Assessing Hybridization-Dependent Off-Target Risk for Therapeutic Oligonucleotides: Updated Industry Recommendations
Patrik Andersson1, Sebastien A Burel2, Heather Estrella3
1AstraZeneca R&D, Gothenburg, Sweden.
Abstract:
Hybridization-dependent off-target (OffT) effects, occurring when oligonucleotides bind via Watson-Crick-Franklin hybridization to unintended RNA transcripts, remain a critical safety concern for oligonucleotide therapeutics (ONTs). Despite the importance of OffT assessment of clinical trial ONT candidates, formal guidelines are lacking, with only brief mentions in Japanese regulatory documents (2020) and US Food and Drug Administration (FDA) recommendations for hepatitis B virus treatments (2022). This article presents updated industry recommendations for assessing OffTs of ONTs, building upon the 2012 Oligonucleotide Safety Working Group (OSWG) recommendations and accounting for recent technological advancements. A new OSWG subcommittee, comprising industry experts in RNase H-dependent and steric blocking antisense oligonucleotides and small interfering RNAs, has developed a comprehensive framework for OffT assessment. The proposed workflow encompasses five key steps: (1) OffT identification through in silico complementarity prediction and transcriptomics analysis, (2) focus on cell types with relevant ONT activity, (3) in vitro verification and margin assessment, (4) risk assessment based on the OffT biological role, and (5) management of unavoidable OffTs. The authors provide detailed considerations for various ONT classes, emphasizing the importance of ONT-specific factors such as chemistry, delivery systems, and tissue distribution in OffT evaluation. The article also explores the potential of machine learning models to enhance OffT prediction and discusses strategies for experimental verification and risk assessment. These updated recommendations aim to improve the safety profile of ONTs entering clinical trials and to manage unavoidable OffTs. The authors hope that these recommendations will serve as a valuable resource for ONT development and for the forthcoming finalization of the FDA draft guidance and the International Council for Harmonization S13 guidance on Nonclinical Safety Assessment of Oligonucleotide-Based Therapeutics.
Insights
Updated guidelines address oligonucleotide therapeutics (ONTs) safety by detailing a five-step framework to identify, assess, and manage hybridization-dependent off-target effects, crucial for clinical trial progression.
Area of Science:
- Pharmacology
- Molecular Biology
- Drug Safety
Background:
- Off-target effects (OffT) from oligonucleotide therapeutics (ONTs) binding unintended RNA are a safety concern.
- Current OffT assessment guidelines are limited, with recent updates from Japan (2020) and the US FDA (2022).
- Technological advancements necessitate updated industry recommendations for robust OffT evaluation.
Purpose of the Study:
- To present updated industry recommendations for assessing OffT in oligonucleotide therapeutics (ONTs).
- To establish a comprehensive five-step framework for OffT identification, verification, risk assessment, and management.
- To provide guidance for various ONT classes, considering factors like chemistry and delivery.
Main Methods:
- Developed a five-step workflow: in silico prediction/transcriptomics, relevant cell type focus, in vitro verification/margin assessment, risk assessment, and OffT management.
- Incorporated expertise from a new Oligonucleotide Safety Working Group (OSWG) subcommittee.
- Considered ONT-specific factors (chemistry, delivery, tissue distribution) and machine learning for enhanced prediction.
Main Results:
- A comprehensive framework for OffT assessment in ONTs is proposed.
- Detailed considerations are provided for different ONT classes and their specific evaluation needs.
- Strategies for experimental verification, risk assessment, and management of unavoidable OffTs are discussed.
Conclusions:
- Updated recommendations aim to enhance the safety profile of ONTs in clinical trials.
- The proposed framework will aid in managing unavoidable OffTs and inform regulatory guidance.
- These recommendations serve as a valuable resource for ONT development and regulatory harmonization.
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