Journal
EUROPEAN JOURNAL OF HEART FAILURE
Volume 14, Issue 11, Pages 1230-1239Publisher
WILEY
DOI: 10.1093/eurjhf/hfs118
Keywords
Heart Failure; Autoimmune disease; Beta-adrenergic receptor
Categories
Funding
- German Federal Research Ministry (BMBF, GoBio) [0315363]
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A novel concept for the treatment of heart failure is the neutralization of antibodies against the (1)-adrenergic receptor (anti-(1)AR-ab). In a rat model of autoimmune cardiomyopathy, the cyclic peptide COR-1 (given i.v. once monthly) neutralized anti-(1)AR-abs and prevented anti-(1)AR-ab-induced myocardial damage, and completely reverted cardiac dysfunction over 36 months. A clinical phase I trial was designed as a single-blinded, placebo-controlled study. Fifty human volunteers received COR-1 or matching placebo as a single i.v. administration with ascending doses (10240 mg). Primary endpoints were safety and tolerability, while the pharmacokinetic profile of COR-1 was assessed as a secondary endpoint. All five investigated dose groups were well tolerated; no drug-related side effects occurred. Pharmacokinetics revealed a favourable profile with an almost complete plasma clearance within 60 min after administration. Pharmacodynamic investigation showed dose-dependent efficacy with almost complete scavenging of pathological anti-(1)AR-abs ex vivo at the two highest doses. No anti-COR-1 autoantibodies occurred. No other effects on the immune system (such as an increase of crucial cytokines) were observed up to 43 days after drug administration, nor upon incubation of anti-(1)AR-ab-positive patient blood samples with COR-1 ex vivo. COR-1 was shown to be safe after i.v. administration in vivo; no relevant side effects occurred. Efficacy was estimated from ex vivo investigation of the potency to neutralize specific anti-(1)-AR-abs. Trial registration: NCT 01043146, Eudra CT 2008-007745-31.
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