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BCS

Current Report · Items 2.02 · 8-K

Atara Biotherapeutics, Inc.

ATRANASDAQEQUITYCurrent

Results of Operations and Financial Condition

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.…

Filed Aug 12, 2026Accepted Aug 12, 2026, 4:10 PM EDTCIK 1604464Accession 0001193125-26-346857
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Company context

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.

Current securities

Recent company filings

  1. 4 filingSep 4, 2026
  2. 144 filingAug 26, 2026
  3. 10-Q filingAug 12, 2026
  4. 3 filingJul 6, 2026
  5. Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory ArrangementsJun 26, 2026

Registered securities in this filing

Atara Biotherapeutics, Inc. · 8-K · Filed 2026-08-12

As filed in this accession. Current/historical status below comes from the governed listing record; the cover itself remains exact to this filing.

Common Stock, par value $0.0001 per share

Symbol
ATRA
Exchange
NASDAQ
Classification
COMMON
Status
Current
Filing context

Context: C_99781c6f-a593-493d-adc1-cb49c44956da

Dimensions: Not supplied

Accession 000119312526346857 · 1 registered-security cover member

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Disclosure sections

Items 2.02

Select an item to read the extracted section. The as-filed document remains the primary evidence.

Item 2.02Item 2.02 - Results of Operations
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.
Filed exhibits (1)
EX-99.1 (by filename) atra-ex99_1.htm

EX-99.1 2 atra-ex99_1.htm EX-99.1 EX-99.1 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 th…

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