Panacea Biotec Joins DENSTAR Project to Advance DengiAll Dengue Vaccine Licensure in Africa
Panacea Biotec has joined the DENSTAR project, a 48-month EU-funded initiative backed by €11,091,138.75, aimed at advancing the licensure of its single-dose tetravalent dengue vaccine DengiAll in sub-Saharan Africa. The consortium, coordinated by Italy's Sclavo Vaccines Association, comprises 10 partners from nine countries and will conduct Phase I/III clinical studies while evaluating vaccine efficacy against DENV-4 using Controlled Human Infection Models.

*this image is generated using AI for illustrative purposes only.
Panacea Biotec has joined the DENSTAR project to advance the licensure of its tetravalent dengue vaccine, DengiAll, in sub-Saharan Africa and facilitate its broader global access. The four-year initiative, funded under the Global Health European & Developing Countries Clinical Trials Partnership 3 Joint Undertaking (GH EDCTP3 JU) and supported by the European Union, aims to combat Neglected Tropical Diseases and reduce the disease burden across Africa. The project is scheduled to run for 48 months starting June 1, 2026.
DENSTAR Consortium
The DENSTAR consortium unites 10 partners from nine countries, including universities, research organizations, and a biotech company. It is coordinated by the Sclavo Vaccines Association, a non-profit organization based in Italy. Panacea Biotec, the developer of DengiAll, serves as a key partner in this public-private partnership. The consortium will conduct Phase I/III studies in healthy African adults and children to confirm the vaccine's safety and efficacy. The project also seeks to address critical knowledge gaps by evaluating vaccine efficacy against Dengue Virus serotype 4 (DENV-4) using Controlled Human Infection Models (CHIMs).
DengiAll is a single-dose, live-attenuated vaccine targeting all four dengue virus serotypes, currently in late-stage development in India. The vaccine is designed to be cost-efficient to manufacture and suitable for large-scale deployment without requiring prior serological testing.
Project Details
The following table outlines the key parameters of the DENSTAR project:
| Feature: | Details |
|---|---|
| Project Title: | Dengue Efficacy and Safety Trial in African Region |
| Acronym: | DENSTAR |
| Duration: | 48 months from June 1, 2026 |
| Coordinator: | Sclavo Vaccines Association ETS (Italy) |
| EDCTP Contribution: | €11,091,138.75 |
| Grant Number: | 101249135 |
Key Participants
The consortium brings together leading institutions across nine countries:
- Sclavo Vaccines Association ETS (Italy)
- Panacea Biotec Limited (India)
- Kwame Nkrumah University of Science and Technology (Ghana)
- Universitätsklinikum Heidelberg (Germany)
- National Institute of Allergy and Infectious Diseases (United States)
- International Vaccine Institute (Republic of Korea)
- Centre de Recherches Medicales de Lambaréné (Gabon)
- Instituto Nacional de Saúde (Mozambique)
- Johns Hopkins University (United States)
- Institut National De Recherche Biomedicale Du Zaire (Democratic Republic of the Congo)
Historical Stock Returns for Panacea Biotec
| 1 Day | 5 Days | 1 Month | 6 Months | 1 Year | 5 Years |
|---|---|---|---|---|---|
| -0.62% | +3.53% | +32.14% | +54.18% | +30.56% | +45.97% |
How will the outcomes of the Phase I/III studies in Africa influence the regulatory approval strategy for DengiAll in other global markets?
What are the potential commercial and public health implications if DengiAll proves effective without requiring prior serological testing?
How might the success of the DENSTAR project impact Panacea Biotec's competitive position in the global dengue vaccine market?































