Beta Cell Rescue in New Onset Type 1 Diabetes With Efalizumab (BRiTE)

Emory University

Status and phase

Withdrawn

Phase 2

Conditions

Diabetes Mellitus, Type 1

Treatments

Drug: placebo

Drug: efalizumab

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00737763

IRB0007365

BRiTE Trial for T1DM (Other Identifier)

Details and patient eligibility

About

In this single-center therapeutic study, we will study the ability of efalizumab to protect remaining beta cells in teenagers and young adults who have been newly diagnosed with type 1 diabetes mellitus. Efalizumab is a monoclonal antibody which prevents the activation of antigen specific T lymphocytes to sites of inflammation. Efalizumab was approved by the FDA in 2003 for the treatment of psoriasis. It has been proven to be safe, well tolerated and effective in targeting T cell mediated disorders like those seen in autoimmunity.

Full description

Since there is data that shows that early intervention can prevent further destruction of insulin producing beta cells, the patients who will be enrolled in this study will have been diagnosed with Type 1 diabetes within 6 weeks of enrolling and starting therapy. Patients who meet the screening criteria will be randomized at a 2 to 1 ratio to either get weekly subcutaneous injections of efalizumab for 26 weeks versus a placebo injection. The researchers and patients will be blinded to the treatment group assignment. All patients will be followed for two years.

The primary endpoint for this study will be the difference from baseline in the body's ability to respond to a Mixed Meal Tolerance Test at 12 months after enrollment. The Mixed Meal Tolerance test will help test the production of insulin by the pancreas. By comparing the results of these tests between the treated group and the placebo group, we hope to be able to show preservation of beta cell function in the group treated with efalizumab.

Sex

All

Ages

12 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Males or females 12-35 years old, no preference nor discrimination will be made based on ethnicity.
Recent diagnosis of Type 1Diabetes Mellitus, participant can be enrolled in the trial within 6 weeks of diagnosis.
Positive for at least one diabetes autoantibody. Insulin autoantibody positivity will only be used as a selection criterion if insulin has not been used in at least the preceding 10 days.
Willingness to provide written informed consent (either the subject or the subject's legally authorized representative)
Have routine diabetic care under an endocrinologist and ability to follow study protocol for the duration of the 2-year study.
Although no preference or discrimination will be made based on ethnicity or gender, participants (and family and/or guardians when applicable) must demonstrate comprehension of the trial, including its obligations and potential risks.
If a female of childbearing potential, a negative pregnancy test and commitment to the use of two forms of effective contraception or abstinence for the duration of the study are necessary.
If a non-sterile male, commitment to the use of two forms of effective contraception (birth control) for the duration of the study is necessary.

Exclusion criteria

Severe allergic allergy or anaphylaxis to human monoclonal antibodies
Hospital admission for cardiac disease, stroke, or pulmonary disease within the past year
History of substance abuse within last 5 years
History of ongoing uncontrolled bacterial, viral, or fungal or atypical mycobacterium infections
History of opportunistic infections
Diagnosis with hepatic cirrhosis regardless of cause or severity
Diagnosis, history, or laboratory evidence of Hepatitis B or C infection
Hepatic enzymes 2 > times the upper limit of normal
History of active or treatment for tuberculosis or skin test positive
History of malignancy over the past 5 years
Recent initiation or change in treatment regimen of beta-blockers, angiotensin-converting enzyme inhibitors, interferons, quinidine anti-malarial drugs, or lithium in the past month
Seropositivity for human immunodeficiency virus (HIV)
Serologic or clinical evidence of recent or acute infection with Epstein-Barr Virus or Cytomegalovirus
Females who are pregnant, lactating, or planning on pregnancy during the 2 year study period
Progressive hearing loss
History of organ or bone marrow transplantation, sickle cell disease, cystic fibrosis, autoimmune anemia, seizures, autoimmune thrombocytopenia, leuko/lymphopenia, vasculitis, other autoimmune disease.
Current use of immunosuppressive medications
Plan or requirement of receiving new immunization of any type within the first 12 months of the study, or booster or completion vaccines with live or live-attenuated vaccines
Any condition that, in judgment of the investigator, could jeopardize the subject-safety following exposure to the drug.
Participation in another simultaneous medical investigation or trial