- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07584967
A Study to Evaluate the Safety and Efficacy of AC01 Compared to Placebo in Participants With Chronic Heart Failure (GOAL-HF2)
11. September 2026 aktualisiert von: AnaCardio AB
Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Safety and Efficacy of 2 Dose Levels of the Oral Ghrelin Receptor Agonist AC01 Over 12 Weeks in Patients With Chronic Advanced Heart Failure With Reduced Ejection Fraction (HFrEF)
The primary purpose of the study is to evaluate the safety and efficacy of 2 doses of AC01 compared to placebo over 12 weeks in participants with chronic advanced HFrEF.
Studienübersicht
Status
Noch keine Rekrutierung
Intervention / Behandlung
Detaillierte Beschreibung
This is a randomized, double-blind, placebo-controlled, parallel-group, multicenter study designed to evaluate the safety and efficacy of the ghrelin-receptor agonist AC01 compared to placebo in participants with chronic advanced HFrEF.
Approximately 400 participants will be randomized to 1 of 3 treatment arms: 3 milligram (mg) AC01, 1 milligram (mg) AC01, or placebo twice daily for 12 weeks.
The primary objective is to evaluate the effect of AC01 compared to placebo on cardiac structure and function assessed by echocardiography.
Studientyp
Interventionell
Einschreibung (Geschätzt)
400
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Robert Edfors, MD, PhD
- Telefonnummer: +46 760 542 609
- E-Mail: studyinfo@anacardio.com
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
Key Inclusion Criteria:
- History of Chronic Heart Failure (CHF) diagnosed greater than or equal to (>=6) months before screening, and in NYHA Class II to IV at screening.
Chronic advanced HFrEF defined as:
- LVEF less than or equal to (<=) 35 percentage (%) by local reading >=6 months before screening or a record of LVEF qualitatively described as severely reduced or moderately-severely reduced >=6 months before screening, and
- LVEF <=35% at the screening echocardiography (confirmed by core lab), and
- no known LVEF greater than (>) 35% (or qualitatively described as less than moderately-severely reduced) between the 2 readings.
- Sinus rhythm or permanent, persistent, or paroxysmal atrial fibrillation flutter (AFF) (AFF at screening is capped at maximum 15% of participants enrolled) with mean resting heart rate of >=55 and <=90 beats per minute (bpm) at screening, and >=50 and <=95 bpm at randomization, regardless of rhythm.
- NT-proBNP >=400 picograms per milliliter (pg/mL) in sinus rhythm and >=800 pg/mL in AFF at screening (confirmed by central laboratory).
- Transvenous implantable cardioverter-defibrillator (ICD) for primary prevention with back-up pacing set at 40 bpm.
- Treated with optimal, stable, medical therapy for HF consistent with prevailing local and international guidelines unless contraindicated or not tolerated, as judged and documented by the investigator.
Key Exclusion Criteria:
- Any acute or serious co-morbid condition that could lead to premature termination of study participation or interfere with the measurement or interpretation of the efficacy and safety assessments in the study.
- Admitted to hospital with the primary reason of HF within 24 hours before randomization or currently hospitalized with the primary reason of HF for more than 10 days. Current hospitalization (>24 hours and <=10 days) is capped at a maximum of 15% of participants enrolled.
- Acute coronary syndrome, stroke or transient ischemic attack, severe ventricular arrhythmia, or major cardiac intervention, percutaneous coronary intervention, valvuloplasty/other cardiac valve repair or implantation, or cardiac surgery within 60 days before randomization.
- Systolic blood pressure >130 or ˂90 millimeters of mercury (mmHg) at screening, or >140 or ˂85 mmHg at randomization.
- Uncontrolled diabetes mellitus, defined as Hemoglobin A1c (HbA1c) >=9.0% (>=75 millimoles per mole [mmol/mol]) at screening, or severe complications of diabetes.
- Body weight <50 kilogram (kg) or body mass index (BMI) <18 kilograms per square meter (kg/m^2) or >45 kg/m^2 at screening.
- Any of the following electrocardiogram (ECG) findings at screening: Corrected QT interval using Fridericia's formula (QTcF) >450 milliseconds (ms), 1st degree atrioventricular (AV) block with PQ >240 ms, or AV block 2nd or 3rd degree.
- History of aborted cardiac arrest, sustained ventricular tachycardia, or Torsades-de Pointes, or congenital long QT syndrome. Family history of sudden cardiac death, unexplained death, long QT syndrome, or death from a primary dysrhythmia.
- Cardiac resynchronization therapy, Cardiac Contractility Modulation, or pacemaker device other than the back-up pacing function of the ICD.
- Mechanical hemodynamic support, kidney support, or ventilation within 7 days before randomization.
- Treatment with i.v. inotropes, i.v. vasodilators, or i.v. vasopressors within 3 days before randomization.
- Treatment with any i.v. diuretics or supplemental oxygen within 6 hours before randomization.
- Use of any drugs or substances known to be strong inducers of Cytochrome P450 3A4 (CYP3A4) enzyme within 28 days before randomization or planned to be used during the study period or strong inhibitors of CYP3A4 within 7 days before randomization or planned to be used during the study period.
- Use of any drug that is known to prolong the QT interval (for example, sotalol, dofetilide, macrolides, some antidepressants, and some antipsychotics) within 28 days before randomization or planned to be used during the study period.
- Treatment changes in glucose lowering therapy within 28 days before randomization.
- Estimated glomerular filtration rate (eGFR) <20 milliliters per minute per 1.73 square meters (mL/min/1.73 m2) according to the Chronic Kidney Disease Epidemiology Collaboration formula, planned renal replacement therapy within the next 6 months, or receiving dialysis at screening.
- Serum potassium <3.5 or >5.2 milliequivalents per liter (mEq/L) at screening.
- Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >3 *upper limit of normal (ULN) or total bilirubin >2 * ULN, or known cirrhosis, severe liver, or pancreatic disease at screening.
- Use of any anti-arrhythmic drugs within 28 days before randomization or planned to be used during the study period, except for amiodarone, ivabradine, digoxin, and beta blockers.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: AC01 3 mg
Participants will receive AC01 orally twice daily (BID) for 12 weeks.
|
AC01 tablets for oral administration.
|
|
Experimental: AC01 1 mg
Participants will receive AC01 orally BID for 12 weeks.
|
AC01 tablets for oral administration.
|
|
Placebo-Komparator: Placebo
Participants will receive matching placebo orally BID for 12 weeks.
|
AC01 matching placebo tablets for oral administration.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Absolute Change from Baseline in Composite Echocardiography Z-Score at Week 12
Zeitfenster: Baseline and Week 12
|
The composite echocardiography Z-score integrates left ventricular stroke volume (LVSV), left ventricular end systolic volume (LVESV), left ventricular ejection fraction (LVEF), and left atrial minimal volume index (LAVImin).
|
Baseline and Week 12
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Absolute Change from Baseline in LVSV at Week 12
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Absolute Change from Baseline in LVEF at Week 12
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Absolute Change from Baseline in LVESV at Week 12
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Absolute Change From Baseline in LAVImin at Week 12
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Absolute Change from Baseline in N-terminal prohormone of Brain Natriuretic Peptide (NT-proBNP)
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Absolute Change From Baseline in Kansas City Cardiomyopathy Questionnaire Total Symptom Score (KCCQ-TSS) at Week 12
Zeitfenster: Baseline and Week 12
|
The KCCQ is a validated, 23-item, self-administered questionnaire designed to assess health status in participants with congestive heart failure.
It evaluates six domains: symptoms, physical function, quality of life, social limitation, self-efficacy, and symptom stability.
Each domain score is transformed to a scale of 0 to 100, with higher scores indicating better health status.
The KCCQ-TSS is derived from the domain scores.
|
Baseline and Week 12
|
|
Absolute Change From Baseline in Patient Global Impression of Severity (PGIS) at Week 12
Zeitfenster: Baseline and Week 12
|
PGIS is 1-item questionnaire used to rate the severity of a specific condition.
Participants record their perceived severity of heart failure (HF) symptoms, specifically shortness of breath, fatigue, and swelling, and choose 1 response that best described the extent of their symptoms based on a 5-point scale.
Response options include none, mild, moderate, severe, and very severe.
Higher PGIS scores indicate more severe HF symptoms; lower scores indicate less severe symptoms.
|
Baseline and Week 12
|
|
Patient Global Impression of Change (PGIC) at Week 12
Zeitfenster: At Week 12
|
The PGIC questionnaire is administered to assess the participant's impression of change in HF symptoms since the initiation of study treatment, specifically changes in shortness of breath, fatigue, and swelling.
Participants select one response to describe the overall change (if any) in HF symptoms on a 7-category scale: 7=very much improved, 6 =much improved, 5 =minimally improved, 4 =no change, 3 =minimally worse, 2 =much worse, and 1 =very much worse.
Higher PGIC scores indicate greater improvement in HF symptoms, while lower scores indicate worsening or no change.
|
At Week 12
|
|
Number of Participants With Death, Cardiovascular Death, Hospitalization, Cardiovascular Hospitalization, Heart Failure Hospitalization, Heart Failure Events, Other Adjudicated Events, and Listed for Heart Transplantation
Zeitfenster: At Week 12
|
At Week 12
|
|
|
Change From Baseline in Guideline-directed Medical Therapy (GDMT) Use for HFrEF at Week 12
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Absolute Change from Baseline in Estimated Glomerular Filtration Rate (eGFR)
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Number of Participants With Dialysis
Zeitfenster: At Week 12
|
At Week 12
|
|
|
Absolute Change from Baseline in Council on Nutrition Appetite Questionnaire (CNAQ) Total Score
Zeitfenster: Baseline and Week 12
|
The CNAQ is an 8-item, self-administered questionnaire used to assess appetite over time.
Each item is scored on a scale of 1 to 5, and the total score is calculated as the sum of all item scores.
The instrument has demonstrated acceptable psychometric properties, including internal consistency, construct validity, and predictive validity, for assessing appetite in participants with heart failure.
Higher CNAQ scores indicate better appetite.
|
Baseline and Week 12
|
|
Absolute Change From Baseline in New York Heart Association (NYHA) Class
Zeitfenster: Baseline and Week 12
|
Baseline and Week 12
|
|
|
Number of Participants With Treatment-emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESIs)
Zeitfenster: From first dose of study drug up to end of follow up (up to Week 16)
|
From first dose of study drug up to end of follow up (up to Week 16)
|
|
|
AUC,ss: Area Under the Concentration-Time Curve at Steady State of AC01 and its Metabolite M6
Zeitfenster: At Week 4 and Week 12
|
Population pharmacokinetic parameters
|
At Week 4 and Week 12
|
|
Cmax,ss: Maximum Observed Concentration at Steady State of AC01 and its Metabolite M6
Zeitfenster: At Week 4 and Week 12
|
Population pharmacokinetic parameters
|
At Week 4 and Week 12
|
|
Tmax,ss: Time to Reach Maximum Concentration at Steady State
Zeitfenster: At Week 4 and Week 12
|
Population pharmacokinetic parameters
|
At Week 4 and Week 12
|
|
Ctrough: Trough concentration at steady state of AC01 and its Metabolite M6
Zeitfenster: At Week 4 and Week 12
|
Population pharmacokinetic parameters
|
At Week 4 and Week 12
|
|
Rac (Cmax): Accumulation Ratio of Cmax for AC01 and its Metabolite M6
Zeitfenster: At Week 4 and Week 12
|
Population pharmacokinetic parameters.
Accumulation ratio of Cmax calculated as Cmax at Week 12/Cmax at Week 4.
|
At Week 4 and Week 12
|
|
Rac (AUC): Accumulation Ratio of AUC for AC01 and its Metabolite M6
Zeitfenster: At Week 4 and Week 12
|
Population pharmacokinetic parameters.
Accumulation ratio of AUC calculated as AUC at Week 12/AUC at Week 4.
|
At Week 4 and Week 12
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
15. November 2026
Primärer Abschluss (Geschätzt)
30. Juli 2028
Studienabschluss (Geschätzt)
30. August 2028
Studienanmeldedaten
Zuerst eingereicht
4. Mai 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
8. Mai 2026
Zuerst gepostet (Tatsächlich)
13. Mai 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
14. September 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
11. September 2026
Zuletzt verifiziert
1. September 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- AC01-02
- 2025 (US NIH Stipendium/Vertrag: Faculty of Social Sciences Scientific Grant at the University of Gdańsk)
- 2025-524469-25-00 (Ctis)
- PIP number (Andere Kennung: EMA/PE/0000267875)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
JA
Beschreibung des IPD-Plans
Individual de-identified participant data will be shared with qualified scientific and medical researchers whose proposed use of data has been approved by the study executive committee, beginning 9 months and ending 36 months following article publication.
Proposals should be directed to the Central Contact Person.
IPD-Sharing-Zeitrahmen
Links to the Study Protocol and Statistical Analysis Plan will be made available on ClinicalTrials.gov
Art der unterstützenden IPD-Freigabeinformationen
- STUDIENPROTOKOLL
- SAFT
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Ja
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Nein
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .