๐ŸŽ—๏ธ Cancer Vaccine Tracker

Tracking Therapeutic & Preventive Cancer Immunotherapy Vaccines

Cancer vaccines represent a paradigm shift in oncology, harnessing the immune system to fight cancer. Unlike traditional vaccines that prevent infectious diseases, most cancer vaccines are therapeutic (treating existing cancer) rather than preventive. Two vaccines are FDA-approved: Provenge (sipuleucel-T) for prostate cancer and T-VEC (talimogene laherparepvec) for melanoma. The field has exploded with personalized mRNA vaccines tailored to individual tumors, neoantigen vaccines targeting tumor-specific mutations, and combinations with checkpoint inhibitors. BioNTech, Moderna, and Gritstone are leading personalized vaccine development for melanoma, pancreatic, and lung cancers. This tracker monitors both therapeutic vaccines (treating cancer) and preventive vaccines (like HPV vaccine preventing cervical cancer).

Cancer Vaccines by Development Phase

2
FDA Approved
5
Phase 3 Trials
40+
Total Pipeline
๐Ÿ”

Cancer Vaccine Candidates

Provenge (Sipuleucel-T)
FDA Approved 2010

Developer: Dendreon Pharmaceuticals

Platform: Autologous cellular immunotherapy (dendritic cell vaccine)

Target: Metastatic castration-resistant prostate cancer

Mechanism: Patient's immune cells are collected, exposed to prostatic acid phosphatase (PAP) antigen, activated, and reinfused to stimulate immune response against prostate cancer cells

Efficacy: 4.1 month median survival benefit in Phase 3 trial. First therapeutic cancer vaccine approved by FDA.

Administration: Three infusions over one month. Personalized to each patient.

Status: Approved and available, though high cost (~$93,000) limits widespread use.

๐ŸŽฏ Prostate cancer ๐Ÿงฌ Personalized โœ… FDA approved
T-VEC (Talimogene Laherparepvec)
FDA Approved 2015

Developer: Amgen

Platform: Oncolytic virus therapy (modified herpes simplex virus)

Target: Advanced melanoma (unresectable stage IIIB-IV)

Mechanism: Genetically modified herpes virus injected directly into tumors, where it replicates in cancer cells, kills them, and releases antigens that stimulate systemic anti-tumor immunity

Efficacy: 16% objective response rate, improved durable response compared to GM-CSF

Administration: Direct intratumoral injection. Often combined with checkpoint inhibitors.

๐ŸŽฏ Melanoma ๐Ÿฆ  Oncolytic virus ๐Ÿ’‰ Intratumoral
mRNA-4157/V940 (Personalized Melanoma Vaccine)
Phase 3

Developer: Moderna + Merck

Platform: Personalized mRNA neoantigen vaccine

Target: High-risk melanoma (adjuvant treatment post-surgery)

Innovation: Tumor is sequenced to identify patient-specific mutations (neoantigens), mRNA vaccine is custom-designed and manufactured within 8 weeks, encoding up to 34 neoantigens

Breakthrough: Phase 2b showed 44% reduction in recurrence/death when combined with Keytruda vs. Keytruda alone

Status: Phase 3 trial (KEYNOTE-942) enrolling 1,089 patients. Could be approved 2025-2026 if successful.

Significance: First personalized cancer vaccine to show major clinical benefit. Platform applicable to multiple cancer types.

๐Ÿงฌ Personalized ๐ŸŽฏ 34 neoantigens ๐Ÿ“Š 44% benefit
BNT122 (Individualized Neoantigen Therapy)
Phase 2

Developer: BioNTech

Platform: Personalized mRNA vaccine encoding patient-specific neoantigens

Targets: Multiple solid tumors (melanoma, pancreatic, colorectal cancers)

Innovation: Manufacturing time reduced to 6-7 weeks. Can encode up to 20 neoantigens per patient.

Status: Phase 2 trials ongoing in combination with checkpoint inhibitors. Pancreatic cancer trial showed promising T-cell responses in preliminary data.

๐Ÿงฌ Personalized mRNA ๐ŸŽฏ Multi-cancer โšก 6-week production
GVAX Pancreas
Phase 2

Developer: Johns Hopkins / Aduro Biotech

Platform: Whole-cell vaccine with GM-CSF

Target: Pancreatic ductal adenocarcinoma

Mechanism: Irradiated pancreatic cancer cells engineered to secrete GM-CSF, stimulating dendritic cell activation

Status: Phase 2 trials in combination with checkpoint inhibitors and chemotherapy

๐ŸŽฏ Pancreatic ๐Ÿงช Whole-cell ๐Ÿ’‰ Combination therapy
Tedopi (OSE-2101)
Phase 3

Developer: OSE Immunotherapeutics

Platform: Peptide-based cancer vaccine

Target: Advanced non-small cell lung cancer (NSCLC) in HLA-A2+ patients

Mechanism: 10 optimized tumor-associated peptides designed to activate cytotoxic T cells

Status: Phase 3 trial (Atalante-1) in 2nd/3rd line NSCLC patients after checkpoint inhibitor failure

๐Ÿซ Lung cancer ๐Ÿงฌ 10 peptides ๐Ÿ“Š Phase 3
GRANITE (Personalized Neoantigen Vaccine)
Phase 2

Developer: Gritstone bio

Platform: Prime-boost strategy using heterologous vectors (viral vector prime + mRNA boost)

Targets: Colorectal, gastric, and other solid tumors with microsatellite instability

Innovation: Uses AI to predict which neoantigens will generate strongest immune responses

Status: Phase 2 trials ongoing, particularly in MSI-high tumors

๐Ÿค– AI-designed ๐Ÿ’‰ Prime-boost ๐ŸŽฏ MSI-high tumors
CIMAvax-EGF
Phase 3

Developer: Center of Molecular Immunology, Cuba / Roswell Park (USA trials)

Platform: Therapeutic vaccine targeting epidermal growth factor (EGF)

Target: Advanced non-small cell lung cancer

Mechanism: Induces antibodies against EGF, blocking EGFR signaling pathway in tumors

Status: Approved in Cuba, Peru, Paraguay. Phase 3 trials in USA.

๐Ÿซ Lung cancer ๐ŸŽฏ EGFR pathway ๐ŸŒŽ Cuba-developed
DPX-Survivac
Phase 2

Developer: IMV Inc.

Platform: DepoVax lipid-based vaccine targeting survivin

Target: Ovarian cancer, diffuse large B-cell lymphoma

Mechanism: Targets survivin protein overexpressed in cancer cells

Status: Phase 2 trials in combination with checkpoint inhibitors

๐ŸŽฏ Ovarian cancer ๐Ÿงฌ Survivin target ๐Ÿ’‰ DepoVax platform
NeoVax (Personalized Peptide Vaccine)
Phase 1

Developer: Dana-Farber Cancer Institute / Neon Therapeutics

Platform: Personalized peptide-based neoantigen vaccine

Targets: Glioblastoma, melanoma

Innovation: Up to 20 personalized neoantigens formulated as long peptides

Status: Phase 1 trials showed strong T-cell responses in glioblastoma patients

๐Ÿง  Glioblastoma ๐Ÿงฌ Personalized ๐Ÿ”ฌ Peptide-based
UV1
Phase 2

Developer: Ultimovacs

Platform: Peptide vaccine targeting telomerase (hTERT)

Targets: Prostate cancer, malignant mesothelioma, ovarian cancer

Mechanism: Telomerase is active in 85-90% of cancers but not normal cells, making it ideal target

Status: Phase 2 trials in multiple cancer types, often combined with checkpoint inhibitors

๐ŸŽฏ Pan-cancer target ๐Ÿงฌ Telomerase ๐Ÿ’‰ Combination therapy
AlloStim
Phase 2

Developer: Immunovative Therapies

Platform: Allogeneic cellular immunotherapy (off-the-shelf immune cells)

Targets: Metastatic colorectal, ovarian, breast cancers

Innovation: Uses donor cells (not patient-specific), allowing immediate treatment

Status: Phase 2 trials in late-stage cancers

๐Ÿงช Off-the-shelf โšก Immediate use ๐ŸŽฏ Metastatic cancer

๐Ÿ’ก Cancer Vaccine Revolution

Cancer vaccines are entering a golden age driven by three breakthroughs: (1) Personalized medicine - sequencing individual tumors to create custom vaccines, (2) mRNA technology - rapid manufacturing of personalized vaccines within 6-8 weeks, and (3) Combination therapy - pairing vaccines with checkpoint inhibitors (anti-PD-1, anti-CTLA-4) dramatically improves efficacy. The Moderna/Merck melanoma vaccine's 44% benefit represents a paradigm shift. Unlike infectious disease vaccines that prevent infection, cancer vaccines primarily treat existing disease by reactivating the immune system against tumors. The future involves: multi-cancer vaccines, AI-designed neoantigens, off-the-shelf allogeneic products, and combinations creating "cancer vaccination + immunotherapy" as standard of care.