A Pilot Study of CC-220 to Treat Systemic Lupus Erythematosus.

Completed · Phase 2 · Has a placebo group

Conditions studied: Systemic Lupus Erythematosus

In brief

The purpose of this study is to determine whether CC-220 is effective for the treatment of skin, joint and serological manifestations of systemic lupus erythematosus.

Key facts

Study ID

NCT02185040

Run by

Celgene

People needed

42

Starts

2014-09-16

Expected to finish

2018-09-25

Last updated by the study team

2020-03-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Part 1
• The subject has an established diagnosis of systemic lupus erythematosus (SLE) as defined by the 1997 Update of the 1982 ACR Revised Criteria for Classification of SLE at screening. The diagnosis is fulfilled provided that at least 4 criteria are met.
• Disease history of SLE ≥ 6 months at baseline
• Females of childbearing potential (FCBP) must:
• Have two negative pregnancy tests as verified by the study doctor prior to starting study therapy. She must agree to ongoing pregnancy testing during the course of the study, and after end of study therapy. This applies even if the subject practices true abstinence from heterosexual contact.
• Either commit to true abstinence from heterosexual contact (which must be reviewed on a monthly basis) or agree to use, and be able to comply with, effective contraception without interruption, 28 days prior to starting IP, during the study therapy (including dose interruptions), and for 28 days after discontinuation of study therapy.
• Male subjects must:
• Must practice true abstinence or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential while participating in the study, during dose interruptions and for at least 28 days following IP discontinuation, even if he has undergone a successful vasectomy.
• If the subject is using oral corticosteroids, the daily dose must be less than or equal to 10 mg of prednisone or equivalent during the study; the dose must be stable over the 4 weeks preceding screening and throughout the study.
• All subjects taking hydroxychloroquine, chloroquine and/or quinacrine during the study must have documentation of a normal ophthalmologic examination performed within 1 year of the Baseline Visit.
• For subjects not taking corticosteroids, or antimalarials, the last dose (in case of previous use) must be at least 4 weeks prior to screening.
• ATEP
• Male or female 18 years of age or older
• Understand and voluntarily sign an ICD prior to the initiation of any study related assessments/procedures
• Able to adhere to the study visit schedule and other protocol requirements. Pregnancy
• Females of childbearing potential (FCBP) must:
• Have two negative pregnancy tests as verified by the study doctor prior to starting study therapy. She must agree to ongoing pregnancy testing during the course of the study, and after end of study therapy. This applies even if the subject practices true abstinence* from heterosexual contact.
• Either commit to true abstinence* from heterosexual contact (which must be reviewed on a monthly basis) or agree to use, and be able to comply with, effective contraception without interruption, 28 days prior to starting IP, during the study therapy (including dose interruptions), and for 28 days after discontinuation of study therapy.
• Male subjects must:
• Practice true abstinence or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential while participating in the study, during dose interruptions and for at least 28 days following IP discontinuation, even if he has undergone a successful vasectomy. True abstinence is acceptable when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence [eg, calendar, ovulation, symptothermal, post-ovulation methods] and withdrawal are not acceptable methods of contraception.)
• Male subjects must agree not to donate semen or sperm during therapy and for at least 90 days following the discontinuation of IP.
• All subjects must:
• Understand that the IP could have potential teratogenic risk
• Agree to abstain from donating blood while taking IP and for 28 days following discontinuation of the IP
• Agree not to share IP with another person

You may not qualify if…

• The subject has been treated with intra-articular, intramuscular or IV pulse corticosteroids within 4 weeks of screening.
• The subject has received high dose oral prednisone (> 100 mg/day) within 4 weeks of screening.
• The subject has received cyclophosphamide, azathioprine or mycophenolate mofetil within 12 weeks of screening.
• The subject has participated in a clinical trial and has received an investigational product within 30 days, 5 pharmacokinetic half-lives or twice the duration of the biological effect of the investigational product (whichever is longer) prior to screening; OR participation in two or more investigational drug trials within 12 months of screening.
• Unstable lupus nephritis defined as: proteinuria > 1.0 g/24 hour /1.73 m2 OR eGFR of less than 60 mL/1.73 m2 CNS disease, including active severe CNS lupus (including seizures, psychosis, organic brain syndrome, cerebrovascular accident (CVA), cerebritis or CNS vasculitis) requiring therapeutic intervention within 6 months of screening.
• The subject has New York Heart Association (NYHA) Class III or IV congestive heart failure.
• Presence of hepatitis B surface antigen (HBsAG). Subjects may have a positive anti-hepatitis B core antibody (anti-HBc) if the anti-hepatitis B surface antibody (anti-HBs) is positive as well.
• Antibodies to hepatitis C at Screening.
• The subject has a known positive history of antibodies to human immunodeficiency virus (HIV) or HIV disease or acquired immune deficiency syndrome (AIDs).
• Has a history of an organ transplant (e.g., heart, lung, kidney, liver) or hematopoietic stem cell/marrow transplant.
• Malignancy or history of malignancy, except for:
• treated (ie, cured) basal cell or squamous cell in situ skin carcinomas;
• treated (ie, cured) cervical intraepithelial neoplasia (CIN) or carcinoma in situ of the cervix with no evidence of recurrence within 5 years of Screening
• Systemic bacterial infections requiring treatment with oral or injectable antibiotics, or significant viral or fungal infections, within 4 weeks of Screening. Any treatment for such infections must have been completed and the infection cured, at least 2 weeks prior to Screening and no new or recurrent infections prior to the Baseline visit.
• History of venous thrombosis or any thromboembolic events within 2 years of screening.
• Clinical evidence of significant unstable or uncontrolled acute or chronic disease not due to SLE (ie, cardiovascular, pulmonary, hematologic, gastrointestinal, hepatic, renal, neurological, malignancy, psychiatric or infectious disease) which in the opinion of the investigator could put the subject at undue risk or confound study results.
• Presence of active uveitis or any other clinically significant ophthalmological finding.
• History or current diagnosis of peripheral or radicular neuropathy. Any clinically significant abnormalities on ECG, which, in the opinion of the investigator would interfere with safe participation in the study.

Where it is running

• University of Alabama at Birmingham — Birmingham, Alabama, United States
• Arizona Arthritis and Rheumatology Research, PLLC — Paradise Valley, Arizona, United States
• University of Arizona Clinical and Translational Science Research Center — Tucson, Arizona, United States
• UCSD Center for Innovative Therapy — La Jolla, California, United States
• Dermatology Research Associates — Los Angeles, California, United States
• East Bay Rheumatology Medical Group Inc. — San Leandro, California, United States
• Clinical Science Institute — Santa Monica, California, United States
• Los Angeles Biomedical Research Institute at Harbor - UCLA — Torrance, California, United States
• Inland Rheumatology Clinical Trials — Upland, California, United States
• Vipul Joshi, MD, PA, dba Bay Area Arthritis and Osteoporosis — Brandon, Florida, United States
• Emory University School of Medicine — Atlanta, Georgia, United States
• Advanced Medical Research — Atlanta, Georgia, United States
• Arthritis Research and Treatment Center — Stockbridge, Georgia, United States
• Northwestern Medical Group; Department of Dermatology — Chicago, Illinois, United States
• Northshore University Health System — Skokie, Illinois, United States
• Southern Illinois University School of Medicine — Springfield, Illinois, United States
• Tulane University Health Sciences Center — New Orleans, Louisiana, United States
• Northwell Health / Division of Rheumatology — Lake Success, New York, United States
• Feinstein Institute For Medical Research — Manhasset, New York, United States
• NYU Langone Medical Center — New York, New York, United States
• Columbia Presbyterian Medical Center — New York, New York, United States
• Univ of Rochester Medical Center — Rochester, New York, United States
• DJL Clinical Research — Charlotte, North Carolina, United States
• MetroHealth Medical Systems — Cleveland, Ohio, United States
• Ohio State University Medical Center — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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