Study to Assess the Safety and the Phosphate Binding Capacity of Renazorb
Completed · Phase 1 · Has a placebo group
Conditions studied: Safety, Phosphate Binding Capacity
In brief
The purpose of this trial is to study safety, tolerability, and phosphate binding capacity of Renazorb (SPI-014) in healthy volunteers before conducting trials in patients with renal failure. Renal excretion of phosphate is expected to decrease and fecal excretion of phosphate is expected to increase after treatment.
Key facts
- Study ID
- NCT01560884
- Run by
- Spectrum Pharmaceuticals, Inc
- People needed
- 32
- Starts
- 2012-04-01
- Expected to finish
- 2012-09-01
- Last updated by the study team
- 2013-11-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male and female volunteers ≥ 18 years of age without history of significant medical disease will be enrolled.
Where it is running
- PAREXEL International - Baltimore Early Phase Clinical Unit — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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