A Research Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of DUR-928 in Patients With Alcoholic Hepatitis
Status: | Recruiting |
---|---|
Conditions: | Hepatitis |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 21 - Any |
Updated: | 10/26/2018 |
Start Date: | April 18, 2018 |
End Date: | March 2019 |
Contact: | Deborah Scott, MS |
Email: | deborah.scott@durect.com |
Phone: | 408-777-1417 |
An Open- Label, Dose Escalation Study to Assess the Safety, Pharmacokinetics and Pharmacodynamic Signals of DUR-928 in Patients With Alcoholic Hepatitis
This is a research trial testing DUR-928 (an experimental medication). The purpose of this
trial is to assess the dose related safety, Pharmacokinetics, and Pharmacodynamics of DUR 928
in patients with moderate and severe alcoholic hepatitis (AH).
trial is to assess the dose related safety, Pharmacokinetics, and Pharmacodynamics of DUR 928
in patients with moderate and severe alcoholic hepatitis (AH).
Inclusion Criteria:
1. Able to provide written informed consent (either from patient or patient's legally
acceptable representative)
2. Male or female patients 21 years of age or older with BMI ≥ 20 to ≤ 40 kg/m2
3. Patients with alcoholic hepatitis defined as:
1. History of heavy alcohol abuse: > 40 g/day in females or > 60 g/day in males for
a minimum period of 6 months, AND
2. Consumed alcohol within 12 weeks of entry into the study, AND
3. Serum bilirubin > 3 mg/dL AND AST > ALT, but less than 300 U/L AND
4. MELD score between 11-30, inclusive
4. No evidence of active infection as determined by the investigator.
5. Women of child-bearing potential must utilize appropriate birth control throughout the
study duration.
6. Male patients must agree to use a medically acceptable method of contraception/birth
control throughout the study duration
Exclusion Criteria:
1. Other or concomitant cause(s) of liver disease as a result of:
1. Autoimmune liver disease
2. Wilson disease
3. Vascular liver disease
4. Drug induced liver disease
2. Co-infection with human immunodeficiency virus (HIV) or Hepatitis B
3. Any active malignancies other than curatively treated skin cancer (basal cell or
squamous cell carcinomas)
4. If female, known pregnancy, or has a positive serum pregnancy test, or
lactating/breastfeeding
5. Serum creatinine > 2.5 mg/dL
6. Patients who have had organ transplantation (such as liver, kidney, lung, heart, bone
marrow, or stem cell etc.), other than cornea transplant
7. Stage 3 or greater encephalopathy by West Haven criteria
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