Atara Biotherapeutics, Inc. is a pioneering allogeneic T-cell immunotherapy company focused on developing transformative therapies for patients with serious medical conditions including solid tumors, hematologic cancers, and autoimmune diseases. Leveraging their novel allogeneic Epstein-Barr virus (EBV) T-cell platform, Atara aims to deliver readily available treatments to patients from healthy donor T-cells. Their leading candidate, tabelecleucel (tab-cel®), is in development for EBV-positive post-transplant lymphoproliferative disease (EBV+ PTLD).
The South San Francisco headquarters serves as the central hub for Atara's corporate strategy, executive leadership, administrative functions, and clinical development oversight.
Modern office spaces designed to foster collaboration and innovation, likely equipped with advanced communication technology to connect with global teams and research sites.
The work culture at Atara Biotherapeutics emphasizes scientific rigor, patient-centricity, collaboration, and innovation. Employees are driven by the mission to develop life-changing therapies for patients with limited treatment options.
Its location in the San Francisco Bay Area provides access to a rich ecosystem of talent, research institutions, and potential partners, crucial for a biotech company.
While headquartered and with primary operations in the United States (California and Colorado), Atara Biotherapeutics conducts clinical trials in multiple countries across North America, Europe, and potentially other regions. Their global presence is primarily driven by their clinical development programs and collaborations with international research institutions and healthcare providers to bring their innovative therapies to patients worldwide. They also have a presence in Zug, Switzerland, for European operations.
611 Gateway Blvd, Suite 900
South San Francisco
CA
USA
Address: One Atara Bio Way, Thousand Oaks, CA 91320
Leverages the strong biotech talent pool in Southern California and supports preclinical research, process development, and operational activities.
Address: Atara Cell Therapy Manufacturing Facility (ATOM), 14100 E. 35th Place, Aurora, CO 80011
Establishes in-house manufacturing capabilities, ensuring quality control and supply chain reliability for their innovative cell therapies. Provides access to a skilled manufacturing workforce.
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As of April 2025, Atara Biotherapeutics' leadership includes:
Atara Biotherapeutics has been backed by several prominent investors over the years, including:
Atara Biotherapeutics has seen key appointments and departures in its executive team over the past year, reflecting strategic shifts and a focus on advancing its pipeline and commercial readiness. Notable changes include appointments in medical and technical leadership and a departure in the commercial team.
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Atara Biotherapeutics commonly uses the email format of first initial followed by the last name. Other formats might exist but this is the most frequently observed pattern.
[first_initial][last]@atarabio.com
Format
jdoe@atarabio.com
Example
85%
Success rate
Atara Biotherapeutics Press Release • January 4, 2024
Atara announced a strategic update to prioritize ATA3219 (allogeneic CD19 CAR T) and ATA3431 (allogeneic CD20 CAR T) programs. The company will reduce its workforce by approximately 25% and streamline operations to extend cash runway into Q2 2026. This includes wind-down of tab-cel® and ATA188 activities in the U.S. while continuing to seek a commercialization partner for tab-cel® in the U.S....more
Atara Biotherapeutics Press Release • November 2, 2023
Atara Biotherapeutics announced the appointment of Danelle James, M.D., M.A.S., as Executive Vice President, Chief Medical Officer. Dr. James brings extensive experience in global clinical development and medical affairs in oncology and rare diseases....more
European Medicines Agency (EMA) • October 24, 2023
The European Commission granted Marketing Authorization for Ebvallo™ (tabelecleucel) as a monotherapy for the treatment of adult and pediatric patients two years of age and older with relapsed or refractory Epstein-Barr virus positive post-transplant lymphoproliferative disease (EBV+ PTLD) who have received at least one prior therapy. For solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate. This was a major regulatory milestone for the company. (Note: Commercialization partner is Pierre Fabre in Europe)....more
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