The Efficacy of CASAD in Patients With Diarrhea Related to Medullary Thyroid Cancer
Primary Purpose
Diarrhea, Medullary Thyroid Cancer
Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
CASAD
Sponsored by
About this trial
This is an interventional treatment trial for Diarrhea focused on measuring Diarrhea, Medullary thyroid cancer
Eligibility Criteria
Inclusion Criteria:
- Patients with medullary thyroid cancer
- Men and women from all ethnic and racial groups
- Diarrhea ( >=3 loose bowel movements per day)
- Duration of diarrhea of at least 1 week
Exclusion Criteria:
- Patients with MEN 2b (since these patients may have megacolon)
- Patients taking any clay products
- History of significant neurological or psychiatric disorders that would impede giving consent, treatment, or follow up.
- Patients who cannot comply with medications
- Patients whose current medication schedule would not permit an approximate 2 hour window between administration of CASAD and other scheduled medications.
- Pregnancy or lactation
- Patients receiving systemic chemotherapy (includes tyrosine kinase inhibitors)
Sites / Locations
- MD Anderson Cancer CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Active Drug
Arm Description
After a 1 week run-in period CASAD will be administered TID for 1 week. Each dose will be 2 500mg CASAD capsules. Patients will be followed for two weeks post active drug administration.
Outcomes
Primary Outcome Measures
Efficacy in treatment of diarrhea
To evaluate the efficacy of CASAD 3 grams per day in reducing the severity of diarrhea after 1 week of treatment in patients with MTC.
Secondary Outcome Measures
Functional impact of CASAD
To explore the functional impact of CASAD and the relative impact of diarrhea in relation to other symptom issues using MDASI-THY (M.D. Anderson Symptom Inventory-Thyroid, appendix D)
Effect on thyroid function tests
To explore the effect of CASAD on thyroid function tests, thyroid hormone and calcium absorption
Changes in MDASI-THY scores
To examine changes in MDASI-THY scores after treatment with CASAD
Full Information
NCT ID
NCT01739634
First Posted
November 29, 2012
Last Updated
November 29, 2012
Sponsor
Salient Pharmaceuticals Incorporated
1. Study Identification
Unique Protocol Identification Number
NCT01739634
Brief Title
The Efficacy of CASAD in Patients With Diarrhea Related to Medullary Thyroid Cancer
Official Title
The Efficacy of CASAD in Patients With Diarrhea Related to Medullary Thyroid Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
November 2012
Overall Recruitment Status
Unknown status
Study Start Date
November 2012 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Salient Pharmaceuticals Incorporated
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Diarrhea in patients with MTC (Medullary Thyroid Cancer) can be debilitating and, in some cases life threatening. Findings in such patients include volume depletion, renal insufficiency, and electrolyte disorders. Diarrhea can also lead to increased cost of care, reduced quality of life, and treatment delays. Not all patients benefit from conventional anti-diarrheal therapy. CASAD is proven to reduce diarrhea in humans and animals. Clays have water-binding effects, increase the absorptive capacity of the intestinal mucosa, and absorb the excess cytokines which are possible mechanisms of diarrhea in MTC. In this study, we will investigate if starting 1 g CASAD three times a day will ameliorate the severity of diarrhea in patients with MTC. Diarrhea in patients with MTC can be debilitating and, in some cases life threatening. Findings in such patients include volume depletion, renal insufficiency, and electrolyte disorders. We hypothesize that adding CASAD 3 grams/day will reduce the incidence and ameliorate the severity of diarrhea in patients with MTC.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea, Medullary Thyroid Cancer
Keywords
Diarrhea, Medullary thyroid cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Active Drug
Arm Type
Experimental
Arm Description
After a 1 week run-in period CASAD will be administered TID for 1 week. Each dose will be 2 500mg CASAD capsules. Patients will be followed for two weeks post active drug administration.
Intervention Type
Drug
Intervention Name(s)
CASAD
Other Intervention Name(s)
Calcium Aluminosilicate Anti-Diarrheal.
Intervention Description
CASAD is provided in 500mg capsules.
Primary Outcome Measure Information:
Title
Efficacy in treatment of diarrhea
Description
To evaluate the efficacy of CASAD 3 grams per day in reducing the severity of diarrhea after 1 week of treatment in patients with MTC.
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Functional impact of CASAD
Description
To explore the functional impact of CASAD and the relative impact of diarrhea in relation to other symptom issues using MDASI-THY (M.D. Anderson Symptom Inventory-Thyroid, appendix D)
Time Frame
1 week
Title
Effect on thyroid function tests
Description
To explore the effect of CASAD on thyroid function tests, thyroid hormone and calcium absorption
Time Frame
1 week
Title
Changes in MDASI-THY scores
Description
To examine changes in MDASI-THY scores after treatment with CASAD
Time Frame
1 week
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with medullary thyroid cancer
Men and women from all ethnic and racial groups
Diarrhea ( >=3 loose bowel movements per day)
Duration of diarrhea of at least 1 week
Exclusion Criteria:
Patients with MEN 2b (since these patients may have megacolon)
Patients taking any clay products
History of significant neurological or psychiatric disorders that would impede giving consent, treatment, or follow up.
Patients who cannot comply with medications
Patients whose current medication schedule would not permit an approximate 2 hour window between administration of CASAD and other scheduled medications.
Pregnancy or lactation
Patients receiving systemic chemotherapy (includes tyrosine kinase inhibitors)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maria E Cabanillas, MD
Email
mcabani@mdanderson.org
Facility Information:
Facility Name
MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria E Cabanillas, MD
First Name & Middle Initial & Last Name & Degree
Ramona Dadu, MD
12. IPD Sharing Statement
Learn more about this trial
The Efficacy of CASAD in Patients With Diarrhea Related to Medullary Thyroid Cancer
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