Therapeutic vaccines (cancer and chronic disease)
Vaccines given to treat an existing disease — antigen-specific DNA, mRNA or cell-based products — with one approved cell-based product since 2010 and a cancer-vaccine market valued at USD 10.21 billion in 2023.
1 · What it gives
Therapeutic vaccines treat a disease that is already present, with high specificity, fewer side effects and potentially longer-lasting effect and no drug resistance compared with chemical or other biological drugs. Sipuleucel-T (Provenge), approved by the FDA in 2010, is the commercial-scale example. The global cancer-vaccine market was valued at USD 10.21 billion in 2023 and is projected to reach USD 30.16 billion by 2033.
2 · What it replaces 6
3 · How to implement 4 steps
- 1Identify antigensIdentify the specific antigens to target.
- 2Design the vaccineDesign the vaccine as DNA, mRNA or a cell-based product.
- 3GMP manufacturingManufacture under GMP conditions.
- 4Clinical trialsRun clinical trials to establish safety, dosage and efficacy.
4 · Who delivers
Matched suppliers (matched automatically)
| Vaxxinova Norway | Norway | Not classified | active |
| Esco Aster | Singapore | Services / consulting | active |
| EGAVET | Egypt | Research / RTO | active |
| Avani | Indonesia | Producer | active |
| Liselo Labs | South Africa | Research / RTO | active |
| MSD Animal Health Poultry and Swine Sub Sahara Africa | South Africa | Services / consulting | active |
| Biocamp Laboratórios Ltda | Brazil | Research / RTO | active |
| Abtec | India | Research / RTO | active |
| Aristogene Biosciences Pvt. Ltd. | India | Producer | active |
| EcoFix Kenya Ltd (EFK) | Kenya | Producer | active |
| PT. Central Proteina Prima, Tbk | Indonesia | Producer | active |
| Vland Biotech 蔚蓝生物 (SSE 603739) | China | Research / RTO | active |
Leading companies and institutes (from the brief)
Companies and institutions developing or delivering therapeutic vaccines in the sources: Genoa Biotechnologia, CreaGene, Northwest Biotherapeutics, APAC Biotech, Merck & Co., SK Bioscience and GlaxoSmithKline.
5 · Rules & route to market
expert examination up to 70 working days plus registration steps
Information, not legal advice — confirm the procedure for your product. (2026-10-06)
United States
In the US the FDA regulates these products.
European Union
The sources reviewed on 2026-10-16 identified no the EU regulator or standard specific to this technology. Treat the route as case-by-case and ask for a check.
China
In China the NMPA Center for Drug Evaluation (CDE) oversees regulation.
6 · Money: tenders & grants
7 · Tech stack & innovations
Main risks from the sources: manufacturing complexity of personalised products, high production cost, immune-related toxicity, and the lack of standardised regulatory frameworks or global harmonisation.
Sources 6
- Acrpnet.org — acrpnet.org 2026-10-16
- Pmc.ncbi.nlm.nih.gov — pmc.ncbi.nlm.nih.gov 2026-10-16
- Mdpi.com — www.mdpi.com 2026-10-16
- Pharmews.xyz — www.pharmews.xyz 2026-10-16
- Pmc.ncbi.nlm.nih.gov — pmc.ncbi.nlm.nih.gov 2026-10-16
- Pmc.ncbi.nlm.nih.gov — pmc.ncbi.nlm.nih.gov 2026-10-16