Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
RSVPreF3 + dTpa is a combination vaccine regimen consisting of the respiratory syncytial virus (RSV) fusion protein stabilized in the prefusion conformation (RSVPreF3) and the diphtheria, tetanus, and acellular pertussis vaccine (dTpa, marketed as Boostrix)[1][2][3]. RSVPreF3 is designed as a maternal vaccine to induce robust immune responses and prevent RSV-associated illness in infants, primarily via maternal antibody transfer[1][2][3]. dTpa provides immunity against diphtheria, tetanus, and pertussis and is routinely recommended for pregnant women to protect newborns from pertussis. The combination is administered intramuscularly and tested in phase 2 studies for its safety and immunogenicity in healthy women of childbearing age. Mechanistically, RSVPreF3 induces neutralizing antibodies against the RSV-F (fusion) protein and dTpa induces immune responses against diphtheria toxin, tetanus toxin, and pertussis antigens (pertussis toxin, filamentous hemagglutinin, and pertactin)[1][2][3].
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 RSVPreF3 + dTpa.