Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DSP-0546LP is a novel vaccine adjuvant developed as part of a universal influenza vaccine candidate. It is a synthetic compound that specifically activates Toll-like receptor 7 (TLR7), which senses virus-derived RNA and induces innate immune responses. As an adjuvant, DSP-0546LP enhances the quantity, quality, and durability of immune responses when combined with antigens such as post-fusion hemagglutinin (fH1). Preclinical studies have shown that formulations containing DSP-0546LP induce cross-reactive antibodies more efficiently than non-adjuvanted formulations, strongly promote Th1-polarized immune responses (evidenced by increased interferon-gamma and IgG2c production), and enhance antibody-dependent cellular cytotoxicity (ADCC) against diverse influenza strains. The mechanism does not primarily rely on neutralizing antibodies but rather on functional antibody induction and Th1-mediated immunity. The universal influenza vaccine candidate fH1/DSP-0546LP is being jointly developed by Sumitomo Pharma and the National Institutes of Biomedical Innovation, Health and Nutrition (NIBIOHN), with clinical development currently in Phase 1 trials for prophylaxis against influenza[1][3][5][8].
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 DSP-0546LP.