Release
Savara Reports First Quarter 2021 Financial Results and Provides Business Update
- Cash Balance of ~$193M; Company Estimates it is Sufficiently Capitalized through 2025
- Clinical Trial Site Activation Process Underway for Pivotal Phase 3 IMPALA-2 Trial of Molgramostim Nebulizer Solution (Molgramostim) in Autoimmune Pulmonary Alveolar Proteinosis (aPAP)
- Patient Randomizations Expected to Begin by End of 2Q or Early 3Q 2021
- Dhaval Desai, M.D. Appointed Head of Clinical Development, Brian Maurer Appointed Head of Clinical Operations
“We made considerable progress in the first quarter of the year,” said
“We are pleased to announce that the IMPALA-2 site activation process has begun,” said
First Quarter Financial Results (Unaudited)
Savara’s net loss attributable to common stockholders for the three months ended
Research and development expenses decreased by
General and administrative expenses decreased by approximately
As of
About Savara
Savara is a clinical stage biopharmaceutical company focused on rare respiratory diseases. Our lead program, molgramostim nebulizer solution, is an inhaled granulocyte-macrophage colony-stimulating factor (GM-CSF) in Phase 3 development for autoimmune pulmonary alveolar proteinosis (aPAP). Our management team has significant experience in rare respiratory diseases and pulmonary medicine, identifying unmet needs, and effectively advancing product candidates to approval and commercialization. More information can be found at www.savarapharma.com. (Twitter: @SavaraPharma, LinkedIn: www.linkedin.com/company/savara-pharmaceuticals/).
Forward Looking Statements
Savara cautions you that statements in this press release that are not a description of historical fact are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words referencing future events or circumstances such as “expect,” “intend,” “plan,” “anticipate,” “believe,” and “will,” among others. Such statements include, but are not limited to, our belief our cash runway extends through 2025; the expected timing of top line results of IMPALA-2 in Q2 2024; that trial sites will be activated on a rolling basis; that approximately 10-15 trial sites are expected to be active by the end of June; and that patients could be randomized and dosed by the end of 2Q or early 3Q 2021. Savara may not actually achieve any of the matters referred to in such forward-looking statements, and you should not place undue reliance on these forward-looking statements. These forward-looking statements are based upon Savara’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, the risks and uncertainties relating to the impact of the COVID-19 pandemic on our business and operations, the outcome of our ongoing and planned clinical trials for our product candidates, the ability to project future cash utilization and reserves needed for contingent future liabilities and business operations, the availability of sufficient resources for Savara’s operations and to conduct or continue planned clinical development programs, the ability to obtain the necessary patient enrollment for our product candidates in a timely manner, the ability to successfully develop our product candidates, the risks associated with the process of developing, obtaining regulatory approval for and commercializing drug candidates such as molgramostim that are safe and effective for use as human therapeutics, and the timing and ability of Savara to raise additional capital as needed to fund continued operations. All forward-looking statements are expressly qualified in their entirety by these cautionary statements. For a detailed description of our risks and uncertainties, you are encouraged to review our documents filed with the
Condensed Consolidated Statements of Operations and Comprehensive Loss | |||||||||
(in thousands, except for share and per share amounts) | |||||||||
(Unaudited) | |||||||||
Three months ended | |||||||||
|
2021 |
|
|
2020 |
|
||||
Operating expenses: | |||||||||
Research and development |
$ |
7,589 |
|
$ |
13,200 |
|
|||
General and administration |
|
2,778 |
|
|
2,982 |
|
|||
Depreciation and amortization |
|
47 |
|
|
58 |
|
|||
Total operating expenses |
|
10,414 |
|
|
16,240 |
|
|||
Loss from operations |
$ |
(10,414 |
) |
$ |
(16,240 |
) |
|||
Other income, net |
|
197 |
|
|
819 |
|
|||
Net loss attributable to common stockholders |
$ |
(10,217 |
) |
$ |
(15,421 |
) |
|||
Net loss per share - basic and diluted |
$ |
(0.13 |
) |
$ |
(0.27 |
) |
|||
Weighted average shares - basic and diluted |
|
76,992,407 |
|
|
57,364,265 |
|
|||
Other comprehensive loss |
|
(457 |
) |
|
(111 |
) |
|||
Total comprehensive loss |
$ |
(10,674 |
) |
$ |
(15,532 |
) |
Condensed Consolidated Balance Sheet Data | ||||||
(in thousands) | ||||||
(Unaudited) | ||||||
|
|
|
||||
2021 |
|
2020 |
||||
Cash, cash equivalents, and short-term investments |
$ |
192,713 |
$ |
82,188 |
||
Working capital |
|
187,595 |
|
76,947 |
||
Total assets |
|
207,630 |
|
97,745 |
||
Total liabilities |
|
32,509 |
|
33,362 |
||
Stockholders' equity |
|
175,121 |
|
64,383 |
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