A Phase I Study of Pyrimethamine in Patients With GM2 Gangliosidosis

Withdrawn before enrolling · Phase 1

Conditions studied: G(M2) Ganglioside, Tay-Sachs Disease Ganglioside, Sandhoff Disease Ganglioside

In brief

Adult Tay-Sachs disease and Sandhoff diseases are caused by deficiency of an enzyme called β-hexosaminidase A, or Hex A in short. This enzyme is located in a particular cellular component, called lysosomes, inside the brain cells. The reason that Hex A of patients with Adult Tay-Sachs disease or Sandhoff disease is deficient is because this enzyme had gone through mutation, resulting in it not working very well. In healthy people, Hex A efficiently breaks down GM2-ganglioside, which is a by-product from cells of our body. However, patients with Adult Tay-Sachs disease or Sandhoff disease cannot efficiently break down GM2-ganglioside in the body. Therefore, these patients have high levels of this by-product in the brain cells, which causes the brain to be unable to function normally. There is a drug called Pyrimethamine. This drug is used by doctors to treat specific types of infections called malaria and toxoplasmosis. Our laboratory test tube studies have shown that Pyrimethamine can help the Hex A enzyme to function in a normal manner. If Hex A can function normally in presence of Pyrimethamine, this drug should be able restore the brain malfunction of these patients since Hex A can now efficiently break down GM2-ganglioside with Pyrimethamine treatment. Although results from laboratory test tube studies are promising and Pyrimethamine should theoretically restore brain function of these patients, we do not know if Pyrimethamine is safe or if it would actually work in patients. This study is the first study (a Phase I study) of testing Pyrimethamine to treat Adult Tay-Sachs and Sandhoff diseases. The objective of this study is to see if Pyrimethamine is safe in these patients and to see if it can restore the brain function of these patients.

Key facts

Study ID

NCT00679744

Run by

Exsar Corporation

People needed

0

Starts

2008-05-01

Last updated by the study team

2013-02-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Biochemically and genetically confirmed diagnosis of GM2 Gangliosidosis caused by β-hexosaminidase deficiency resulting from mutations in the HEX-A or HEX-B genes, which has been shown to respond to Pyrimethamine treatment in previous cell culture experiments (Maegawa et al. 2006).
• Must be 18 years of age or older to participate in the study.
• Able to understand and cooperate with the requirements of the study protocol.
• Mentally competent, have ability to understand and willingness to sign the informed consent form.
• Able to travel to the participating study site.
• Women of child-bearing potential must use accepted contraceptive methods, and must have a negative serum or urine pregnancy test within 2 days prior to treatment initiation.
• Fertile men must practice effective contraceptive methods during the study period, unless documentation of infertility exists.
• Laboratory values ≤2 weeks prior to randomization must be within acceptable range.
• Body weight >40 kg (88 pounds).

You may not qualify if…

• Serious medical illness, significant cardiac disease that would increase patients' risk for toxicity.
• Any hematologic or related abnormality, especially megaloblastic anemia, leukopenia, thrombocytopenia, pancytopenia, atrophic glossitis, hematuria, and disorders of cardiac rhythm, pulmonary eosinophilia, etc.
• Any active uncontrolled bleeding, and any patients with a bleeding diathesis (e.g., active peptic ulcer disease).
• Possible folate deficiency, such as individuals with malabsorption syndrome, alcoholism, or pregnancy, and those receiving therapy (such as phenytoin) affecting folate levels.
• Any complex disease that may confound treatment assessment.
• Pregnant women, or women of child-bearing potential not using reliable means of contraception (because Pyrimethamine is a "Pregnancy Category C" product).
• Lactating females because of the potential for serious adverse reactions in nursing infants.
• Fertile men unwilling to practice contraceptive methods during the study period.
• Unwilling or unable to follow protocol requirements.
• Known hypersensitivity reactions, intolerance or adverse reactions to Pyrimethamine or to the inactive ingredients (corn and potato starch, lactose, and magnesium stearate).
• Evidence of systemic infection, or anyone who in the opinion of the investigator would not be suitable for the study.
• Test positive for HIV.
• Test positive for hepatitis B or hepatitis C.
• Patients with a history of convulsive disorders, since these patients are very susceptible to the nervous system toxicity of Pyrimethamine.
• Patients receiving any other investigational treatment for any indication within the past 4 weeks prior to initiation of Pyrimethamine treatment.
• A history of cancer of any type, since Pyrimethamine may be carcinogenic.
• Patients who have received immunotherapy of any type within the past 4 weeks prior to initiation of Pyrimethamine treatment.
• Patients who are receiving antifolic drugs and drugs associated with myelosuppression, or patients who are receiving drugs, when used in combination with Pyrimethamine, have been reported to induce some degree of hepatotoxicity:
• Any condition or abnormality which may, in the opinion of the investigator, compromise the safety of patients.

Where it is running

• New York University, School of Medicine, Department of Neurology — New York, New York, United States
• University Hospitals of Cleveland — Cleveland, Ohio, United States
• Division of Clinical & Metabolic Genetics, Hospital for Sick Children — Toronto, Ontario, Canada

Full record on ClinicalTrials.gov

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