So be ready for that at the time.Got it. Location field must contain 'city, state' or a zip code to perform a radius search (e.g., The Regulatory Project Manager is responsible for the coordination, prioritization and tracking regulatory deliverables and submissions associated with the company’s research, development, and post-marketing activities for a variety of therapeutic areas. So part of the question there is what is a non-responder? Our next question comes from the line of Ben Burnett from Stifel.

And again, there is a slide that explain the protocol on our new investor deck based on already existing clinical data that clearly showing that there is some efficacy in a few patients and an acceptable safety as presented at ASH 2019. So we have a number of patient samples from the clinical trial where we're looking at the phenotypes of the cells, before and after treatment which is cellular therapy with the combination of the checkpoint inhibitors as well. And then just lastly on the OLE, can you just give us a little bit more color about how many patients we can expect to see and from which of the cohorts are those patients coming from? You were asking what we would consider good for that population. Personal Finance ft., state-of-the-art Atara T-Cell Operations and Manufacturing (ATOM) facility in Thousand Oaks, California.Our mission – “Transform the lives of patients with serious medical conditions through pioneering science, teamwork, and a commitment to excellence.”Our vision - “T-Cell Immunotherapy for every patient, any time.”Atara Bio is an equal opportunity employer and makes employment decisions on the basis of merit and other lawful factors. Your line is now open.Operator, it seems like John is having some technical difficulties. The average salary for Atara Biotherapeutics is $120,178 per year, ranging from $72,823 to $149,360.

We have worked with our clinical trial sites to implement remote study visits, leverage telemedicine, home healthcare and other methods to ensure continuity of care for patients and to preserve key endpoint data.From a supply chain perspective, we continue to deliver product to patients from our inventory on time, which is a clear advantage of such off-the-shelf, allogeneic EBV T cells.
So this is Jakob.

Notice that we haven't presented data on AID PID and that's coming in September.

The CNS-PTLD for example, is -- that's quite a medical emergency. So on the NPC, just want to correct, we're not discontinuing the development.

Stock Market So it's based on data that we want to accelerate. And certainly what we've seen in the previous cohorts is the -- is when we have sustained stability, we continue to see that. Obviously, COVID-19 is a major concern at this point in the world and as Pascal has alluded to as well.
Just a few for me.

A few from me on multiple sclerosis, if I can. As mentioned here, the multi-cohort study is quite a straightforward experiment from the perspective these are all EBV driven tumors, we are treating with tab-cel.

Competitive salary.

So with the AID and PID LPDs, I think AJ explained well, the value proposition there and the opportunity with the new data that we've generated.

Apply on company website. So Pascal or AJ or Jakob, can you just confirm if you've submitted the abstract already, or if not, if you plan on doing it by that deadline?Number two, on the Cohort 4 data that we're going to get later this year, I'm curious what your thinking is around moving to a Cohort 4 dose for the randomized portion.

And we think it's important also as we were to answer these types of questions for the field in general, because we are just at the beginning of these clinical experiments, combining a checkpoint inhibitor with a cell therapy as well.So clearly we think that we can go faster to address an important medical need with a relatively large population of a few thousand patients in the US with a multi-cohort, particularly the AID PID cohort there, and we want to go fast. Thanks very much for taking the question.Thank you.

When you think about adding that information from the multi-cohort, that information will already have on PTLD. They only delay progression by a few months and clearly do not alter the course of disease. Now from a regulatory point of view, maybe AJ want to comment of the possibility that we are either to have a specific cohort as BLA type of indication or tumor agnostic later.Yeah, sure. So we've actually had a very good engagement from the agency, even during this period of COVID.Thank you.

Thank you. So we can do, we're just simply applying it similarly to the 188 program. This concludes our question-and-answer session for today.

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