aTyr Pharma Announces Second Quarter 2019 Results and Provides Corporate Update
aTyr to report interim safety results from Phase 1b/2a proof-of-concept trial of ATYR1923 in pulmonary sarcoidosis patients in Q4 2019
Company to host conference call and webcast today,
“Our recent key opinion leader webinar featuring Dr.
Second Quarter 2019 and Subsequent Period Highlights
- Continued to advance its ongoing Phase 1b/2a clinical trial of ATYR1923 in patients with pulmonary sarcoidosis, with interim safety data planned for Q4 2019.
- Strengthened its Board of Directors with the appointments of two seasoned biopharmaceutical executives,
Jane Gross, Ph.D. and Svetlana Lucas, Ph.D.
- Hosted a key opinion leader educational webinar featuring Dr.
Daniel Culver, DO, Director of the Interstitial Lung Disease Program in the Department of Pulmonary Medicineat Cleveland Clinicwho discussed the current standard of care and unmet medical need in treating patients with pulmonary sarcoidosis.
- Appointed leading immunobiology researcher Dr.
David Briscoe, Professor of Pediatrics at Harvard Medical School, as strategic advisor to consult on the ongoing development of therapeutics based on the NRP2 co-receptor and related signaling pathways.
Second Quarter 2019 Financial Results and Cash Position
Net loss for the three and six months ended
For the six months ended
Conference Call and Webcast Details
aTyr is developing ATYR1923 as a potential therapeutic for patients with interstitial lung diseases. ATYR1923, a fusion protein comprised of the immuno-modulatory domain of histidyl tRNA synthetase fused to the FC region of a human antibody, is a selective modulator of Neuropilin-2 that downregulates the innate and adaptive immune response in inflammatory disease states. aTyr is currently enrolling a proof-of-concept Phase 1b/2a trial evaluating ATYR1923 in patients with pulmonary sarcoidosis. This Phase 1b/2a study is a multi-ascending dose, placebo-controlled, first-in-patient study of ATYR1923 that has been designed to evaluate the safety, tolerability, steroid sparing effect, immunogenicity and pharmacokinetics profile of multiple doses of ATYR1923.
About Neuropilin-2 (NRP2)
NRP2 is a pleiotropic cell surface receptor that plays a key role in lymphatic development and in regulating inflammatory responses. In many forms of cancer, high NRP2 expression is associated with worse outcomes. NRP2 can interact with multiple ligands and coreceptors to influence their functional roles. aTyr is actively investigating NRP2 receptor biology, both internally and in collaboration with key academic thought leaders, to identify new product candidates for a variety of disease settings, including cancer, inflammation, and lymphangiogenesis.
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 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.
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 our projected cash expenditures, the potential therapeutic benefits and applications of our product candidates; our ability to successfully advance our 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; 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. All forward-looking statements are based on estimates and assumptions by our management that, although we believe to be reasonable, are inherently uncertain. 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
|Managing Director, LifeSci Advisors, LLC|
|ATYR PHARMA INC.|
|Condensed Consolidated Statements of Operations|
|(in thousands, except share and per share data)|
|Three Months Ended June 30,||Six Months Ended June 30,|
|Research and development||$||3,314||$||6,484||$||6,659||$||12,634|
|General and administrative||2,421||3,476||4,953||7,546|
|Total operating expenses||5,735||9,960||11,612||20,180|
|Loss from operations||(5,641||)||(9,960||)||(11,518||)||(20,180||)|
|Total other expense, net||(207||)||(452||)||(467||)||(899||)|
|Net loss per share attributable to common stock holders, basic and diluted||$||(1.80||)||$||(4.88||)||$||(4.23||)||$||(9.89||)|
|Weighted average common stock shares outstanding, basic and diluted||3,244,920||2,133,790||2,834,079||2,132,113|
|ATYR PHARMA INC.|
|Condensed Consolidated Balance Sheets|
|June 30,||December 31,|
|Cash, cash equivalents and available-for-sale investments||$||42,398||$||49,545|
|Property and equipment, net||1,512||1,853|
|Accounts payable, accrued expenses and other liabilities||$||2,782||$||3,066|
|Current portion of operating lease liability||705||—|
|Long-term operating lease liability, net of current portion||2,632||—|
|Current portion of long-term debt, net of issuance costs and discount||7,817||7,767|
|Long-term debt, net of current portion and issuance costs and discount||4,600||8,263|
|Total liabilities and stockholders’ equity||$||48,762||$||52,746|
Source: aTyr Pharma, Inc.