Anti-Claudin-1 antibodies target bile duct epithelial damage in PSC to reduce fibrosis, cholestasis, and liver inflammation.
A body-temperature gelling ECM hydrogel coats the esophagus to curb inflammation and stricture without invasive late-stage procedures.
Mild heat-aging boosts parsnip polyphenols, enabling lower-temperature extraction and liver-protective effects against MASLD and MASH.
A water or alcohol extract of radix actinidiae chinensis suppresses IL-8, IL-17, and TNFα to treat ulcerative colitis with lower side effects.
An injectable hyaluronic acid-Pluronic hydrogel extends DFO nanochelator release to improve iron chelation compliance and reduce toxicity.
Citrate-buffered mepolizumab compositions control deamidation, oxidation, and aggregation to preserve IL-5 antibody function and efficacy.
Using imeglimin, metformin, and phosphoenolpyruvic acid to inhibit ATP secretion while avoiding the low absorption and severe side effects of clodronate.
Receptor-targeted antibody binders internalize into hepatic stellate cells to deliver antifibrotic agents while reducing systemic toxicity.
Lauryl sulfate cabozantinib compositions improve fasted oral bioavailability, reduce food effect variability, and lower adverse events.
Function-blocking α11β1 antibodies disrupt collagen binding to attenuate fibrotic microenvironments and slow cancer progression.
Fc-region α4β7 antibody variants extend serum half-life, maintain therapeutic levels, and reduce dosing frequency in IBD treatment.
A bovine milk fat and vegetable lipid blend controls TAG fatty acid positions to reduce calcium and magnesium soaps and ease infant constipation.
A composite liver-specific promoter element boosts and stabilizes hepatocyte gene expression for AAV-based gene delivery.
Fermented cereal gruel with Lp299 and Lp299v helps restore gut barrier integrity, modulate permeability, and reduce inflammation.
A natural oil ear drop composition targets inner ear balance structures to relieve motion sickness without the side effects of systemic drugs.
DPP-IV inhibitors modulate immune responses in PBC, PSC, and AIH to slow liver disease progression with fewer side effects.
Combining an LPA1 receptor antagonist with pirfenidone and/or nintedanib improves anti-fibrotic activity while helping reduce side effects.