MRI Evaluation Assessing Synovitis to Address the Unmet Need for Reliable Endpoints in SLE

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 joints in the hands and wrists. Patients who are already taking methotrexate
/= 2.5 mg/week dose increase at baseline,
receiving subcutaneous dosing whether on oral or sc dosing prior to entry. Those not taking
methotrexate at baseline will initiate open label treatment in ascending doses beginning at
15 mg/week. All patients will increase methotrexate weekly up to 25 mg as tolerated or until
resolution of arthritis. Decreases are allowed as needed.

After randomization, patients may choose to stop or continue any NSAIDs, hydroxychloroquine,
or up to 10 mg prednisone if these were being used at screening. All other lupus-specific
treatments or medications will be withdrawn. Optimization of methotrexate dose must be
completed by Month 2. If additional immune- suppressive medications or steroids become
necessary during the trial, patients remain evaluable for the primary endpoint, which is
defined by clinical response regardless of treatment. In secondary analyses of Depomedrol vs.
placebo, patients treated with rescue interventions will be censored when comparing changes
in mean/median synovitis, osteitis RAMRIS or tendinitis scores in the two treatment groups,
and they will be included as non- responders in dichotomous endpoints (SRI-4, BICLA). These
analyses will also provide useful data for many of the other endpoints (comparisons of MRI vs
joint counts and other measures which are valid regardless of treatment). Thus, although off
protocol medications will not be encouraged, they will not require removal from the study.

Inclusion Criteria:

1. Meeting 4 1997 revised ACR classification criteria or SLICC criteria for SLE.

2. 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.

3. Willing and able to receive weekly subcutaneous methotrexate and intramuscular steroid
injections (or placebo injection) as per the protocol.

4. Willing and able to stop current immunosuppressants.

5. Willing and able to undergo MRI and other study procedures (including no known allergy
to contrast material).

6. 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.

7. People of any sex or gender 18 to 70 years of age.

Exclusion Criteria:

1. 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.

2. Medical History and Concurrent Diseases:

1. Patients incapable of understanding or completing study-related assessments.

2. 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.

3. 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.

4. Patients who, in the opinion of the investigator, currently abuse drugs or
alcohol.

5. Patients with herpes zoster or cytomegalovirus (CMV) that resolved less than 2
months before the informed consent document was signed.

6. Patients who have received any live vaccines within 2 months of the anticipated
first dose of study medication.

7. 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).

8. 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).

3. Physical and Laboratory Test Findings:

1. Patients must not be known to be positive for hepatitis B surface antigen.

2. 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.

3. 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

4. WBC < 1500/mm3 (< 1.5 x 109/L) unless due to chronic lupus activity and stable
for at least one month

5. 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.

6. Serum creatinine > 2 times the ULN or estimated glomerular filtration rate (eGFR)
<40 mL/min/1.73 m2

7. 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.

8. Any other laboratory test results that, in the opinion of the investigator, might
place a patient at unacceptable risk for participation in the study.

4. 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.

5. Prohibited Treatments and/or Therapies:

1. 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.

2. Patients who have received cyclophosphamide within 3 months of the Day 1 dose or
bolus parenteral steroids >/= 500 mg within 1 month of screening.

3. 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).

4. 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.

5. 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.

6. Other Exclusion Criteria:

1. Prisoners or patients who are involuntarily incarcerated.

2. Patients who are compulsorily detained for treatment of either a psychiatric or
physical (eg, infectious disease) illness.

3. Known contraindication or intolerance or risk of MRI procedures (e.g. permanent
pacemakers, cardioverter-defibrillators, other implanted electronic devices,
aneurysm clips and other metal implants, procedure-limiting claustrophobia
(unless mitigated by the circumstances of the testing MRI for small joints) and
severe renal impairment (estimated GFR < 40 mL/min/1.73 m2).