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Atara Biotherapeutics Provides Regulatory and Business Updates on Tabelecleucel (Tab-cel®)

1. Atara has resubmitted a BLA for tabelecleucel to the FDA. 2. This FDA submission aims for approval in cancer and autoimmune treatments.

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FAQ

Why Bullish?

The resubmission of the BLA can lead to future revenue and product approval, historically contributing to stock price increases in biotech firms. ATRA's position as a leader in T-cell immunotherapy may appeal to investors anticipating growth.

How important is it?

The FDA's decision on this BLA could significantly influence ATRA's market position. Given that progress towards FDA approval tends to attract investor interest and drive stock prices, this is a significant development.

Why Long Term?

FDA approval processes typically take several months, impacting revenue over the long term, especially with potential new market access if approved, much like other successful biotech approvals that bolstered company valuations over time.

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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 announced that it has resubmitted a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for tabelecleucel (EBVALLO™ or tab-cel®) indicated as monotherapy for treatment of adult and pedi.

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