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A Phase 2 Clinical Trial Investigating the Safety and Efficacy of ADX-629 in Subjects with Moderate Alcohol Associated Hepatitis (Part 1)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ADX-629 (125 mg twice daily) | Experimental |
| |
| ADX-629 (250 mg twice daily) | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ADX-629 | Drug | 125 mg twice daily for 28 days |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Treatment-Emergent Adverse Event Query | Incidence and severity of treatment-emergent adverse events | Day 1 to Day 28 |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Synergry Healthcare | Bradenton | Florida | 34209 | United States | ||
| Florida Health Sciences Center/Tampa General Hospital/USF |
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| ADX-629 |
| Drug |
250 mg twice daily for 28 days |
|
| Tampa |
| Florida |
| 33606 |
| United States |
| The Liver Institute at Methodist Dallas Medical Center | Dallas | Texas | 75203 | United States |
| UDL Clinical Research, LLC | Houston | Texas | 77057 | United States |
| Methodist Specialty and Transplant Hospital | San Antonio | Texas | 78229 | United States |
| Bon Secours Liver Institute of Newport News | Richmond | Virginia | 23221 | United States |
| ID | Term |
|---|---|
| D006519 | Hepatitis, Alcoholic |
| ID | Term |
|---|---|
| D006505 | Hepatitis |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D008108 | Liver Diseases, Alcoholic |
| D020751 | Alcohol-Induced Disorders |
| D019973 | Alcohol-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
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| ID | Term |
|---|---|
| C000716647 | ADX-629 |
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