Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The tetanus-CMV fusion peptide vaccine is a candidate therapeutic and prophylactic vaccine designed to elicit cytotoxic T-lymphocyte (CTL) responses against cytomegalovirus (CMV), particularly in immunocompromised individuals such as hematopoietic cell transplant recipients. It consists of the HLA A*0201-specific CMV pp65(495-503) cytotoxic CD8+ T-cell epitope fused to a universal T-helper epitope derived from the natural tetanus toxin sequence. This design aims to enhance both helper and cytotoxic T-cell responses for improved protection against CMV infection or reactivation[1][5][3]. Clinical trials have demonstrated its safety and ability to expand pp65(495-503)-specific T cells, especially when coadministered with the adjuvant PF03512676[1][5]. The primary indication is prevention or control of CMV complications in high-risk populations.
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 tetanus-cmv fusion peptide vaccine.