Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ALB-408 is a synthetic peptide developed by Pharis Biotec that functions as an antagonist of the C-X-C chemokine receptor type 4 (CXCR4). It is an optimized derivative of the endogenous peptide EPI-X4, which is a fragment of human serum albumin (residues 408-423) naturally found in human blood. ALB-408 works by binding to and blocking the CXCR4 co-receptor, which is essential for the entry of X4-tropic HIV-1 strains into target CD4+ T lymphocytes. By preventing the interaction between the viral envelope glycoprotein gp120 and the host cell receptor, ALB-408 acts as an entry inhibitor, thereby reducing viral fusion and replication. The drug has been investigated in early-stage clinical settings for the treatment of HIV infections, particularly to target viral variants that utilize the CXCR4 receptor for cellular entry.
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 ALB-408.