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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05749068
Other study ID # EB-03
Secondary ID 1R21CA260665-01A
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2022
Est. completion date October 30, 2022

Study information

Verified date February 2024
Source Envivo Bio Inc
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of the CapScan intestinal collection device in characterizing the metabolism of sulfasalazine in the digestive tracts of healthy volunteers.


Description:

The objective is to evaluate the effectiveness of the CapScan intestinal collection device in characterizing the regional distribution of sulfasalazine, the metabolic breakdown products of sulfasalazine, and the gut microbiota in the digestive tracts of healthy volunteers.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date October 30, 2022
Est. primary completion date October 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Males or females 18 years of age or older and 70 years of age or younger at the time of the first Screening Visit. Physical Status Classification System 1 or 2. For women of childbearing potential, negative urine pregnancy test within 7 days of Screening Visit and agreement to remain abstinent (refrain from heterosexual intercourse) or use adequate contraception during the treatment period and for 14 days after the final dose of sulfasalazine. Subject is fluent in English and understands the study protocol and informed consent and is willing and able to comply with study requirements and sign the informed consent form Exclusion Criteria: - • Known or suspected gastrointestinal obstructions, strictures or fistula - Known or suspected moderate to severe dysmotility, by the judgement of the principal investigator - Gastroparesis - A swallowing disorder - Known intolerance, reaction or hypersensitivity to sulfasalazine, its metabolites, sulfonamides, or salicylates - Urinary obstruction - Porphyria - Glucose-6-phosphate dehydrogenase deficiency - Known or suspected infection with severe acute respiratory syndrome, HIV, hepatitis B virus or hepatitis C virus - Pregnancy or planned pregnancy within 30 days from Screening Visit, or breast-feeding. - Use of concomitant medications, such as aspirin, antibiotics, laxatives and proton pump inhibitors that may interfere with the study in the judgement of the investigator. - Any form of active substance abuse or dependence (including drug or alcohol abuse), unstable medical or psychiatric disorder, or any chronic condition susceptible, in the opinion of the principal investigator, to interfere with the conduct of the study. - A clinical condition that, in the judgment of the principal investigator, could potentially pose a health risk to the subject while involved in the study

Study Design


Related Conditions & MeSH terms


Intervention

Device:
CapScan intestinal sampling device
CapScan is an intestinal collection device used to characterize the regional distribution of sulfasalazine, the metabolic breakdown products of sulfasalazine, and the gut microbiota in the digestive tracts of healthy volunteers.

Locations

Country Name City State
United States Silicon Valley Gastroenterology Mountain View California

Sponsors (2)

Lead Sponsor Collaborator
Envivo Bio Inc National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Regional Collection of Metabolites and Gut Microbiota Regional measurement of sulfasalazine in the intestinal lumen, the metabolic breakdown products of sulfasalazine and the gut microbiota in the digestive tracts of healthy volunteers. 2 days
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