1. Select homogenous patients with inflammatory variants (arthritis and cutaneous manifestations) |
2. Evaluate potential renal protective effects |
3. Evaluate the effect on SLE related metabolic syndrome |
4. Evaluate the effect on cardiovascular (CV) morbidity and mortality |
5. Evaluate an anti-osteoclastogenic property |
6. Evaluate its value as a glucocorticoid sparing agent (will have protective effect on metabolic syndrome, CV morbidity and osteoporosis) |
7. Cost advantage over newer agents |
1. Select homogenous patients with inflammatory variants (arthritis and cutaneous manifestations) |
2. Evaluate potential renal protective effects |
3. Evaluate the effect on SLE related metabolic syndrome |
4. Evaluate the effect on cardiovascular (CV) morbidity and mortality |
5. Evaluate an anti-osteoclastogenic property |
6. Evaluate its value as a glucocorticoid sparing agent (will have protective effect on metabolic syndrome, CV morbidity and osteoporosis) |
7. Cost advantage over newer agents |
1. Select homogenous patients with inflammatory variants (arthritis and cutaneous manifestations) |
2. Evaluate potential renal protective effects |
3. Evaluate the effect on SLE related metabolic syndrome |
4. Evaluate the effect on cardiovascular (CV) morbidity and mortality |
5. Evaluate an anti-osteoclastogenic property |
6. Evaluate its value as a glucocorticoid sparing agent (will have protective effect on metabolic syndrome, CV morbidity and osteoporosis) |
7. Cost advantage over newer agents |
1. Select homogenous patients with inflammatory variants (arthritis and cutaneous manifestations) |
2. Evaluate potential renal protective effects |
3. Evaluate the effect on SLE related metabolic syndrome |
4. Evaluate the effect on cardiovascular (CV) morbidity and mortality |
5. Evaluate an anti-osteoclastogenic property |
6. Evaluate its value as a glucocorticoid sparing agent (will have protective effect on metabolic syndrome, CV morbidity and osteoporosis) |
7. Cost advantage over newer agents |
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