Trial of Novel Oral Zinc Cysteine Preparation in Alzheimer's Disease

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2011 by Adeona Pharmaceuticals.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Adeona Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT01099332
First received: March 30, 2010
Last updated: January 27, 2011
Last verified: January 2011

March 30, 2010
January 27, 2011
November 2009
January 2011   (final data collection date for primary outcome measure)
Biometal levels will be measured in serum by atomic absorption spectrometry [ Time Frame: 6 to 12 months ] [ Designated as safety issue: No ]
Active comparator material orally administered will be associated with better tolerability than oral zinc acetate, and will produce a reduction in serum non-ceruloplasmin bound copper levels and an elevation in serum zinc levels
Biometal levels will be measured in serum by atomic absorption spectrometry [ Time Frame: 6 to 12 months ] [ Designated as safety issue: No ]
Active material oral administration associated with better tolerability than oral inorganic zinc acetate, and produces a reduction in serum non-ceruloplasmin bound copper levels and elevate serum zinc levels
Complete list of historical versions of study NCT01099332 on ClinicalTrials.gov Archive Site
  • Serum zinc levels after oral administration of two different zinc-containing compounds and placebo will be determined by atomic absorption spectrometry [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    The change in serum zinc levels over time after oral administration of the active comparator of the study as well as the placebo and for certain subjects an inorganic zinc salt will be compared
  • Comparison of mental status functions at baseline, 3 and 6 months in active comparator versus placebo groups. [ Time Frame: 6 to 12 months ] [ Designated as safety issue: No ]
    All subjects will perform standard and standardized tests of mental function, ranging from a general dementia rating scale (Mini Mental Status Exam) to more Alzheimer's specific tests (ADAS-cognitive). Daily living and caregiver assessments of overall daily functioning will be noted. Test results will be compared statistically in a two-point fashion, and correlated with biometal ststus.
Serum zinc levels after oral administration of two different zinc-containing compounds and placebo will be determined by atomic absorption spectrometry [ Time Frame: 3 months ] [ Designated as safety issue: No ]
The change in serum zinc levels over time after oral administration of the active component of the Study as well as the placebo and for certain Subjects an inorganic zinc salt will be compared
Not Provided
Not Provided
 
Trial of Novel Oral Zinc Cysteine Preparation in Alzheimer's Disease
CopperProof-2: Prospective, Randomized, Double-Blind Placebo-Controlled Clinical Trial Comparing the Effects of a Novel Once-Daily Oral Zinc Cysteine Preparation on Zinc and Copper Parameters in Mild Cognitive Impairment and Alzheimer's Disease

This trial aims to test the hypothesis that 1) a single dose of zinc cysteine in a proprietary gastro-retentive form will produce sustained blood levels of zinc giving a larger bioavailable amount of zinc than an FDA approved preparation of inorganic zinc acetate; and 2) that the zinc cysteine gastro-retentive, sustained-release preparation will be better tolerated with significantly less gastrointestinal side effects than the zinc acetate capsules. The trial also tests the hypothesis that, after 6 months of once daily administration, the zinc cysteine subjects will show reduced serum non-ceruloplasmin copper. Additionally, subjects will perform tests of mental function,including the dementia rating scale, the Mini Mental Status Examination and the ADAS-cognitive performance test aimed at Alzheimer's status assessment. Tests will be administered at baseline, 3 and 6 months, and the performance results compared. Care-giver assessments will also be noted.

This multi-center study aims to determine the pharmacokinetics and pharmacodynamics of a novel gastro-retentive, sustained-release zinc cysteine preparation on the blood and urine measures of copper and zinc balance in Alzheimer's disease and mild cognitive impairment. Data expected to be derived include tolerability of the novel preparation in comparison with oral inorganic zinc salt, and long-term effects on primarily blood-measured copper-zinc balance. The study design is that of a prospective, randomized, double blind placebo-controlled clinical trial, with a duration for individual subjects of 6 months. The study will be performed at a total of 3 sites, under the direction of a single principal investigator, with a sub-investigator. The statistical plan calls for a comparison of data from the two long-term parallel groups using ANOVA and other applicable techniques. In addition to blood parameters, mental function assessments obtained at baseline, 3 and 6 months will be evaluated statistically.

Interventional
Phase 1
Phase 2
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
  • Alzheimer's Disease
  • Mild Cognitive Impairment
  • Other: Gastro-retentive zinc cysteine tablet
    Oral, one tablet, once daily with water for 6 months.
    Other Name: Zinthionein ZC
  • Other: Tablet identical physically to active comparator containing some lactose
    Oral, once daily, with water, 6 months.
    Other Name: Placebo Tablet
  • Active Comparator: Gastro-retentive zinc cysteine tablet
    Once daily administration by mouth of a gastro-retentive, sustained-release preparation of zinc cysteine with excipients, all G.R.A.S., with adequate water.
    Intervention: Other: Gastro-retentive zinc cysteine tablet
  • Placebo Comparator: Identical appearance of placebo with active comparator
    Once daily administration of placebo of identical physical appearance to that of active comparator with similar amount of water.
    Intervention: Other: Tablet identical physically to active comparator containing some lactose
Arnal N, Cristalli DO, de Alaniz MJ, Marra CA. Clinical utility of copper, ceruloplasmin, and metallothionein plasma determinations in human neurodegenerative patients and their first-degree relatives. Brain Res. 2010 Mar 10;1319:118-30. doi: 10.1016/j.brainres.2009.11.085. Epub 2009 Dec 22.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
60
January 2011
January 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Alzheimer's disease mild to moderate as diagnosed by standard clinical, functional and NINDA-ADRDA criteria
  • Mild cognitive impairment diagnosed by standard clinical, functional and NINDA-ADRDA criteria
  • All subjects able to swallow Tablets
  • Subjects taking copper or zinc containing supplements must have a 30-day wash out before starting study materials
  • Screening laboratory values either within normal limits or deemed not clinically significant by investigator

Exclusion Criteria:

  • Subjects or their study companions/care givers unable to give adequate informed consent
  • Presence of a disease or condition known to affect biometal homeostasis
  • Presence of psychosis, substance abuse or other major medical or neurological issues
  • Presence of vascular dementia
  • Clinically significant anemia at the time of the screening visit
  • Current use of a decoppering drug such as trientine or penicillamine
Both
55 Years to 90 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01099332
CopperProof-2
Yes
Diana Pollock, M.D., P.I., Neurology Research Unit of Clearwater FL
Adeona Pharmaceuticals
Not Provided
Study Director: David Newsome, M.D. Senior Vice President of Research and Development, Adeona Pharmaceuticals, Inc.
Adeona Pharmaceuticals
January 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP