Human safety & anti-inflammatory trial
Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid
Gandy et al. · Clinical Pharmacology: Advances and Applications · 2012
This randomized, double-blind, placebo-controlled phase 1 trial in 30 adults evaluated escalating oral doses of a carbohydrate-derived fulvic acid (CHD-FA) solution. Across acute and subacute dosing up to 40 mL of 3.8% CHD-FA twice daily, comprehensive safety labs, ECG, and clinical assessments remained within normal limits, while skin-prick reactivity was significantly reduced. For readers looking for a strong human entry point into the fulvic-acid literature, it is one of the most relevant safety and anti-inflammatory proof-of-concept studies available.