Atara Biotherapeutics, Inc 8-K, filed Aug 12, 2026
Atara Biotherapeutics, Inc. (ATRA)
About this 8-K
Atara Biotherapeutics, Inc filed this 8-K on August 12, 2026.
Items reported
- Item 2.02: Financial results
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
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Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
Securities registered pursuant to Section 12(b) of the Act:
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Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).
Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On August 12, 2026, Atara Biotherapeutics, Inc. (the “Company”) announced certain financial results for the quarter ended June 30, 2026. A copy of the Company’s press release titled “Atara Biotherapeutics Announces Second Quarter 2026 Financial Results and Operational Progress” is furnished as Exhibit 99.1 hereto.
The information set forth in this Item 2.02 and in the press release included as Exhibit 99.1 shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of Section 11 and 12(a)(2) of the Securities Act of 1933, as amended, and shall not be incorporated by reference into any filing with the U.S. Securities and Exchange Commission, whether made before or after the date hereof, except as shall be expressly set forth by specific reference in such filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits.
Exhibit No. |
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Description |
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99.1 |
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104 |
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Cover Page Interactive Data File (embedded within the Inline XBRL document) |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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ATARA BIOTHERAPEUTICS, INC. |
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Date: |
August 12, 2026 |
By: |
/s/ Kevin G. Sarney |
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Kevin G. Sarney |
Exhibit 99.1
Atara Biotherapeutics Announces Second Quarter 2026 Financial Results and Operational Progress
Productive Type A Meeting with FDA for tabelecleucel
FDA guidance provided on resubmission of tabelecleucel BLA
Year over Year costs and operating expenses reduction of 87%
THOUSAND OAKS, Calif.--(BUSINESS WIRE)-- Atara Biotherapeutics, Inc. (Nasdaq: ATRA), a leader in T-cell immunotherapy, leveraging its novel allogeneic Epstein-Barr virus (EBV) T-cell platform to develop transformative therapies for patients with cancer and autoimmune diseases, today reported financial results for the second quarter 2026 and business updates.
“This was an important quarter for Atara. We and our partners, Pierre Fabre Pharmaceuticals (PFP), had a productive Type A meeting with the FDA where we confirmed the opportunity to resubmit the tabelecleucel BLA based on the existing Phase 3 single arm ALLELE trial. We are actively working with and supporting PFP in a resubmission that includes an updated dataset with additional patients and longer follow-up. Patients are still dying from EBV-driven PTLD, and we remain fully committed to ensuring that they have access to this new medicine,” said Cokey Nguyen, President and Chief Executive Officer of Atara. "We continue to believe that tab-cel has significant commercial potential in the US, and we have taken steps to control expenses with the goal of protecting and maximizing shareholder value and enhancing our strategic flexibility."
Tabelecleucel (tab-cel® or EBVALLO™) for Post-Transplant Lymphoproliferative Disease (PTLD)
As previously communicated, PFP has indicated they intend to submit an updated dataset with additional patients and longer follow-up from the pivotal Phase 3 single arm ALLELE study as well as supportive data. Atara anticipates providing a further regulatory update later this quarter.
Under its commercialization agreement with Pierre Fabre Laboratories, Atara is eligible to receive a $31 million milestone payment upon FDA approval of the tabelecleucel BLA, as well as significant double-digit tiered royalties as a percentage of net sales, and milestones related to commercial sales of EBVALLO.
Second Quarter 2026 Financial Results:
2026 Outlook and Cash Runway:
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 that can be rapidly delivered to patients from inventory. 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 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. Atara is headquartered in Southern California. For more information, visit atarabio.com and follow @Atarabio on X and LinkedIn.
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) the development, timing and progress of tab-cel, including the timing of PFP’s resubmission, the potential characteristics and benefits of tab-cel, and the results of, and prospects for bringing tab-cel to U.S. patients with EBV+ PTLD, the global partnership with Pierre Fabre Medicament involving tab-cel, and the potential financial benefits to Atara as a result of the global partnership with Pierre Fabre Medicament, including the receipt, timing and amount of any payments to be received by Atara thereunder; and (2) Atara’s cash runway, receipt of potential milestone payments, and estimated reduction in operating expenses, including Atara’s ability to fund its planned operations into mid-2027. Because such statements deal with future events and are based on Atara’s current expectations, they are subject to various risks and uncertainties and actual results, performance or achievements of Atara could differ materially from those described in or implied by the statements in this press release. These forward-looking statements are subject to risks and uncertainties, including, without limitation, risks and uncertainties associated with the costly and time-consuming pharmaceutical product development process and the uncertainty of clinical success; risks related to FDA’s review of tab-cel, including the risk that a resubmission of the tab-cel BLA may not address the deficiencies identified in the Complete Response Letter received on January 9, 2026 or other issues that may be raised by the FDA on review; the fact that PFP, and not Atara, holds the tab-cel BLA and controls the timing, content and strategy of any resubmission and related FDA interactions, and Atara's ability to influence the resubmission process is limited; Atara’s ability to access capital, and the sufficiency of Atara’s cash resources and access to additional capital on favorable terms or at all; and other risks and uncertainties affecting Atara, including those discussed in Atara’s filings with the Securities and Exchange Commission, including in the “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” sections of Atara’s most recently filed periodic reports on Form 10-K and Form 10-Q and subsequent filings and in the documents incorporated by reference therein. Except as otherwise required by law, Atara disclaims any intention or
obligation to update or revise any forward-looking statements, which speak only as of the date hereof, whether as a result of new information, future events or circumstances or otherwise.
Atara Biotherapeutics, Inc.
Condensed Consolidated Balance Sheets
(Unaudited)
(In thousands, except per share amounts)
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June 30, |
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December 31, |
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2026 |
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2025 |
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Assets |
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Current assets: |
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Cash and cash equivalents |
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$ |
3,221 |
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$ |
8,482 |
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Short-term investments |
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6,652 |
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- |
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Accounts receivable |
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318 |
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1,253 |
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Other current assets |
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3,339 |
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2,477 |
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Total current assets |
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13,530 |
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12,212 |
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Property and equipment, net |
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41 |
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73 |
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Operating lease assets |
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6,688 |
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7,064 |
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Other assets |
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765 |
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886 |
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Total assets |
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$ |
21,024 |
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$ |
20,235 |
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Liabilities and stockholders’ equity (deficit) |
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Current liabilities: |
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Accounts payable |
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$ |
824 |
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$ |
127 |
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Accrued compensation |
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699 |
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1,271 |
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Accrued research and development expenses |
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57 |
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82 |
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Deferred revenue |
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775 |
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716 |
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Liability related to the sale of future revenues – current portion |
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1,032 |
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9,750 |
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Other current liabilities |
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3,460 |
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2,976 |
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Total current liabilities |
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6,847 |
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14,922 |
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Operating lease liabilities – long-term |
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8,782 |
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9,347 |
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Liability related to the sale of future revenues – long-term |
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40,506 |
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32,673 |
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Other long-term liabilities |
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1,885 |
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1,795 |
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Total liabilities |
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58,020 |
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58,737 |
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Commitments and contingencies |
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Stockholders’ equity (deficit): |
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Common stock—$0.0001 par value, 500,000 shares authorized as of June 30, 2026 and December 31, 2025; 9,443 and 7,324 shares issued and outstanding as of June 30, 2026 and December 31, 2025, respectively |
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1 |
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1 |
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Additional paid-in capital |
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1,993,849 |
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1,983,361 |
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Accumulated other comprehensive income (loss) |
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(2 |
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1 |
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Accumulated deficit |
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(2,030,844 |
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(2,021,865 |
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Total stockholders’ equity (deficit) |
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(36,996 |
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(38,502 |
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Total liabilities and stockholders’ equity (deficit) |
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$ |
21,024 |
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$ |
20,235 |
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Atara Biotherapeutics, Inc.
Condensed Consolidated Statements of Operations and Comprehensive (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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2026 |
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2025 |
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2026 |
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2025 |
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Commercialization revenue |
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$ |
630 |
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$ |
17,575 |
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$ |
1,146 |
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$ |
115,724 |
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Costs and operating expenses: |
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Cost of commercialization revenue |
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191 |
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554 |
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315 |
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20,993 |
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Research and development expenses |
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1,345 |
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7,310 |
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1,509 |
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34,743 |
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General and administrative expenses |
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3,814 |
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6,514 |
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7,411 |
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17,989 |
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Total costs and operating expenses |
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5,350 |
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14,378 |
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9,235 |
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73,725 |
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Income (loss) from operations |
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(4,720 |
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3,197 |
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(8,089 |
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41,999 |
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Other income (expense), net: |
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Interest income |
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78 |
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143 |
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132 |
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379 |
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Interest expense |
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(191 |
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(972 |
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(1,021 |
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(1,989 |
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Other income (expense), net |
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— |
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22 |
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— |
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11 |
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Total other income (expense), net |
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(113 |
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(807 |
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(889 |
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(1,599 |
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Income (loss) before provision for (benefit from) income taxes |
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(4,833 |
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2,390 |
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(8,978 |
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40,400 |
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Provision for (benefit from) income taxes |
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1 |
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3 |
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1 |
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3 |
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Net income (loss) |
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$ |
(4,834 |
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$ |
2,387 |
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$ |
(8,979 |
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$ |
40,397 |
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Other comprehensive gain (loss): |
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Unrealized gain (loss) on available-for-sale securities |
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(2 |
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— |
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(3 |
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(8 |
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Comprehensive income (loss) |
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$ |
(4,836 |
) |
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$ |
2,387 |
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$ |
(8,982 |
) |
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$ |
40,389 |
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Basic (loss) earnings per common share |
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$ |
(0.32 |
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$ |
0.20 |
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$ |
(0.62 |
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$ |
3.52 |
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Diluted (loss) earnings per common share |
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$ |
(0.32 |
) |
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$ |
0.19 |
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$ |
(0.62 |
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$ |
3.49 |
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Basic and diluted weighted-average shares outstanding |
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15,033 |
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12,197 |
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14,560 |
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11,484 |
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Diluted weighted-average shares outstanding |
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15,033 |
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12,310 |
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14,560 |
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11,576 |
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Investor and Media Relations
Amber Daugherty
Sr. Director, Strategy and Operations
adaugherty@atarabio.com