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healthcare, and it serves patients who need customized formulations or cannot access commercially available products - but it operates under different oversight standards than FDA-approved manufacturing

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Patients were randomly assigned in a 2:1 ratio to receive vandetanib or placebo.[11][Level of evidence B1] With a median follow-up of 24 months, progression-free survival (PFS) favored vandetanib (hazard ratio [HR], 0.46

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