Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cyd dengue virus serotype 3 live (attenuated) antigen is a component of the tetravalent, live attenuated chimeric dengue vaccine known as CYD-TDV or Dengvaxia. This vaccine is designed to prevent infection by all four major serotypes of the dengue virus and is based on a yellow fever 17D backbone with the pre-membrane (prM) and envelope (E) genes from each respective dengue virus serotype inserted in place of those from yellow fever. The mechanism of action involves stimulating an immune response against all four types of the dengue virus, thereby providing protective immunity. The primary indication for this drug is prevention of dengue disease in individuals aged 9–45 years who have had prior infection with any type of the dengue virus[1][2][5]. It was developed by Sanofi Pasteur.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Cyd dengue virus serotype 3 live (attenuated) antigen.