Table 2.
Clinical trials registered in Clinical Trials.gov evaluating efficacy and safety of Tranilast in a variety of diseases.
Condition or disease | Intervention/treatment | Phase | Participants | Clinical trial identifier |
---|---|---|---|---|
Mucinoses | 0.1g each time, three times a day,12 months | Early Phase 1 | 56 | NCT03490708 |
Scleredema Adultorum | 0.1g each time, three times a day,6 months | Early Phase 1 | 56 | NCT03512873 |
Sarcoidosis | 0.1g each time, three times a day | Early Phase 1 | 56 | NCT03528070 |
Gout Hyperuricemia | Combination Tranilast and Febuxostat | Phase 2 | 24 | NCT00995618 |
Active Rheumatoid Arthritis | Tranilast, 300 mg/day Tranilast, 150 mg/day |
Phase 2 | 250 | NCT00882024 |
Gout Hyperuricemia | Tranilast and Allopurinol | Phase 2 | 24 | NCT01052987 |
Gout Hyperuricemia | 1-Tranilast 300 mg QD Allopurinol 400 mg QD. 2-Tranilast, 300 mg QD Allopurinol 600 mg QD | Phase 2 | 112 | NCT01109121 |
Allergic Conjunctivitis | Olopatadine 0.1% one drop in one eye Tranilast 0.5% one drop in one eye |
Phase 4 | 50 | NCT00818805 |