To determine the efficacy of 10 20 and 30 mg dose of Sandostatin-LAR compared to subcutaneous Sandostatin in providing continuous symptomatic control of malignant carcinoid syndrome when given at intervals of four weeks. To test the safety and tolerability of sequential doses of Sandostatin-LAR in carcinoid patients. To investigate the pharmacokinetic/pharmacodynamic profile of Sandostatin-Lar. To assess the dose proportionally of serum octreotide concentrations of Sandostatin-LAR at doses of 10,20, 30 mg when given at intervals of four weeks.

Project Start
1997-01-27
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
37
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
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