aTyr Pharma Announces Second Quarter 2018 Operating Results and Provides Corporate Update
“We have made important advancements in the development of our lead product candidate, ATYR1923, during the recent months,” said
Clinical Highlights & Upcoming Milestones
- In
June 2018 , aTyr announced results of its Phase 1, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, immunogenicity and pharmacokinetics (PK) of intravenous ATYR1923 in 36 healthy volunteers.- ATYR1923 was generally well-tolerated with no significant adverse events and its PK profile supports the potential for a once-monthly dosing regimen.
- In the fourth quarter of 2018, aTyr plans to initiate a Phase 1b/2a multiple-ascending dose, placebo-controlled, first-in-patient study with ATYR1923 for the treatment of patients with immune-mediated interstitial lung disease.
- The study will be designed to evaluate safety, tolerability, and immunogenicity of multiple doses of ATYR1923 and to evaluate several established functional pulmonary endpoints, imaging endpoints, patient reported outcome measures and potential biomarkers.
Research Highlights
- In
May 2018 , aTyr presented a mechanistic update on the Resokine pathway at theAmerican Academy of Immunology Annual Meeting inAustin, TX. - Identification of a T cell Immunomodulatory Domain in Histidyl-tRNA Synthetase.
- In
May 2018 , aTyr presented preclinical data in a lung injury model demonstrating that ATYR1923 improves lung function and reduces inflammation in rats after bleomycin induced lung injury at the 2018American Thoracic Society Annual Meeting inSan Diego, CA. - Preclinical Characterization of ATYR1923 (iMod.Fc), an Immune-Modulatory Therapeutic with Potentially Broad Application in Interstitial Lung Diseases.
- In
July 2018 , aTyr presented positive lung and skin findings with ATYR1923 in a translational animal model at theScleroderma Foundation National Patient Education Conference inPhiladelphia, PA. - ATYR1923 Ameliorates Dermal and Pulmonary Fibrosis in a Murine Model of Sclerodermatous Chronic Graft vs. Host Disease.
- In
July 2018 , the publication titled “Bi-allelic Mutations in the Phe-tRNA Synthetase Associated with Multi-system Pulmonary Disease Supports Non-Translation Function” was published in theAmerican Journal of Human Genetics .- This was a collaborative effort between aTyr, The
Scripps Research Institute ,Hong Kong University of Science and Technology ,Pangu Biopharma andColumbia University among others.
- This was a collaborative effort between aTyr, The
- In
August 2018 , the publication titled “Tyrosyl-tRNA Synthetase Stimulates Thrombopoietin-Independent Hematopoiesis Accelerating Recovery from Thrombocytopenia” was published in the Proceedings of theNational Academy of Sciences .- This research was supported in part by aTyr in collaboration with The
Scripps Research Institute andKyoto University among others.
- This research was supported in part by aTyr in collaboration with The
Corporate Highlights
- In
July 2018 , aTyr appointedJill Broadfoot as Chief Financial Officer.
Second Quarter 2018 Financial Results and Cash Position
Research and development expenses were
General and administrative expenses were
Year-to-Date 2018 Financial Results
Research and development expenses were
General and administrative expenses were
As of
Conference Call and Webcast Details
About ATYR1923
aTyr scientists successfully engineered the first fusion protein with a Resokine protein, ATYR1923, designed to enhance the immuno-modulatory properties in vivo. aTyr is developing ATYR1923 as a potential therapeutic for patients with immune-mediated interstitial lung diseases. aTyr announced data from a first-in-human Phase 1 clinical trial of ATYR1923 in
About the Resokine Pathway
The Resokine pathway is comprised of extracellular proteins derived from the histidyl tRNA synthetase (HARS) gene family. The gene for HARS gives rise to a number of splice variants, many of which have lost their catalytic activity, but which retain the N-terminal domain of 59 amino acids. This domain was appended to HARS during evolution of multicellular organisms and is not essential for protein synthetic activity but is retained with high homology across mammalian species. Proteins derived from the HARS gene, both full-length and splice variants, are present in human circulation and appear to play a role in modulating immune responses. We refer to the extracellular HARS proteins as Resokine, to differentiate them from the intracellular enzyme involved in protein synthesis.
About aTyr
aTyr is a biotherapeutics company engaged in the discovery and development of innovative medicines based on novel immunological pathways. aTyr’s research and development efforts are concentrated on a newly discovered area of biology, the extracellular functionality of tRNA synthetases. aTyr has built a global intellectual property estate directed to a potential pipeline of protein compositions derived from 20 tRNA synthetase genes. aTyr is focused on the therapeutic translation of the Resokine pathway, comprised of extracellular proteins derived from the histidyl tRNA synthetase gene family. ATYR1923 is a clinical-stage product candidate, based on the Resokine pathway, which binds to the neuropilin-2 receptor and is designed to down-regulate immune engagement in interstitial lung diseases and other immune-mediated diseases. For more information, please visit http://www.atyrpharma.com.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Litigation Reform Act. Forward-looking statements are usually identified by the use of words such as “anticipates,” “believes,” “estimates,” “expects,” “intends,” “may,” “plans,” “projects,” “seeks,” “should,” “will,” and variations of such words or similar expressions. We intend these forward-looking statements to be covered by such safe harbor provisions for forward-looking statements and are making this statement for purposes of complying with those safe harbor provisions. These forward-looking statements, including statements regarding the potential therapeutic benefits and applications of our product candidates; our ability to successfully advance our pipeline or product candidates, undertake certain development activities (such as the initiation of clinical trials, clinical trial enrollment, the conduct of clinical trials and the announcement of top-line results) and accomplish certain development goals, and the timing of such events; the anticipated benefits and cost-savings relating to the corporate restructuring; and the scope and strength of our intellectual property portfolio. These forward-looking statements also reflect our current views about our plans, intentions, expectations, strategies and prospects, which are based on the information currently available to us and on assumptions we have made. Although we believe that our plans, intentions, expectations, strategies and prospects, as reflected in or suggested by these forward-looking statements, are reasonable, we can give no assurance that the plans, intentions, expectations or strategies will be attained or achieved. Furthermore, actual results may differ materially from those described in these forward-looking statements and will be affected by a variety of risks and factors that are beyond our control including, without limitation, risks associated with the discovery, development and regulation of our product candidates, the risk that we may cease or delay preclinical or clinical development activities for any of our existing or future product candidates for a variety of reasons (including difficulties or delays in patient enrollment in planned clinical trials), and the risk that we may not be able to raise the additional funding required for our business and product development plans, as well as those risks set forth in our most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and in our other
ATYR PHARMA INC. | ||||||||||||||||
Condensed Consolidated Statements of Operations | ||||||||||||||||
(unaudited, in thousands, except share and per share data) | ||||||||||||||||
Three Months Ended | Six Months Ended | |||||||||||||||
June 30, | June 30, | |||||||||||||||
2018 | 2017 | 2018 | 2017 | |||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | $ | 6,484 | $ | 8,420 | $ | 12,634 | $ | 17,624 | ||||||||
General and administrative | 3,476 | 3,487 | 7,546 | 7,494 | ||||||||||||
Total operating expenses | 9,960 | 11,907 | 20,180 | 25,118 | ||||||||||||
Loss from operations | (9,960 | ) | (11,907 | ) | (20,180 | ) | (25,118 | ) | ||||||||
Total other expense, net | (452 | ) | (231 | ) | (899 | ) | (425 | ) | ||||||||
Net loss | $ | (10,412 | ) | $ | (12,138 | ) | $ | (21,079 | ) | $ | (25,543 | ) | ||||
Net loss per share attributable to common stock holders, basic and diluted | $ | (0.35 | ) | $ | (0.51 | ) | $ | (0.71 | ) | $ | (1.07 | ) | ||||
Weighted average common stock shares outstanding, basic and diluted | 29,842,721 | 23,810,112 | 29,819,224 | 23,774,736 |
ATYR PHARMA INC. | ||||||||
Condensed Consolidated Balance Sheets | ||||||||
(in thousands) | ||||||||
June 30, | December 31, | |||||||
2018 | 2017 | |||||||
(unaudited) | ||||||||
Cash, cash equivalents and available-for-sale investments | $ | 64,329 | $ | 85,119 | ||||
Other assets | 1,758 | 1,956 | ||||||
Property and equipment, net | 2,221 | 2,280 | ||||||
Total assets | $ | 68,308 | $ | 89,355 | ||||
Accounts payable and accrued expenses | $ | 3,367 | $ | 5,379 | ||||
Current portion of long-term loans, net of debt issuance costs and discount | 7,717 | 5,012 | ||||||
Term loans, net of current portion and debt issuance costs and discount | 11,848 | 14,719 | ||||||
Stockholders’ equity | 45,376 | 64,245 | ||||||
Total liabilities and stockholders’ equity | $ | 68,308 | $ | 89,355 |
Contact: |
Mark Johnson |
Sr. Director, Investor Relations |
mjohnson@atyrpharma.com |
858-223-1163 |
Source: aTyr Pharma, Inc.