Atara Biotherapeutics Announces Second Quarter 2023 Financial Results and Operational Progress
- Progress in discussions with FDA and potential commercial partners
- IND cleared for ATA3219
- Primary analysis of EMBOLD study in progressive MS to be communicated in early November
- Net loss of $71.1 million
Discussions With FDA Progressing on Potential BLA Submission for Tab-cel® With Meeting Scheduled To Resolve Remaining Topic of Comparability
ATA188 Phase 2 EMBOLD Study Primary Analysis and Communication Will Now Occur in Early November To Include the Last Patient Visits From More Than 90 Patients
IND Cleared for Atara's First Allogeneic CAR T, ATA3219, in Relapsed/Refractory B-Cell NHL
“We are pleased to announce IND clearance for ATA3219, our first allogeneic CAR-T cell product candidate expected to enter the clinic in the coming months as a potential best-in-class treatment for patients with certain B-cell malignancies,” said Pascal Touchon, President and Chief Executive Officer of Atara. “Building on this momentum, our discussions with FDA and potential commercial partners for tab-cel in the
Tabelecleucel (tab-cel® or EBVALLO™) for Post-Transplant Lymphoproliferative Disease (PTLD)
- Continued productive discussions between Atara and FDA have addressed outstanding chemistry, manufacturing, and controls (CMC) questions. A meeting is scheduled to resolve the remaining topic of comparability between clinical and intended commercial process versions which should provide clarity on timing for a potential BLA submission
-
Following significant levels of engagement, discussions with potential
U.S. commercialization partners are advancing -
Patients in
Europe are now receiving treatment with EBVALLO in the commercial setting, as Pierre Fabre is progressively launching on a country-by-country basis - Atara is investigating label expansion opportunities with its ongoing Phase 2 multi-cohort study with initial data expected in Q4 2023
ATA188 for Progressive Multiple Sclerosis (MS)
- Atara plans to communicate data from the primary analysis of the double-blind placebo-controlled Phase 2 EMBOLD study in progressive MS in early November
- This communication will include data from more than 90 patients, covering the primary endpoint of confirmed disability improvement (CDI) based on expanded disability status scale (EDSS) at 12 months, other clinical endpoints, and additional biomarkers
- In addition, the Company anticipates sharing longer-term results for patients that have completed study visits beyond the 12-month primary endpoint
- Atara will present new biomarker analyses from its ongoing Phase 1 trial of ATA188 at the International Society of Neuroimmunology (ISNI) congress taking place August 20-24. The data show ATA188-treated patients who achieved CDI by EDSS exhibited reduced accumulation of plasma Glial Fibrillary Acidic Protein (GFAP), a potential biomarker of disease progression in MS. Additionally, a novel application of TCRβ-sequencing allowed for detection of ATA188-derived EBV-specific TCRβ clonotypes in patients
ATA3219: Allogeneic CD19 CAR T for Various Indications
- A Phase 1 study in relapsed/refractory B-cell non-Hodgkin’s lymphoma (NHL) is expected to start in the coming months following Atara’s receipt of a Safe to Proceed letter from FDA in response to an Investigational New Drug Application (IND) submitted for ATA3219. ATA3219 is an allogeneic CD19-1XX CAR+ EBV T cell immunotherapy that incorporates multiple clinically validated technologies designed for T-cell memory, robust expansion and persistence, and potent anti-tumor efficacy
- A large unmet medical need remains for CD19-directed CAR T products that can be reliably manufactured at scale, are available in advance of patient need, and are enabling more complete and durable responses with favorable safety
Second Quarter 2023 Financial Results
-
Cash, cash equivalents and short-term investments as of June 30, 2023, totaled
, as compared to$153.6 million as of March 31, 2023$205.4 million -
Net cash used in operating activities was
for the second quarter 2023, as compared to$52.8 million in the same period in 2022$64.0 million - Atara believes that its cash and investments as of June 30, 2023, will be sufficient to fund the Company’s planned operations into second quarter 2024
-
Atara reported a net loss of
, or$71.1 million per share for the second quarter 2023, as compared to net income of$0.68 , or$18.5 million per share for the same period in 2022. Second quarter 2022 net income included$0.18 of deferred revenue recognized due to the termination of the Bayer Collaboration Agreements and a gain on the sale of the ATOM facility of$50.9 million .$50.2 million -
Total costs and operating expenses include non-cash stock-based compensation, depreciation and amortization expenses of
for the second quarter 2023, as compared to$13.8 million for the same period in 2022$15.6 million -
Research and development expenses were
for the second quarter 2023, as compared to$56.1 million for the same period in 2022$64.9 million -
Research and development expenses include
of non-cash stock-based compensation expenses for the second quarter 2023 as compared to$7.2 million for the same period in 2022$7.9 million
-
Research and development expenses include
-
General and administrative expenses were
for the second quarter 2023, as compared to$13.3 million for the same period in 2022$18.8 million -
General and administrative expenses include
of non-cash stock-based compensation expenses for the second quarter 2023, as compared to$5.4 million for the same period in 2022$6.2 million
-
General and administrative expenses include
About Atara Biotherapeutics, Inc.
Atara is harnessing the natural power of the immune system to develop off-the-shelf cell therapies for difficult-to-treat cancers and autoimmune conditions, including multiple sclerosis, that can be rapidly delivered to patients within days. With cutting-edge science and differentiated approach, Atara is the first company in the world to receive regulatory approval of an allogeneic T-cell immunotherapy. Our advanced and versatile Epstein-Barr virus (EBV) T-cell platform does not require T-cell receptor or HLA gene editing and forms the basis of a diverse portfolio of investigational therapies that target EBV, the root cause of certain diseases, in addition to next-generation AlloCAR-Ts designed for best-in-class opportunities across a broad range of non-EBV-associated liquid and solid tumors. Atara is headquartered in
Forward-Looking Statements
This press release contains or may imply "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. For example, forward-looking statements include statements regarding: (1) dialogue with the FDA regarding a potential BLA submission for tab-cel (2) tab-cel clinical trials, and the occurrence, timing and outcome of Atara’s interactions and discussions with the FDA regarding a BLA submission for tab-cel; (3) the potential submission of a BLA for tab-cel; (4) the timing and progress of ATA188, including data and analyses from the EMBOLD study and the timing of when such data will be received and communicated; (5) the timing and progress of Atara’s CAR T programs, including the timing of the start of any clinical trials, and the safety and efficacy of product candidates emerging from such programs, including ATA3219; (6) Atara’s cash runway; (7) Pierre Fabre’s activities relating to the commercialization of Ebvallo™ in
Financials
ATARA BIOTHERAPEUTICS, INC. Condensed Consolidated Balance Sheets (Unaudited) (In thousands) |
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June 30, |
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December 31, |
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||
|
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2023 |
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|
2022 |
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Assets |
|
|
|
|
|
|
|
|
Current assets: |
|
|
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
45,898 |
|
|
$ |
92,942 |
|
Short-term investments |
|
|
107,744 |
|
|
|
149,877 |
|
Restricted cash |
|
|
146 |
|
|
|
146 |
|
Accounts receivable |
|
|
507 |
|
|
|
40,221 |
|
Inventories |
|
|
7,861 |
|
|
|
1,586 |
|
Other current assets |
|
|
10,164 |
|
|
|
10,308 |
|
Total current assets |
|
|
172,320 |
|
|
|
295,080 |
|
Property and equipment, net |
|
|
5,349 |
|
|
|
6,300 |
|
Operating lease assets |
|
|
62,195 |
|
|
|
68,022 |
|
Other assets |
|
|
6,575 |
|
|
|
7,018 |
|
Total assets |
|
$ |
246,439 |
|
|
$ |
376,420 |
|
|
|
|
|
|
|
|
|
|
Liabilities and stockholders’ equity |
|
|
|
|
|
|
|
|
Current liabilities: |
|
|
|
|
|
|
|
|
Accounts payable |
|
$ |
4,138 |
|
|
$ |
6,871 |
|
Accrued compensation |
|
|
12,556 |
|
|
|
17,659 |
|
Accrued research and development expenses |
|
|
20,737 |
|
|
|
24,992 |
|
Deferred revenue |
|
|
11,949 |
|
|
|
8,000 |
|
Other current liabilities |
|
|
25,172 |
|
|
|
21,394 |
|
Total current liabilities |
|
|
74,552 |
|
|
|
78,916 |
|
Deferred revenue - long-term |
|
|
75,565 |
|
|
|
77,000 |
|
Operating lease liabilities - long-term |
|
|
51,754 |
|
|
|
58,064 |
|
Liability related to the sale of future revenues - long-term |
|
|
32,091 |
|
|
|
30,236 |
|
Other long-term liabilities |
|
|
5,023 |
|
|
|
5,564 |
|
Total liabilities |
|
$ |
238,985 |
|
|
$ |
249,780 |
|
|
|
|
|
|
|
|
|
|
Stockholders’ equity: |
|
|
|
|
|
|
|
|
Common stock |
|
|
10 |
|
|
|
10 |
|
Additional paid-in capital |
|
|
1,847,280 |
|
|
|
1,821,721 |
|
Accumulated other comprehensive (loss) income |
|
|
(933 |
) |
|
|
(2,067 |
) |
Accumulated deficit |
|
|
(1,838,903 |
) |
|
|
(1,693,024 |
) |
Total stockholders’ equity |
|
|
7,454 |
|
|
|
126,640 |
|
Total liabilities and stockholders’ equity |
|
$ |
246,439 |
|
|
$ |
376,420 |
|
ATARA BIOTHERAPEUTICS, INC. Condensed Consolidated Statements of Operations and Comprehensive Income (Loss) (Unaudited) (In thousands, except per share amounts) |
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Three Months Ended June 30, |
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Six Months Ended June 30, |
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2023 |
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2022 |
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|
2023 |
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|
2022 |
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Commercialization revenue |
|
$ |
793 |
|
|
$ |
— |
|
|
$ |
1,677 |
|
|
$ |
— |
|
License and collaboration revenue |
|
|
164 |
|
|
|
51,579 |
|
|
|
506 |
|
|
|
58,893 |
|
Total revenue |
|
|
957 |
|
|
|
51,579 |
|
|
|
2,183 |
|
|
|
58,893 |
|
Costs and operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of commercialization revenue |
|
|
2,895 |
|
|
|
— |
|
|
|
3,111 |
|
|
|
— |
|
Research and development expenses |
|
|
56,141 |
|
|
|
64,898 |
|
|
|
118,297 |
|
|
|
139,861 |
|
General and administrative expenses |
|
|
13,335 |
|
|
|
18,813 |
|
|
|
27,207 |
|
|
|
39,384 |
|
Total costs and operating expenses |
|
|
72,371 |
|
|
|
83,711 |
|
|
|
148,615 |
|
|
|
179,245 |
|
Loss from operations |
|
|
(71,414 |
) |
|
|
(32,132 |
) |
|
|
(146,432 |
) |
|
|
(120,352 |
) |
Gain on sale of ATOM Facility |
|
|
— |
|
|
|
50,237 |
|
|
|
— |
|
|
|
50,237 |
|
Interest and other income, net |
|
|
307 |
|
|
|
361 |
|
|
|
576 |
|
|
|
476 |
|
Total other income, net |
|
|
307 |
|
|
|
50,598 |
|
|
|
576 |
|
|
|
50,713 |
|
Income (loss) before provision for income taxes |
|
|
(71,107 |
) |
|
|
18,466 |
|
|
|
(145,856 |
) |
|
|
(69,639 |
) |
Provision for income taxes |
|
|
1 |
|
|
|
— |
|
|
|
23 |
|
|
|
— |
|
Net income (loss) |
|
$ |
(71,108 |
) |
|
$ |
18,466 |
|
|
$ |
(145,879 |
) |
|
$ |
(69,639 |
) |
Other comprehensive gain (loss): |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Unrealized gain (loss) on available-for-sale securities |
|
|
304 |
|
|
|
(726 |
) |
|
|
1,134 |
|
|
|
(2,250 |
) |
Comprehensive income (loss) |
|
$ |
(70,804 |
) |
|
$ |
17,740 |
|
|
$ |
(144,745 |
) |
|
$ |
(71,889 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic net earnings (loss) per common share |
|
$ |
(0.68 |
) |
|
$ |
0.18 |
|
|
$ |
(1.40 |
) |
|
$ |
(0.69 |
) |
Diluted net earnings (loss) per common share |
|
$ |
(0.68 |
) |
|
$ |
0.18 |
|
|
$ |
(1.40 |
) |
|
$ |
(0.69 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Weighted-average basic shares outstanding |
|
|
105,091 |
|
|
|
101,601 |
|
|
|
104,533 |
|
|
|
101,166 |
|
Weighted-average diluted shares outstanding |
|
|
105,091 |
|
|
|
101,866 |
|
|
|
104,533 |
|
|
|
101,166 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20230808955684/en/
Investors
Eric Hyllengren
805-395-9669
ehyllengren@atarabio.com
Media
Alex Chapman
805-456-4772
achapman@atarabio.com
Source: Atara Biotherapeutics, Inc.
FAQ
What progress has Atara made with the FDA and potential commercial partners?
What is the latest update on ATA3219?
When will the primary analysis of the EMBOLD study in progressive MS be communicated?