A recombinant antibody with optimized CDR binding improves NT-proBNP detection sensitivity and specificity for earlier heart failure diagnosis.
Point mutations in NT-proBNP can disrupt standard assays; these variant-specific antibodies improve heart failure diagnosis by detecting R46H and E43D forms.
Conjugating pramlintide analogues to albumin-binding moieties extends half-life while reducing amyloid fibril formation and preserving amylin activity.
Antibodies targeting kallidin and des-Arg10-kallidin block bradykinin B1 receptor binding to address inflammation, pain, and fibrosis.
OCN-derived oral peptides reduce fat absorption, liver fat, and blood lipids to address NAFLD and related metabolic disorders with fewer side effects.
Glycoengineered FSTL1 with O-linked glycosylation and no N-linked glycosylation supports cardiomyocyte survival, growth, and scar reduction.
Gradual weekly tirzepatide titration helps patients who miss HbA1c or weight goals on GLP-1 RAs improve control with better tolerability.
Sequence-modified amylin analogs improve solubility, thermal stability, and half-life to enable less frequent dosing with fewer side effects.
Amino acid changes plus a half-life extending group improve PYY analogue solubility near pH 6-7 and prolong NPY2 receptor action for obesity treatment.
Human cell line production adds α2,6 and α2,3 sialylation to recombinant FSH, improving natural-like pharmacokinetics and activity.
Modified CRF2 agonist peptides extend half-life and stability, enabling once-daily subcutaneous dosing instead of continuous infusion.
Modified UCN2-derived peptides improve stability and solubility, enabling once-daily subcutaneous CRF2 therapy instead of continuous infusion.
Modified MIS protein arrests folliculogenesis to preserve ovarian reserve and protect ovarian and uterine tissue during chemotherapy.
Cyclized hepcidin analogue conjugates improve solubility, stability, and half-life while preserving iron regulation for iron overload treatment.
Modified hepcidin peptides target sickle cell complications by reducing spleen and liver size while improving blood cell indices.
Targeted amino acid substitutions and a methylene bridge improve hAMY3R agonist stability, reduce dimerization, and extend half-life.
Engineered hepcidin analogues improve solubility and synthesis while binding ferroportin to lower serum iron in iron overload diseases.