Atara Biotherapeutics is halving its head count as it navigates the fallout from the FDA’s move to halt trials of the allogeneic T-cell immunotherapy Ebvallo and a CAR-T candidate. Atara ...

The revision follows concerns related to the delayed approval of Atara's Ebvallo and the possibility that the company may discontinue its CAR-T development in the first quarter of 2025.

The company's off-the-shelf or 'allogeneic' therapy tabelecleucel – now given the Ebvallo trade name – has been approved by the European Commission as a second-line treatment for a rare and ...

Chief Executive Cokey Nguyen said the restructuring will allow the company to further narrow its focus on Ebvallo, a treatment candidate for Epstein-Barr virus positive post-transplant ...

The approval of Ebvallo reflects the tremendous growth and momentum we see across the CGT industry, as developers continue to usher in new therapies that offer life-extending and potentially ...

Atara is working closely with its partners and the FDA to lift clinical hold and support EBVALLO™ BLA resubmission in the U.S. Atara remains focused on delivering on the future financial value ...

Reports Q4 revenue $32.75M vs. $4.25M last year. “We will further narrow our focus on the future financial value of EBVALLO for the benefit of all stakeholders. Atara continues to productively ...

FDA halts Atara's EBVALLO and ATA3219 trials over manufacturing issues. Atara eyes $60 million milestone from Pierre Fabre upon EBVALLO approval.

“We will further narrow our focus on the future financial value of EBVALLO for the benefit of all stakeholders. Atara continues to productively engage with our partner Pierre Fabre Laboratories ...