A Randomized, Double-Blind, Placebo-Controlled, Multiple Dose Escalation Study to Evaluate the Safety and Pharmacokinetics of ELX-02 in Healthy Subjects

Andi Leubitz, Frederic Vanhoutte, Ming-Yi Hu, Kaela Porter, Efrat Gordon, Kathleen Tencer, Kathleen Campbell, Kate Banks, Tom Haverty, Andi Leubitz, Frederic Vanhoutte, Ming-Yi Hu, Kaela Porter, Efrat Gordon, Kathleen Tencer, Kathleen Campbell, Kate Banks, Tom Haverty

Abstract

ELX-02 is an investigational compound being developed as a therapy for genetic diseases caused by nonsense mutations such as cystic fibrosis. Structurally, ELX-02 is an aminoglycoside analogue that induces read-through of nonsense mutations through interaction with the ribosome, resulting in the production of full-length functional proteins. This phase 1 multiple-ascending-dose trial evaluated the safety and pharmacokinetics of ELX-02 in 62 healthy volunteers. ELX-02 plasma exposure was dose proportional, with no apparent accumulation, and followed by renal elimination. The most reported adverse event was injection site reactions that were mild to moderate in severity. At the top dose of 5.0 mg/kg, 1 of 6 subjects experienced auditory threshold changes in which ototoxicity could not be clearly ruled out, and 2 of 6 had hearing threshold changes consistent with possible ototoxicity. Two of 3 subjects receiving placebo in the 5.0 mg/kg group also had significant hearing threshold changes. All observed hearing threshold changes resolved or were trending toward resolution after withdrawal of the study drug. No severe or serious adverse events were reported.The results of this study support the evaluation of ELX-02 in phase 2 clinical trials with patients that have genetic diseases caused by nonsense mutations.

Keywords: ELX-02; cystic fibrosis; nonsense mutations; pharmacokinetics; phase 1; safety.

Conflict of interest statement

A.L., M.‐Y.H., E.G., K.T., K.B., and T.H. are employees of Eloxx Pharmaceuticals, Inc. F.V. was a principal investigator for the study. K.P. and K.C. are consultants to Eloxx Pharmaceuticals, Inc.

© 2021 Eloxx Pharmaceuticals. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.

Figures

Figure 1
Figure 1
Mean (standard deviation) plasma ELX‐02 concentration vs time by cohort on day 1 from 0 to 12 hours (A), from 0 to 36 hours (B), day 29 from 0 to 12 hours (C), and from 0 to 36 hours (D).
Figure 2
Figure 2
Mean (standard deviation) plasma ELX‐02 1‐hour postdose concentration vs study day by cohort.
Figure 3
Figure 3
Mean (standard deviation) ELX‐02 fraction excreted vs midpoint of urinary collection time interval by cohort on days 1 (upper panel) and 29 (lower panel).

References

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Source: PubMed

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