A Two Arm Randomised, Open-label Study to Investigate the Persistence of Autoantibody Neutralisation, the Safety, and Pharmacokinetics of BC 007 in Patients With Chronic Heart Failure With Reduced Ejection Fraction (HFrEF) and Autoantibodies Directed Against the beta1 Adrenergic Receptor
Overview
- Phase
- Phase 2
- Intervention
- BC 007
- Conditions
- Cardiomyopathy, Dilated
- Sponsor
- Berlin Cures GmbH
- Enrollment
- 30
- Locations
- 3
- Primary Endpoint
- Proportion of β1 AAb negative participants at month 12
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
Chronic heart failure (CHF) is one of the major causes of death in Western societies. Evidence has accumulated that functionally active autoantibodies directed against the beta1 adrenergic receptor (β1 AAb) are of pathophysiological relevance for the development and progression of cardiomyopathy and associated CHF. BC 007 is under development for targeted neutralisation of autoantibodies directed against G protein coupled receptors, including β1 AAb. This is an open label, three-centre, randomised phase 2a study in participants with chronic HFrEF. The study will evaluate whether BC 007 causes a persistent neutralisation of the β1 AAb demonstrated by a negative β1 AAb status up to 12 months. Participants will be randomised in a 2:1 ratio to the treatment arm (BC 007) or the control arm (untreated). Treatment is repeated once up to month 11 if the participant's β1 AAb were not neutralised after 1st dosing on day 1 or reoccur.
Detailed Description
Primary objective is: - To compare the efficacy of an intravenous (i.v.) infusion of BC 007 with an untreated control arm in removal of β1 AAb at month 12 in participants with chronic heart failure with reduced ejection fraction (HFrEF) Secondary objectives are: * To evaluate the time to recurrence of β1 AAb after a single i.v. infusion of BC 007 * To evaluate the response rate and time to recurrence of β1 AAb after a repeated single i.v. infusion of BC 007 after the first recurrence of β1 AAb * To evaluate the safety and tolerability of BC 007 after a single and a repeated single i.v. infusion * To determine the pharmacokinetic (PK) plasma and urine profiles of BC 007 * To investigate the PK plasma profiles of BC 007 metabolites * To investigate the β aminoisobutyric acid (β-AIBA) plasma and urine, and uric acid serum and urine concentration as a marker for BC 007 degradation * To investigate the spontaneous conversion of β1 AAb status from positive to negative in untreated participants (control arm) Exploratory objective is: - To evaluate the change of the left ventricular ejection fraction (LVEF) after a single and a repeated single i.v. infusion
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or female participant ≥18 years of age, at the time of signing the informed consent.
- •Participant has CHF class II III, according to the NYHA classification.
- •Participant has a chronic HFrEF with a left ventricular ejection fraction (LVEF) ≤40 % during screening (as assessed by in-hospital echocardiography).
- •Participant screened positive for β1 AAb by a validated functional assay.
Exclusion Criteria
- •Participant has a sustained systolic blood pressure ≥160 mmHg prior to randomisation.
- •Participant has a sustained bradycardia with resting heart rate \<45 beats per minute (bpm) or tachycardia with resting heart rate \>100 bpm prior to randomisation.
- •Participant has an untreated primary valvular disease, considered clinically significant by the Investigator.
- •Participant has any condition or therapy, which would make the participant unsuitable for the study, or life expectancy less than 12 months (e.g., active malignancy).
Arms & Interventions
BC 007
The treatment arm will comprise 20 randomly allocated β1-AAb positive dilative cardiomyopathy (DCM) patients. Participants will receive a continuous 75 minute infusion of 1350 mg BC 007 at day 1. The β1-AAb status will be monitored 10 days after treatment and every month. Treatment is repeated once up to month 11 if the participant's β1-AAbs were not neutralized after 1st dosing on day 1 or reoccur.
Intervention: BC 007
Outcomes
Primary Outcomes
Proportion of β1 AAb negative participants at month 12
Time Frame: 12 month
Secondary Outcomes
- Maximum observed plasma concentration (Cmax) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Persistence of response defined as the time from initial β1 AAb neutralisation to β1 AAb recurrence.(12 month)
- Response rate defined as the percentage of β1 AAb negative participants after a second treatment and persistence of response defined as the time from subsequent β1 AAb neutralisation to β1 AAb recurrence(12 month)
- Comparative conversion rate of β1 AAb from positive to negative status measured by a cardiomyocyte beat rate assay in untreated participants (control arm)(12 month)
- Number of Participants with abnormal laboratory values and/or adverse events that are related to treatment(12 month)
- Area under the plasma concentration time curve (AUC) from time zero to the last quantifiable concentration (AUC0-t) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Area under the plasma concentration time curve (AUC) from time zero extrapolated to infinity (AUC0-inf) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Apparent terminal half-life (t1/2) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Nominal time of Cmax (tmax) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Plasma clearance (CL) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Volume of distribution during terminal phase (Vz) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Terminal elimination rate constant (λz) derived from BC 007 and BC 007 metabolite (N-1, N-2 and N-3) plasma concentrations(6 hour post start of infusion)
- Cumulative amount of unchanged drug excreted into urine (Ae)(6 hour post start of infusion)
- Fraction of intravenous administered drug that is excreted unchanged in urine (fe)(6 hour post start of infusion)
- Renal clearance (CLR) of BC 007(6 hour post start of infusion)
- Area under the plasma concentration time curve (AUC) from time zero to the last quantifiable concentration (AUC0-t) derived from β-aminoisobutyric acid and uric acid plasma concentrations(6 hour post start of infusion)
- Area under the plasma concentration time curve (AUC) from time zero to the concentration after 4 hours (AUC0-4h) derived from β-aminoisobutyric acid and uric acid plasma concentrations(4 hour post start of infusion)
- Area under the plasma concentration time curve (AUC) from time zero to the concentration after 6 hours (AUC0-6h) derived from β-aminoisobutyric acid and uric acid plasma concentrations(6 hour post start of infusion)
- Area under the plasma concentration time curve (AUC) from time zero extrapolated to infinity (AUC0-inf) derived from β-aminoisobutyric acid and uric acid plasma concentrations(6 hour post start of infusion)
- Maximum observed plasma concentration (Cmax) derived from β-aminoisobutyric acid and uric acid plasma concentrations(6 hour post start of infusion)
- Nominal time of Cmax (tmax) derived from β-aminoisobutyric acid and uric acid plasma concentrations(6 hour post start of infusion)
- Cumulative amount of β-aminoisobutyric acid and uric acid excreted into urine (Ae)(6 hour post start of infusion)
- Renal clearance (CLR) of β-aminoisobutyric acid and uric acid(6 hour post start of infusion)