Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Sifuvirtide is a synthetic 36-amino acid peptide and a potent HIV fusion inhibitor designed to block the entry of HIV into host cells. It acts by binding to the N-terminal heptad repeat (NHR) region of the gp41 transmembrane glycoprotein on the HIV envelope, thereby preventing the conformational changes required for viral and cellular membrane fusion. This mechanism inhibits replication across diverse HIV strains, including those resistant to other fusion inhibitors such as enfuvirtide. Sifuvirtide demonstrates high potency, broad anti-HIV activity against multiple subtypes (A, B, C, B', CRF07_BC, CRF01_AE), low cytotoxicity in vitro, and favorable pharmacokinetic properties. It was rationally designed with engineered salt bridges and hydrogen bonds that enhance its stability and affinity for gp41. The drug has reached phase 2 clinical trials in China for treatment of acquired immunodeficiency syndrome (AIDS)[1][2][4].
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 sifuvirtide.