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Safety and Efficacy of ALV003 for the Treatment of Celiac Disease

Primary Purpose

Celiac Disease

Status
Completed
Phase
Phase 2
Locations
Finland
Study Type
Interventional
Intervention
ALV003
ALV003 placebo
Sponsored by
Alvine Pharmaceuticals Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Celiac Disease focused on measuring Celiac Disease, Coeliac Disease, Celiac Sprue, Keliakia

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • History of biopsy-proven celiac disease
  • Adherence to a gluten-free diet
  • TG2 antibody negative
  • Signed informed consent

Exclusion Criteria:

  • Active dermatitis herpetiformis
  • History of IgE-mediated reactions to gluten
  • Use of specific medications 6 months prior to entry
  • History of alcohol abuse or illicit drug use
  • Current untreated or GI disease
  • Positive pregnancy test
  • Received any experimental drug within 14 days of randomization
  • Uncontrolled chronic disease or condition
  • Uncontrolled complications of celiac disease
  • Any medical condition, which could adversely affect participation

Sites / Locations

  • FINN-MEDI Research - Clinical Trials Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

ALV003

Placebo comparator

Arm Description

ALV003 is an orally administered mixture of two recombinant proteases (cysteine endoprotease B-isoform 2 and prolyl endopeptidase) engineered to degrade gluten into non-immunogenic fragments, by targeting the glutamine and proline residues common in gluten.

Excipients for ALV003 absent the experimental compounds

Outcomes

Primary Outcome Measures

Efficacy: Intestinal mucosal morphology
Safety: Tolerability of ALV003

Secondary Outcome Measures

Efficacy: Change in intestinal intraepithelial lymphocyte numbers/phenotype
Efficacy: Change in serological markers of celiac disease

Full Information

First Posted
August 13, 2009
Last Updated
July 30, 2012
Sponsor
Alvine Pharmaceuticals Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00959114
Brief Title
Safety and Efficacy of ALV003 for the Treatment of Celiac Disease
Official Title
A Phase 2a, Double-Blind, Placebo Controlled Study of the Efficacy, Safety and Tolerability of 6-weeks Treatment With ALV003 In Patients With Well-Controlled Celiac Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
August 2010 (Actual)
Study Completion Date
October 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Alvine Pharmaceuticals Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A phase 2a study to evaluate the safety and efficacy of ALV003 to treat celiac disease.
Detailed Description
Double-blind, placebo controlled study of the efficacy, safety and tolerability of 6-weeks treatment of ALV003 in patients with well-controlled celiac disease. Approximately 110 biopsy proven celiac disease patients will be randomized to treatment with ALV003 or placebo in a 1:1 ratio. Patients will be required to have a pre-dose and a post-treatment intestinal biopsy, and also will be required to ingest a foodstuff that contains a specified amount of gluten during the active phase of the study along with the study treatment. Patients will return to the clinic weekly for the first two weeks, then every two weeks thereafter for safety visits. Patients will return to the clinic 28 days after completion of treatment for final safety and follow-up. Safety will be closely monitored throughout the study including laboratory parameters and clinical assessment of adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Celiac Disease
Keywords
Celiac Disease, Coeliac Disease, Celiac Sprue, Keliakia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
74 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ALV003
Arm Type
Experimental
Arm Description
ALV003 is an orally administered mixture of two recombinant proteases (cysteine endoprotease B-isoform 2 and prolyl endopeptidase) engineered to degrade gluten into non-immunogenic fragments, by targeting the glutamine and proline residues common in gluten.
Arm Title
Placebo comparator
Arm Type
Placebo Comparator
Arm Description
Excipients for ALV003 absent the experimental compounds
Intervention Type
Biological
Intervention Name(s)
ALV003
Intervention Description
ALV003 is an orally administered mixture of two enzymes (cysteine endoprotease B-isoform 2 and prolyl endopeptidase).
Intervention Type
Biological
Intervention Name(s)
ALV003 placebo
Intervention Description
ALV003 is an orally administered mixture of two enzymes (cysteine endoprotease B-isoform 2 and prolyl endopeptidase).
Primary Outcome Measure Information:
Title
Efficacy: Intestinal mucosal morphology
Time Frame
6 weeks
Title
Safety: Tolerability of ALV003
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Efficacy: Change in intestinal intraepithelial lymphocyte numbers/phenotype
Time Frame
6 weeks
Title
Efficacy: Change in serological markers of celiac disease
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: History of biopsy-proven celiac disease Adherence to a gluten-free diet TG2 antibody negative Signed informed consent Exclusion Criteria: Active dermatitis herpetiformis History of IgE-mediated reactions to gluten Use of specific medications 6 months prior to entry History of alcohol abuse or illicit drug use Current untreated or GI disease Positive pregnancy test Received any experimental drug within 14 days of randomization Uncontrolled chronic disease or condition Uncontrolled complications of celiac disease Any medical condition, which could adversely affect participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marja-Leena Lähdeaho, MD, PhD
Organizational Affiliation
FINN-MEDI Research
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Markku Mäki, Prof, MD, PhD
Organizational Affiliation
Tampere University
Official's Role
Study Chair
Facility Information:
Facility Name
FINN-MEDI Research - Clinical Trials Center
City
Tampere
Country
Finland

12. IPD Sharing Statement

Citations:
PubMed Identifier
24583059
Citation
Lahdeaho ML, Kaukinen K, Laurila K, Vuotikka P, Koivurova OP, Karja-Lahdensuu T, Marcantonio A, Adelman DC, Maki M. Glutenase ALV003 attenuates gluten-induced mucosal injury in patients with celiac disease. Gastroenterology. 2014 Jun;146(7):1649-58. doi: 10.1053/j.gastro.2014.02.031. Epub 2014 Feb 25.
Results Reference
derived

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Safety and Efficacy of ALV003 for the Treatment of Celiac Disease

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