Developing Treatment, Treatment Validation and Treatment Scope in the Setting of an Autism Clinical Trial

This is an interventional treatment trial for Autism Read More

Inclusion Criteria:

• Meets DSM-IV, ADI, and ADOS criteria for autistic disorder
• Age 5-17.
• Outpatients
• Parent or legal guardian signing informed consent, and assent documented for patient with demonstrated capacity to provide it.
• Sexually active females of childbearing potential must use an acceptable method of birth control (oral contraceptive medications [the administration of which must be supervised by a parent or guardian], IUD, depot medication, double barrier or tubal ligation) and have a negative serum pregnancy test prior to entry into the study.
• Subjects with history of seizures, who have been seizure-free for more than or equal to 6 months on a stable dose of anticonvulsant medication.Non-medicated subjects with a history of seizures who have been seizure-free for more than or equal to 6 months.Subjects with abnormal EEG but no clinical seizures.

Exclusion Criteria:

• Subjects who are pregnant or nursing mothers.
• Sexually active females of childbearing potential who are not using adequate birth control measures (detailed above in inclusion criteria).
• Subjects with overall adaptive behavior scores below the age of two years on the Vineland Adaptive Behavior Rating Scale.
• Subjects with active or unstable epilepsy.
• Subjects with any of the following past or present mental disorders: schizophrenia, schizoaffective disorder, major depressive disorder, bipolar I or II disorders or substance abuse disorders.
• Subjects who are a serious suicidal risk.
• Subjects with clinically significant or unstable medical illness that would contraindicate participation in the study, including hematopoietic or cardiovascular disease, pancreatitis, liver toxicity, and polycystic ovary syndrome
• Subjects reporting history of encephalitis, phenylketonuria, tuberous sclerosis, fragile X syndrome, anoxia during birth, pica, neurofibromatosis, hypomelanosis of Ito, hypothyroidism, Duchenne muscular dystrophy, and maternal rubella.
• Patients with history of the following:gastrointestinal, liver, or kidney, or other known conditions which will presently interfere presently with the absorption, distribution, metabolism, or excretion of drugs, cerebrovascular disease or brain trauma, clinically significant unstable endocrine disorder, such as hypo- or hyperthyroidism, recent history or presence of any form of malignancy
• Treatment within the previous 30 days with any drug known to a well-defined potential for toxicity to a major organ
• Subjects with clinically significant abnormalities in laboratory tests or physical exam
• Subjects likely to require ECT.
• Subjects unable to tolerate taper from psychoactive medication if necessary.
• Subjects with a history of hypersensitivity or severe side effects associated with the use of divalproex sodium, or other an ineffective prior therapeutic trial of omega three fatty acids.
• Subjects who have received any of the following interventions within the prescribed period before starting treatment-investigational drugs within the previous 30 days.
• Subjects who have begun any new alternative non-medication treatments, such as diet, vitamins, and psychosocial therapy, within the previous three months.
• Subjects with any organic or systemic disease or patients who require a therapeutic intervention, not otherwise specified, which would confound the evaluation of the safety of the study medication.
• Subjects who reside in a remote geographical area who do not have regular access to transportation to the clinical facility.
• If a patient is not doing well enough (defined by CGI-AD Severity score of 3-"mildly ill" or better)