A Study to Evaluate Safety and Tolerability of Subcutaneous Doses of MEDI-545 in Subjects With Lupus

NCT ID: NCT00657189

Last Updated: 2016-08-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 87 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-07-31
• Study Completion Date: 2010-05-31

Brief Summary

The primary objective of this study is to evaluate the safety and tolerability of multiple doses of MEDI-545 in subjects with moderately to severely active Lupus.

Detailed Description

The primary objective of this study is to evaluate the safety and tolerability of multiple SC doses of MEDI-545 in subjects ≥ 18 years of age with moderately to severely active SLE despite standard of care.

Conditions

Lupus Erythematosus, Systemic; Lupus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

1

MEDI-545

Group Type: EXPERIMENTAL

MEDI-545

Intervention Type: DRUG

100 mg once; SC Placebo × 12 doses on other weeks

2

MEDI-545

Group Type: EXPERIMENTAL

MEDI-545

Intervention Type: DRUG

100 mg every 4 weeks × 4 doses; SC Placebo × 9 doses on other weeks

3

MEDI-545

Group Type: EXPERIMENTAL

MEDI-545

Intervention Type: DRUG

100 mg every 2 weeks × 7 doses; SC Placebo × 6 doses on other weeks

4

MEDI-545

Group Type: EXPERIMENTAL

MEDI-545

Intervention Type: DRUG

100 mg every week × 13 doses

5

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

SC Placebo every week × 13 doses

Interventions

MEDI-545

100 mg once; SC Placebo × 12 doses on other weeks

Intervention Type: DRUG

MEDI-545

100 mg every 4 weeks × 4 doses; SC Placebo × 9 doses on other weeks

Intervention Type: DRUG

MEDI-545

100 mg every 2 weeks × 7 doses; SC Placebo × 6 doses on other weeks

Intervention Type: DRUG

MEDI-545

100 mg every week × 13 doses

Intervention Type: DRUG

Placebo

SC Placebo every week × 13 doses

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female subjects ≥ 18 years at the time of the first dose of study drug;
• Written informed consent and HIPAA authorization (applies to covered entities in the US only) obtained from the subject or subject's legal representative;
• Meet at least 4 of the 11 revised ACR classification criteria for SLE
• Have positive antinuclear antibody test (ANA) at ≥ 1:80 serum dilution documented in the past or at screening;
• Have at least 1 system with a score of A or 2 systems with a score of B on the BILAG index at screening, or have a SELENA-SLEDAI score ≥ 6;
• Treatment for SLE with antimalarials, oral prednisone or another systemic corticosteroid, mycophenolate mofetil, methotrexate, leflunomide, azathioprine, or dapsone;
• Women, unless surgically sterile or at least 2 years post-menopausal, must use an effective method of avoiding pregnancy (including oral, injectable, transdermal, or implanted contraceptives, intrauterine device, diaphragm with spermicide, cervical cap, abstinence, or sterile sexual partner) in addition to the use of condoms (male or female condoms with spermicide) from screening through the end of the study. Cessation of birth control after this point should be discussed with a responsible physician. Men unless surgically sterile, must likewise practice 2 effective methods of birth control (condom with spermicide or abstinence) from Study Day 0 through the end of the study;
• Ability to complete the study period, including the follow-up period through Study Day 168; and
• Willing to forego other forms of experimental treatment during the study.

Exclusion Criteria

• Have received MEDI-545 within 120 days prior to screening;
• History of allergy or reaction to any component of the study drug formulation;
• Have received the following medications within 28 days before randomization:

• Systemic cyclophosphamide at any dose
• Cyclosporine at any dose
• Thalidomide at any dose
• Hydroxychloroquine > 600 mg/day
• Mycophenolate mofetil > 3 g/day
• Methotrexate > 25 mg/week
• Azathioprine > 3 mg/kg/day
• Have received fluctuating doses of the following within 28 days before randomization:

• Antimalarials
• Mycophenolate mofetil
• Methotrexate
• Leflunomide
• Azathioprine
• Dapsone
• Have received Leflunomide > 20mg/day in the 6 months prior to Study Day 0;
• Have received prednisone > 20 mg/day or in fluctuating doses within 14 days before randomization;
• Have received fluctuating doses of non-steroidal anti-inflammatory drugs within 14 days before randomization;
• Treatment with any investigational drug therapy within 28 days before randomization into the study, B cell-depleting therapies within 12 months before randomization, or biologic therapies within 30 days or 5 half-lives of the biologic agent, whichever is longer, before randomization into the study;
• In the investigator's opinion, evidence of clinically significant active infection, including ongoing, chronic infection, within 28 days before randomization;
• A history of severe viral infection as judged by the investigators, including severe infections of either cytomegalovirus or the herpes family such as disseminated herpes, herpes encephalitis, ophthalmic herpes;
• Herpes zoster infection within 3 months before randomization;
• Evidence of infection with hepatitis B or C virus, or human immunodeficiency virus (HIV)-1 or HIV-2, or active infection with hepatitis A, as determined by results of testing at screening
• Vaccination with live attenuated viruses within 28 days before randomization;
• Pregnancy (women, unless surgically sterile or at least 2 years post-menopausal, must have a negative serum pregnancy test within 28 days before receiving the study drug and a negative urine pregnancy test on days of study drug administration before receiving the study drug);
• Breastfeeding or lactating women;
• History of primary immunodeficiency;
• History of alcohol or drug abuse < 1 year prior to randomization;
• History of cancer (except basal cell carcinoma or in situ carcinoma of the cervix treated with apparent success with curative therapy > 1 year prior to randomization);
• History of active tuberculosis (TB) infection or newly positive TB skin test (defined as a reaction ≥ 10 mm in diameter if not on systemic immunosuppressive medication or ≥ 5 mm if on systemic immunosuppressive medication;
• History of latent TB infection without completion of an appropriate course of treatment;
• Elective surgery planned from the time of screening through Study Day 168;
• At screening blood tests (within 28 days before randomization), any of the following:

• AST > 2.5 x upper limit of the normal range (ULN), unless caused by SLE
• ALT > 2.5 x ULN, unless caused by SLE
• Creatinine > 4.0 mg/dL
• Neutrophils < 1,500/mm3
• Platelet count < 50,000/mm3
• History of any disease, evidence of any current disease (other than SLE), any finding upon physical examination, or any laboratory abnormality that, in the opinion of the investigator or medical monitor, may compromise the safety of the subject in the study or confound the analysis of the study; or
• Any employee of the research site who is involved with the conduct of the study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

MedImmune LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Warren Greth, M.D.

Role: STUDY_DIRECTOR

MedImmune LLC

Locations

Research Site

Anniston, Alabama, United States

Research Site

Huntington Beach, California, United States

Research Site

Upland, California, United States

Research Site

Colorado Springs, Colorado, United States

Research Site

Farmington, Connecticut, United States

Research Site

Clearwater, Florida, United States

Research Site

Ocala, Florida, United States

Research Site

Atlanta, Georgia, United States

Research Site

Decatur, Georgia, United States

Research Site

Marrietta, Georgia, United States

Research Site

West Fayetteville, Georgia, United States

Research Site

Baltimore, Maryland, United States

Research Site

Lansing, Michigan, United States

Research Site

Brooklyn, New York, United States

Research Site

Charlotte, North Carolina, United States

Research Site

Cincinnati, Ohio, United States

Research Site

Oklahoma City, Oklahoma, United States

Research Site

Charleston, South Carolina, United States

Research Site

Columbia, South Carolina, United States

Research Site

Houston, Texas, United States

Research Site

Sugarland, Texas, United States

Research Site

Seattle, Washington, United States

Countries

United States

References

Merrill JT, Wallace DJ, Petri M, Kirou KA, Yao Y, White WI, Robbie G, Levin R, Berney SM, Chindalore V, Olsen N, Richman L, Le C, Jallal B, White B; Lupus Interferon Skin Activity (LISA) Study Investigators. Safety profile and clinical activity of sifalimumab, a fully human anti-interferon alpha monoclonal antibody, in systemic lupus erythematosus: a phase I, multicentre, double-blind randomised study. Ann Rheum Dis. 2011 Nov;70(11):1905-13. doi: 10.1136/ard.2010.144485. Epub 2011 Jul 27.

Reference Type: RESULT

PMID: 21798883 (View on PubMed)

Other Identifiers

MI-CP179

Identifier Type: -

Identifier Source: org_study_id