Study to Evaluate Hepatic Artery Injection of Autologous Human Bone Marrow-Derived MSCs in Patients With Alcoholic LC

Status unconfirmed · Phase 1

Conditions studied: Alcoholic Liver Cirrhosis

In brief

This study is to evaluate the safety and efficacy of a single dose of Cellgram™ delivered via hepatic artery in patients with decompensated alcoholic liver cirrhosis.

Key facts

Study ID

NCT03838250

Run by

Pharmicell Co., Ltd.

People needed

10

Starts

2019-06-20

Expected to finish

2021-06-01

Last updated by the study team

2020-10-22

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Alcoholic liver cirrhosis as diagnosed by clinical, biochemical, radiological, or histological evidence.
• Male or female, 18 to 70 years of age, inclusive.
• Child-Pugh class B (7 to 9 points)
• Capable, in the Investigators opinion, of undergoing hepatic artery catheterization.
• No consumption of alcohol or other potentially hepatotoxic substances considered clinically relevant in the opinion of the Investigator, within 6 months prior to screening and throughout the study.
• Provision of informed consent by the patient (or their legal representative) to participate in the clinical study.
• Able, in the Investigator's opinion, to comply with the requirements of the protocol (including the follow-up period).
• Females of childbearing potential must test negative on standard urine pregnancy test and must be willing to practice appropriate contraceptive methods for the duration of the study. Highly effective methods of birth control include hormonal birth control, intrauterine devices (IUDs), or any double-barrier method (sponges, female condoms) used by the woman in addition to contraception used by their male partner such as vasectomy or condom supplemented with spermicide.

You may not qualify if…

• Current diagnosis of malignant hematologic disease (e.g., acute myeloid leukemia, acute lymphoblastic leukemia, non-Hodgkin's lymphoma, Hodgkin's lymphoma, multiple myeloma).
• Etiology other than alcohol for underlying liver cirrhosis.
• Baseline creatinine >1.7 mg/dL and/or estimated glomerular filtration rate (eGFR) <30 mL/min/1.73 m2
• Clinical history of a solid cancer within 5 years prior to screening or current diagnosis of a solid cancer (including hepatocellular carcinoma assessed by ultrasonography and elevated AFP level) and currently receiving cancer treatment.
• Continuous use of a clinically relevant amount of steroids or antibiotics within 1 month prior to screening. Clinical relevance will be determined by the Investigator.
• Model for End-Stage Liver Disease score >20.
• International normalized ratio >3.0 and/or platelet counts <30,000/mm3
• Major operation within 3 months prior to screening.
• Presence of extrahepatic biliary stricture.
• Participant has undergone transjugular intrahepatic portosystemic shunt.
• Active hepatic artery or portal vein thrombosis.
• Presence of advanced hepatic encephalopathy Stages 3-4 (West Haven criteria) at the time of screening.
• Active variceal bleeding during the last 6 months before screening.
• Severe cardiac, renal, or respiratory failure.
• Positive serological test results for human immunodeficiency virus (HIV), HCV, hepatitis B surface antigen (HBsAg) and/or syphilis.
• Patient is pregnant or breast feeding, or planning to become pregnant while enrolled in the study, up to the EOS visit.
• Positive urine pregnancy test at Screening.
• Drug abuse within the past 2 years (as confirmed by patient disclosure or a urine drug screen conducted at Screening).
• Participation in an interventional clinical study within 30 days prior to screening.

Where it is running

• University of Utah — Salt Lake City, Utah, United States (enrolling)

Full record on ClinicalTrials.gov

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