Safety Study of Larazotide Acetate to Treat Celiac Disease.

Celiac Disease Clinical Trial

Official title:

A Phase Ib, Randomized, Double-Blind, Placebo Controlled Study to Determine the Safety, Tolerance, Pharmacokinetic and Pharmacodynamic Effects of Single Doses of Larazotide Acetate (AT-1001) in Celiac Disease Subjects.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00386165
• Other study ID #: CLIN1001-002
• Status: Completed
• Phase: Phase 1
• First received: October 9, 2006
• Last updated: September 8, 2017
• Start date: November 29, 2005
• Est. completion date: January 26, 2006

Study information

• Verified date: September 2017
• Source: Innovate Biopharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To demonstrate the safety, pharmacokinetics and efficacy of larazotide acetate in patients with controlled celiac disease on a gluten-free diet following a gluten challenge.

Description:

CLIN1001-002 was a Phase 1b, randomized, double-blind, placebo controlled study to determine the safety, tolerance, pharmacokinetic and pharmacodynamic effects of single doses of larazotide acetate in subjects with celiac disease subjects. Study subjects were randomized (2:1) to receive single oral doses of larazotide acetate 12 mg or matching placebo once daily for 3 days. Subjects received a single-blinded gluten challenge (5 mg amygluten) on Day 2. Intestinal permeability was measured each day following dosing. Intestinal permeability was measured by administration of an oral sucrose, lactulose and mannitol solution followed by a 6-hour urine collection. Serial blood samples were collected for pharmacokinetic determinations at baseline and 2 and 3 hours post dose; for zonulin determinations at baseline (prior to first dose) and 3 hours post dose; and for cytokine determination at baseline and 3 hours post dose (Days 2 and 3 only) and on Day 7. Sucrose, lactulose, mannitol, zonulin and larazotide acetate concentrations were determined by validated analytical methods.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 21
• Est. completion date: January 26, 2006
• Est. primary completion date: January 26, 2006
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 59 Years

Eligibility

Inclusion Criteria:

• Subject must have been diagnosed with celiac disease by biopsy for = 6 months (attending physician confirmation will be accepted in lieu of a biopsy report).

• Subject must be on a gluten-free diet for at least the past 6 months.

Exclusion Criteria:

• Subject has Anti-Tissue Transglutaminase (tTG) > 10 EU as measured by serology

• Subject intermittently consumes clinically significant quantities of non-steroidal anti-inflammatory agents ("NSAIDs") and proton-pump inhibitors, within the last 3 days prior to the treatment visit.

Related Conditions & MeSH terms

• Celiac Disease

Intervention

Drug:
• larazotide acetate
larazotide acetate 4 mg capsules

Locations

Country	Name	City	State
United States	Parexel	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
Innovate Biopharmaceuticals

Country where clinical trial is conducted

United States, 

References & Publications (1)

Paterson BM, Lammers KM, Arrieta MC, Fasano A, Meddings JB. The safety, tolerance, pharmacokinetic and pharmacodynamic effects of single doses of AT-1001 in coeliac disease subjects: a proof of concept study. Aliment Pharmacol Ther. 2007 Sep 1;26(5):757-6 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Demonstrate the safety and tolerance of single doses of larazotide acetate in patients with controlled celiac disease on a gluten-free diet.	Safety assessments included scheduled monitoring of adverse events (AEs), vital sign measurements, 12-lead ECG measurements, physical examinations, and clinical laboratory testing (chemistry, hematology, and urinalysis).	AEs were monitored throughout the study. Clinical laboratory testing was performed at scheduled times throughout the study. ECGs were measured at baseline, 3 hours post-dose on all study days and at the follow-up visit.
Primary	Determine whether quantifiable concentrations of larazotide acetate are present in plasma following single oral doses and to characterize the pharmacokinetic behavior of larazotide acetate in celiac disease subjects that are gluten-free and in remission	Pharmacokinetic samples were taken to determine whether quantifiable concentrations of larazotide acetate were present in plasma following single oral doses and to characterize the pharmacokinetic behavior of larazotide acetate in celiac disease subjects.	erial blood samples were collected for pharmacokinetic determinations at baseline and 2 and 3 hours post dose.
Primary	Evaluate the effects of single doses of larazotide acetate on intestinal permeability ratios and zonulin levels	Intestinal permeability was measured by administration of an oral sucrose, lactulose and mannitol solution followed by urine and serum collection to measure urinary lactulose and mannitol, and serum zonulin concentrations as biomarkers.	Intestinal permeability was measured each day following dosing. A gluten challenge was administered on Day 2.
Secondary	Self-reported measures of GI discomfort	GI discomfort was reported by marking an "X" on a 10 cm linear line. Other GI Symptoms were assessed by subjects answering three questions related to bowel function.	Once daily on dosing days
Secondary	Patient Global Assessment of Disease Status	Subjects chose one of seven ordinal levels in response to a question related to any change in their disease status since being admitted to the clinic	At discharge from the clinic