Study on the Effectiveness and Safety of ALXN2220 for Adults with Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

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What is this study about?

This clinical trial is focused on studying a condition known as Transthyretin Amyloid Cardiomyopathy (ATTR-CM). ATTR-CM is a heart disease caused by the buildup of abnormal proteins called amyloids in the heart tissue, which can lead to heart failure. The study is testing a new treatment called ALXN2220, which is a type of medication known as a monoclonal antibody. Monoclonal antibodies are proteins made in a lab that can bind to specific substances in the body, in this case, the amyloid proteins, to help remove them.

The purpose of this study is to evaluate the effectiveness and safety of ALXN2220 in adults with ATTR-CM. Participants in the study will receive either the ALXN2220 treatment or a placebo, which is a substance with no active medication. The study will be conducted over a period of time, during which participants will receive regular injections of the treatment or placebo. Throughout the study, participants will be monitored for any changes in their heart condition and overall health.

The study aims to determine if ALXN2220 can help reduce the symptoms and progression of ATTR-CM by comparing the health outcomes of those receiving the treatment to those receiving the placebo. Participants will undergo various health assessments, including heart function tests and physical examinations, to track their progress. The study will provide valuable information on whether ALXN2220 is a safe and effective treatment option for people with ATTR-CM.

1 randomization

Upon joining the study, participants are randomly assigned to receive either the ALXN2220 medication or a placebo. This process is double-blind, meaning neither the participant nor the study team knows which treatment is being administered.

2 treatment administration

Participants receive the assigned treatment as a solution for infusion. The specific dosage and frequency are determined by the study protocol and are administered under medical supervision.

3 blinded treatment period

During this period, the effectiveness and safety of ALXN2220 are evaluated. Participants continue to receive their assigned treatment and undergo regular assessments to monitor their health and any potential side effects.

4 primary endpoint evaluation

The main goal is to assess the difference in the occurrence of cardiovascular events and overall health status between the ALXN2220 and placebo groups. This includes monitoring for any adverse events and changes in health indicators.

5 secondary endpoint evaluation

Additional outcomes are measured, such as changes in physical function and quality of life over a 24-month period, as well as the incidence of any treatment-related adverse effects.

6 study completion

The study is expected to conclude by October 31, 2028. Participants will have contributed valuable data to assess the potential benefits and risks of ALXN2220 for treating transthyretin amyloid cardiomyopathy.

Who Can Join the Study?

  • Must be a male or female aged between 18 and 90 years old.
  • If using a treatment for ATTR amyloidosis, the dose must be stable for at least 90 days before the study starts.
  • Participants must use contraception according to local rules. Women must not be pregnant or breastfeeding and should use effective birth control if they can have children. Men must agree to use contraception and not donate sperm.
  • Must have a confirmed diagnosis of ATTR-CM (a type of heart condition) with specific tests showing heart involvement.
  • The thickness of the heart’s septal wall must be 12 mm or more, as measured by an ultrasound of the heart.
  • Must have a NT-proBNP level greater than 2000 pg/mL, which is a blood test that helps assess heart function.
  • Must have been treated with a loop diuretic (a type of medication that helps remove excess fluid) for at least 30 days before the study.
  • Must have a history of heart failure, shown by events like hospitalization for heart failure, urgent visits for heart failure, or episodes of fluid overload.
  • Must be classified as NYHA Class II-IV, which describes the severity of heart failure symptoms.
  • Must have a life expectancy of at least 6 months, as judged by the study doctor.

Who Cannot Join the Study?

  • Patients who are not adults cannot participate.
  • Patients who do not have Transthyretin Amyloid Cardiomyopathy (ATTR-CM) cannot participate. ATTR-CM is a condition where a protein called transthyretin builds up in the heart, affecting its function.
  • Patients who are part of a vulnerable population, such as those who cannot make decisions for themselves, cannot participate.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Medical University Of Vienna Vienna Austria
Hospital Universitario De Salamanca Salamanca Spain
Medical University Of Graz Graz Austria
Medizinische Universitaet Innsbruck Innsbruck Austria
Azienda Ospedaliero Universitaria Careggi Florence Italy
Oncopole Claudius Regaud Toulouse France
Oslo Universitetssykehus HF Oslo Norway
Medizinische Hochschule Hannover Hanover Germany
Bellvitge University Hospital L'hospitalet De Llobregat Spain
Hospital Universitario De Navarra Pamplona Spain
Université Libre de Bruxelles – Hôpital Erasme Brussels Belgium
Centre Hospitalier Universitaire De Bordeaux Bordeaux France

Other Sites

Site Name City Country Status
Karolinska University Hospital Solna Sweden
Centre Hospitalier Universitaire De Nantes Nantes France
Hopital Beaujon Clichy France
Klinikum Wels-Grieskirchen GmbH Wels Austria
Universitätsklinikum des Saarlandes – Homburg/Saar, Klinik für Urologie und Kinderurologie Homburg Germany
Az St-Jan Brugge-Oostende A.V. Brugge Belgium
Hospital Son Llatzer Palma Spain
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
A.O.U. Policlinico G. Martino Di Messina Messina Italy
Annmlst Oolpbqdpqjd dc Pzpnns Padua Italy
Hdcjlsat Vdab dhlcvfxt Barcelona Spain
Hcpnqrbe Ukyelwjbvflhx dg A Culxbz A Coruna Galicia Spain
Unzrqxbryf Hoidjann Cjyluuj Cologne Germany
Oyvfpd Uswnisrfgx Hszffwcg Odense Denmark
Fbkvewjlvk Iywsx Co Gbxxvx Otkikszf Mlqjdjck Pzxwxgzlszy Milan Italy
Fouihoolrt Idcbx Psjwiiddlng Srs Mjmejq Pavia Italy
Axaqxcxxlm Pkvmpspa Hxnyfsub Do Mxbbrkycq Marseille France
Rjuchq Saluz Sagsks Ugdwfkozsxamvbwhljo Lund Sweden
Uuheuycihzgm Mzcqqes Cthwgip Uinxvzb Utrecht The Netherlands
Aongjsplq Hwwcfzpx Athens Greece
Awqhrndy Unmjpotxtw Hnpusxwy Lorenskog Norway
Cdhsmvs Uthknlcgovmsgtxtkkft Bqkdfr Kuu Berlin Germany
Emhnhsr Uebvvjjzrsbn Meumnds Cmwulgt Rtqlbcarx (fvphixo Mql Rotterdam The Netherlands
Cpkyzi Hfjfvmnvrqo Rpghvhar Uripdbehuqhlg Dd Tupdw Tours France
Ugiebgevsu Cfwkuotj Hvojbcnd Vxjjth Db Ln Azcfycwf Murcia Spain
Cusdlr Hznetyzzado Uhagdtczxhxhd De Mancszhzdeb Montpellier France
Ujmgkaytgzxg Dt Smvunwgr Dq Ccjbpvpwzl Santiago De Compostela Spain
Uxqlxozgssbxbllpvxsov Mpvhrdig Agh Munster Germany
Alumbqq Ovanwldsvwy Udhomuxiexpwm Fsyizvwv Iq Dy Nvlquw Naples Italy
Udpglkvtxlzqtvxiiicxb Hekncjheru Apj Heidelberg Germany
Jvdsrzsaijlilwcmuhsogqlevt Gqafaet Giessen Germany
Kogoxruu ddo Ulxgtztmlemb Meylorgx Afa Munich Germany
Uvvziumuhcewjejlkvhnt Wwhttlwnc Arq Wuerzburg Germany
Vivhsouou Frfkgcbz Nvnzrpgxs V Pifsv Prague Czechia
Uvgvyoeyso Hgyhchof Mhsgiswehi Maastricht The Netherlands
Uyttmpzwoaen Lelhrtu Leipzig Germany
Cdimsx Hvuawefgnhw Urusabjlzieza Db Rsvbib Rennes France
Rktutirhhshcdk Copenhagen Denmark
Acxozlh Ulnrc Seuslwicw Lgvzgz Dp Bfrthjx Bologna Italy
Ulkbqhwuqhlxud Cgvajvh Kgfdacmat Gdansk Poland
Udfcggfmkihdwugtihsgn Emfct Afv Essen Germany
Iltajrbmi Fdc Ccqhkpcc Ahm Eyabushtcvtj Mjoeqkxs Prague Czechia
Umnnumzdxxwu Mjzapxh Cvjixgr Gloesdecv Groningen The Netherlands
Unqfblimvuzuwxqmqpvyy Swiadccocnonsycvwo Aqv Kiel Germany
Cntrkj Hoqlvifqkga Lkjo Sfs Pierre Benite France
Hvyxpfoe Uaphhjhvunmke Pqhsyn Ds Hrbhkv Dn Mwxtaypihsi Majadahonda Spain
Uxlcgjdgxjchhgwxd Dbqsx Sfgxp Du Fvpihjm Ferrara Italy
Qzeha Smcfkf Ctjjkkgfl Hdrzuecn &pwbuaa Serdienxgcc Uwsveffuxt Hicoibwu &kxuaig Vzonfnp Gkguxxsxohpohncbkd Gothenburg Sweden
Srbmd Wxzx Wbxpbk Gvpbgogtlxooelunkg Vienna Austria
Hxtqwlwc Ueihfyfdievik Vqkdhk Dm Lx Vnhmwxty Malaga Spain
Aqgxfqy Sqmfkizcs Uethctgkyybex Grwkkafu Ihuxtwzj Trieste Italy
Aqlrjd Upwtbjtgcd Hmnffjfo Aarhus Denmark
Oijapuvk Sdk Ghcsndbw Bvkbh Turin Italy
Forfbhhw Nbykswehj U Ss Ajvv V Bqfj Brno-Stred Czechia
Zjfblerlid Otyc Lvvhiww Genk Belgium
Hxktz Msacl Od Rglkcmp Hx Aalesund Norway
Afqxgpx Onwzmwozxvqrjuswbmnmioxjs Sdig Aixbn Rome Italy
Fuuecsmnkd Tbkvpqg Gmebrrqi Maxspxneaa Pisa Italy
Cjffty Hcnepserrdn Uytlsvisynwfj Da Pdmomanq Poitiers France
Rqfzqd Vntxednoknyho Umea Sweden
Szu Ogdmy Howloagx Hy Trondheim Norway
Hldvtphr Uziwxrwprcrjw Dq Jawg Jaen Spain
Hqta Mxp Gdqx Hamburg Germany
Umqjymaeuoptia Colfcqc Kyizjqxdt Wqektbpcnntjc Uorkxrwotwid Mzazejxfsi Warsaw Poland
Owhnhbof Gcebwa Bxeegsre Metgrslihyrgce Pbzuunbetu Dr Fazuo Forli' Italy

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
23.04.2024
Belgium Belgium
Not recruiting
23.04.2024
Czechia Czechia
Not recruiting
23.04.2024
Denmark Denmark
Not recruiting
23.04.2024
France France
Not recruiting
23.04.2024
Germany Germany
Not recruiting
23.04.2024
Greece Greece
Not recruiting
23.04.2024
Ireland Ireland
Not recruiting
23.04.2024
Italy Italy
Not recruiting
23.04.2024
Norway Norway
Not recruiting
23.04.2024
Poland Poland
Not recruiting
23.04.2024
Spain Spain
Not recruiting
23.04.2024
Sweden Sweden
Not recruiting
23.04.2024
The Netherlands The Netherlands
Not recruiting
23.04.2024

Trial locations

Investigated Drugs:

ALXN2220 is a medication being studied for its potential to treat transthyretin amyloid cardiomyopathy (ATTR-CM). This condition involves the buildup of abnormal protein deposits in the heart, which can lead to heart problems. ALXN2220 is designed to help reduce these protein deposits, potentially improving heart function and reducing related health issues. The study aims to evaluate how effective and safe ALXN2220 is for patients with this condition.

Investigated Diseases:

Transthyretin Amyloid Cardiomyopathy (ATTR-CM) – This is a rare heart condition caused by the buildup of abnormal protein deposits called amyloid in the heart tissue. These deposits can lead to the stiffening of the heart muscle, making it difficult for the heart to pump blood effectively. Over time, this can result in symptoms such as fatigue, shortness of breath, and swelling in the legs and feet. The disease typically progresses slowly, but the accumulation of amyloid can eventually lead to more severe heart problems. ATTR-CM is often seen in older adults and can be hereditary or occur without a family history. The condition requires careful monitoring to manage its impact on heart function.

Trial ID:
2023-506669-70-00
Protocol code:
ALXN2220-ATTRCM-301
Trial Phase:
Therapeutic confirmatory (Phase III)

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