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Avoid vigorous shaking, which can break the delicate peptide bonds

We received the application for a new device category for transitional pass-through payment status for the aprevo Cervical ACDF System on March 3, 2025, which is within 3 years of the date of the initial FDA marketing authorization

0.1% RGN-259 (Thymosin 4) ophthalmic solution promotes healing and improves comfort in neurotrophic keratopathy patients in a randomized, placebo-controlled, double-masked Phase III clinical trial

Without human trials, clinicians cannot reliably determine appropriate dosing, long-term risks or whether benefits outweigh risks