A Thorough QT/QTc Study With Laquinimod, a Novel Immunomodulator in Development for Multiple Sclerosis and Huntington Disease.


Journal

Clinical pharmacology in drug development
ISSN: 2160-7648
Titre abrégé: Clin Pharmacol Drug Dev
Pays: United States
ID NLM: 101572899

Informations de publication

Date de publication:
01 2019
Historique:
received: 27 09 2017
accepted: 20 12 2017
pubmed: 23 5 2018
medline: 24 3 2020
entrez: 23 5 2018
Statut: ppublish

Résumé

In this randomized double-blind study, 4 groups of healthy subjects (50 per arm) participated to evaluate the effect of laquinimod, an oral treatment in development for multiple sclerosis and Huntington disease, on the QTc interval. Subjects received a dose of either 0.6 or 1.2 mg/day laquinimod for 14 days, placebo for 14 days, or 13 days of placebo followed by a dose of 400 mg moxifloxacin on day 14. Continuous 12-lead electrocardiograms were recorded on day -1 (baseline) and days 14 to 17,  and quadruplicate electrocardiograms were extracted at predefined time points. The primary measure was time-matched change from baseline in individual QTc (QTcI), and an analysis of variance was conducted on the placebo-corrected change from baseline data (ddQTcI). Pharmacokinetic-pharmacodynamic and safety assessments were included. Results showed that the upper limits of the 2-sided 90%CI for ddQTcI for both laquinimod doses were below 10 millisconds at all time points, whereas lower limits for moxifloxacin were above 5 milliseconds. No notable changes in ECG parameters were observed. Pharmacokinetic/pharmacodynamic analysis showed no positive correlation between laquinimod plasma levels and QTcI. In conclusion, laquinimod was not found to affect cardiac repolarization or to cause prolongation of QTcI at doses of 0.6 and 1.2 mg/day.

Identifiants

pubmed: 29786964
doi: 10.1002/cpdd.442
doi:

Substances chimiques

Immunologic Factors 0
Quinolones 0
laquinimod 908SY76S4G

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

49-59

Informations de copyright

© 2018, The American College of Clinical Pharmacology.

Auteurs

Ofer Spiegelstein (O)

Clinical Pharmacology and Pharmacometrics, Teva Pharmaceutical Industries Ltd, Netanya, Israel.

Dorit Mimrod (D)

Project Leadership, Teva Pharmaceutical Industries Ltd, Netanya, Israel.

Laura Rabinovich (L)

Clinical Pharmacology and Pharmacometrics, Teva Pharmaceutical Industries Ltd, Frazer, PA, USA.

Eli Eyal (E)

Global Biostatistics Unit, TEVA Pharmaceutical Industries Ltd, Netanya, Israel.

Craig Sprenger (C)

Novum, Fargo, ND, USA.

Anna Elgart (A)

Clinical Pharmacology and Pharmacometrics, Teva Pharmaceutical Industries Ltd, Netanya, Israel.

Emil Samara (E)

PharmaPolaris International, Davis, CA, USA.

Joel Morganroth (J)

eResearch Technology, Inc, Philadelphia, PA, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH