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While the research was conducted at Seoul National University with IRB approval, commercial funding is a standard disclosure to note

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70% of patients reported at least one adverse event, most commonly skin reactions (16.4% hypericin PDT vs 10.5% placebo), pruritus (cycle 1, 5.2% hypericin PDT vs 4.0% placebo), application-site pain and/or irritation (cycle 1, 6.9% hypericin PDT vs 4.0% placebo), application-site pruritus (cycle 1, 4.3% hypericin PDT vs 2.0% placebo)

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