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The outstanding 17% ( n = 6), not in full compliance, is comprised of patients lost to follow-up (6%, n = 2), and a patient who was deemed to be under treated based on the standard but was clinically stable on oral replacement (3%, n = 1)

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Efficacy and safety of LX9211 for relief of diabetic peripheral neuropathic pain (RELIEF-DPN 1): results of a double-blind, randomized, placebo-controlled, proof-of-concept study