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Tuesday, June 4, 2019

AbbVie Presents Data on Venetoclax Chemo-Free Leukemia Combo

AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, today presented data from the CLL14 trial, the first randomized clinical trial to examine stopping an oral-based, chemotherapy-free combination after 12 months in previously untreated patients with CLL and coexisting medical conditions. The results demonstrate that venetoclax plus obinutuzumab prolonged progression-free survival (PFS) and achieved higher rates of complete response and minimal residual disease (MRD)-negativity compared to a commonly used standard of care obinutuzumab plus chlorambucil.1
These data were presented today in an oral presentation at the American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago (abstract #7502) and were simultaneously published in the New England Journal of Medicine (NEJM).
“Conducting CLL14 was another collaborative and bold attempt to continue pushing the boundaries of treatment in CLL,” said Mohamed Zaki, M.D., Ph.D., vice president, global head of hematology development, AbbVie. “The combination of venetoclax plus obinutuzumab significantly prolonged progression-free survival and patients maintained that benefit after stopping treatment. After the recent approval in the U.S., we look forward to continue working with health authorities worldwide as we aim to bring venetoclax plus obinutuzumab to patients with previously untreated CLL.”
The venetoclax and obinutuzumab combination was recently approved by the U.S. Food and Drug Administration (FDA) for previously untreated patients with CLL or small lymphocytic lymphoma (SLL) based on results from the CLL14 clinical trial.
In the CLL14 trial, investigator-assessed results demonstrated that patients with CLL who were treated with venetoclax plus obinutuzumab achieved superior PFS compared to patients treated with obinutuzumab plus chlorambucil. Twenty-four-month PFS estimates were 88.2 percent and 64.1 percent, respectively (hazard ratio [HR]: 0.35, 95% confidence interval [CI]: 0.23, 0.53; P<0.001). Higher rates of MRD-negativity were observed with venetoclax plus obinutuzumab compared to obinutuzumab plus chlorambucil in both peripheral blood (75.5 percent versus 35.2 percent, P<0.001) and bone marrow (56.9 percent versus 17.1 percent [P<0.001]) three months after treatment completion, and complete response rates were significantly higher with venetoclax plus obinutuzumab than with chlorambucil plus obinutuzumab (49.5 percent versus 23.1 percent [P<0.001]).1 
“The combination of venetoclax plus obinutuzumab is a new and rational approach to treat patients with previously untreated CLL and coexisting medical conditions based on the results of the CLL14 trial,” said Michael Hallek, M.D., chairman of the German CLL Study Group (DCLLSG), Department of Internal Medicine and Center of Integrated Oncology at the University Hospital Cologne in Germany, and lead study investigator. “The CLL14 trial results show that a finite treatment duration induces a longer time without progression when compared to a conventional chemoimmunotherapy.”

Beyond glucose in type 2 diabetes: Novo Nordisk addresses chronic kidney disease

After moving from academia to industry, Stephen Gough is now Novo Nordisk’s global chief medical officer, working on putting patients at the centre of the company and providing medical leadership to its R&D strategy, as well as seeking out pre-competitive partnerships. We speak to him about the company’s drive to tackle the complications of type 2 diabetes, such as chronic kidney disease, and how they see the future unfolding with GLP-1 agonists and beyond.
What are some of the major challenges still facing diabetes patients today?
There are currently 425 million people globally estimated to have type 2 diabetes. Over the next 20 years, that could rapidly increase to over 600 million, maybe as high as 700 million.
Cardiovascular disease is the number one cause of morbidity and mortality in people with type 2 diabetes. We also know that cardiovascular disease and chronic kidney disease are inextricably linked. Both conditions are very common, both are associated with significant morbidity and mortality, and there’s a massive unmet need. We don’t have any specific treatments currently for diabetic kidney disease or chronic kidney disease.
“Chronic kidney disease is a global healthcare problem in its own right but we also know that people with chronic kidney disease have a 30-fold higher cardiovascular mortality”
People with diabetes have a whole range of other complications, and we’re looking into those too. For example, diabetic retinopathy is the centre of our FOCUS trial, which has just started. We are continuing to invest in areas such as cardiovascular disease as well as metabolic conditions associated with type 2 diabetes and obesity like non-alcoholic steatohepatitis (NASH).
We’re committed to tackling these complications because they are important for patients. Our commitment is clear in many ways, not least through our investment in several big outcomes trials. In this regard Novo Nordisk is leading the way.
What is Novo Nordisk’s approach to chronic kidney disease?
We’ve become increasingly committed to chronic conditions that include cardiovascular disease and chronic kidney disease – the reason being, as previously mentioned, that diabetes is the leading cause of both conditions.
Around one in three adults with type 2 diabetes has chronic kidney disease, and unfortunately around 50% of those patients don’t have a clear laboratory diagnosis.  Chronic kidney disease is a global healthcare problem in its own right but we also know that people with chronic kidney disease have a 30-fold higher cardiovascular mortality.
Novo Nordisk has had at least two large trials with our two main GLP-1 agonists – LEADER with liraglutide and SUSTAIN-6 with semaglutide – in which we included important renal endpoints. Liraglutide showed over a 20% reduction in chronic renal disease composite endpoints and SUSTAIN-6 showed a 36% reduction.
These exciting results have driven us into conducting the first ever dedicated outcomes trial with a GLP-1 receptor agonist in chronic kidney disease, called the FLOW trial, which will be starting within the next month.
Although it is important to look at the future pipeline, it is also important to recognise that we are making a significant investment in our GLP-1 receptor agonists, because of the strong data that we have shown in recent outcome trials.
Novo Nordisk are world leaders in diabetes and obesity and our ambition is to continue to lead in these important areas. Clearly we also wish to establish ourselves as leaders in cardiovascular disease and chronic kidney disease. Regarding  a dedicated real outcomes trial with respect to GLP-1 receptor agonists in type 2 diabetes, our FLOW trial will be a first.
What kinds of public-private partnerships can help tackle unmet needs in diabetes?
In terms of public-private partnerships, the largest initiative within Europe has been the Innovative Medicines Initiative (IMI). As part of the second IMI, we are the lead pharma partner in Hypo-Resolve as we aim to reduce the burden of hypoglycemia along with other major pharma and academic partners. We’ve also just put out a call for a substantial obesity programme, as we endeavor to learn more about obesity as a chronic disease. Obesity is a chronic disease associated with numerous comorbidities not just impacting on diabetes, but also on kidney disease, and on so many other different areas. As part of the third IMI, I think we will continue to look strategically at some of the big unmet medical needs that I have been discussing.
Do you think a more preventative approach to diabetes, through tackling areas like obesity, is going to become more important?
Absolutely. If you look at why the prevalence of type 2 diabetes is going up, it has undoubtedly been driven by obesity. So for us, targeting obesity is not just the right thing to do in its own right, but it also has the potential to have a big impact on the development of type 2 diabetes.
An important ambition within Novo Nordisk is to “bend the curve of obesity”, so that we can in turn “bend the curve of type 2 diabetes”, and really try to reduce the global burden of both diseases.
How do you see the future of this area developing?
We see that GLP-1 receptor agonists are going to be one of the major therapies for people with type 2 diabetes over the next 15 years or so. If we look at our R&D horizon, I think it’s fair to say that GLP-1 receptor agonists figure very highly in that. Our recent PIONEER programme with oral semaglutide has shown that we can, for the first time, provide a GLP-1 receptor agonist as an oral therapy with a similar level of efficacy and safety to that seen with injectable semaglutide. We believe that this offers the patient a new opportunity when it comes to improving glycemic control and ultimately reducing diabetes related outcomes. Of course, there continue to be other areas that we’re focusing on and we’re always looking at new therapies in type 2 diabetes with new mechanisms of action.
If you look back at the management of type 2 diabetes and developments over the last 5 to 10 years, many of us have now moved beyond glycemic control. Clearly, helping to manage obesity and overweight must also be central to what we do in type 2 diabetes. I think we’ve reached the stage now where glycemic control and beneficial effects on weight are almost a given. As we have seen in LEADER, SUSTAIN 6 and PIONEER 6 with liraglutide and semaglutide, cardiovascular benefits are also being established and this is now reflected in recent international diabetes and cardiovascular guidelines.
These are setting the bar for what we should be striving for when we develop new treatments. We at Novo Nordisk believe we’re going to have to offer something extra. The unmet need of chronic kidney disease is, to my mind, one of the next major complications that should be addressed.
And how do you think the disease area will develop once GLP-1 agonists are more established?
We’ve still got lots to learn, and I think there will be further developments within GLP-1 receptor agonists. I think they will form the backbone of treatment in type 2 diabetes for at least another 15 years and beyond.
We also know however that there are other gut hormones that may also be important in combination with GLP-1 receptor agonists.
Looking even further ahead, we could be looking to change the course of the disease, perhaps by harnessing disease modifying therapies, and this will include stem cells.
Developing therapies that are easier to take, so that we can improve adherence to therapies, will continue to be a big area.
We spend a lot of time listening to, and working with patients, through our patient relations department and expert panels involving patients. An important topic of discussion is the difficulty of taking medicines on a regular basis. Diabetes isn’t something you treat for a week or a month – it’s for life, and we need to be part of the solution, not the problem.
Part of that solution is making medicine easier to take, whether it’s through less frequent injections or switching injections to oral therapies. Digital health programmes are also aimed at helping patients take their medicines on a regular basis, and this is an equally important area of research for us at Novo Nordisk.
Digital health can support patients and health care professionals in several ways. One way is connecting our delivery systems, such as our pens, to your mobile phone to tell you what dose you’ve taken and when you’ve taken it. That will serve as a reminder to take your medicine or to let you know if you’ve already taken it. Linking this to other features such as blood glucose self-measurements will help make appropriate adjustments to treatment, in a more timely manner.
To sum up, I don’t think that there has been a more exciting time in diabetes and obesity research and Novo Nordisk is at the forefront in helping patients deal with the burden of chronic disease.

ASCO live day 5

Exclusive live coverage from day five of the American Society of Clinical Oncology’s annual meeting in Chicago.
• To view all of our coverage from the preeminent cancer event, produced in association with Kantar Health, as well as additional content, visit the Spotlight on ASCO 2019 and the future of oncology
On the agenda for Tuesday:
  • An oral presentation will discuss results of a phase 2 trial of Ipsen/Exelixis’ cabozantinib vs. chemotherapy, based on data from the phase 2 Alliance A091201 study in metastatic and primary uveal melanoma.


View the live coverage from day five at ASCO 2019 below (the live blog may take a few seconds to load):
Joan Mancuso@2020VisionGirl
Dr. Jeff Peppercorn discussing the constant struggle between access to treatment and development of evidence in the interest of time in MBC, at the controversies in MBC session this morning. ⁦@EthicsdoctorP⁩ ⁦@ASCO⁩   pic.twitter.com/AwpAYxqqeu
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Prof Patel also mentioned data from Eli Lilly’s Verzenio (abemaciclib), which is showing promise in dedifferentiated liposarcomas.
Privately held biotech Aadi Bioscience is also developing nab-Sirolimus in a rare sarcoma called advanced PEComa (perivascular epithelioid cell tumour) where there is no approved therapy.
This produced a 42% overall response rate in 31 patients and 62% of patients were still on trial after a year. 35% of patients had stable disease, and disease control rate was 77%.
Aadi expects to file data with the FDA late this year or early next year, and the drug has already been earmarked as a Breakthrough Therapy, setting up a potential six-month priority review.
Just
attended a session on sarcoma, from Professor Shreyaskumar Patel, of the University of Texas MD Anderson Center, on the rare cancer sarcoma. There are some target-specific treatments that are under investigation.
One of these in Epizyme’s taxemetostat, which the biotech just filed with the FDA in epithelioid sarcomas.
Findings of a phase 2 study used for the filing include a 15% objective response rate (ORR) and a 26% disease control rate (DCR).
The median duration of response (DOR) has not yet been reached.

AstraZeneca has presented three-year overall survival (OS) results from the Phase III PACIFIC trial of Imfinzi (durvalumab) in unresectable, Stage III non-small cell lung cancer (NSCLC).
Latest results show a durable and sustained OS benefit in patients with unresectable, Stage III NSCLC who had not progressed following concurrent chemoradiation therapy (CRT), a previous standard-of-care (SoC) treatment.
The OS rate was 57% at three years for patients receiving Imfinzi vs. 43.5% for placebo following concurrent CRT. Median OS was not yet reached with the Imfinzi arm vs. 29.1 months for placebo.

Good morning from Chicago. ASCO is winding up now but there is still some late breaking data coming through.
Bristol-Myers Squibb just announced results of the phase 1/2 CheckMate – 040 study, testing Opdivo (nivolumab) and Yervoy (ipilimumab) in hepatocellular carcinoma (HCC) previously treated with Bayer’s Nexavar (sorafenib).
After 28-month follow up the objective response rate was 31% based on a standard tumour evaluation.
Data were featured on a poster display summarising findings of the study of 148 patients, split into three arms testing different doses.
The best overall survival came from an arm with a lower dose of nivo, and a higher dose of ipi, where overall survival was 22.8 months. At 30 months the overall survival rate was 44% and responses were achieved regardless of PD-L1 status.
There were the usual safety issues expected from this combination such as itchy skin and diarrhoea.
Merry-Jennifer Markham@DrMarkham
I may say this every year, but it’s worth repeating. Thank you to all patients who participated in the research that makes  and progress in cancer care possible. We owe you our gratitude, and we’ll continue to work hard to make outcomes better.
Only 3% of patients with cancer in the US enrol on a clinical trial – and the American Society of Clinical Oncology (ASCO) is concerned that outdated and restrictive eligibility criteria could be hindering research.
The organisaton has used its annual meeting in Chicago to call for some of these outmoded eligibility criteria to be dropped after a study showed that relaxing three rules used to screen patients almost doubled the number of patients on a dummy lung cancer trial.

Antonio Passaro MD PhD@APassaroMD
  
💡One of the best presentstion of this ASCO. A very excellent discussion of @christine_lovly about EGFR exon 20 insertions.
Yesterday orphan, today very potentially druggable mutations!! 💥
The power of clinical and translational pic.twitter.com/muTiRryExX
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At ASCO 2019, results were presented from the phase II EV-201 trial, which evaluated antibody drug conjugate (ADC) enfortumab vedotin in relapsed patients with locally advanced or metastatic bladder cancer.
The data presented were from Cohort 1 of the trial, which evaluated enfortumab in relapsed patients who had been treated with a platinum and a checkpoint inhibitor. Kantar’s Len Kusdra reviews the study in this video.
Sanofi’s plans for a comeback in cancer have taken a step forward with new data on its anti-CD38 candidate isatuximab in multiple myeloma, already filed in the US and Europe.
Headline results from the first phase 3 ICARIA-MM trial of isatuximab were reportedearlier this year, but the actual data was revealed for the first time at the ASCO congress in Chicago – and according to analyst Vamil Divan at Credit Suisse looks “strong” and “pivotal”, likely setting up approvals.

Puma Presents on Phase 3 Neratinib Breast Cancer Trial Results at ASCO

 Puma Biotechnology Inc. (Nasdaq: PBYI), a biopharmaceutical company, announced that results from the Phase III NALA trial of PB272 (neratinib) in patients with HER2-positive metastatic breast cancer who have failed two or more prior lines of HER2-directed treatments (third-line disease) in the setting of metastatic disease, were presented at the American Society of Clinical Oncology (ASCO) 2019 Annual Meeting in Chicago. “Neratinib + capecitabine versus lapatinib + capecitabine in patients with HER2+ metastatic breast cancer previously treated with ≥ 2 HER2-directed regimens: Findings from the multinational, randomized, phase III NALA trial,” was presented as an oral presentation by Adam M. Brufsky, MD, PhD, Professor of Medicine, Co-Director, Comprehensive Breast Cancer Center, Magee Women’s Hospital of the University of Pittsburgh Medical Center. Slides from the presentation are available on the Puma Biotechnology website.
The Phase III NALA trial is a randomized controlled trial of neratinib plus capecitabine versus Tykerb® (lapatinib) plus capecitabine in patients with third-line HER2-positive metastatic breast cancer. The trial enrolled 621 patients who were randomized (1:1) to receive either neratinib plus capecitabine or lapatinib plus capecitabine. The trial was conducted globally at sites in North America, Europe, Asia-Pacific and South America. The co-primary endpoints of the trial are centrally confirmed progression free survival (PFS) and overall survival (OS). An alpha level of 1% was allocated to the PFS and 4% allocated to OS. The study was to be considered positive if either of the co-primary endpoints was positive. Puma reached agreement with the U.S. Food and Drug Administration (FDA) under a Special Protocol Assessment (SPA) for the design of the Phase III clinical trial and the European Medicines Agency (EMA) also provided follow-on scientific advice (SA) consistent with that of the FDA regarding the Company’s Phase III trial design and endpoints used in the trial.
For the primary analysis of centrally confirmed PFS, treatment with neratinib plus capecitabine resulted in a statistically significant improvement in centrally confirmed PFS (hazard ratio=0.76, p=0.0059) compared to treatment with lapatinib plus capecitabine. Because the proportional hazard assumption did not hold, the statistical analysis plan for the NALA trial prespecified that a restricted means survival analysis at 24 months would be performed. In this prespecified analysis the mean PFS for the patients treated with neratinib plus capecitabine was 8.8 months and the mean PFS for the patients treated with lapatinib plus capecitabine was 6.6 months.
For the primary analyses of OS, neratinib plus capecitabine resulted in an improvement in OS that trended positively in favor of the neratinib plus capecitabine arm of the study (hazard ratio = 0.88, p=0.21). The median OS for the patients treated with neratinib plus capecitabine was 21.0 months and the median OS for the patients treated with lapatinib plus capecitabine was 18.7 months. In the prespecified restricted means analysis the mean OS at 48 months for the patients treated with neratinib plus capecitabine was 24.0 months and the mean OS for the patients treated with lapatinib plus capecitabine was 22.2 months.
For the secondary endpoint of time to intervention for symptomatic central nervous system disease (also referred to as brain metastases), the results of the trial showed that treatment with neratinib plus capecitabine led to an improvement over the combination of lapatinib plus capecitabine. The overall cumulative incidence of CNS metastases was 22.8% for the neratinib plus capecitabine arm and 29.2% for the lapatinib plus capecitabine arm (p=0.043, descriptive). For the secondary enpoint of duration of response, neratinib plus capecitabine treatment resulted in a longer duration of response compared to lapatinib and capecitabine treatment, with a median response of 8.54 months compared to a median response of 5.55 months (HR = 0.495, p = 0.0004, descriptive).

Cerner Calls for App Ideas That Improve Consumer Access to Health Records

Cerner, a global health platform and innovation company, challenges innovators and application developers to advance consumers’ access to electronic health records (EHRs) with the 2019 code App Challenge. Participants will join Cerner’s pursuit of the next groundbreaking advancement, with a focus on helping consumers easily access and understand health records.
Cerner’s 40-year history of innovation and technological developments has helped reduce the complexities of health care and drive breakthrough advancements, directly benefiting providers and consumers. By creating a single patient record with a complete picture of a person’s health and financial information, providers can engage people in meaningful and informed discussions to improve health and well-being. Following health care’s digitization era, the focus is on shaping the future with a person-centered mission that requires joint efforts among developers, technology companies and provider organizations. Cerner’s platforms, technology and culture of openness emphasize the importance of collaboration to advance health care.
With the 2019 code App Challenge, Cerner encourages innovators to build apps on its industry-leading platforms that further transform health care. Proposed apps must focus on consumers’ ability to access, understand and use health information in the EHR.
“We challenge innovators and organizations across the industry to join us in advancing interoperability, secure data exchange and consumer access to health records. People should be able to access and understand their own health information regardless of facility or EHR, which is why collaboration through open platforms and shared data is critical to our mission,” said John Gresham, senior vice president, Health Networks, Cerner. “Putting the person at the center of care by improving consumer access to medical information encourages active participation in health care. Embedding consumer-centric apps in the EHR can drive patient engagement, increase awareness of health care costs and improve overall health outcomes.”
Innovation and collaboration are fostered through openness and transparency, exemplified by the launch of the Cerner Open Developer Experience (code) in 2016. The code program provides third-party developers with tools and resources to realize ideas and create software apps that can be embedded across all EHRs, not only Cerner’s platform. The Cerner code App Gallery now has more than 30 apps accessed by nearly 53,000 unique and active monthly users. Cerner’s rigorous validation process helps ensure providers and consumers access high-quality and secure apps that bring differentiated benefits to the delivery of care and the patient experience. Cerner’s open platforms and technology provide new ways for organizations to adjust to health care’s rapidly evolving demands.
Submissions for the 2019 code App Challenge can be at any stage of development, from an idea to a working demo. Developers can create apps independently, as a team, or in collaboration with hospitals or health systems. The winning individual or team will receive a one-year membership to the code program, with Cerner engineers helping guide the app through the validation process. If the app completes validation, it will be added to the code App Gallery. The deadline for submissions is Aug. 16, 2019.
For more information, including official rules and the submission form, click the following link.

Atara: Positive Phase 1 for Mesothelioma CAR T Immunotherapy

Memorial Sloan Kettering Cancer Center collaborators presented results demonstrating that a regionally delivered mesothelin-targeted, autologous CAR T was well tolerated and showed encouraging anti-tumor activity in combination with pembrolizumab, a PD-1 checkpoint inhibitor
 In a subset of 16 malignant pleural mesothelioma patients with minimum follow-up time of 3 months who also received pembrolizumab and lymphodepleting chemotherapy, 12-month overall survival was 80% and best overall response rate was 63%, including 3 investigator-assessed complete responses
Clinical findings presented at the American Society of Clinical Oncology (ASCO) Annual Meeting 2019
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 that the Company’s collaborators at Memorial Sloan Kettering Cancer Center (MSK), Prasad S. Adusumilli, M.D. and Michel Sadelain, M.D., Ph.D., presented an update on encouraging results from an ongoing MSK investigator-sponsored Phase 1 clinical study (NCT02414269) of a mesothelin-targeted CAR T immunotherapy for patients with mesothelin-associated malignant pleural solid tumors, primarily mesothelioma, who progressed following platinum-containing chemotherapy. Mesothelin-targeted, autologous CAR T cells delivered regionally were well-tolerated and showed encouraging anti-tumor activity in combination with pembrolizumab, a PD-1 checkpoint inhibitor. The findings were presented today at the American Society of Clinical Oncology (ASCO) Annual Meeting 2019 in Chicago.

Genentech Phase 3: Xofluza Effective at Preventing Influenza Infection

– Compared with placebo, XOFLUZA treatment significantly reduced the likelihood of people developing influenza (flu) after exposure to an infected household member
– Data from the Phase III BLOCKSTONE study will be submitted to health authorities globally
* * *
Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced that the Phase III BLOCKSTONE study, conducted by Shionogi & Co., Ltd., met its primary endpoint showing that people exposed to a household member with influenza (flu) and treated preventatively with XOFLUZA(TM) (baloxavir marboxil) were significantly less likely to develop the disease compared to those treated with placebo (1.9% versus 13.6%, p&lt;0.0001). Furthermore, XOFLUZA was well tolerated with no safety signals identified. Full results from the BLOCKSTONE study will be presented at an upcoming medical meeting.
” This positive Phase III study adds to robust existing clinical data for XOFLUZA, and is the first to show that a single treatment with XOFLUZA reduced the likelihood that people living with an infected household member would develop the flu,” said Sandra Horning, M.D., chief medical officer and head of Global Product Development. “Preventing otherwise healthy people from developing the flu virus will reduce the overall societal burden of disease, and we look forward to sharing these data with health authorities around the world. ”
XOFLUZA is the first and only one-dose oral medicine approved to treat the flu, and the first new flu medicine approved by the U.S. Food and Drug Administration (FDA) with a novel proposed mechanism of action in nearly 20 years. XOFLUZA is also the only flu treatment with a new mechanism of action shown to be efficacious in both otherwise healthy people with the flu (in the CAPSTONE-1 study) and people at high risk of flu complications (in the CAPSTONE-2 study).
XOFLUZA is currently approved in Japan for the treatment of influenza types A and B in children, adolescents and adults, and in the U.S. for the treatment of acute, uncomplicated influenza in people 12 years of age and older. In addition, the FDA recently accepted a supplemental New Drug Application (sNDA) for XOFLUZA as a one-dose oral treatment for people at high risk of complications from the flu, which includes adults 65 years of age or older, or those who have conditions such as asthma, chronic lung disease, morbid obesity or heart disease – for these people the flu can be particularly serious or deadly. The FDA is expected to decide on whether to approve this additional indication by November 4, 2019.