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Head to Head Study Against Sevelamer Hydrochloride
This study has been completed.
Study NCT00441545   Information provided by Shire Pharmaceutical Development
First Received: February 27, 2007   Last Updated: October 1, 2009   History of Changes
Study Type: Interventional
Study Design: Randomized, Open Label, Active Control, Crossover Assignment
Condition: Chronic Kidney Disease, Stage 5
Interventions: Drug: Fosrenol (Lanthanum Carbonate)
Drug: Sevelamer hydrochloride

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Following Washout 1, eligible subjects with serum phosphorus levels greater than or equal to 6.0mg/dL (greater than or equal to 1.94mmol/L) and calcium levels greater than or equal to 8.4mg/dL (greater than or equal to 2.10mmol/L) were randomized in a 1:1 ratio to receive either Fosrenol or sevelamer hydrochloride (HCl) for 4 weeks.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
The study consisted of the following phases: screening (1 week), washout 1 (2 weeks), treatment (4 weeks), Washout 2 (2 weeks), crossover treatment (4 weeks), and a 30-day follow-up

Reporting Groups
  Description
Fosrenol First Fosrenol (Lanthanum carbonate) dosing began at 2250mg/day, administered orally as one 750mg tablet taken three times per day with meals for 1 week. After receiving this dose for 1 week, subjects received the final dose of 3000mg/day, administered orally as one 1000mg tablet three times per day with meals. Subjects were to remain on the final Fosrenol dose of 3000mg/day for 3 weeks. After washout, patients then crossover to receive Sevelamer HCl for 4 weeks (see below).
Sevelamer HCl First Sevelamer HCl dosing began at 4800mg/day, administered orally as two 800mg tablets taken three times per day with meals for 1 week. After receiving this dose for 1 week, subjects received the final dose of 6400mg/day, administered orally as three 800mg tablets taken two times per day with meals and two 800mg tablets taken once per day with the lighter meal (i.e., a total of eight 800mg tablets per day). Subjects were to remain on the final sevelamer HCl dose of 6400mg/day for 3 weeks. After washout, patients then crossover to receive Fosrenol for 4 weeks (see above).

Participant Flow for 3 periods

Period:   First Intervention
  Fosrenol First Sevelamer HCl First
STARTED   95     87  
COMPLETED   77     75  
NOT COMPLETED   18     12  
      Adverse Event               6                 5  
      Protocol Violation               2                 2  
      Withdrawal by Subject               3                 3  
      Kidney transplant               1                 1  
      Lack of Efficacy               2                 0  
      Subject exceeded safety criteria               0                 1  
      Subject met an exclusionary criteria               1                 0  
      Extended hospitalization               1                 0  
      Site error               1                 0  
      Sponsor's request               1                 0  

Period:   Washout
  Fosrenol First Sevelamer HCl First
STARTED   77     75  
COMPLETED   77     75  
NOT COMPLETED   0     0  

Period:   Second Intervention
  Fosrenol First Sevelamer HCl First
STARTED   77     75  
COMPLETED   65     68  
NOT COMPLETED   12     7  
      Adverse Event               5                 2  
      Protocol Violation               4                 1  
      Withdrawal by Subject               1                 1  
      Kidney Transplant               1                 1  
      Lack of Efficacy               0                 1  
      Subject exceeded safety criteria               1                 0  
      Subject moved               0                 1  



  Baseline Characteristics
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  Outcome Measures
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1.  Primary:   Change From Baseline in Serum Phosphorus Levels at 4 Weeks   [ 4 weeks ]

2.  Secondary:   Change From Baseline in Serum Calcium Levels at 4 Weeks   [ 4 weeks ]

3.  Secondary:   Levels of Intact Parathyroid Hormone (iPTH) at Baseline and 4 Weeks   [ Baseline and 4 weeks ]

4.  Secondary:   Patients Achieving Kidney Disease Outcomes Quality Initiative (KDOQI) Target for Serum Phosphorous at 4 Weeks   [ 4 weeks ]


  Serious Adverse Events
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  Other Adverse Events
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  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Limitations and Caveats
Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
No text entered.  


Results Point of Contact:  
Name/Title: Timothy Whitaker, MD
Organization: Shire
e-mail: twhitaker@shire.com


No publications provided


Responsible Party: Shire Pharmaceutical ( Timothy Whitaker, M.D. )
Study ID Numbers: SPD405-319
Study First Received: February 27, 2007
Results First Received: June 29, 2009
Last Updated: October 1, 2009
ClinicalTrials.gov Identifier: NCT00441545     History of Changes
Health Authority: United States: Food and Drug Administration