Eidos Therapeutics Reports First Quarter 2019 Financial Results
“The initiation of our Phase 3 ATTRibute-CM study in the first quarter of
Recent Achievements and Upcoming Milestones
- Initiated Phase 3 study of AG10 in ATTR-CM (ATTRibute-CM)
- Published Phase 2 data of AG10 in ATTR-CM in the
Journal of the American College of Cardiology(JACC)
- Presented sub-group analysis of Phase 2 data in ATTR-CM at
American College of Cardiology (ACC) Scientific Sessions
- Plan to initiate Phase 3 study of AG10 in ATTR-PN (ATTRibute-PN) in the second half of 2019
- Plan to present data from the open label extension of the Phase 2 study of AG10 in ATTR-CM in the fourth quarter of 2019
First Quarter Financial and Operating Results
Cash and cash equivalents totaled
Eidos reported a net loss attributable to common stockholders of $11.7 million or
Research and development expenses for the first quarter of 2019 were $8.5 million, as compared to $5.7 million for the same period in the prior year. Research and development expenses for the first quarter included costs related to contract manufacturing, the preparation for and conduct of AG10 clinical trials.
General and administrative expenses for the first quarter of 2019 were $4.0 million, as compared to $2.3 million for the same period in the prior year. The increase in general and administrative expense in these periods was due primarily to an increase in professional service fees, salaries and employee-related expense primarily due to an increase in headcount to support the growth of our operations, and other administrative expenses.
AG10 is an investigational, orally-administered small molecule designed to potently stabilize tetrameric transthyretin, or TTR, thereby halting at its outset the series of molecular events that give rise to amyloidosis, or ATTR. In a Phase 2 clinical trial in subjects with symptomatic ATTR-CM, AG10 was generally well tolerated, demonstrated >90% average TTR stabilization at day 28, and increased serum TTR concentrations, a prognostic indicator of survival in a retrospective study of ATTR-CM patients, in a dose-dependent manner. AG10 is currently being studied in an open-label extension of a Phase 2 clinical trial in patients with ATTR-CM, and patient enrollment has begun for a Phase 3 clinical trial of AG10 in patients with ATTR-CM (ATTRibute-CM).
AG10 was designed to mimic a naturally-occurring variant of the TTR gene (T119M) that is considered a rescue mutation because co-inheritance has been shown to prevent ATTR in individuals also inheriting a pathogenic, or disease-causing, mutation in the TTR gene. To our knowledge, AG10 is the only TTR stabilizer in development that has been observed to mimic the stabilizing structure of this rescue mutation.
About transthyretin amyloidosis (ATTR)
ATTR represents a significant unmet medical need with a large patient population and an inadequate current standard of care. ATTR is caused by the destabilization of TTR due to inherited mutations or aging and is commonly divided into three distinct categories: wild-type ATTR cardiomyopathy (ATTRwt-CM), mutant ATTR cardiomyopathy (ATTRm-CM), and ATTR polyneuropathy (ATTR-PN). The worldwide prevalence of each disease is approximately 400,000 patients, 40,000 patients and 10,000 patients, respectively.
All three forms of ATTR are progressive and fatal. For patients with ATTRwt-CM and ATTRm-CM, symptoms usually manifest later in life (age 50+), with median survival of three to five years from diagnosis. ATTR-PN either presents in a patient's early 30s or later (age 50+), and results in a median life expectancy of five to ten years from diagnosis. Progression of all forms of ATTR causes significant morbidity, impacts productivity and quality of life, and creates a significant economic burden due to the costs associated with progressively greater patient needs for supportive care.
This release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act. All statements other than statements of historical facts, including the statements about the potential therapeutic and clinical benefits of AG10, the potential to accelerate the development and registration of AG10, the design of the ATTRibute-CM trial, our ability to enroll patients in and conduct the ATTRibute-CM trial in accordance with our plans, future clinical and regulatory milestones of AG10, the timing of these events, the indications we intend to pursue and our possible clinical or other business strategies, and our ability to fund our clinical development plans, are forward-looking statements. Forward-looking statements can be identified by terms such as “believes,” “expects,” “plans,” “potential,” “would” or similar expressions and the negative of those terms. These forward-looking statements are based on our management’s current beliefs and assumptions about future events and on information currently available to management. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. These risks include, but are not limited to, risks and uncertainties related to: our limited operating history and historical losses, our liquidity to fund the development of AG10 through current and future milestones, our ability to raise additional funding to complete the development of AG10, our dependence on the success of AG10, our ability to enroll patients in the ATTRibute-CM trial, results from our clinical trials and pre-clinical studies and those of third parties working in the same area as our product candidate, our ability to advance AG10 in clinical development in accordance with our plans, and our dependence on third parties in connection with our manufacturing, clinical trials and pre-clinical studies. Additional risks and uncertainties that could affect our future results are included in the section titled “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in our Quarterly Report on Form 10-Q for the quarter ended
Condensed Statements of Operations
(In thousands, except share and per share data)
|Three months ended|
|Research and development||$||8,549||$||5,652|
|General and administrative||4,035||2,345|
|Total operating expenses||12,584||7,997|
|Loss from operations||(12,584||)||(7,997||)|
|Other income (expense), net||851||(879||)|
|Net and comprehensive loss||(11,733||)||(8,876||)|
|Deemed dividend related to redemption feature embedded in Convertible Promissory Notes payable to stockholders||-||(6,523||)|
|Gain on extinguishment of Convertible Promissory Notes payable to stockholders||-||7,436|
|Net loss attributable to common stockholders||$||(11,733||)||$||(7,963||)|
|Net loss per share attributable to common stockholders, basic and diluted||$||(0.32||)||$||(1.81||)|
|Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted||36,175,523||4,392,435|
|* Includes stock-based compensation as follows|
|Research and development||$||452||$||178|
|General and administrative||512||210|
|Total stock-based compensation expense||$||964||$||388|
Condensed Balance Sheets
|March 31,||December 31,|
|Cash and cash equivalents||$||147,064||$||157,147|
|Related party receivable||72||34|
|Prepaid expenses and other current assets||2,160||1,789|
|Total current assets||149,296||158,970|
|Property and equipment, net||196||209|
|Operating lease, right of use asset||1,053||-|
|Liabilities, Redeemable Convertible Preferred Stock and Stockholders’ Equity|
|Related party payable||407||256|
|Accrued expenses and other current liabilities||3,953||2,577|
|Total current liabilities||7,841||4,789|
|Lease liabilities, non-current||854||-|
|Additional paid-in capital||221,267||220,240|
|Total stockholders’ equity||144,301||155,007|
|Total liabilities, redeemable convertible preferred stock and stockholders’ equity||$||153,197||$||160,112|
Source: Eidos Therapeutics, Inc.