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

Acute-On-Chronic Liver Failure Clinical Trial

— APACHE  

Official title:

Effects of Plasma Exchange With Human Serum Albumin 5% (PE-A 5%) on Short-term Survival in Subjects With "Acute-On-Chronic Liver Failure" (ACLF) at High Risk of Hospital Mortality

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03702920
• Other study ID #: IG1407
• Status: Recruiting
• Phase: Phase 3
• Start date: February 21, 2019
• Est. completion date: October 2026

Study information

• Verified date: April 2024
• Source: Grifols Therapeutics LLC
• Contact: Mireia Torres
• Phone: +34 93 5710500
• Email: approach_apache[@]grifols.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

Approximately 380 subjects with cirrhosis, ACLF, and high risk of hospital mortality (ACLF-1b, ACLF-2, or ACLF-3a) will be included in this study after obtaining written informed consent. In case of hepatic encephalopathy (HE), written informed consent will be obtained from a relative or a legally authorized representative if the subject is considered incompetent to consent. Randomization of subjects will be stratified by region (European Union [EU] or North America [NA]) and the 3 ACLF grades (ACLF-1b, ACLF-2, or ACLF-3a). Within each stratum (ie, each unique combination of region and ACLF grade), subjects will be randomized in a 1:1 ratio into 2 treatment groups below: - SMT+PE-A 5% (treatment group) - SMT (control group) SMT + PE-A 5% Treatment Group: PE-A 5% will be performed using 5% albumin (Albutein® 5%) as the main replacement fluid administered intravenously. Fresh frozen plasma (FFP) will be given after each PE-A 5% session to prevent coagulopathy. The exact number of sessions will be determined by the pattern of response (achieving complete response or no improvement/deterioration of ACLF) to PE-A 5% therapy. IVIGs will be administered to prevent the development of hypogammaglobulinemia and infection. SMT Control Group: The Treatment Period will be 7 days for all subjects and will be prolonged depending on subject's ACLF evolution to up to 17 days. Subjects in both the SMT+ PE-A 5% treatment group and the SMT control group will be followed for 90 days after randomization. During the entire study, the safety of both groups will be monitored by a Data Safety Monitoring Board.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 380
• Est. completion date: October 2026
• Est. primary completion date: October 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 79 Years

Eligibility

Inclusion Criteria:

• 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.

Exclusion Criteria:

• Subjects without ACLF.
• Subjects with ACLF-1a or ACLF-3b (See Table 2-1 for ACLF grades) 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 (=20×109/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 [Appendix 5]), 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 COVID19, those who are less than 14 days post recovery or those who have clinical signs and symptoms consistent with COVID19 infection.

Related Conditions & MeSH terms

• Acute-On-Chronic Liver Failure
• End Stage Liver Disease
• Hepatic Insufficiency
• Liver Failure

Intervention

Biological:
• SMT + PE-A 5%
Plasma exchange treatment (PE-A 5%) will be performed using 5% albumin solution (Albutein 5%). Fresh frozen plasma will be given to prevent coagulopathy. IVIGs will be administered intravenously to prevent the development of hypogammaglobulinemia and infection.

Other:
• Standard Medical Treatment
Standard medical treatment according to the institution's standard practice

Locations

Country	Name	City	State
Austria	Medical University of Vienna	Vienna
Belgium	Université libre de Bruxelles	Bruxelles
Belgium	UZ Leuven - Campus Gasthuisberg	Leuven
Denmark	Rigshospitalet	Copenhagen
France	Hôpital Beaujon	Clichy
France	Centre Hépato-Biliaire - Hôpital Universitaire Paul Brousse	Villejuif
Germany	Universitätsklinikum Bonn	Bonn
Germany	Universitätsklinikum Frankfurt	Frankfurt
Germany	Hannover Medical School	Hannover
Germany	Universitaetsklinikum Leipzig	Leipzig
Germany	Klinikum der Universitaet Muenchen	Muenchen
Germany	Klinikum der Universitaet Muenchen	München
Italy	ASST Papa Giovanni XXIII	Bergamo
Italy	Milano Hospital Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico	Milan
Italy	ASST Grande Ospedale Metropolitano Niguarda	Milano
Italy	Azienda Ospedaliera di Padova	Padova
Italy	Azienda Ospedaliero-Universitaria Policlinico Umberto I	Roma
Portugal	Centro Hospitalar Lisboa Norte	Lisboa
Portugal	Centro Hospitalar do Porto	Porto
Spain	Hospital Clínic de Barcelona	Barcelona
Spain	Hospital Universitario del Valle Hebron	Barcelona
Spain	Hospital General Gregorio Marañón	Madrid
Spain	Hospital Universitario Ramón y Cajal	Madrid
United Kingdom	King's College Hospital NHS Foundation Trust	London
United Kingdom	Royal Free NHS Foundation Trust Hospital	London
United Kingdom	Nottingham University Hospital	Nottingham
United States	University of New Mexico	Albuquerque	New Mexico
United States	Emory University	Atlanta	Georgia
United States	University of Alabama at Birmingham (UAB) Hospital	Birmingham	Alabama
United States	Ohio State University Wexner Medical Center	Columbus	Ohio
United States	Southern California Research Center	Coronado	California
United States	University of Kansas	Kansas City	Kansas
United States	Cedars-Sinai Medical Center	Los Angeles	California
United States	Aurora Health Care, Inc.	Milwaukee	Wisconsin
United States	Rutgers-New Jersey Medical School	Newark	New Jersey
United States	University of Pennsylvania	Philadelphia	Pennsylvania
United States	Mayo Clinic Phoenix	Phoenix	Arizona
United States	University of Pittsburgh Medical Center	Pittsburgh	Pennsylvania
United States	McGuire VA Medical Center	Richmond	Virginia
United States	Mayo Clinic Rochester	Rochester	New York
United States	University of Washington Medical Center	Seattle	Washington

Sponsors (2)

Lead Sponsor	Collaborator
Grifols Therapeutics LLC	Instituto Grifols, S.A.

Countries where clinical trial is conducted

United States,  Austria,  Belgium,  Denmark,  France,  Germany,  Italy,  Portugal,  Spain,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to death through Day 90	Time to death through Day 90 after randomization of SMT+PE-A 5% versus SMT alone	Day 1 to Day 90
Secondary	Time to transplant or death through Day 90	Time to transplant or death through Day 90 after randomization of SMT+PE-A 5% versus SMT alone	Day 1 to Day 90
Secondary	Time to death through Day 28	Time to death through Day 28 after randomization of SMT+PE-A 5% versus SMT alone	Day 1 to Day 28