Study of Olezarsen (ISIS 678354) in Patients with Severe Hypertriglyceridemia: Testing Effects on Triglyceride Levels

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What is this study about?

This clinical trial focuses on patients with Severe Hypertriglyceridemia, a condition characterized by very high levels of triglycerides (fats) in the blood. The study will test a medication called ISIS 678354 (also known as olezarsen), which is an antisense oligonucleotide – a type of drug that can influence how genes work in the body.

The purpose of this research is to determine how well ISIS 678354 works compared to placebo in reducing triglyceride levels in the blood. During the study, participants will receive either ISIS 678354 or placebo as an injection under the skin (subcutaneous injection). The treatment will continue for approximately 12 months, with regular monitoring of blood triglyceride levels and other health parameters.

The medication will be given alongside standard lipid-lowering treatments that patients are already taking. Throughout the study, researchers will measure various factors related to blood fats, including substances called Apolipoprotein C-III and different types of cholesterol. They will also monitor patients for potential health complications and check the amount of fat in the liver.

1 Initial medical assessment

Your fasting triglyceride levels will be checked to confirm they are at least 500 mg/dL

Your current lipid-lowering medications will be reviewed – they should be stable for at least 4 weeks before starting

2 Treatment assignment

You will be randomly assigned to receive either olezarsen (ISIS 678354) or placebo

Neither you nor your doctor will know which treatment you are receiving

3 Treatment period – first 6 months

You will receive subcutaneous injections (shots under the skin)

Your triglyceride levels will be measured regularly

Key measurements will be taken at weeks 25 and 27

4 Treatment period – months 7-12

Treatment continues with regular injections

Additional measurements will include:

Triglyceride levels

Apolipoprotein C-III (a protein that affects fat processing)

Remnant cholesterol

Non-HDL cholesterol

Your liver fat content will be measured

5 Final assessment

Final measurements will be taken at week 53

Your overall response to treatment will be evaluated

Your triglyceride levels will be compared to the starting values

Who Can Join the Study?

  • Must be 18 years of age or older
  • Must have high levels of triglycerides (fats in the blood) of at least 500 mg/dL when measured after fasting
  • Must be currently taking lipid-lowering medications (medicines that help reduce fats in the blood) according to standard medical guidelines
  • Must have been on a stable dose of lipid-lowering medications for at least 4 weeks before starting the screening process
  • Both men and women can participate in the study
  • Must be willing to continue taking current lipid-lowering medications throughout the study period
  • Must be able to provide fasting blood samples (not eating or drinking anything except water for several hours before blood tests)

Who Cannot Join the Study?

  • Age below 18 years or above 75 years
  • Pregnant or breastfeeding women
  • History of acute pancreatitis (inflammation of the pancreas) within the past 6 months
  • Current use of medications that can significantly affect triglyceride levels (blood fats)
  • Uncontrolled diabetes (blood sugar levels not well managed)
  • Severe kidney disease or requiring dialysis
  • Severe liver disease
  • History of heart attack or stroke within the past 6 months
  • Active cancer or cancer treatment within the past 5 years
  • Participation in another clinical trial within the past 30 days
  • Known allergies to the study medication or its components
  • Alcohol or substance abuse within the past year
  • Mental conditions that could interfere with study compliance
  • Unstable medical conditions that could affect study results

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Technische Universitaet Dresden Dresden Germany
Oslo Universitetssykehus HF Oslo Norway
Bellvitge University Hospital L'hospitalet De Llobregat Spain
Ośrodek Badań Klinicznych “METABOLICA” lek. Robert Witek Tarnow Poland
Sydvestjysk Sygehus Esbjerg Denmark
Azienda Ospedaliera Universitaria Federico II Di Napoli Naples Italy
Centro Hospitalar Universitario Sao Joao E.P.E. Porto Portugal
Futuremeds Sp. z o.o. Wroclaw Poland
Unidade Local De Saude De Lisboa Ocidental E.P.E. Carnaxide Portugal
Hospital Universitario De Navarra Pamplona Spain
Hospitais da Universidade de Coimbra Coimbra Portugal

Other Sites

Site Name City Country Status
Ziekenhuis Gelderse Vallei Stichting Ede The Netherlands
Central Hospital Of Northern Pest Military Hospital Budapest Hungary
University Multiprofile Hospital For Active Treatment Sofiamed OOD Sofia Bulgaria
Hospital Universitario 12 De Octubre Madrid Spain
Unidade Local De Saude De Gaia/Espinho E.P.E. Vila Nova De Gaia Portugal
Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo Italy
Instytut Centrum Zdrowia Matki Polki Lodz Poland
Borbanya Praxis Egeszsegugyi Kft. Nyiregyhaza Hungary
Hospital Universitari Joan XXIII De Tarragona Tarragona Spain
Umbal – Prof. D-R Stoyan Kirkovich AD Stara Zagora Bulgaria
DRC Kft. Balatonfured Hungary
Edumed s.r.o. Nachod Czechia
Kalimat Medical Center Ltd. Sofia Bulgaria
Cardio D&R s.r.o. Kosice Kosice Slovakia
MUDr. Nina Zemkova s.r.o. Uherske Hradiste Czechia
Diamedical Medical Center 2013 Ltd. Dimitrovgrad Bulgaria
Medical Center Smolyan Clinical Research OOD Smolyan Bulgaria
Evangelisches Krankenhaus Witten gGmbH Witten Germany
Multiprofile Hospital For Active Treatment Blagoevgrad AD Blagoevgrad Bulgaria
Frederiksberg Hospital Frederiksberg Denmark
Azienda Socio Sanitaria Territoriale Nord Milano Cinisello Balsamo Italy
Army Hospital General L. Svoboda Svidnik a.s. Svidnik Slovakia
Belinus Bt. Debrecen Hungary
Fejer Varmegyei Szent Gyoergy Egyetemi Oktato Korhaz Szekesfehervar Hungary
University Of Debrecen Debrecen Hungary
Medicus Services s.r.o. Brandys Nad Labem Czechia
Medical Center Doctor Staykov EOOD Burgas Bulgaria
Human-Care s.r.o. Kosice Slovakia
Hospital Universitario Reina Sofía Cordoba Spain
Virgen del Rocío University Hospital Sevilla Spain
ASST Grande Ospedale Metropolitano Niguarda Milan Italy
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Hospital Clinic De Barcelona Barcelona Spain
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Karolinska University Hospital Solna Sweden
Stichting Radboud University Medical Center Nijmegen The Netherlands
Turku University Hospital Turku Finland
Centre Hospitalier Universitaire De Montpellier Montpellier France
Aalborg University Hospital Aalborg Denmark
Multiprofile Hospital For Active Treatment Dr. Tota Venkova AD Gabrovo Bulgaria
Centre Hospitalier Universitaire De Nantes Nantes France
Medical Center Dr. Kalchev Ltd. Sofia Bulgaria
Centro Hospitalar Do Baixo Vouga E.P.E. (CHBV E.P.E.) Aveiro Portugal
Region Midtjylland Aarhus Denmark
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Medifarma-98 Kft. Nyiregyhaza Hungary
Salvia Lekston I Madej Sp. J. Katowice Poland
Centre Hospitalier Lyon Sud Pierre Benite France
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Medical Center Teodora EOOD Ruse Bulgaria
University Hospital Ostrava Ostrava Czechia
Vychodoslovensky Ustav Srdcovych A Cievnych Chorob a.s. Kosice Slovakia
Medical Centre Nevromedics EOOD Veliko Tirnovo Bulgaria
Ruxqacilf Znfflueais Ssvmylilb Arnhem The Netherlands
Ulpgxboogz Hvlsgnmgx Prlmi Siadfbrnghw Cfnmzcx Ffkq Paris France
Npxawktrt S Pjygaosylhpq Bugafy Nufc Brezno Slovakia
Duowtyofqj Cpjcdytfsv Cmnula 1 Siqsxv Egrv Sliven Bulgaria
Sbpl Shaewws Mzvbi Owv Plovdiv Bulgaria
Slifnctt Cr sxxoei Prague Czechia
Pjzk Ttkji Hvdfbdfl Utpfwwwxuifz Sabadell Spain
Uqczajhxgx Hbtxcqkl Cvitpsp Cologne Germany
Cxllrt Hjejfjpdeic Unfohgyphmiqm Db Duezz Dijon France
Aembmihnbw Phkkbdgv Hkxsvdta De Mtbjhpglw Marseille France
Eevvvpi Uokxownnwgoq Muurcmz Cgplnyz Rsicwlrnk (rwfsguj Mrl Rotterdam The Netherlands
Ahtsra Ueohlvamyq Htyahwrm Aarhus Denmark
Azybrjble Utt Amsterdam The Netherlands
Aprkkac Ultxu Sjteyeauu Lrbged Da Bhyndky Bologna Italy
Mcmzvjgw Mboptzf Azpzvps Pleven Bulgaria
Udsgocflmg Dvohk Sqiup De Raqw Lj Skzpqbfp Rome Italy
Cak Hfylilj Khis Encs Hungary
Hxbzptoz Ulwgtiigqlufi da A Ckwbaj A Coruna Galicia Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Bulgaria Bulgaria
Not recruiting
01.08.2021
Czechia Czechia
Not recruiting
01.08.2021
Denmark Denmark
Not recruiting
01.08.2021
Finland Finland
Not recruiting
01.08.2021
France France
Not recruiting
01.08.2021
Germany Germany
Not recruiting
01.08.2021
Hungary Hungary
Not recruiting
01.08.2021
Italy Italy
Not recruiting
01.08.2021
Norway Norway
Not recruiting
01.08.2021
Poland Poland
Not recruiting
01.08.2021
Portugal Portugal
Not recruiting
01.08.2021
Slovakia Slovakia
Not recruiting
01.08.2021
Spain Spain
Not recruiting
01.08.2021
Sweden Sweden
Not recruiting
01.08.2021
The Netherlands The Netherlands
Not recruiting
01.08.2021

Trial locations

Investigated drugs:

Olezarsen (also known as ISIS 678354) is a medication being studied for treating severe hypertriglyceridemia, a condition where there are very high levels of triglycerides (fats) in the blood. This medication is given as an injection under the skin (subcutaneously) and works by helping to reduce triglyceride levels in the bloodstream. It represents a new approach to treating patients who have difficulty controlling their triglyceride levels with currently available treatments.

Investigated diseases:

Severe Hypertriglyceridemia – A metabolic disorder characterized by abnormally high levels of triglycerides (fat molecules) in the blood, specifically above 500 mg/dL. The condition develops when the body produces too many triglycerides or cannot break them down effectively. Excess triglycerides can accumulate in various organs, particularly the liver and pancreas. The condition can be inherited genetically or develop due to other health conditions. People with this disorder often have difficulty processing fats from their diet, leading to their accumulation in the bloodstream.

Trial ID:
2024-510696-38-00
Protocol code:
ISIS 678354-CS5
NCT ID:
NCT05681351
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

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  • Study of ISIS 678354 for Patients with Severe High Triglycerides

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    Belgium Bulgaria Czechia France Greece Hungary +9