PepFold

Condition Database

Warfarin Sensitivity

Prevalence: ~2 million US patients on warfarin, ~30% experience dosing complications

Genetic variation in VKORC1 and CYP2C9 determines warfarin dose requirements. FDA recommends pharmacogenomic testing, and genotype-guided dosing reduces bleeding events by 30%. It is the most established pharmacogenomic application in clinical practice.

Peptide Therapeutics

Peptide anticoagulants targeting thrombin (bivalirudin class), Factor Xa inhibitor peptides, and VKORC1-selective peptide modulators offer genotype-independent alternatives to warfarin.

Current Treatments

Warfarin (with pharmacogenomic dosing), DOACs (rivaroxaban, apixaban, dabigatran), bivalirudin (peptide-based, IV only).

Key Genetic Variants

Associated Genes

Explore peptide candidates for Warfarin Sensitivity

Submit rs9923231, rs1799853, rs1057910 to PepFold. Full report with 3D structures and synthesis protocols in under 2 minutes.