Wave Life Sciences to Highlight Advancements from PRISM Platform at Upcoming Scientific Congresses
Six presentations and posters between
First presentation in a scientific congress of preclinical data supporting WVE-006 as a potential best-in-class therapeutic approach in alpha-1 antitrypsin deficiency
“Wave continues to expand its genetic medicines toolkit of modalities and novel chemistries, enabling both the flexibility to optimally address disease biology, as well as the ability to fine-tune potency, durability of effect, and tissue distribution of our stereopure oligonucleotides. Our data at
18th Annual Meeting of the Oligonucleotide Therapeutics Society
- Tuesday, October 4 at 8:30 a.m. MDT
Phosphoryl-guanidine backbone chemistry: understanding its impact on stereopure oligonucleotides (Chandra Vargeese, PhD, Chief Technology Officer and Head of Platform Discovery Sciences at Wave Life Sciences)
Session IV: Preclinical
- Wednesday, October 5 at 10:00 a.m. MDT
RNA base editing for the treatment of Alpha-1 antitrypsin deficiency (
Prashant Monian, PhD, Senior Scientist I at Wave Life Sciences)
Session VI: Genome & RNA Editing
- Monday, October 3 at 4:00 p.m. MDT
Stereopure oligonucleotides incorporating phosphoryl guanidine backbone increase durability of gene silencing by RNAi (
Naoki Iwamoto, PhD, Senior Director, Oligo Chemistry and Biochemistry Researchat Wave Life Sciences)
Poster Session I (Poster #101)
- Tuesday, October 4 at 4:30 p.m. MDT
Effect of stereochemistry and backbone chemistry on AIMer RNA editing efficiency (
Jack Godfrey, PhD, Senior Scientist I at Wave Life Sciences)
Poster Session II (Poster #52)
- Tuesday, October 4 at 4:30 p.m. MDT
Synthesis of stereopure chimeric oligonucleotides containing PN and PS backbone: A systematic evaluation of chiral auxiliaries (
Jayakanthan Kumarasamy, PhD, Principal Scientist, Medicinal Chemistry at Wave Life Sciences)
Poster Session II (Poster #58)
- Thursday, October 13 at 5:30 p.m. BST
Application of ADAR-mediated RNA editing to modulate protein-protein interactions (
Ian Harding, PhD, Scientist II at Wave Life Sciences)
Poster session II (poster #424)
Wave’s scientific presentations and posters can be accessed after the conferences at the “Events & Publications” section of the company’s Investor Relations website: ir.wavelifesciences.com.
Wave’s AIMers are designed to correct mutations in an RNA transcript, thereby avoiding permanent changes to the genome that occur with DNA-targeting approaches. Rather than using an exogenous editing enzyme, AIMers recruit proteins that exist in the body, called ADAR enzymes, which naturally edit certain adenine (A) bases to inosine (I). Because I is read as G (guanine) by the cellular translational machinery, sequence-directed editing with ADAR has the potential to revert transcripts with single G-to-A point mutations that cause genetic diseases. This approach redirects a natural system for therapeutic purposes, enables simplified delivery without viral particles or liposomes, and avoids the risk of irreversible off-target effects of DNA-targeting approaches. AIMers are short in length, fully chemically modified, and use novel chemistry, including proprietary PN backbone modifications and chiral control, that make them distinct from other ADAR-mediated editing approaches.
PRISM is Wave Life Sciences’ proprietary discovery and drug development platform that enables genetically defined diseases to be targeted with stereopure oligonucleotides across multiple therapeutic modalities, including silencing, splicing, and editing. PRISM combines the company’s unique ability to construct stereopure oligonucleotides with a deep understanding of how the interplay among oligonucleotide sequence, chemistry and backbone stereochemistry impacts key pharmacological properties. By exploring these interactions through iterative analysis of in vitro and in vivo outcomes and machine learning-driven predictive modeling, the company continues to define design principles that are deployed across programs to rapidly develop and manufacture clinical candidates that meet pre-defined product profiles.
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, our expectations for our GalNAc-conjugated A-to-I(G) RNA base editing oligonucleotides (AIMers) and the anticipated therapeutic benefits thereof; our expectations regarding the ability of our AIMers to address diseases of many different tissues and cell types; our research of unconjugated AIMers for delivery to organs that are not reachable by other editing approaches; the potential benefits of our AIMers compared with other RNA base editing approaches; and the potential benefits of PRISM, including our AIMers and our stereopure oligonucleotides. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management's current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release and actual results may differ materially from those indicated by these forward-looking statements as a result of these risks, uncertainties and important factors, including, without limitation, the risks and uncertainties described in the section entitled “Risk Factors” in Wave’s most recent Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC), as amended, and in other filings Wave makes with the SEC from time to time. Wave undertakes no obligation to update the information contained in this press release to reflect subsequently occurring events or circumstances.
Source: Wave Life Sciences USA, Inc.