Literature DB >> 25782535

Impact of dosing regimen of custirsen, an antisense oligonucleotide, on safety, tolerability and cardiac repolarization in healthy subjects.

Laura Rabinovich-Guilatt1, Anna Elgart1, Lavi Erisson2, Sandra K Willsie3, Shoshi Tessler1, Ofra Barnett-Griness1, Amitkumar Pande4, Ofer Spiegelstein1.   

Abstract

AIMS: Custirsen (OGX-011/TV-1011), a second-generation antisense oligonucleotide (ASO) that reduces clusterin production, is under investigation with chemotherapy in patients with solid tumours. Custirsen is associated with constitutional symptoms (CS) that may interfere with clinical pharmacology investigations, such as QT interval studies. Experience with other ASOs suggests NSAID premedication may ameliorate CS, but we observed suboptimal outcomes in healthy subjects given custirsen and NSAIDs. We sought to establish a custirsen regimen for future clinical pharmacology studies in healthy subjects.
METHODS: Subjects received custirsen (640 mg intravenously over 120 min) with dexamethasone premedication or increasing doses (320, 480, 640 mg over 6 days) of custirsen with dexamethasone premedication, then one full custirsen dose without premedication on day 8. Incidence/severity of adverse events (AEs) and extensive electrocardiogram readings were evaluated. Pharmacokinetic parameters were estimated.
RESULTS: AEs included CS, elevated transaminases and prolonged activated partial thromboplastin time (aPTT) that were predominantly grade 1/2. Administration of increasing custirsen doses and dexamethasone premedication reduced the incidence of CS associated with full dose custirsen. Transaminase elevation showed a dose-dependent effect (0% at days 2, 4, 27% at day 6) with the highest custirsen doses. Increasing doses of custirsen may have mitigated the severity but not incidence of aPTT prolongation. Neither regimen was associated with cardiac repolarization changes in QT values or concentration-effect analyses. The custirsen pharmacokinetic profile was consistent with previous experience.
CONCLUSION: Escalation of custirsen dose combined with dexamethasone premedication reduced CS associated with full dose custirsen and should be considered in future clinical pharmacology studies of custirsen.
© 2015 The British Pharmacological Society.

Entities:  

Keywords:  antisense oligonucleotides; cardiac safety; custirsen; healthy subjects; pharmacokinetics; thorough QT

Mesh:

Substances:

Year:  2015        PMID: 25782535      PMCID: PMC4574829          DOI: 10.1111/bcp.12633

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  27 in total

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6.  Antitumor activity of antisense clusterin oligonucleotides is improved in vitro and in vivo by incorporation of 2'-O-(2-methoxy)ethyl chemistry.

Authors:  T Zellweger; H Miyake; S Cooper; K Chi; B S Conklin; B P Monia; M E Gleave
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  4 in total

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Authors:  Rosie Z Yu; Rudy Gunawan; Zhaoyang Li; Robert S Mittleman; Asif Mahmood; John S Grundy; Walter Singleton; Richard Geary; Yanfeng Wang
Journal:  Eur J Clin Pharmacol       Date:  2015-12-09       Impact factor: 2.953

2.  A population pharmacokinetic meta-analysis of custirsen, an antisense oligonucleotide, in oncology patients and healthy subjects.

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3.  Lack of QT Prolongation for 2'-O-Methoxyethyl-Modified Antisense Oligonucleotides Based on Retrospective Exposure/Response Analysis of Ten Phase 1 Dose-Escalation Placebo-Controlled Studies in Healthy Subjects.

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