Study on the Effects of Pegozafermin and Simvastatin for Patients with Severe High Triglycerides

3 1 1

What is this study about?

This clinical trial is focused on studying a condition known as Severe Hypertriglyceridemia, which is characterized by very high levels of triglycerides in the blood. The study will evaluate a treatment called Pegozafermin, which is a solution for injection. Pegozafermin is also known by its code name BIO89-100. The purpose of the study is to determine how Pegozafermin affects triglyceride levels in people with Severe Hypertriglyceridemia after 26 weeks of treatment. Participants in the study will receive either Pegozafermin or a placebo, which is a substance with no active medication.

In addition to Pegozafermin, the study involves the use of Simvastatin, a medication commonly used to lower cholesterol levels. Simvastatin will be provided in the form of film-coated tablets. Participants will continue their usual lipid-modifying therapy, which helps manage cholesterol levels, throughout the study. The study will last for a total of 52 weeks, with the main focus on changes in triglyceride levels at the 26-week mark.

Throughout the study, participants will have regular check-ups to monitor their health and the effects of the treatment. The study will also look at changes in other cholesterol levels, such as non-high-density lipoprotein cholesterol (non-HDL-C) and high-density lipoprotein cholesterol (HDL-C), as well as liver fat content using MRI scans. The goal is to gather information on the safety and effectiveness of Pegozafermin in managing Severe Hypertriglyceridemia.

1 initial visit

Upon joining the study, an initial visit is scheduled. During this visit, eligibility is confirmed based on specific criteria, such as age and current health status.

Participants are informed about the need to maintain stable medication, eating, and exercise habits throughout the study.

2 medication stabilization period

A period is designated for stabilizing medication and lifestyle. This involves maintaining consistent habits related to medication, diet, and exercise.

3 treatment phase

Participants receive the study medication, pegozafermin, administered as a solution for injection under the skin (subcutaneous use).

The treatment lasts for 26 weeks, during which the effect on fasting serum triglyceride levels is monitored.

4 additional medication

Participants may also be on a stable background of simvastatin, taken orally as a 10 mg film-coated tablet, to manage cholesterol levels.

5 monitoring and assessments

Regular assessments are conducted to monitor changes in triglyceride levels and other cholesterol-related measures.

These assessments occur at specified intervals, including at week 26 and week 52.

6 end of treatment evaluation

At the end of the 26-week treatment period, a final evaluation is conducted to assess the primary and secondary outcomes of the study.

This includes measuring changes in triglyceride levels and other health indicators.

Who Can Join the Study?

  • Must be at least 22 years old.
  • Must be willing to maintain stable medication, eating, and exercise habits during the study.
  • Must be on stable background Lipid Modifying Therapy (LMT) for at least 4 weeks before the study. This means taking medication to help manage cholesterol and fat levels in the blood.

Who Cannot Join the Study?

  • Patients with Severe Hypertriglyceridemia cannot participate. This means having very high levels of triglycerides, which are a type of fat found in your blood.
  • Patients who are not within the specified age range for the study cannot participate. The study is open to certain age groups only.
  • Patients who are part of a vulnerable population cannot participate. This includes groups of people who might need special protection or care.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Bellvitge University Hospital L'hospitalet De Llobregat Spain
Hospital Universitario De Navarra Pamplona Spain
Osteo-Medic s.c. Artur Racewicz, Jerzy Supronik Bialystok Poland
Futuremeds Łódź Lodz Poland
Multiprofile Hospital For Active Treatment Hadji Dimitar OOD Sliven Bulgaria
Futuremeds Sp. z o.o. Wroclaw Poland
Krakowskie Centrum Medyczne Sp. z o.o. Cracow Poland

Other Sites

Site Name City Country Status
Diagnostic Consultation Center XX-Sofia EOOD Sofia Bulgaria
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Mbal Lyulin EAD Sofia Bulgaria
Semmelweis University Budapest Hungary
Klinik Hietzing Vienna Austria
CHU Helora La Louviere Belgium
Instytut Centrum Zdrowia Matki Polki Lodz Poland
Dwopbprhxttebkkyconqtbi cqfqhq “rrvycrvhapzffjs Erhy Sofia Bulgaria
Fquiqdbf ngbxvwifr Mxocc a Hkiyzoz Prague Czechia
Axsbcmnrwd Pkecgwtg Hkuxizln Df Mgiszprgd Marseille France
Heahhnic Cjsvnx Dc Bbygpnalk Barcelona Spain
Mfmryrs Utsdkkzasy Or Guon Graz Austria
Vlywhnlgy Frincnho Nqgemfqqe V Pqbnr Prague Czechia
Uwvdldjvwtqk Lqvwfaq Leipzig Germany
Hhkuhswx Dr Lq Siqfs Cjdc I Srie Ppq Barcelona Spain
Usqlkjdfvt Ol Alvbwpu Edegem Belgium
Uqvbjnvyknixhkmtstfik Eszng Awv Essen Germany
Ijhquuwrs Fqq Clypmyqx Aoo Edpssnpafkhh Muptqnwc Prague Czechia
Ukvijudffytq Zfwqgmkyds Gmka Gent Belgium
Hgarxhiw Uswqctzyctqns 1v Dl Onkoxiy Madrid Spain
Cwante Hsbdizjxdzo Uyavigmjixjyl Dxxpie Goyvaie Sgglcoonwvaeehlaqaiskbjlns Namur Belgium
Hirsbyjm Uhtesavcebwkl Vxuyyv Df Lah Ncxkcq Granada Spain
Egehmj swfsiw Nachod Czechia
Piytm Slusklzo Czgbpkrk Uorkiclfnz Hiezzkka Riga Latvia
Dhgdcvxctd Cjmigegrltok Chypyf Amxhbuscu Owg Sofia Bulgaria
Eieedcmlhrg Csehti Oza Sofia Bulgaria
Rcrgd Azmvxjrf kgkvakoq uxcprrxqvnetg selpgipy Skj Riga Latvia
Mwrswxygbcqj Rfwsgdye Hknmneos Fnc Afveqp Tljmpeaff Doe Sdwabw Cgvifuoyd Ah Veliko Tirnovo Bulgaria
Mfernmabixck Hjejnwaq Ftc Acvags Ttgyzubhd Bzzvbfocd Lfze Botevgrad Bulgaria
Febfjdxj Nfhkzwdhk U Ss Apjk V Bmwp Brno-Stred Czechia
Kygwwv Cqibcf Kwkdiztaf Sah z ohrz Zamosc Poland
Lmmvjqe Kzqw Baja Hungary
Prozzlzajfri Vjbysu Valenciennes France
Uyrcrqokge Mxlwfugdqtvn Hwmaveyw Fox Asidzj Tffqgzvhd Eywropuuarxz Prfmwuz Lgpv Plovdiv Bulgaria
Ecqms Dczallwzjgwwdyj Pbbhdusx Bgioqyquh Sucdioyj Ssznnq Barcelona Spain
Hqdbawcv Urggwnsluhshv Pajdgd Dhj Mtm Cadiz Spain
Kjnbuj Lxdfkknnwts Vienna Austria
Uigkmhqlap Hlglmvmwh Pfuum Ssrxqxmhgib Cojjrxf Fual Paris France
Hlkmzkqr Qxuszlldtpx Meljze Malaga Spain
Dsiqsqugyq rcdilmhvu shooinoi Sme Daugavpils Latvia
Dmt Klut Balatonfured Hungary
Djhvawmsdi Mulnjoo Czjfpv 2dxs Lghv Dimitrovgrad Bulgaria

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

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
18.09.2023
Belgium Belgium
Not recruiting
18.09.2023
Bulgaria Bulgaria
Not recruiting
18.09.2023
Czechia Czechia
Not recruiting
18.09.2023
France France
Not recruiting
18.09.2023
Germany Germany
Not recruiting
18.09.2023
Hungary Hungary
Not recruiting
18.09.2023
Italy Italy
Not recruiting
18.09.2023
Latvia Latvia
Not recruiting
18.09.2023
Poland Poland
Not recruiting
18.09.2023
Spain Spain
Not recruiting
18.09.2023

Trial locations

Investigated Drugs:

Pegozafermin is a medication being studied for its potential to help people with a condition called Severe Hypertriglyceridemia, which means having very high levels of triglycerides in the blood. Triglycerides are a type of fat, and having too much of them can increase the risk of heart disease and other health problems. Pegozafermin is designed to lower these triglyceride levels, which might help reduce these risks. In this clinical trial, researchers are looking at how well pegozafermin works and how safe it is for people to use over a period of 26 weeks.

Investigated Diseases:

Severe Hypertriglyceridemia – Severe Hypertriglyceridemia is a condition characterized by extremely high levels of triglycerides in the blood. Triglycerides are a type of fat that circulates in the bloodstream, and when their levels become excessively high, it can lead to various health issues. The condition often progresses with the accumulation of fat in the liver and other tissues, which can cause inflammation and damage. Over time, severe hypertriglyceridemia can contribute to the development of pancreatitis, a painful inflammation of the pancreas. It may also be associated with other metabolic disorders, such as insulin resistance and obesity. The progression of the disease can be influenced by genetic factors, lifestyle, and dietary habits.

Trial ID:
2023-503576-25-00
Protocol code:
BIO89-100-231
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • Study of Plozasiran to prevent acute pancreatitis in adults with severe hypertriglyceridemia

    Recruiting

    3 1
    Austria Belgium Bulgaria Croatia Czechia Hungary +6
  • Long-Term Safety Study of Plozasiran for Adults with High Triglycerides

    Recruiting

    3 1 1
    Investigated Diseases:
    Belgium Bulgaria Croatia Czechia France Germany +8