Atara Biotherapeutics Announces Plan to Initiate Tab-cel® FDA Biologics License Application Submission Next Year
Atara Biotherapeutics, Inc. (ATRA)
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Source: GlobeNewswire
SOUTH SAN FRANCISCO, Calif., July 16, 2019 (GLOBE NEWSWIRE) -- Atara Biotherapeutics, Inc. (Nasdaq: ATRA), a leading off-the-shelf, allogeneic T-cell immunotherapy company developing novel treatments for patients with cancer, autoimmune and viral diseases, today announced an updated development plan for the Phase 3 tab-cel® (tabelecleucel) program for patients with Epstein-Barr virus-associated post-transplant lymphoproliferative disease (EBV+ PTLD). Based on Atara’s recent discussions with the U.S. Food & Drug Administration (FDA), the Company plans to initiate a tab-cel® biologics license application (BLA) submission for patients with EBV+ PTLD in the second half of 2020. “We believe focusing on the initiation of an FDA BLA submission next year is the best strategic development and value creation opportunity for tab-cel®,” said Pascal Touchon, President and Chief Executive Officer of Atara Biotherapeutics. “We remain diligently committed to addressing the critical need for new t
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ATRA
Earnings
- 11/12/24 - Beat
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Analyst Actions
- 11/13/24 - Canaccord Genuity
ATRA
Sec Filings
- 11/20/24 - Form 4
- 11/20/24 - Form 4
- 11/20/24 - Form 4
- ATRA's page on the SEC website