Efficacy of Phosphate Binding in Healthy Volunteers: Chewed Versus Crushed Lanthanum Carbonate
Primary Purpose
Hyperphosphatemia in Chronic Kidney Disease
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Lanthanum carbonate (chewed vs. crushed)
Sponsored by
About this trial
This is an interventional treatment trial for Hyperphosphatemia in Chronic Kidney Disease
Eligibility Criteria
Inclusion Criteria:
- Men and women at least 18 years of age
- No clinically significant abnormal findings on clinical laboratory evaluation and medical history
- Within 15% of ideal body weight for height and build according to the Metropolitan Life tables5
- Women of child-bearing potential (premenopausal and not surgically sterilized) who have a negative pregnancy test
- Women who are sexually active must be using effective means of contraception
Exclusion Criteria:
- History of dysphagia or swallowing disorders
- Clinically significant illness within 3 months of study enrollment
- Concomitant use of medication that might interact with lanthanum carbonate
- Pregnant or intends to become pregnant within 30 days of completing the study
- Breast feeding
- Alcohol or controlled substance abuse
- Use of an investigational agent within 30 days of study entry
Sites / Locations
- University of Illinois at Chicago, Dept of Pharmacy Practice
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
Active Comparator
Active Comparator
Arm Label
1
2
3
Arm Description
P-containing meal alone
P-containing meal AND single 1 g oral dose of chewed lanthanum carbonate
P-containing meal and single 1 g oral dose of lanthanum carbonate crushed into a fine powder
Outcomes
Primary Outcome Measures
Serum phosphorous concentration
Secondary Outcome Measures
Full Information
NCT ID
NCT00458289
First Posted
April 6, 2007
Last Updated
December 18, 2019
Sponsor
University of Illinois at Chicago
Collaborators
Shire
1. Study Identification
Unique Protocol Identification Number
NCT00458289
Brief Title
Efficacy of Phosphate Binding in Healthy Volunteers: Chewed Versus Crushed Lanthanum Carbonate
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
August 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Illinois at Chicago
Collaborators
Shire
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with end-stage renal disease (ESRD) commonly have high concentrations of phosphorous, a mineral, in the blood (hyperphosphatemia). This is a result of their inability to excrete phosphorous by the kidneys. This in turn may result in the development of a condition known as secondary hyperparathyroidism and renal osteodystrophy or bone disease. As such, these patients often receive medications known as phosphate binders such as calcium carbonate or acetate, sevelamer, aluminum hydroxide and lanthanum carbonate to manage and treat hyperphosphatemia.
Lanthanum carbonate is a newly available phosphate binding agent that is effective in the management of hyperphosphatemia and preventing secondary hyperparathyroidism. It works in the gastrointestinal tract by binding to the phosphorus in the diet. ESRD patients taking lanthanum carbonate are counseled to chew the tablets completely before swallowing, with or immediately after meals. However, patients who are intubated or receiving nutrition via feeding tubes are unable to chew the tablets. For these patients, medications are commonly crushed and administered via the tube. Moreover, some patients prefer to crush the tablets and mix it with food instead of chewing. To date, it is not known if crushing the lanthanum carbonate tablets prior to administration and taking it with food would be as effective as chewing them.
The purpose of this study is to compare the efficacy of phosphate binding between chewed and crushed lanthanum carbonate tablets.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperphosphatemia in Chronic Kidney Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
No Intervention
Arm Description
P-containing meal alone
Arm Title
2
Arm Type
Active Comparator
Arm Description
P-containing meal AND single 1 g oral dose of chewed lanthanum carbonate
Arm Title
3
Arm Type
Active Comparator
Arm Description
P-containing meal and single 1 g oral dose of lanthanum carbonate crushed into a fine powder
Intervention Type
Drug
Intervention Name(s)
Lanthanum carbonate (chewed vs. crushed)
Intervention Description
single 1 g oral dose of lanthanum carbonate either chewed or crushed into a fine powder
Primary Outcome Measure Information:
Title
Serum phosphorous concentration
Time Frame
Hourly from time=0-8 h after administration of meal and drug
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Men and women at least 18 years of age
No clinically significant abnormal findings on clinical laboratory evaluation and medical history
Within 15% of ideal body weight for height and build according to the Metropolitan Life tables5
Women of child-bearing potential (premenopausal and not surgically sterilized) who have a negative pregnancy test
Women who are sexually active must be using effective means of contraception
Exclusion Criteria:
History of dysphagia or swallowing disorders
Clinically significant illness within 3 months of study enrollment
Concomitant use of medication that might interact with lanthanum carbonate
Pregnant or intends to become pregnant within 30 days of completing the study
Breast feeding
Alcohol or controlled substance abuse
Use of an investigational agent within 30 days of study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan H Lau, Pharm.D.
Organizational Affiliation
University of Illinois at Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Illinois at Chicago, Dept of Pharmacy Practice
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Efficacy of Phosphate Binding in Healthy Volunteers: Chewed Versus Crushed Lanthanum Carbonate
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