based vaccines such as BNT111 and mRNA-4157, emerging innate immune adjuvants including Toll-like receptor (TLR) and stimulator of interferon genes (STING) agonists, and rational combination strategies with immune checkpoint blockade. Key safety and quality consideration including immunotoxicity, off-target immune activation, and batch heterogeneity are critically evaluated alongside emerging engineering solutions. Finally, future directions integrating AI-guided neoantigen prediction, modular microfluidic manufacturing, and multi-omic biomarker frameworks are discussed to accelerate next generation cancer nanovaccine translation.
Review • Journal • IO biomarker
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STING (stimulator of interferon response cGAMP interactor 1)
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BNT111 • intismeran autogene (mRNA-4157)
3ms
Trial completion
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BRAF (B-raf proto-oncogene)
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BRAF mutation • BRAF V600
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Libtayo (cemiplimab-rwlc) • BNT111
6ms
Innovative therapeutic cancer vaccine PDC∗lung01 with or without anti-PD-1: an open-label, dose-escalation phase I/II study in non-small-cell lung cancer. (PubMed, ESMO Open)
PDC∗lung01 was immunogenic and had a manageable safety profile in all cohorts and met the predefined clinical objectives when combined with anti-PD-1 in metastatic NSCLC. Median PFS was positively correlated with antigen-specific T-cell expansions.
P1/2 data • Journal
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PD-L1 (Programmed death ligand 1) • MUC1 (Mucin 1) • BIRC5 (Baculoviral IAP repeat containing 5) • CTAG1B (Cancer/testis antigen 1B) • MAGEA4 (Melanoma antigen family A, 4)
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PDC*lung
10ms
Trial completion date
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BRAF (B-raf proto-oncogene)
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BRAF mutation • BRAF V600
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Libtayo (cemiplimab-rwlc) • BNT111
over1year
PDC-LUNG-101: Safety, Immunogenicity and Preliminary Clinical Activity Study of PDC*lung01 Cancer Vaccine in NSCLC (clinicaltrials.gov)
P1/2, N=73, Active, not recruiting, PDC*line Pharma SAS | Trial primary completion date: Dec 2025 --> Jul 2024
Trial primary completion date
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CD8 (cluster of differentiation 8) • HLA-A (Major Histocompatibility Complex, Class I, A)
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HLA-A*02
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Keytruda (pembrolizumab) • pemetrexed • PDC*lung
over1year
Trial primary completion date
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BRAF (B-raf proto-oncogene)
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Libtayo (cemiplimab-rwlc) • BNT111
almost2years
Expression of the tumor antigens NY-ESO-1, tyrosinase, MAGE-A3, and TPTE in pediatric and adult melanoma: a retrospective case control study. (PubMed, Virchows Arch)
BNT111, an investigational lipoplex-formulated mRNA-based therapeutic cancer vaccine encoding melanoma TAAs NY-ESO-1, tyrosinase, MAGE-A3, and TPTE, is undergoing clinical testing in adults. All four TAAs were expressed in pediatric melanoma, albeit NY-ESO-1 and MAGE-A3 to a lesser extent than in adult melanoma. These data support the possibility of investigating vaccines targeting these TAAs for the treatment of pediatric melanoma.
Retrospective data • Journal • IO biomarker
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CTAG1B (Cancer/testis antigen 1B)
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BNT111
over2years
PDC-LUNG-101: Safety, Immunogenicity and Preliminary Clinical Activity Study of PDC*lung01 Cancer Vaccine in NSCLC (clinicaltrials.gov)
P1/2, N=73, Active, not recruiting, PDC*line Pharma SAS | Recruiting --> Active, not recruiting | Trial completion date: Sep 2025 --> Dec 2025 | Trial primary completion date: Sep 2025 --> Dec 2025
Enrollment closed • Trial completion date • Trial primary completion date
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CD8 (cluster of differentiation 8) • HLA-A (Major Histocompatibility Complex, Class I, A)
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HLA-A*02
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Keytruda (pembrolizumab) • pemetrexed • PDC*lung
over2years
Enrollment closed
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BRAF (B-raf proto-oncogene)
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BRAF mutation • BRAF V600
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Libtayo (cemiplimab-rwlc) • BNT111
over2years
PDC-LUNG-101: Safety, Immunogenicity and Preliminary Clinical Activity Study of PDC*lung01 Cancer Vaccine in NSCLC (clinicaltrials.gov)
P1/2, N=64, Recruiting, PDC*line Pharma SAS | Trial completion date: Aug 2024 --> Sep 2025 | Trial primary completion date: Aug 2024 --> Sep 2025
Trial completion date • Trial primary completion date
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CD8 (cluster of differentiation 8) • HLA-A (Major Histocompatibility Complex, Class I, A)
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HLA-A*02
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Keytruda (pembrolizumab) • pemetrexed • PDC*lung