Release
Savara Reports Third Quarter Financial Results and Provides Business Update
-
Top Line Data from the Pivotal Phase 3 IMPALA-2 Trial Remains On-Track to
Read Out by End of 2Q 2024
— 48-week placebo-controlled trial is evaluating molgramostim nebulizer solution (molgramostim), a novel inhaled biologic, for the treatment of autoimmune Pulmonary Alveolar Proteinosis (aPAP), a rare lung disease -
Company Expects to Launch an aPAP Antibody Blood Test and Disease Awareness Campaign in the
U.S. by End of Year -
Following the Close of an
~$80M Equity Financing, the Company Ended the Quarter with~$168.3M in Cash, Cash Equivalents, and Short-term Investments
“We remain on track to report top line data from the pivotal, Phase 3 IMPALA-2 trial by the end of the second quarter 2024,” said
Third Quarter Financial Results (Unaudited)
Savara's net loss for the third quarter of 2023 was
Research and development expenses increased by
General and administrative expenses increased by
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). Molgramostim is delivered via an investigational eFlow® Nebulizer System (
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, statements related to the expected timing of reporting top line data from the IMPALA-2 trial, statements regarding the aPAP antibody blood test and disease awareness campaign, including the expected timing of the launches in the
Financial Information to Follow
Condensed Consolidated Statements of Operations and Comprehensive Loss | ||||||||||||||||
(in thousands, except for share and per share amounts) | ||||||||||||||||
Unaudited | ||||||||||||||||
Three months ended |
|
Nine months ended |
||||||||||||||
|
|
|
||||||||||||||
2023 |
|
2022 |
|
2023 |
|
2022 |
||||||||||
Operating expenses: | ||||||||||||||||
Research and development |
$ |
13,867 |
|
$ |
8,151 |
|
$ |
31,516 |
|
$ |
20,253 |
|
||||
General and administrative |
|
4,147 |
|
|
2,376 |
|
|
10,816 |
|
|
7,687 |
|
||||
Depreciation and amortization |
|
30 |
|
|
8 |
|
|
45 |
|
|
24 |
|
||||
Total operating expenses |
|
18,044 |
|
|
10,535 |
|
|
42,377 |
|
|
27,964 |
|
||||
Loss from operations |
|
(18,044 |
) |
|
(10,535 |
) |
|
(42,377 |
) |
|
(27,964 |
) |
||||
Other income, net: |
|
1,445 |
|
|
149 |
|
|
3,778 |
|
|
114 |
|
||||
Net loss attributable to common stockholders |
$ |
(16,599 |
) |
$ |
(10,386 |
) |
$ |
(38,599 |
) |
$ |
(27,850 |
) |
||||
Net loss per share - basic and diluted |
$ |
(0.10 |
) |
$ |
(0.07 |
) |
$ |
(0.24 |
) |
$ |
(0.18 |
) |
||||
Weighted average shares - basic and diluted |
|
164,342,634 |
|
|
152,773,015 |
|
|
158,444,739 |
|
|
152,771,302 |
|
||||
Other comprehensive loss |
|
(323 |
) |
|
(591 |
) |
|
(337 |
) |
|
(1,612 |
) |
||||
Total comprehensive loss |
$ |
(16,922 |
) |
$ |
(10,977 |
) |
$ |
(38,936 |
) |
$ |
(29,462 |
) |
Condensed Consolidated Balance Sheet Data | ||||||||
(in thousands) | ||||||||
(Unaudited) | ||||||||
|
|
|
||||||
2023 |
|
2022 |
||||||
Cash, cash equivalents, and short-term investments |
$ |
168,251 |
$ |
125,876 |
||||
Working capital |
|
161,133 |
|
|
123,087 |
|
||
Total assets |
|
182,072 |
|
|
139,777 |
|
||
Total liabilities |
|
35,528 |
|
|
31,999 |
|
||
Stockholders’ equity |
|
146,544 |
|
|
107,778 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20231109539209/en/
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Source: