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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05852431
Other study ID # BIO89-100-231
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date June 15, 2023
Est. completion date September 2026

Study information

Verified date April 2024
Source 89bio, Inc.
Contact ENTRUST clinical trial
Phone 415.432.9270
Email entrustinfo@89bio.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine the effect of Pegozafermin on fasting serum triglyceride levels in subjects with Severe Hypertriglyceridemia (TG ≥500 to ≤2000 mg/dL) after 26 weeks of treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 360
Est. completion date September 2026
Est. primary completion date August 2025
Accepts healthy volunteers No
Gender All
Age group 22 Years and older
Eligibility Inclusion Criteria: - Age =22 years - Willing to enter a medication/lifestyle stabilization period during the screening period, which means maintaining those stable medication, eating, and exercise habits for the duration of the study - Subjects should be on stable background Lipid Modifying Therapy (LMT) to manage ASCVD for a minimum of 4 weeks prior to first qualifying TG Exclusion Criteria: - Positive for hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV) - Uncontrolled or newly diagnosed (=3 months since diagnosis) Type 2 diabetes mellitus as determined by the Principal Investigator. Subjects must have HbA1c level =9.5% at Screening. Medications for glucose management must be stable for at least 4 weeks prior to Screening - Type 1 diabetes mellitus - A history of symptomatic gallstone disease, gallstone pancreatitis (unless treated with cholecystectomy), or any other ongoing symptomatic biliary disease - Acute pancreatitis within 6 months prior to Screening - Subjects with chronic pancreatitis - Known or suspected familial chylomicronemia syndrome (FCS) (Type 1 hyperlipoproteinemia) Other inclusion and exclusion criteria may apply.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Pegozafermin
Subcutaneous injection
Placebo
Subcutaneous injection

Locations

Country Name City State
Argentina 89bio Clinical Study Site Buenos Aires
Argentina 89bio Clinical Study Site Buenos Aires
Argentina 89bio Clinical Study Site Buenos Aires
Argentina 89bio Clinical Study Site Córdoba
Argentina 89bio Clinical Study Site Córdoba
Argentina 89bio Clinical Study Site Rosario Santa Fe
Argentina 89bio Clinical Study Site San Miguel De Tucumán
Austria 89bio Clinical Study Site Graz
Austria 89bio Clinical Trial Site Vienna
Austria 89bio Clinical Trial Site Wien
Belgium 89bio Clinical Study Site Gent
Belgium 89bio Clinical Study Site Haine-Saint-Paul
Belgium 89bio Clinical Study Site Yvoir
Bulgaria 89bio Clinical Trial Site Botevgrad
Bulgaria 89bio Clinical Study Site Dimitrovgrad
Bulgaria 89bio Clinical Trial Site Plovdiv
Bulgaria 89bio Clinical Study Site Sliven
Bulgaria 89bio Clinical Trial Site Sliven
Bulgaria 89bio Clinical Study Site Sofia
Bulgaria 89bio Clinical Study Site Sofia
Bulgaria 89bio Clinical Study Site Sofia
Bulgaria 89bio Clinical Study Site Sofia
Bulgaria 89bio Clinical Trial Site Sofia
Bulgaria 89bio Clinical Study Site Veliko Tarnovo
Bulgaria 89bio Clinical Trial Site Veliko Tarnovo
Canada 89bio Clinical Study Site Brampton Ontario
Canada 89bio Clinical Study Site Chicoutimi Quebec
Canada 89bio Clinical Study Site Laval Quebec
Canada 89bio Clinical Study Site Montréal Quebec
Canada 89bio Clinical Study Site North Vancouver British Columbia
Chile 89bio Clinical Study Site Concepcion
Chile 89bio Clinical Study Site Santiago
Chile 89bio Clinical Study Site Santiago
Chile 89bio Clinical Study Site Viña Del Mar
Czechia 89bio Clinical Study Site Brno
Czechia 89bio Clinical Study Site Brno
Czechia 89bio Clinical Study Site Praha
Czechia 89bio Clinical Study Site Praha
Czechia 89bio Clinical Study Site Praha
France 89bio Clinical Study Site Marseille
France 89bio Clinical Study Site Paris
France 89bio Clinical Study Site Valenciennes
Georgia 89bio Clinical Study Site Batumi
Georgia 89bio Clinical Trial Site Kutaisi
Georgia 89bio Clinical Study Site Tbilisi
Georgia 89bio Clinical Study Site Tbilisi
Georgia 89bio Clinical Study Site Tbilisi
Georgia 89bio Clinical Trial Site Tbilisi
Germany 89bio Clinical Study Site Leipzig
Hungary 89bio Clinical Trial Site Balatonfüred
Hungary 89bio Clinical Trial Site Budapest
Hungary 89bio Clinical Trial Site Puspokladany
Latvia 89bio Clinical Study Site Daugavpils
Latvia 89bio Clinical Trial Site Riga
Latvia 89bio Clinical Study Site Zemgale
Poland 89bio Clinical Study Site Kraków
Poland 89bio Clinical Study Site Lódz
Poland 89bio Clinical Study Site Lódz
Poland 89bio Clinical Study Site Lublin
Poland 89bio Clinical Study Site Warszawa
Puerto Rico 89Bio Clinical Study Site San Juan
Spain 89bio Clinical Study Site Barcelona
Spain 89bio Clinical Study Site Cadiz
Spain 89bio Clinical Study Site Cordoba
Spain 89bio Clinical Study Site Granada
Spain 89bio Clinical Study Site Huelva
Spain 89bio Clinical Study Site Madrid
Spain 89bio Clinical Study Site Málaga
Spain 89bio Clinical Study Site Pamplona
United Kingdom 89bio Clinical Study Site Cardiff
United Kingdom 89bio Clincal Study Site London
United States 89bio Clinical Study Site Amarillo Texas
United States 89bio Clinical Study Site Atlanta Georgia
United States 89 Clinical Study Site Austin Texas
United States 89bio Clinical Study Site Bridgeport Connecticut
United States 89Bio Clinical Study Site Burke Virginia
United States 89bio Clinical Study Site Chandler Arizona
United States 89bio Clinical Study Site Charleston South Carolina
United States 89Bio Clinical Study Site Chattanooga Tennessee
United States 89Bio Clinical Study Site Chicago Illinois
United States 89bio Clinical Study Site Cincinnati Ohio
United States 89bio Clinical Trial Site Clarksville Tennessee
United States 89Bio Clinical Study Site Clearwater Florida
United States 89bio Clinical Study Site Clearwater Florida
United States 89Bio Clinical Study Site Columbus Georgia
United States 89bio Clinical Trial Site Columbus Ohio
United States 89bio Clinical Study Site Conway Arkansas
United States 89bio Clinical Study Site Dallas Texas
United States 89bio Clinical Study Site East Syracuse New York
United States 89Bio Clinical Study Site Eugene Oregon
United States 89bio Clinical Study Site Graham Texas
United States 89bio Clinical Study Site Hialeah Gardens Florida
United States 89Bio Clinical Study Site Homestead Florida
United States 89bio Clinical Study Site Houston Texas
United States 89bio Clinical Trial Site Huntington Park California
United States 89bio Clinical Study Site Jonesboro Arkansas
United States 89bio Clinical Trial Site Kansas City Missouri
United States 89bio Clinical Study Site Kissimmee Florida
United States 89Bio Clinical Study Site Lampasas Texas
United States 89bio Clinical Study Site Las Vegas Nevada
United States 89Bio Clinical Study Site Lawrenceville Georgia
United States 89bio Clinical Study Site Little Rock Arkansas
United States 89Bio Clinical Study Site Long Beach California
United States 89bio Clinical Study Site Los Angeles California
United States 89Bio Clinical Study Site Marrero Louisiana
United States 89Bio Clinical Study Site Miami Lakes Florida
United States 89bio Clinical Study Site Middleburg Heights Ohio
United States 89Bio Clinical Study Site Morganton North Carolina
United States 89bio Clinical Trial Site New Windsor New York
United States 89bio Clinical Trial Site New York New York
United States 89Bio Clinical Study Site North Massapequa New York
United States 89bio Clinical Trial Site Northridge California
United States 89Bio Clinical Study Site Orlando Florida
United States 89Bio Clinical Study Site Oviedo Florida
United States 89Bio Clinical Study Site Oxon Hill Maryland
United States 89bio Clinical Study Site Panama City Florida
United States 89bio Clinical Trial Site Panorama City California
United States 89bio Clinical Study Site Peoria Arizona
United States 89bio Clinical Trial Site Port Orange Florida
United States 89bio Clinical Trial Site Richmond Virginia
United States 89bio Clinical Trial Site Richmond Hill New York
United States 89bio Clinical Study Site Saint Louis Missouri
United States 89bio Clinical Trial Site Salt Lake City Utah
United States 89bio Clinical Study Site San Antonio Texas
United States 89bio Clinical Trial Site San Antonio Texas
United States 89bio Clinical Study Site Santa Ana California
United States 89bio Clinical Trial Site Santa Ana California
United States 89bio Clinical Trial Site Shreveport Louisiana
United States 89bio Clinical Study Sites Sparta New Jersey
United States 89bio Clinical Trial Site Syracuse New York
United States 89Bio Clinical Study Site Tampa Florida
United States 89bio Clinical Study Site Thousand Oaks California
United States 89Bio Clinical Study Site Tucson Arizona
United States 89bio Clinical Study Site Tullahoma Tennessee
United States 89Bio Clinical Study Site Tustin California
United States 89bio Clinical Study Site West Des Moines Iowa
United States 89bio Clinical Study Site Wheat Ridge Colorado
United States 89bio Clinical Trial Site Wheat Ridge Colorado
United States 89Bio Clinical Study Site Wichita Kansas
United States 89bio Clinical Study Site Wichita Falls Texas

Sponsors (1)

Lead Sponsor Collaborator
89bio, Inc.

Countries where clinical trial is conducted

United States,  Argentina,  Austria,  Belgium,  Bulgaria,  Canada,  Chile,  Czechia,  France,  Georgia,  Germany,  Hungary,  Latvia,  Poland,  Puerto Rico,  Spain,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent change from baseline in fasting TG 26 weeks
Secondary Percent change from baseline in non-high-density lipoprotein cholesterol (non-HDL-C) 26 weeks
Secondary Percent change from baseline in high-density lipoprotein cholesterol (HDL-C) 26 weeks
Secondary Percent change from baseline in very low-density lipoprotein cholesterol (VLDL-C) 26 weeks
Secondary Percent change from baseline in total cholesterol (TC) 26 weeks
Secondary Change from baseline in liver fat by magnetic resonance imaging - whole liver proton density fat fraction (MRI-PDFF) 26 weeks
Secondary Percent change from baseline in apolipoprotein B (apo-B) 26 weeks
Secondary Change in HbA1c at Week 26 for those with baseline =7.0% 26 weeks
Secondary Percent change from baseline in fasting TG 52 weeks
See also
  Status Clinical Trial Phase
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Completed NCT04541186 - Study to Explore the Efficacy and Safety of BIO89-100 in Subjects With Severe Hypertriglyceridemia Phase 2
Recruiting NCT05079919 - A Study of Olezarsen (ISIS 678354) Administered to Participants With Severe Hypertriglyceridemia Phase 3
Completed NCT02189252 - An Open-Label Crossover Study to Compare the Relative Bioavailability, Efficacy and Safety of Epanova® and Lovaza® in Men and Women With a History of Pancreatitis Phase 1
Active, not recruiting NCT01229566 - Efficacy Study to Treat Subjects With Severe Hypertriglyceridemia Phase 3
Completed NCT03001817 - Study to Evaluate the Efficacy and Safety of K-877 in Adult Patients With Fasting High Triglyceride Levels and Normal Renal Function Phase 3
Completed NCT03011450 - Study to Evaluate the Efficacy and Safety of K-877 in Adult Patients With Fasting High Triglyceride Levels and Mild or Moderate Renal Impairment Phase 3
Completed NCT05355402 - A Study of Olezarsen (Formerly Known as AKCEA-APOCIII-LRx) in Adults With Hypertriglyceridemia and Atherosclerotic Cardiovascular Disease (Established or at Increased Risk for), and/or With Severe Hypertriglyceridemia Phase 2
Completed NCT04720534 - Study to Evaluate ARO-APOC3 in Adults With Severe Hypertriglyceridemia Phase 2
Recruiting NCT06347003 - Study of Plozasiran (ARO-APOC3) in Adults With Severe Hypertriglyceridemia Phase 3
Recruiting NCT06347016 - Study of Plozasiran in Adults With Severe Hypertriglyceridemia Phase 3
Withdrawn NCT04662528 - Safety and Efficacy of MAT9001(Omega-3-pentaenoic Acid) in Subjects With Triglycerides ≥500 mg/dL and <2000 mg/dL Phase 3
Completed NCT01242527 - Epanova® for Lowering Very High Triglycerides Phase 2/Phase 3
Completed NCT02944383 - A 12-Week Study to Assess the Efficacy Safety and Tolerability of Gemcabene in Subjects With Severe Hypertriglyceridemia Phase 2
Recruiting NCT05681351 - A Study of Olezarsen (ISIS 678354) Administered Subcutaneously to Participants With Severe Hypertriglyceridemia (SHTG) Phase 3
Recruiting NCT05552326 - A Study of Olezarsen Administered Subcutaneously to Participants With Severe Hypertriglyceridemia Phase 3
Withdrawn NCT01997268 - The Efficacy of EPA+DHA (SC401B) for Lowering Triglyceride Levels (≥ 500 mg/dL) Phase 3