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PDR for Nutritional Supplements

Hyper-homocysteinemia as a risk factor and potential nutraceutical target for certain pathologies

In 2-year feeding studies, F344/N rats and B6C3F1 mice were fed a diet containing acetaminophen up to 6,000 ppm

Inclusion Criteria Timeline for a Trial Participant Screening Participants are screened for eligibility to participate in the trial Treatment Participants receive either glutathione alone or glutathione plus AdiaVita during the initial three-month treatment phase Crossover/Extension Children in the glutathione-only group may cross over to receive AdiaVita infusions if safety checks at month 6 are satisfactory Follow-up Participants are monitored for safety and effectiveness after treatment using repeated Autism Treatment Evaluation Checklist assessments What Are the Treatments Tested in This Trial