Wave Life Sciences Reports Third Quarter 2017 Financial Results and Provides Business Update
“Through the growth of talent and capabilities in our organization and
excellent execution throughout the quarter, we achieved our ambitious
clinical and research goals. Importantly, we initiated our third
clinical program of 2017 with a Phase 1 study investigating our DMD Exon
51 program, WVE-210201,” said
Business Update
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DMD Exon 51 (WVE-210201) program initiates clinical trial
OnNovember 6 , Wave announced the initiation of clinical development for WVE-210201, Wave’s lead program for Duchenne muscular dystrophy (DMD) patients amenable to exon 51 skipping. We expect that data from the Phase 1 trial for WVE-210201 will be available in Q3 2018 and will facilitate the rapid transition to an open-label extension study and efficacy study. Both studies following the Phase 1 are designed to include an interim efficacy readout of dystrophin expression from muscle biopsies in 2H 2019. The company is exploring both intravenous and subcutaneous administration.
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Huntington’s disease allele selective programs (WVE-120101,
WVE-120102) clinical trials on track
The company’s PRECISION-HD program, which includes two Phase 1b/2a global clinical trials evaluating WVE-120101 and WVE-120102 for patients with Huntington’s disease (HD), continues to enroll and it is on track to report topline data in 1H 2019.
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First peer-reviewed publication in Nature Biotechnology
In August, Wave announced its first peer-reviewed publication in the September issue of Nature Biotechnology, representing a significant scientific advancement for the oligonucleotide field. The paper, entitled "Control of phosphorothioate stereochemistry substantially increases the efficacy of antisense oligonucleotides," describes a breakthrough method to produce antisense oligonucleotide (ASO) therapeutics with high stereochemical purity as well as rational drug design to control pharmacologic properties in nucleic acid therapeutics drug development more broadly.
The paper outlines early foundational principles discovered by Wave to engage RNase H1 that can be applied to any ASO sequence, and demonstrated that stereochemistry plays a central role in oligonucleotide drug design, with the potential to improve stability, duration of activity and specificity. The company’s highly efficient manufacturing process may allow for these key findings to translate into breakthrough treatments by applying nucleic acid therapeutics. Wave is continuing to leverage these initial findings to further build its knowledge base and expand its platform capabilities beyond antisense, including ongoing work in exon skipping, single stranded RNAi and other modalities.
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Pfizer collaboration progress
The collaboration with Pfizer continues to make progress on developing genetically targeted therapies for the treatment of metabolic diseases, including nonalcoholic steatohepatitis (NASH). As an update, our APOC3-GalNAc ASO findings demonstrated a potency equivalent to state-of-the-art GalNAc conjugated double-strand RNAi with a median effective dose of 0.3mg/kg in vivo. In addition to a 7- to 10-fold improvement in potency, an increase was seen in durability over GalNAc conjugated stereorandom APOC3.
The collaboration has accelerated the application of Wave’s stereochemistry platform across antisense and RNAi modalities with the incorporation of GalNAc and Pfizer’s hepatic targeting technology to address disease of the liver. Wave continues to advance its research efforts in this area.
In addition, Wave amended its collaboration agreement with Pfizer to extend the target nomination period fromNovember 5, 2017 toMay 5, 2018 , which provides Pfizer with an additional six months to nominate the two remaining hepatic targets under the agreement.
Third Quarter 2017 Financial Results and Financial Guidance
Wave reported a net loss of
Research and development expenses were
General and administrative expenses were
As of September 30, 2017, Wave had cash and cash equivalents totaling
Wave expects that the capital resources available as of September 30, 2017, together with anticipated milestone payments under its existing collaboration with Pfizer, will be sufficient to fund its operating expenses and capital expenditure requirements into mid-2019.
About
Forward-Looking Information
This press release contains forward-looking statements concerning our
goals, beliefs, expectations, strategies, objectives and plans, and
other statements that are not necessarily based on historical facts,
including statements regarding the following: the anticipated
commencement, data readouts and duration of our clinical trials; the
protocol, design and endpoints of our clinical trials; the future
performance and results of our programs in clinical trials; the progress
and potential benefits of our collaborations with partners; our
identification of future candidates and their therapeutic potential; the
anticipated therapeutic benefits of our potential therapies compared to
others; our advancing of therapies across multiple modalities and the
anticipated benefits of that strategy; the anticipated benefits of our
manufacturing process and our internal manufacturing facility; our
future growth; the potential benefits of our stereopure compounds
compared with stereorandom compounds, our drug discovery platform and
nucleic acid therapeutics generally; and the anticipated duration of our
cash runway. Actual results may differ materially from those indicated
by these forward-looking statements as a result of various important
factors, including the following: the ability of our preclinical
programs to produce data sufficient to support our clinical trial
applications and the timing thereof; our ability to continue to build
and maintain the company infrastructure and personnel needed to achieve
our goals; the clinical results of our programs, which may not support
further development of product candidates; actions of regulatory
agencies, which may affect the initiation, timing and progress of
clinical trials; our effectiveness in managing future clinical trials
and regulatory processes; the success of our platform in identifying
viable candidates; the continued development and acceptance of nucleic
acid therapeutics as a class of drugs; our ability to demonstrate the
therapeutic benefits of our candidates in clinical trials, including our
ability to develop candidates across multiple therapeutic modalities;
our ability to obtain, maintain and protect intellectual property; our
ability to enforce our patents against infringers and defend our patent
portfolio against challenges from third parties; our ability to finance
our drug discovery efforts and to raise additional capital when needed;
and competition from others developing therapies for similar uses, as
well as the information under the caption “Risk Factors” contained in
our most recent Annual Report on Form 10-K filed with the
WAVE LIFE SCIENCES LTD. | ||||||||
UNAUDITED CONSOLIDATED BALANCE SHEETS | ||||||||
(In thousands, except share amounts) |
||||||||
September 30, 2017 | December 31, 2016 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 168,464 | $ | 150,293 | ||||
Prepaid expenses and other current assets | 5,370 | 1,483 | ||||||
Deferred tax assets | — | 214 | ||||||
Total current assets | 173,834 | 151,990 | ||||||
Property and equipment, net | 24,584 | 8,607 | ||||||
Deferred tax assets | — | 560 | ||||||
Restricted cash | 3,608 | 3,601 | ||||||
Other assets | 60 | 53 | ||||||
Total assets | $ | 202,086 | $ | 164,811 | ||||
Liabilities, Series A preferred shares and shareholders’ equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 4,705 | $ | 4,943 | ||||
Accrued expenses and other current liabilities | 6,953 | 4,434 | ||||||
Current portion of capital lease obligation | 31 | 62 | ||||||
Current portion of deferred rent | 50 | — | ||||||
Current portion of deferred revenue | 2,705 | 2,705 | ||||||
Current portion of lease incentive obligation | 678 | 11 | ||||||
Total current liabilities | 15,122 | 12,155 | ||||||
Long-term liabilities: | ||||||||
Capital lease obligation, net of current portion | — | 16 | ||||||
Deferred rent, net of current portion | 3,837 | 680 | ||||||
Deferred revenue, net of current portion | 6,283 | 8,311 | ||||||
Lease incentive obligation, net of current portion | 2,093 | 116 | ||||||
Other liabilities | 1,021 | 796 | ||||||
Total long-term liabilities | 13,234 | 9,919 | ||||||
Total liabilities | $ | 28,356 | $ | 22,074 | ||||
Series A preferred shares, no par value; 3,901,348 shares issued and outstanding at September 30, 2017 and December 31, 2016 |
$ | 7,874 | $ | 7,874 | ||||
Shareholders’ equity: | ||||||||
Ordinary shares, no par value; 27,767,905 and 23,502,169 shares issued and outstanding at September 30, 2017 and December 31, 2016, respectively |
$ | 309,434 | $ | 215,602 | ||||
Additional paid-in capital | 18,995 | 10,029 | ||||||
Accumulated other comprehensive loss | (272 | ) | (291 | ) | ||||
Accumulated deficit | (162,301 | ) | (90,477 | ) | ||||
Total shareholders’ equity | $ | 165,856 | $ | 134,863 | ||||
Total liabilities, Series A preferred shares and shareholders’ equity | $ | 202,086 | $ | 164,811 | ||||
WAVE LIFE SCIENCES LTD. | ||||||||||||||||
UNAUDITED CONSOLIDATED STATEMENTS OF OPERATIONS | ||||||||||||||||
(In thousands, except share and per share amounts) |
||||||||||||||||
Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||||
2017 | 2016 | 2017 | 2016 | |||||||||||||
Revenue | $ | 676 | $ | 392 | $ | 2,028 | $ | 809 | ||||||||
Operating expenses: | ||||||||||||||||
Research and development | 20,097 | 13,686 | 53,940 | 26,823 | ||||||||||||
General and administrative | 7,571 | 3,939 | 20,088 | 10,809 | ||||||||||||
Total operating expenses | 27,668 | 17,625 | 74,028 | 37,632 | ||||||||||||
Loss from operations | (26,992 | ) | (17,233 | ) | (72,000 | ) | (36,823 | ) | ||||||||
Other income (expense): | ||||||||||||||||
Dividend income | 515 | — | 1,287 | — | ||||||||||||
Interest income (expense), net | 1 | 118 | 5 | 328 | ||||||||||||
Other income (expense), net | (75 | ) | (36 | ) | (211 | ) | (25 | ) | ||||||||
Total other income (expense), net | 441 | 82 | 1,081 | 303 | ||||||||||||
Loss before income taxes | (26,551 | ) | (17,151 | ) | (70,919 | ) | (36,520 | ) | ||||||||
Income tax benefit (provision) | 416 | (384 | ) | (905 | ) | (427 | ) | |||||||||
Net loss | $ | (26,135 | ) | $ | (17,535 | ) | $ | (71,824 | ) | $ | (36,947 | ) | ||||
Net loss per share attributable to ordinary shareholders— basic and diluted |
$ | (0.94 | ) | $ | (0.75 | ) | $ | (2.75 | ) | $ | (1.64 | ) | ||||
Weighted-average ordinary shares used in computing net loss per share attributable to ordinary shareholders—basic and diluted |
27,758,792 | 23,445,673 | 26,078,696 | 22,571,575 | ||||||||||||
View source version on businesswire.com: http://www.businesswire.com/news/home/20171109005459/en/
Source:
Wave Life Sciences
Investors:
Jillian Connell,
617-949-2981
jconnell@wavelifesci.com
or
Media:
Jose
Juves, 617-949-4708
jjuves@wavelifesci.com
or
Patient
Contact:
Wendy Erler, 617-949-2898
werler@wavelifesci.com