A Study to Evaluate the Efficacy and Safety of Concomitant Use of Eplontersen and ALXN2220 Compared With Eplontersen and Placebo for Adults Participants With ATTR-CM (ATTRiumph)
13 juli 2026 bijgewerkt door: AstraZeneca
A Phase IIb, Randomised, Double-blind, Placebo-controlled, Multicentre Study to Evaluate the Efficacy and Safety of Concomitant Use of Eplontersen and ALXN2220 Compared With Eplontersen and Placebo in Adult Participants With Transthyretin-Mediated Amyloid Cardiomyopathy (ATTR-CM)
The purpose of this randomised, double-blind, placebo-controlled, multicenter study is to evaluate the efficacy and safety of concomitant use of eplontersen and ALXN2220 compared with eplontersen and placebo in adult participants with Transthyretin-mediated amyloid cardiomyopathy (ATTR-CM).
Studie Overzicht
Toestand
Actief, niet wervend
Interventie / Behandeling
Gedetailleerde beschrijving
This is a Phase IIb, multicenter, double-blind study in 326 participants, who will be randomized to receive either eplontersen and ALXN2220 or eplontersen and placebo once every four weeks.
Participants will also receive daily supplemental doses of the recommended daily allowance of vitamin A.
Studietype
Ingrijpend
Inschrijving (Geschat)
326
Fase
- Fase 2
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Alberta
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Calgary, Alberta, Canada, T2N 4Z6
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British Columbia
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Vancouver, British Columbia, Canada, V6Z 1Y6
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Nova Scotia
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Halifax, Nova Scotia, Canada, B3H 3A7
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Ontario
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London, Ontario, Canada, N6A 5A5
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Toronto, Ontario, Canada, M5G 2C4
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Quebec
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Montreal, Quebec, Canada, H1T 1C8
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Beijing, China, 100730
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Beijing, China, 100034
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Changsha, China, 410012
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Chongqing, China, 400042
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Guangzhou, China, 510080
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Hangzhou, China, 310009
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Berlin, Duitsland, 10117
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Cologne, Duitsland, 50937
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Essen, Duitsland, 45147
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Hamburg, Duitsland, 22767
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Heidelberg, Duitsland, 69120
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Homburg, Duitsland, 66421
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München, Duitsland, 81377
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Münster, Duitsland, 48149
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Créteil, Frankrijk, 94010
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Marseille, Frankrijk, 13005
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Rennes, Frankrijk, 35033
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Toulouse, Frankrijk, 31059
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Bologna, Italië, 40138
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Florence, Italië, 50134
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Milan, Italië, 20138
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Padova, Italië, 35128
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Pavia, Italië, 27100
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Pisa, Italië, 56124
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Torino, Italië, 10154
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Torrette - Ancona, Italië, 60126
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Trieste, Italië, IT-34149
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Bunkyō City, Japan, 113-8431
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Kurume-shi, Japan, 830-0011
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Sapporo, Japan, 060-8543
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Shinjuku-ku, Japan, 160-8582
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Suita, Japan, 565-8565
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Barcelona, Spanje, 08035
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Jaén, Spanje, 23007
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L'Hospitalet de Llobregat, Spanje, 08907
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Majadahonda, Spanje, 28222
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Málaga, Spanje, 29010
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Pamplona, Spanje, 31008
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Salamanca, Spanje, 37007
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Valencia, Spanje, 46010
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London, Verenigd Koninkrijk, NW3 2QG
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London, Verenigd Koninkrijk, NW10 2PB
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California
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La Jolla, California, Verenigde Staten, 92037
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San Francisco, California, Verenigde Staten, 94115
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Stanford, California, Verenigde Staten, 94305
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Colorado
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Aurora, Colorado, Verenigde Staten, 80045
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District of Columbia
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Washington D.C., District of Columbia, Verenigde Staten, 20010
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Florida
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Jacksonville, Florida, Verenigde Staten, 32224
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Miami, Florida, Verenigde Staten, 33176
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Weston, Florida, Verenigde Staten, 33331
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Illinois
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Chicago, Illinois, Verenigde Staten, 60637
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Massachusetts
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Boston, Massachusetts, Verenigde Staten, 02115
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Missouri
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Kansas City, Missouri, Verenigde Staten, 64111
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St Louis, Missouri, Verenigde Staten, 63110
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New York
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New York, New York, Verenigde Staten, 10032
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North Carolina
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Chapel Hill, North Carolina, Verenigde Staten, 27599
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Durham, North Carolina, Verenigde Staten, 27710
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Ohio
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Cleveland, Ohio, Verenigde Staten, 44195
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Oregon
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Portland, Oregon, Verenigde Staten, 97239
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Pennsylvania
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Danville, Pennsylvania, Verenigde Staten, 17822
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Philadelphia, Pennsylvania, Verenigde Staten, 19104
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Tennessee
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Germantown, Tennessee, Verenigde Staten, 38138
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Texas
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Dallas, Texas, Verenigde Staten, 75390
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Houston, Texas, Verenigde Staten, 77030
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Utah
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Salt Lake City, Utah, Verenigde Staten, 84132
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Virginia
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Falls Church, Virginia, Verenigde Staten, 22042
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Gothenburg, Zweden, 413 45
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Lund, Zweden, 22242
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Stockholm, Zweden, 171 64
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Uppsala, Zweden, 751 85
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Capable of giving informed consent.
Inclusion Criteria:
- Participant must be ≥ 18 years to ≤ 85 years at the time of signing the informed consent.
Participants who have a diagnosis of ATTR-CM with either wild-type or variant TTR genotype based on 1 of the following:
- Endomyocardial biopsy with confirmatory TTR amyloid typing OR
- Grade 2 or 3 cardiac uptake on 99mTc scintigraphy in the absence of monoclonal gammopathy OR
- Grade 2 or 3 cardiac uptake on 99mTc scintigraphy AND confirmatory TTR amyloid typing in the presence of monoclonal gammopathy.
- NYHA Class I to III at Screening and life expectancy of ≥ 1 year as per the Investigator's judgement.
- End-diastolic IVST ≥ 12 mm on echocardiography.
- NT-proBNP ≥ 600pg/mL for participants without ongoing atrial fibrillation/flutter at Screening or NT-proBNP ≥ 1200pg/mL for participants with ongoing atrial fibrillation/flutter at Screening.
Able to complete symptom-limited maximal CPET at Screening based on the following test criteria:
- Able to exercise to near exhaustion during CPET as exhibited by RER ≥ 1.0 during symptom-limited CPET conducted during screening.
- If participant does not achieve RER ≥1.0, the CPET may be repeated once, at least 48 hours but less than 2 weeks (but before randomization) after the initial test.
- Treated according to locally recognised guidelines on standard-of-care treatment for patients with HF. Therapy should have been individually optimised and stable for ≥ 4 weeks (except diuretics) and include, unless contraindicated or not tolerated, treatment of high BP (targeting SBP < 130 mmHg as suggested in 2022 American College of Cardiology/American Heart Association/Heart Failure Society of America HF guidelines), and ischaemic heart disease.
- Willingness to adhere to daily self-administered vitamin A supplementation (3000 IU).
Exclusion Criteria:
- Known leptomeningeal amyloidosis.
- Known light chain (AL) or secondary (amyloid A) amyloidosis, or any other form of systemic amyloidosis.
- Cardiomyopathy not primarily caused by ATTR-CM, for example, cardiomyopathy primarily due to hypertension, valvular heart disease, or ischaemic heart disease per Investigator's assessment.
- Acute coronary syndrome, unstable angina, stroke, transient ischaemic attack, coronary revascularisation, cardiac device implantation, cardiac valve repair, or major surgery within 12 weeks of Screening.
- Uncontrolled hypertension (average resting SBP > 160 mmHg or DBP > 100 mmHg at Screening).
- Average resting SBP < 90 mmHg or symptomatic orthostatic hypotension, despite appropriate treatment, at Screening per Investigator's assessment.
- Uncontrolled ventricular clinically significant cardiac arrhythmia, per Investigator's assessment.
- Left ventricular ejection fraction < 30% on echocardiography measured locally at Screening.
- Severe pulmonary impairment (SpO₂ < 92%) defined as resting SpO₂ below 92% on room air, measured by pulse oximetry, indicative of severe lung disease. Participants requiring supplemental oxygen to maintain SpO₂ ≥ 92%.
- Participants with renal failure requiring dialysis.
- History of solid organ transplantation or ventricular assist device or listing for heart transplantation at Screening. Note: prior history of planned corneal transplant is not an exclusion criterion.
- Suspected or known intolerance/allergy to proteins or any components of the study intervention.
Any of the following results conducted at screening:
i) Haemoglobin <8g/dL for women or <9g/dL for men. ii) Platelet count <125 X10*9/L or other disorder associated with clinically significant thrombocytopenia.
iii) ALT >2.0 X ULN iv) TBL >2.5 X ULN (participants with known Gilbert's syndrome can be included with TBL >2.5 X ULN as long as direct bilirubin is ≤ 1.5 X ULN) v) Serum retinol level < LLN vi) By CKD-EPI formula, eGFR <20 mL/min/1.73 m2 measured by the central laboratory at Screening.
- Current unstable liver or biliary disease per Investigator's assessment.
- Multiple myeloma, lymphoma, leukemia, or any malignancy or clonal stem cell disorder within the past 5 years (except basal cell or squamous epithelial carcinomas of the skin, melanoma in situ or cervical carcinoma in situ that have been curatively resected, Stage I cancer in remission, or adequately treated prostate cancer stage I, IIA, or IIB with Gleason score ≤ 3+4 and prostate-specific antigen < 20 ng/mL).
- Any prior treatment with an ATTR amyloid depleter or a TTR gene silencing agent approved or in clinical development.
- Participated in a structured exercise training programme within the 1 month prior to Screening or planned to start during the trial.
- Participation in another investigational clinical study or intake of another investigational drug within 30 calendar days or 5 half-lives of the IMP, whichever is longer before signing the ICF.
- Judgement by the Investigator that the participant should not participate in the study if the participant has a known medical or psychological condition or other risk factor that might interfere with the participant's full participation in the study, pose any additional risk for the participant, or confound the assessment of the participant or outcome of the study.
- Previous enrolment or randomisation in the present study.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Eplontersen and ALXN2220
Subcutaneous eplontersen and intravenous ALXN2220 every 4 weeks
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Eplontersen delivered subcutaneously, once every 4 weeks
ALXN2220 delivered intravenously, once every 4 weeks
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Placebo-vergelijker: Eplontersen and placebo
Subcutaneous eplontersen and intravenous placebo every 4 weeks
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Eplontersen delivered subcutaneously, once every 4 weeks
Placebo delivered intravenously, once every 4 weeks
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Cardiopulmonary exercise test peak VO2
Tijdsspanne: 52 week
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Change from baseline in Cardiopulmonary exercise test peak VO2 at week 52
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52 week
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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NT-proBNP
Tijdsspanne: 52 week
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Change from baseline in NT-proBNP at week 52
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52 week
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Kansas City Cardiomyopathy Questionnaire-Clinical Summary Score
Tijdsspanne: 52 week
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Change from baseline in Kansas City Cardiomyopathy Questionnaire-Clinical Summary Score at week 52. The minimum score is 0 and maximum score is 100. Higher scores indicate better health status. |
52 week
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Extracellular volume
Tijdsspanne: 52 week
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Change from baseline in Extracellular volume (subgroup) at week 52
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52 week
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
11 juni 2026
Primaire voltooiing (Geschat)
6 februari 2029
Studie voltooiing (Geschat)
6 februari 2029
Studieregistratiedata
Eerst ingediend
12 mei 2026
Eerst ingediend dat voldeed aan de QC-criteria
19 mei 2026
Eerst geplaatst (Werkelijk)
27 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
14 juli 2026
Laatste update ingediend die voldeed aan QC-criteria
13 juli 2026
Laatst geverifieerd
1 juli 2026
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- D8456C00001
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
JA
Beschrijving IPD-plan
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.
IPD-tijdsbestek voor delen
AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles.
For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
IPD-toegangscriteria voor delen
When a request has been approved AstraZeneca will provide access to the de-identified individual patient-level data in an approved sponsored tool .
Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.
Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access.
For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Ja
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .