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Atara Biotherapeutics ATRA · USD

Health Care · US listing · 🇺🇸 United States

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8.18

+3.94%

Close of 9 Nov 2026, in USD

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About Atara Biotherapeutics

From its filings with the US Securities and Exchange Commission

SEC filings

Atara Biotherapeutics is based in Thousand Oaks, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker ATRA. The SEC classifies its business as biological products, (no diagnostic substances). In the fiscal year to 31 December 2025, it reported revenue of $120.8m and net income of $32.7m. At that date it held total assets of $20.2m and shareholders' equity of −$38.5m.

In its own words

Atara Biotherapeutics is 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 disease. Tab-cel®(tabelecleucel), has received marketing authorization approval under the proprietary name Ebvallo™ by the European Commission (EC) for commercial sale and use in the European Economic Area (EEA), by the Medicines and Healthcare products Regulatory Agency (MHRA) for commercial sale and use in the United Kingdom (UK) and by Swissmedic for commercial sale and use in Switzerland. We partnered with Pierre Fabre Medicament (Pierre Fabre) for commercialization of tab-cel in Europe and potential commercialization, if approved, worldwide, including in the U.S. Tab-cel is currently in Phase 3 development in the U.S. for patients with EBV- associated post-transplant lymphoproliferative disease (EBV+ PTLD) who have failed rituximab or rituximab plus chemotherapy, as well as other EBV-driven diseases.

Our pipeline also includes ATA3219, an allogeneic CAR T targeting CD19 intended to target B-cell malignancies and autoimmune diseases, based on a next generation 1XX signaling domain and the innate advantages of EBV T cells as the foundation for an allogeneic CAR T platform, and ATA3431, an allogeneic dual CAR T immunotherapy targeting both CD19 and CD20 for B-cell malignancies; and a potential next generation EBV vaccine which is differentiated from earlier EBV vaccine efforts that solely focused on B cell responses to EBV.

Quoted from its 10-K, filed 16 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
16 Oct 2014
Employees
14
Head office
1280 RANCHO CONEJO BLVD, THOUSAND OAKS, CA, 91320
Incorporated in
DE
Classification
Biological Products, (No Diagnostic Substances)
Filer status
Non-accelerated filer<br>Smaller reporting company

Leadership

Pay as last reported

  • Mr. Gregory CiongoliNon-Executive Chairman of the Board
  • Mr. Anhco NguyenPresident, Chief Executive Officer, Director, since 2023$1.6m
  • Dr. Carol GallagherLead Independent Director$191,552
  • Mr. Matthew FustIndependent Director$169,100
  • Mr. William HeidenIndependent Director$170,762
  • Mr. James HuangIndependent Director
  • Mr. Nachi SubramanianIndependent Director
  • Mr. Amber DaughertySenior Director, Strategy and Operations, since 2024

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
59
Environment
34
Social
99
Governance
45
Carbon reduction policy
No
Human rights policy
Yes

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Company is a clinical stage biotechnology firm focused on developing novel therapeutics for cancer, autoimmune, and viral diseases.
  • Headquartered in South San Francisco, California with a focus on severe and life-threatening diseases.
  • Operates through the development and commercialization of therapeutics, specifically allogeneic T-cell therapies.

Weaknesses

  • Source description states 437 employees, but company data lists 14 employees, indicating a significant discrepancy.
  • Company is clinical stage, meaning it has not yet commercialized any products.
  • Reliance on multiple product candidates in various stages of clinical trials without commercial success.

Opportunities

  • Potential for growth in the biotechnology sector with increasing focus on novel therapies for severe diseases.
  • Expansion of T-cell therapy applications for various diseases including cancer and autoimmune conditions.
  • Opportunity to leverage clinical trial successes to advance product candidates like ATA129 and ATA520.

Threats

  • High risk associated with clinical stage development without commercialized products.
  • Discrepancy in employee count may indicate operational inefficiencies or mismanagement.
  • Competition in the biotechnology sector for similar therapeutic approaches.

Sources and methodology

Data on this tab
Our data supplier
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