Oral Collagen for Rheumatoid Arthritis

Rheumatoid Arthritis Clinical Trial

Official title:

Open Label Multicenter Induction of CII Tolerance in Patients With Rheumatoid Arthritis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00000401
• Other study ID #: R01AR045255
• Secondary ID: R01AR045255NIAMS
• Status: Completed
• Phase: Phase 2
• First received: November 3, 1999
• Last updated: May 28, 2013
• Start date: July 1999
• Est. completion date: August 2005

Study information

• Verified date: May 2013
• Source: University of Tennessee
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Rheumatoid arthritis (RA) is an autoimmune disease characterized by swelling and inflammation of the joints. In RA, the immune system attacks a person's own cells inside joints, eventually leading to joint damage and disability. This study will determine if oral bovine type II collagen (bovine CII) will lead to decreased joint inflammation in RA patients.

Description:

RA is an inflammatory disease that causes pain, swelling, stiffness, and loss of function in the joints. The study will evaluate the effects of using oral bovine CII on RA patients by assessing the levels of inflammation markers such as interferon gamma (IFN-gamma), interleukin-10 (IL-10), and transforming growth factor beta (TGF-beta). This study is a multicenter clinical trial to be conducted at the University of Tennessee, Memphis (the lead center) and the West Tennessee Medical Specialty Clinic (a collaborating site).

Patients enrolled will be allowed to continue a constant dose of disease-modifying anti-rheumatic drugs (DMARDs) and prednisone less than or equal to 7.5 mg/day. Patients will be randomly assigned to one of two groups. The low dose group will receive 30 mcg daily for 10 weeks, then 50 mcg daily for 10 weeks, followed by 70 mcg daily for 10 more weeks; the high dose group will receive 90 mcg daily for 10 weeks, then 100 mcg daily for 10 weeks, followed by 130 mcg daily for 10 more weeks. Blood will be collected at screening and at Weeks 10, 20, and 30. Blood will be analyzed for indicators of inflammation.

Note: this trial is no longer being conducted as an intervention trial. Accrual has been discontinued, although patients previously enrolled are still being followed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 110
• Est. completion date: August 2005
• Est. primary completion date: August 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Note: accrual into this trial has been discontinued, but patients previously enrolled are still being followed.

Inclusion Criteria:

• Clinically stable RA and unlikely to require adjustment of doses of DMARDs, NSAIDs, prednisone, or anti-TNFa therapies for the treatment phase of the study

• Meets American College of Rheumatology (ACR) 1988 revised criteria for RA

• Onset of disease at age 16 or older

• Onset of disease at least 3 months prior to enrollment

• PBMC - IFN? - a1(II)/PBS stimulation index greater than or equal to 1.5 in 6 months prior to baseline visit

• Agree to discontinue herbal remedies described in this protocol

• Agree to use acceptable forms of contraception

Exclusion Criteria:

• Participation in another clinical research study involving the evaluation of another investigational drug within 90 days prior to study entry

• Currently taking greater than 7.5 mg prednisone daily

• Intra-articular corticosteroid injections within 30 days prior to study entry

• Concurrent serious medical condition which, in the opinion of the investigator, makes the patient inappropriate for the study

• Pregnancy

• Beef allergy

• Use of fish oil within 4 weeks of study entry

• Previous use of auranofin or cyclophosphamide (all other DMARDs are allowed)

• Previous autologous or heterologous stem cell transplantation

• Active malignancy or past treatment consisting of antineoplastic drugs or total lymphoid irradiation

• Intolerance to citrus juices or colorless carbonated beverages

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Arthritis
• Arthritis, Rheumatoid
• Rheumatoid Arthritis

Intervention

Drug:
• Oral bovine type II collagen
Drug can be interrupted or stopped for suspected adverse events.

Locations

Country	Name	City	State
United States	The Arthritis Clinic of Jackson, PLLC	Jackson	Tennessee
United States	University of Tennessee, Memphis	Memphis	Tennessee

Sponsors (2)

Lead Sponsor	Collaborator
University of Tennessee	National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Country where clinical trial is conducted

United States, 

References & Publications (2)

Carbone LD, McKown K, Pugazhenthi M, Barrow KD, Warrington K, Somes G, Postlethwaite AE. Dosage effects of orally administered bovine type I collagen on immune function in patients with systemic sclerosis. Arthritis Rheum. 2004 Aug;50(8):2713-5. — View Citation

Postlethwaite AE. Can we induce tolerance in rheumatoid arthritis? Curr Rheumatol Rep. 2001 Feb;3(1):64-9. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Repeated measures analysis of variance with contrasts to determine if the change in the PBMC-IFN gamma-alpha 1(II)/PBS stimulation index is significantly at the 0.05 level and/or greater than or equal to 30%.		Before and after each 10-week treatment	No
Secondary	A Pearson correlation coefficient will be calculated for the change in the PBMC-INF gamma-alpha1(II)/PBS stimulation index and the change in the reactivity to RA CII epitope alpha 1 (II) CB11 for each dose.		Before and after each 10-week treatment	No