Short-term Survival of Subjects With Acute-on-chronic Liver Failure After Plasma Exchange With Human Serum Albumin 5%

Stopped early · Phase 3

Conditions studied: Acute-On-Chronic Liver Failure

In brief

This is a Phase 3, multicenter, randomized, controlled, parallel-group, open-label study to evaluate the effects of plasma exchange using human serum albumin 5% (PE-A 5%) in acute-on-chronic liver failure (ACLF) subjects. The study will involve approximately 40 study centers in the United States, Canada, and Europe with expertise in the management of subjects with ACLF. Subjects with ACLF at a high risk of hospital mortality will be enrolled. The study will consist of a Screening Period during which subjects will be randomized (1:1) to receive either standard medical treatment (SMT) + PE-A 5% (treatment group) or SMT only (control group), followed by a Treatment Period, and a Follow-up Period. The Treatment Period for subjects in the SMT+ PE-A 5% treatment group will be between 7 and 17 days, depending on ACLF evolution. The Treatment Period for subjects in the SMT control group will be a minimum of 7 days for all subjects and up to 17 days depending on the ACLF evolution. Subjects in this group will receive SMT according to the institution's standards. The Follow-up Period for subjects in both groups will be 90 days.

Key facts

Study ID

NCT03702920

Run by

Instituto Grifols, S.A.

People needed

274

Starts

2019-06-17

Expected to finish

2025-04-14

Last updated by the study team

2026-06-04

Who can join

Age: 18 and older, up to 79. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female cirrhotic subjects between 18 and 79 years of age.
• Subjects with ACLF-1b, ACLF-2, or ACLF-3a detected either at admission or during hospitalization (must be ACLF-1b, -2, or -3a within the Screening Period [a maximum of 10 days]).
• Willing and able to provide written informed consent or have an authorized representative able to provide written informed consent on behalf of the subject in accordance with local law and institutional policy.
• In case of HE, informed consent will be provided by a relative or a legally authorized representative if the subject is considered incompetent to consent.

You may not qualify if…

• Subjects without ACLF.
• Subjects with ACLF-1a or ACLF-3b after the Screening Period.
• Subjects fulfilling inclusion criteria that improve to no ACLF or to ACLF-1a or worsen to ACLF-3b during the Screening Period (between initial evaluation and time of randomization).
• Subjects with ACLF for more than 10 days prior to randomization.
• Subjects with acute or subacute liver failure without underlying cirrhosis.
• Subjects with septic shock requiring use of norepinephrine (> 0.3 mcg/kg/min) or need for a second vasopressor (including terlipressin).
• Subjects with active bacterial or fungal infection: who have received less than 24h of appropriate antibiotic treatment.
• Subjects with severe respiratory failure with PaO2/FiO2 ≤200.
• Subjects with active or recent bleeding (unless controlled for >48 hours).
• Subjects with severe thrombocytopenia (≤20×10\^9/L) (based on local laboratory assessment).
• Subjects with chronic renal failure and currently receiving hemodialysis.
• Evidence of current locally advanced or metastatic malignancy. Subjects with hepatocellular carcinoma within the Milan criteria (1 nodule ≤5 cm or 3 nodules ≤3 cm), non-melanocytic skin cancer, and controlled breast or prostate cancer, can be included).
• Subjects with severe chronic heart failure (New York Heart Association [NYHA] class III or IV).
• Subjects with severe pulmonary disease (Global Obstructive Lung Disease [GOLD] stage III or IV).
• Subjects with severe myopathy as defined clinically.
• Subjects with a known infection with human immunodeficiency virus (HIV) or have clinical signs and symptoms consistent with current HIV infection.
• Females who are pregnant, breastfeeding, or if of childbearing potential, unwilling to practice a highly effective method of contraception.
• Subjects with previous liver transplantation.
• Subjects receiving anti-platelet or anti-coagulant therapy (LMWH for DVT prophylaxis is allowed).
• Participation in another clinical study within at least 30 days prior to screening.
• Subjects with active drug addiction (exceptions: active alcoholism or marijuana).
• Subjects with a do-not-resuscitate order.
• In the opinion of the investigator, the subject may have compliance problems with the protocol and the procedures of the protocol.
• Subjects with current infection of COVID-19, those who are less than 14 days post recovery or those who have clinical signs and symptoms consistent with COVID-19 infection.

Where it is running

• Southern California Research Center — Coronado, California, United States
• Cedars-Sinai Medical Center — Los Angeles, California, United States
• Emory University — Atlanta, Georgia, United States
• Rutgers-New Jersey Medical School — Newark, New Jersey, United States
• Mayo Clinic Rochester — Rochester, New York, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States
• University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
• McGuire VA Medical Center — Richmond, Virginia, United States
• University of Washington Medical Center — Seattle, Washington, United States
• Aurora Health Care, Inc. — Milwaukee, Wisconsin, United States
• Medical University of Vienna — Vienna, Austria
• Université libre de Bruxelles — Brussels, Belgium
• UZ Leuven - Campus Gasthuisberg — Leuven, Belgium
• Hôpital Beaujon — Clichy, France
• Centre Hépato-Biliaire - Hôpital Universitaire Paul Brousse — Villejuif, France
• Universitätsklinikum Frankfurt — Frankfurt, Germany
• Hannover Medical School — Hanover, Germany
• Universitaetsklinikum Leipzig — Leipzig, Germany
• Klinikum der Universitaet Muenchen — München, Germany
• Milano Hospital Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico — Milan, Milan, Italy
• Azienda Ospedaliero-Universitaria Policlinico Umberto I — Roma, Roma, Italy
• ASST Grande Ospedale Metropolitano Niguarda — Milan, Italy
• Azienda Ospedaliera di Padova — Padova, Italy
• Centro Hospitalar do Porto — Porto, Portugal
• Hospital Universitario del Valle Hebron — Barcelona, Spain

Full record on ClinicalTrials.gov

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