A Dose Ranging Study of Delayed Release Beclomethasone for Prevention of Acute Enteritis in Patie… (NCT01073384) | Clinical Trial Compass
CompletedPhase 1/2
A Dose Ranging Study of Delayed Release Beclomethasone for Prevention of Acute Enteritis in Patients With Rectal Cancer
United States16 participantsStarted 2009-12
Plain-language summary
The purpose of this study is to evaluate the safety and preliminary efficacy of four doses of SGX201 in subjects with rectal cancer treated with concurrent radiation and chemotherapy.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Primary rectal cancer
* Planned course of conventional neoadjuvant radiation therapy before surgery
* Scheduled to receive chemotherapy
* \>/= 18 years of age
* Negative pregnancy test
Exclusion Criteria:
* History of acute or chronic regional enteritis or inflammatory bowel disease
* Stool incontinence
* Uncontrollable diarrhea
* Abdominal-perineal resection or other surgery leaving patient without a functioning rectum
* Patients using colostomy or ileostomy
* Liver function tests \> 3x upper limit of normal, or bilirubin test result \> 1.5 the upper limit of normal
* Calculated creatinine clearance \<60 mL/minute
* Planned hyperfractionated or split course radiation
* Planned brachytherapy prior to completion of all external beam radiation therapy
* Prior pelvic RT
* An on-going infection
* ECOG score \>/= 3
* Leukopenia \<2,000 WBC/mm3 or Hg \<10.5 g/dL
* Participation in an investigational drug trial within the previous 30 days
* Patients with a medical condition that would interfere with study compliance
* Known hypersensitivity to 5-FU or capecitabine
* Anticipated inability to tolerate oral administration of SGX201
* Pregnant or breastfeeding
What they're measuring
1
Preliminary Efficacy
Timeframe: One day prior to and 7 days after radiation therapy