Status:
TERMINATED
MRI Evaluation Assessing Synovitis to Address the Unmet Need for Reliable Endpoints in SLE
Lead Sponsor:
Oklahoma Medical Research Foundation
Collaborating Sponsors:
Bristol-Myers Squibb
Conditions:
Systemic Lupus Erythematosus Arthritis
Eligibility:
All Genders
18-70 years
Phase:
PHASE2
Brief Summary
This is an exploratory evaluation of MRI as a reliable, sensitive, and accurate outcome measure for clinical trials in SLE arthritis. Forty patients with SLE and moderate to severe synovitis (minimum ...
Detailed Description
This will be a six month, double blind, randomized, placebo- controlled trial of subcutaneous methotrexate vs methotrexate plus baseline Depomedrol in patients with SLE and \>/= 3 tender and 3 swollen...
Eligibility Criteria
Inclusion
- Meeting 4 1997 revised ACR classification criteria or SLICC criteria for SLE.
- Have active polyarticular arthritis with a minimum of 3 tender and 3 swollen joints or tendons in the hands and wrists observed at the screening visit and a history consistent with BILAG 2004 "B" arthritis.
- Willing and able to receive weekly subcutaneous methotrexate and intramuscular steroid injections (or placebo injection) as per the protocol.
- Willing and able to stop current immunosuppressants.
- Willing and able to undergo MRI and other study procedures (including no known allergy to contrast material).
- Women of childbearing potential must have a negative pregnancy test at screening and baseline and be willing to use effective contraception after the screening visit until three months after the end of the study.
- People of any sex or gender 18 to 70 years of age.
Exclusion
- Target Disease Exceptions: Patients with acute nephritis requiring induction therapy, CNS lupus (except chorea, cranial neuropathy, and resolving optic neuritis) or any lupus condition requiring cyclophosphamide, biologics, or IV steroids \>/= 500 mg.
- Medical History and Concurrent Diseases:
- Patients incapable of understanding or completing study-related assessments.
- Patients with any condition, whether or not related to SLE, which, in the opinion of the investigator, might place a patient at unacceptable risk for participation in the study.
- Patients with a history of cancer in the last 5 years, other than non-melanoma skin cell cancers cured by local resection or carcinoma in situ.
- Patients who, in the opinion of the investigator, currently abuse drugs or alcohol.
- Patients with herpes zoster or cytomegalovirus (CMV) that resolved less than 2 months before the informed consent document was signed.
- Patients who have received any live vaccines within 2 months of the anticipated first dose of study medication.
- Patients with any serious bacterial infection within the last 2 months, unless treated and resolved with antibiotics, or any chronic bacterial infection (eg, chronic pyelonephritis, osteomyelitis, or bronchiectasis).
- Patients at risk for tuberculosis (TB). Patients with active TB within 3 years, even if treated; history of active TB \> 3 years ago, unless documented prior anti-TB treatment appropriate in duration and type; current known or suspected active TB; and latent TB not successfully treated (≥ 4 weeks at baseline).
- Physical and Laboratory Test Findings:
- Patients must not be known to be positive for hepatitis B surface antigen.
- Patients who are known to be positive for hepatitis C antibody may participate if the presence of hepatitis C virus can be excluded by polymerase chain reaction or recombinant immunoblot assay at screening.
- Acute hemolytic anemia with hemoglobin \< 7.0 g/dL or known change in Hg by 2.0 g/dL within the last two months unless due to SLE and stable for the past month
- WBC \< 1500/mm3 (\< 1.5 x 109/L) unless due to chronic lupus activity and stable for at least one month
- Platelets \< 40,000/mm3 (\< 3 x 109/L) (If less than 100,000 must have been stable (within a range of 10,000/mm3) either by historical testing of known chronic thrombocytopenic patients within two months of screening or in two tests during the screening period at least one week apart.
- Serum creatinine \> 2 times the ULN or estimated glomerular filtration rate (eGFR) \<40 mL/min/1.73 m2
- Serum ALT or AST \> 2.5 times the ULN. If currently on methotrexate, patients may repeat this test during the screening period or later rescreen.
- Any other laboratory test results that, in the opinion of the investigator, might place a patient at unacceptable risk for participation in the study.
- Allergies and Adverse Drug Reactions: Known allergy or a history, in the opinion of the investigator or patient, of an unacceptable adverse sensitivity to gadolinium, methotrexate or unacceptable difficulties tolerating intramuscular or subcutaneous injections. Patients may elect lower doses of Depomedrol (1/2 or ¼ the dose) however if there is concern about tolerability of the large dose injection.
- Prohibited Treatments and/or Therapies:
- Patients who have received treatment with an investigational biologic within 28 days (or less than 5 terminal half-lives of elimination) of the Day 1 dose.
- Patients who have received cyclophosphamide within 3 months of the Day 1 dose or bolus parenteral steroids \>/= 500 mg within 1 month of screening.
- Use of rituximab within 6 months prior to Day 1; if \> 6 months have elapsed since last rituximab dose, reconstitution of total peripheral B cell counts to predosing range should be documented. If there were no predose levels obtained then B cell counts must be minimally 200 x 106/l which characterizes most SLE patients (Odendahl et al. J Immunol 2000;165:5970-5979).
- Ongoing treatment (after the baseline visit) with immune suppressants (such as azathioprine, mycophenolate mofetil, leflunomide, calcineurin inhibitors or belimumab). These may be stopped or tapered as soon as informed consent procedures have been completed at the screening visit.
- Prednisone \> 20 mg po qd (or equivalent) at the time of the screening visit or \> 10 mg po qd (or equivalent) at or after randomization (steroids will additionally be tapered during the study if tolerated). Hydroxychloroquine is not exclusionary if the investigator or patient is unwilling to stop it, but taper will also be encouraged if the patient improves. NSAIDS are not exclusionary, but patients will be asked not to take them on the morning of each monthly visit, until the visit is concluded.
- Other
Key Trial Info
Start Date :
April 10 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 16 2022
Estimated Enrollment :
9 Patients enrolled
Trial Details
Trial ID
NCT03355482
Start Date
April 10 2017
End Date
December 16 2022
Last Update
February 20 2024
Active Locations (1)
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1
Access Health
Las Vegas, Nevada, United States, 89128