Alpine Immune Sciences Provides Corporate Update and Reports Fourth Quarter and Full Year 2022 Financial Results
Alpine Immune Sciences, Inc. (NASDAQ: ALPN) has initiated patient enrollment in the RUBY-3 study for autoimmune glomerulonephritis and plans to start the RUBY-4 study for autoimmune cytopenias in Q2 2023. The company expects initial data from both studies by the end of 2023. Financially, Alpine reported a net loss of $57.8 million for 2022, with cash reserves of $273.4 million sufficient to fund operations through 2025. Research expenses rose to $18.8 million, reflecting increased headcount for clinical programs. Collaboration revenue decreased to $2.8 million in Q4 2022, down from $4.5 million in Q4 2021.
- Initiation of RUBY-3 and RUBY-4 studies, promising clinical development.
- Strong cash position of $273.4 million, sufficient through 2025.
- Potential first-in-class status of povetacicept as a dual BAFF/APRIL inhibitor.
- Increased net loss of $57.8 million in 2022 compared to $50.3 million in 2021.
- Collaboration revenue declined to $2.8 million in Q4 2022 from $4.5 million in Q4 2021.
- R&D expenses increased to $18.8 million, reflecting higher personnel costs.
- RUBY-3, a basket study of povetacicept in autoimmune glomerulonephritis, has initiated patient enrollment; RUBY-4, a basket study of povetacicept in autoimmune cytopenias, targets initiation in Q2 2023
- Initial data from both basket studies are anticipated by the end of 2023
“With the recent initiation of the RUBY-3 study in autoimmune glomerulonephritis and the imminent initiation of the RUBY-4 study in autoimmune cytopenias, 2023 is on track to be a pivotal year for Alpine and povetacicept, a potential best-in-class dual BAFF/APRIL inhibitor which we are developing for multiple autoantibody-related diseases. We look forward to sharing updates on both studies anticipated by the end of the year,” said
“We are thrilled to be part of povetacicept’s RUBY-3 study for autoimmune glomerulonephritis, especially IgA nephropathy. Povetacicept looks to be the first true dual inhibitor of both the BAFF and APRIL cytokines with the added potential advantage of its unique, convenient dose regimen of subcutaneous administration every four weeks,” said
Fourth Quarter 2022 and Recent Pipeline and Corporate Updates
- RUBY-3, an open-label basket study in autoimmune glomerulonephritis, including IgA nephropathy, lupus nephritis and primary membranous nephropathy, recently initiated enrollment.
- RUBY-4, an open-label basket study in autoimmune cytopenias, including immune thrombocytopenia, warm autoimmune hemolytic anemia, and cold agglutinin disease, is anticipated to begin enrollment in the second quarter.
- The Company plans to launch RUBY-2, a placebo-controlled, dose-ranging, randomized phase 2 study in systemic lupus erythematosus in mid-2024, based on enabling data from the RUBY-3 and RUBY-4 studies.
- Key preclinical data on povetacicept -- demonstrating differentiation from wild-type TACI-Igs, BAFF- or APRIL-only inhibitors and anti-CD20 depletion, as well as efficacy in mouse models of lupus -- were published in the peer-reviewed journal Arthritis & Rheumatology (View Publication).
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The Company presented multiple oral and poster presentations on povetacicept at recent scientific conferences, including an ePoster and oral presentation at the
American Academy of Dermatology Annual Meeting onMarch 18 th (Full List ofCompany Publications and Presentations).
Corporate
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The Company recently announced that it had entered into a strategic collaboration with Truveta to use
Truveta Studio to help rapidly identify and enroll participants in Alpine’s clinical studies for povetacicept, including the RUBY-3 study in autoimmune glomerulonephritis and RUBY-4 study in autoimmune cytopenias. Truveta’s databases are updated daily from its 28 health system members which include more than 20,000 clinics and 700 hospitals from all 50 states and represent16% of the covered lives inthe United States . -
The Company ended the year with
in cash, cash equivalents, restricted cash, and investments as of$273.4 million December 31, 2022 , which the Company anticipates should be sufficient to fund its planned operations through 2025.
Fourth Quarter and Full Year 2022 Financial Results
As of
Collaboration revenue for the quarter ended
Research and development expenses for the quarter ended
General and administrative expenses for the quarter ended
The Company recorded net losses of
Conference Call and Webcast Information
The link to the webcast will be available in the investor relations section of the Company’s website at https://ir.alpineimmunesciences.com/events and a replay will be available on the Company's website for 90 days following the live event.
Povetacicept (ALPN-303) is a dual antagonist of the BAFF (B cell activating factor) and APRIL (a proliferation inducing ligand) cytokines, which play key roles in the activation and survival of B cells, particularly antibody-secreting cells. Based upon an engineered TACI (transmembrane activator and CAML interactor) domain, povetacicept exhibits greater potency in preclinical studies versus wild-type TACI-based comparators, as well as other inhibitors of BAFF and/or APRIL alone. Povetacicept is in development for multiple B cell and/or autoantibody-related diseases, such as systemic lupus erythematosus, autoimmune glomerulonephritis, and autoimmune cytopenias.
About
Forward-Looking Statements
This release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995. These forward-looking statements are not based on historical fact and include statements regarding our platform technology and potential therapies; the timing of and results from clinical trials and preclinical development activities; clinical and regulatory objectives and the timing thereof; expectations regarding the sufficiency of cash, cash equivalents, restricted cash, and investments to fund our planned operations through 2025; the potential efficacy, safety profile, future development plans, addressable market, regulatory success, and commercial potential of our product candidates; our ability to achieve additional milestones in our collaborations and proprietary programs; the progress and potential of our ongoing development programs; the timing of our public presentations and potential publication of future clinical data; the efficacy of our clinical trial designs; anticipated enrollment in our clinical trials and the timing thereof; expectations regarding our ongoing collaborations; and our ability to successfully develop and achieve milestones in our development programs. Forward-looking statements generally include statements that are predictive in nature and depend upon or refer to future events or conditions and include words such as “may,” “will,” “should,” “would,” “expect,” “plan,” “intend,” and other similar expressions, among others. These forward-looking statements are based on current assumptions that involve risks, uncertainties, and other factors that may cause actual results, events, or developments to be materially different from those expressed or implied by such forward-looking statements. These risks and uncertainties, many of which are beyond our control, include, but are not limited to: clinical trials may not demonstrate safety and efficacy of any of our product candidates; our ongoing discovery and preclinical efforts may not yield additional product candidates; our discovery-stage and preclinical programs may not advance into the clinic or result in approved products; any of our product candidates may fail in development, may not receive required regulatory approvals, or may be delayed to a point where they are not commercially viable; we may not achieve additional milestones in our proprietary or partnered programs; the impact of competition; adverse conditions in the general domestic and global economic markets; the impact of the COVID-19 pandemic on our business, research and clinical development plans and timelines and results of operations, including the impact on our clinical trial sites, collaborators, and contractors who act for or on our behalf, may be more severe and prolonged than currently anticipated; as well as the other risks identified in our filings with the
"Synergy," and the Alpine logo are registered trademarks or trademarks of
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Selected Consolidated Balance Sheet Data |
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(In thousands) |
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|
|
|
|
|
|
||
|
|
|
|
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Cash and cash equivalents |
|
$ |
13,376 |
|
$ |
67,907 |
Short-term investments |
|
|
224,265 |
|
|
94,396 |
Total current assets |
|
|
240,993 |
|
|
192,013 |
Long-term investments |
|
|
35,481 |
|
|
52,866 |
Total assets |
|
|
286,686 |
|
|
255,900 |
Total current liabilities |
|
|
57,996 |
|
|
69,778 |
Total stockholders’ equity |
|
|
179,420 |
|
|
120,903 |
Total liabilities and stockholders’ equity |
|
|
286,686 |
|
|
255,900 |
Consolidated Statement of Operations and Comprehensive Income (Loss) Data |
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(In thousands, except share and per share amounts) |
Three Months Ended
|
|
Twelve Months Ended
|
||||||||||||
|
|
2022 |
|
|
|
2021 |
|
|
|
2022 |
|
|
|
2021 |
|
|
(unaudited) |
|
|
|
|
||||||||||
Collaboration revenue |
$ |
2,776 |
|
|
$ |
4,530 |
|
|
$ |
30,064 |
|
|
$ |
23,443 |
|
Operating expenses: |
|
|
|
|
|
|
|
||||||||
Research and development |
|
18,756 |
|
|
|
15,362 |
|
|
|
70,243 |
|
|
|
58,742 |
|
General and administrative |
|
4,389 |
|
|
|
4,544 |
|
|
|
17,968 |
|
|
|
14,560 |
|
Total operating expenses |
|
23,145 |
|
|
|
19,906 |
|
|
|
88,211 |
|
|
|
73,302 |
|
Loss from operations |
|
(20,369 |
) |
|
|
(15,376 |
) |
|
|
(58,147 |
) |
|
|
(49,859 |
) |
Other income (expense): |
|
|
|
|
|
|
|
||||||||
Interest income |
|
2,165 |
|
|
|
93 |
|
|
|
3,288 |
|
|
|
259 |
|
Interest expense |
|
(87 |
) |
|
|
(178 |
) |
|
|
(476 |
) |
|
|
(816 |
) |
Other, net |
|
(25 |
) |
|
|
(4 |
) |
|
|
(97 |
) |
|
|
(4 |
) |
Loss before taxes |
|
(18,316 |
) |
|
|
(15,465 |
) |
|
|
(55,432 |
) |
|
|
(50,420 |
) |
Income tax benefit (expense) |
|
(548 |
) |
|
|
298 |
|
|
|
(2,330 |
) |
|
|
87 |
|
Net loss |
$ |
(18,864 |
) |
|
$ |
(15,167 |
) |
|
$ |
(57,762 |
) |
|
$ |
(50,333 |
) |
Comprehensive income (loss): |
|
|
|
|
|
|
|
||||||||
Unrealized gain (loss) on investments |
|
484 |
|
|
|
(237 |
) |
|
|
(901 |
) |
|
|
(238 |
) |
Unrealized gain (loss) on foreign currency translation |
|
64 |
|
|
|
(51 |
) |
|
|
53 |
|
|
|
(88 |
) |
Comprehensive loss |
$ |
(18,316 |
) |
|
$ |
(15,455 |
) |
|
$ |
(58,610 |
) |
|
$ |
(50,659 |
) |
Weighted-average shares used to compute basic and diluted net loss per share |
|
45,882,437 |
|
|
|
29,354,961 |
|
|
|
33,435,280 |
|
|
|
25,476,889 |
|
Basic and diluted net loss per share |
$ |
(0.41 |
) |
|
$ |
(0.52 |
) |
|
$ |
(1.73 |
) |
|
$ |
(1.98 |
) |
View source version on businesswire.com: https://www.businesswire.com/news/home/20230323005680/en/
Investor and Media Contact:
ir@alpineimmunesciences.com
Source:
FAQ
What studies is Alpine Immune Sciences currently conducting for povetacicept (ALPN)?
What were Alpine's financial results for Q4 2022?
What is the cash position of Alpine Immune Sciences as of December 31, 2022?
When can we expect data from the RUBY-3 and RUBY-4 studies?