Milnacipran in the Treatment of Widespread, Non-Joint Pain in Rheumatoid Arthritis

Despite the development of effective medications to treat inflammation, pain remains a
priority for rheumatoid arthritis (RA) patients. The pain that persists despite
anti-inflammatory treatment is usually widespread and non-articular; it may lead to
diminished quality of life and high medical, psychological and social costs. To develop
better treatments for pain and prevent disability, it is critical to obtain a better
understanding of widespread, non-joint pain in RA.

Milnacipran is a selective serotonin-norepinephrine reuptake inhibitor (SNRI). No studies
have examined the effect of SNRIs on pain in RA. However, several studies have examined the
role of SNRIs in fibromyalgia and related pain conditions. Treatment with milnacipran has
been associated with improvements in clinical pain severity in Phase 2 and Phase 3
randomized placebo-controlled trials of fibromyalgia patients. In animal models, milnacipran
appears to moderate the pain-inducing effects of inflammation and central sensitization.
Thus milnacipran may be an ideal drug to treat pain in RA.

A clinical trial of an SNRI in the treatment of widespread, non-joint pain in RA will
provide more information regarding pain mechanisms and may lead to more targeted, effective
ways of treating pain in RA.

Inclusion Criteria:

- Age 24 years or older

- Primary diagnosis of rheumatoid arthritis from a board-certified rheumatologist

- Willing to maintain stable doses of concurrent non-steroidal anti-inflammatory drugs
or other acceptable medications or therapies for the duration of the study

- Brief Pain Inventory Average Pain >= 4 at the screening visit

- Widespread Pain Index >= 5 at the screening visit

- Able to give informed consent

Exclusion Criteria:

- Diagnosis of primary fibromyalgia

- Diagnosis of cold sensitive conditions such as Raynaud's syndrome, cryoglobulinemia
and paroxysmal cold hemoglobinuria

- Diagnosis of psychotic disorders, such as schizophrenia, schizoaffective disorder,
delusional disorder and shared psychotic disorder

- Patients being treated with SSRIs, MAO inhibitors or tricyclic, tetracyclic or
atypical antidepressants for pain may participate in this study if they are washed
off these medications before study entry. Patients currently receiving therapy with
SSRIs or tricyclic, tetracyclic or atypical antidepressants for depression may be
washed off these medications before study entry pending permission of the prescribing
physician and if they have never received a diagnosis of major depressive disorder or
had a history of suicidal ideation.

- Patients on thioridazine or MAO inhibitors

- Patients taking codeine or other opioids/opiates. Patients who are taking medications
such as pregabalin (Lyrica) and gabapentin (Neurontin) for pain may be enrolled in
this study.

- Known hypersensitivity to milnacipran

- Patients with a significant risk of suicide as assessed by the Beck depression
inventory form

- Patients with a history of suicide

- Pregnant or breast-feeding women

- Patients with an actively pending worker's compensation claim or auto no-fault claim;
patients with current worker's compensation, auto no-fault compensation, or
litigation; or any patient with significant secondary gain issues per discretion of
the researchers.

- Patients with myocardial infarction within the past 12 months, active cardiac disease
(chest pain or evidence of ischemia on stress test), acute congestive heart failure
requiring hospitalization in the past 12 months, clinically significant cardiac
rhythm or conduction abnormalities requiring hospitalization in the past 12 months

- Patients with severe liver impairment (AST or ALT > 3 times the upper limit of
normal)

- For patients 2-3 times the upper limit of normal, we will obtain enrollment
permission from the patient's hepatologist and monitor values at each study
visit. If values increase above 3 times the upper limit of normal, the patient
will be discontinued from the study.

- For patients 1-2 times the upper limit of normal, we will obtain enrollment
permission from the patient's physician and monitor per request of the
physician.

- Patients with severe or end stage renal disease, defined as a GFR < 15 ml/min or on
dialysis

- Patients with a recent (≤ 12 months) history of seizures.

- Patients with uncontrolled narrow-angle glaucoma.

- Patients who have been treated with an experimental agent within the last three
months.