Dose Escalation Study of Cu(II)ATSM in Parkinson's Disease

• Status: Completed
• Trial end date: 2020-02-29
• Target enrollment: 0
• Participant gender: All

Summary

Multicenter, open-label dose-escalation study

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Collaborative Medicinal Development Pty Limited
• Treatments: Copper

Criteria

Inclusion Criteria:

• Signed informed consent prior to initiation of any study-specific procedures

• Early idiopathic Parkinson's disease (PD) with at least two of the cardinal signs of PD (resting tremor, bradykinesia, rigidity, postural instability). If tremor is not present, must have unilateral onset and persistent asymmetry of symptoms.

• Hoehn & Yahr stage ≤ 2

• First PD motor symptoms occurred ≤ 5 years prior to screening visit

• Use of dopaminergic therapy allowed provided dose is stable for at least 8 weeks prior to screening visit

• Use of amantadine and/or anticholinergics allowed provided dose is stable for at least 8 weeks prior to screening visit

• Use of CNS-acting medications allowed provided dose is stable for at least 4 weeks prior to screening visit

• Age ≥ 30 years at time of PD diagnosis

• Adequate bone marrow reserve, liver and renal function:

Absolute neutrophil count ≥ 1500/µL; Platelet count ≥ 150,000/µL; Hemoglobin ≥ 11 g/dL; Creatinine clearance ≥ 6- mL/min (Cockroft & Gault formula); ALT and/or AST ≤ 2 x ULN; total bilirubin ≤ 1.5 x ULN; albumin ≥ 2.8 g/dL

• Women and men with partners of childbearing potential must take effective contraception while on study and women of childbearing potential must have a negative pregnancy test and be non-lactating at screening

Exclusion Criteria:

• Atypical Parkinsonism

• Taking ≥ 3 dopaminergic medications

• Exposure to typical or atypical antipsychotics or other dopamine blocking agents within 6 months prior to screening visit

• Exposure to any other investigational agent within 6 months or 2 investigational agents within 12 months prior to screening visit

• Known immune compromising illness or treatment

• History of brain surgery for PD, including deep brain stimulation and stem cell transplants

• History of cognitive or neuropsychiatric conditions

• Inability to swallow oral medications or presence of a GI disorder (eg, malabsorption) deemed to jeopardize intestinal absorption of study drug

• Active GI disease (excluding GERD) within 30 days prior to screening visit

• Presence of any of the following clinical conditions:

any significant non-PD CNS disorder; drug abuse or alcoholism; unstable cardiac, pulmonary, renal, hepatic, endocrine or hematologic disease; active infectious disease; AIDS or AIDS-related complex; malignancy within 3 years of screening (other than fully excised non-melanoma skin cancer, cured in situ cervical carcinoma, early stage bladder cancer, or DCIS of breast); psychosis or untreated major depression within 30 days of screening; dementia

• Current use of strong inducers or inhibitors of CYPs 2C19 and 2D6