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Fujitsu Launches Ultralight, Secured and Full-Featured LIFEBOOK U9311 Business Notebook Redefine Lightweight Business Ultraportable

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Fujitsu unveils the ultra-mobile business notebook LIFEBOOK U9311, the ultralight LIFEBOOK that weighs from approximately 756 g, it offers convenient mobility and superior security with the super-lightweight form factor.

 

HONG KONG, CHINA – Media OutReach – 13 November 2020 – Fujitsu introduces LIFEBOOK U9311 – the featherweight, powerful and enhanced version of its ultra-mobile premium commercial notebook designed for business professionals. The ultraportable, fully featured business notebook is on the market today1 to support workstyle transformation initiatives. The 13.3″ minimally stylish LIFEBOOK U9311 comprises the latest 11th Generation Intel® Core™ processor, enterprise-grade biometric authentication and excellent connectivity.

[View Image]

FUJITSU LIFEBOOK U9311 Business Notebook

Super-Lightweight without Compromising Performance

Constant change is the new norm in smart workplace. Empowering professionals and teams to work agile is the way to ensure business continuity. The 13.3-inch (33.8cm) LIFEBOOK U9311 is 15.5mm slim and weighs as low as approximately 756 g that can be easily held with one hand. It is packed with up to 11th Generation Intel® Core™ i7-1165G7 processor, specially designed for thin-and-light laptops to accelerate demanding business tasks for quick and responsive performance2.

Available in eye-catching red and matte black, the LIFEBOOK U9311 is designed with an ultra-thin bezel that spots a screen-to-body ratio of 84.1%, it is flawlessly fitted in with an ultra-tiny shutter protected camera.

Thin Bezel and Ultra-Tiny Camera Shutter

Secure and Powerful for Workplace Everywhere

Apart from being ultra-portable, LIFEBOOK U9311 is also highly secure, featuring Fujitsu’s PalmSecure™ advanced biometric authentication system that users can sign-in to Windows in a contactless way, the easy and password-free identity verification is hygienic since no contact is required.

Despite its slimline profile, LIFEBOOK U9311 offers best-in-class connectivity options range from full size LAN, HDMI, USB-A and Thunderbolt™ 4 connector for charging and speedy file transfer. The notebook is equipped with a long battery runtime to ensure all-day productivity, and embedded WLAN supporting Wi-Fi 6. 

 

Pursuit of Excellence in the Japan Way

Every Fujitsu notebook delivers the highest reliability and pursuit of excellence in design and usage experience. Staying true to its Japanese heritage, every piece of design details is carefully articulated to create the finest and quality product through precise engineering, cutting edge innovations and quality assurance.

Pricing and Availability

The LIFEBOOK U9311 is available in selected countries in Asia1, please contact Fujitsu for more details.

Learn more: www.fujitsu.com/hk/lifebook-u9311

 

Remarks:

1.     Product availability may vary depending on country. On-shelf dates may vary by geography.

2.     Please go to www.intel.com/11thgen for details.

About Fujitsu

Fujitsu is the leading Japanese information and communication technology (ICT) company, offering a full range of technology products, solutions, and services. Approximately 130,000 Fujitsu people support customers in more than 100 countries. We use our experience and the power of ICT to shape the future of society with our customers. Fujitsu Limited (TSE: 6702) reported consolidated revenues of 3.9 trillion yen (US $35 billion) for the fiscal year ended March 31, 2020. For more information, please see www.fujitsu.com.

About Fujitsu Business Technologies

Fujitsu Business Technologies Asia Pacific is the Asia Pacific Regional Headquarters for business technologies of Fujitsu Limited, Japan, responsible for wide range of personal computers and solutions for corporate and end-user markets in the Asia Market.

All company or product names mentioned herein are trademarks or registered trademarks of their respective owners. Information provided in this press release is accurate at time of publication and is subject to change without advance notice.

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Sarah Cannon to Present Latest in Blood Cancer Research at the 62nd ASH Annual Meeting & Exposition

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Today, Sarah Cannon announced that 53 abstracts and presentations authored by Sarah Cannon experts have been selected for presentation at the upcoming American Society of Hematology (ASH) Annual Meeting & Exposition. Held virtually December 5-8, 2020, the ASH Annual Meeting & Exposition will bring together thought leaders from across the globe to discuss innovative research in malignant and non-malignant blood cancer.

Our network of experts are excited to share the latest advancements in blood cancer research at this years ASH Annual Meeting and Exposition, including important advances in CAR T-Cell Therapy and data from innovative studies for beta thalassemia and sickle cell disease, says Fred LeMaistre, MD, Physician-in-Chief of Blood Cancers, Sarah Cannon. We look forward to virtually coming together with experts from around the world to discuss the pivotal research and cutting-edge therapies that are changing the way we treat blood cancer.

Haydar Frangoul, MD, MS, Medical Director, Pediatric Hematology/Oncology, Sarah Cannon Center for Blood Cancer at The Childrens Hospital at TriStar Centennial, will present ˜Safety and Efficacy of CTX001 in Patients with Transfusion-Dependent β-Thalassemia and Sickle Cell Disease: Early Results from the Climb THAL-111 and Climb SCD-121 Studies of Autologous CRISPR-CAS9“Modified CD34+ Hematopoietic Stem and Progenitor Cells during the Plenary Scientific Session on December 6 from 7-9am PST. Dr. Frangoul will also discuss this research during a press briefing as part of the 62nd ASH Annual Meeting Press Program taking place on December 5 from 9:30-10 a.m. PST.

Aravind Ramakrishnan, MD, Medical Director of Adult Blood and Marrow Transplant, Texas Transplant Institute at the Sarah Cannon Blood Cancer Center at St. Davids South Austin Medical Center, will present ˜Phase 1 Alexander Study of AUTO3, the First CD19/22 Dual Targeting CAR T Cell Therapy, with Pembrolizumab in Patients with Relapsed/Refractory (r/r) DLBCL in an oral presentation on December 7 from 9-10:30 a.m. PST.

Additionally, Ian Flinn, MD, PhD, Director of Lymphoma Research, Sarah Cannon Research Institute, will chair the Satellite Symposia ˜Addressing the Medical Need in CLL: How BTK Inhibitors Are Improving Outcomes on December 4 from 7:30-9 a.m. PST and Jesus G. Berdeja, MD, Director of Myeloma Research, Sarah Cannon Research Institute, will participate in an Education Session on ˜The Emerging Role of Targeted Therapies and Cell Therapy in Transplant – Live Q&A on December 5 from 2-2:45 p.m. PST.

The 53 abstracts and presentations represent studies being conducted by investigators from Sarah Cannon Blood Cancer Network and Sarah Cannon Research Institute in affiliation with: Colorado Blood Cancer Institute at Presbyterian/St. Lukes Medical Center- HealthONE in Denver, Florida Cancer Specialists, Texas Oncology at Medical City Dallas in Dallas, Private Care at Guys at London Bridge Hospital in London, UK, Sarah Cannon Blood Cancer Center at Research Medical Center in Kansas City, Mo., Sarah Cannon Blood Cancer Center at St. Davids South Austin Medical Center in Austin, Texas, Sarah Cannon Center for Blood Cancer at TriStar Centennial Medical Center in Nashville, Tenn., Texas Transplant Institute at Methodist Hospital in San Antonio, Texas, Tulane Medical Center in New Orleans, and University of Oklahoma Medical Center in Oklahoma City.

Additionally, ASH Annual Meeting & Exposition posters with Sarah Cannon Blood Cancer Network experts as first authors will be presented by:

  • Carlos Bachier, MD, Director of Cellular Therapy Research, Sarah Cannon Research Institute; Program Director, Sarah Cannon Center for Blood Cancer at TriStar Centennial Medical Center, will present on ˜A Phase 1 Study of NKX101, an Allogeneic CAR Natural Killer (NK) Cell Therapy, in Subjects with Relapsed/Refractory (R/R) Acute Myeloid Leukemia (AML) or Higher-Risk Myelodysplastic Syndrome (MDS) on December 5 from 7am-3:30 p.m. PST and ˜Costs and Adverse Events Associated with Ibrutinib or Ruxolitinib in Chronic Graft-Versus-Host Disease on December 7 from 7 a.m.-3:30 p.m. PST.
  • Minoo Battiwalla, MD, MS, Director of Outcomes Research, Sarah Cannon, will present on ˜Reduction in Transplantation Activity without Impairment in Outcomes in the Covid-19 Era- Data from the Sarah Cannon Blood Cancer Network (SCBCN) on December 7 from 7 a.m.-3:30 p.m. PST.
  • Dr. Berdeja will present on ˜Efficacy and Safety of Idecabtagene Vicleucel (ide-cel, bb2121) in Elderly Patients with Relapsed and Refractory Multiple Myeloma: KarMMa Subgroup Analysis on December 5 from 7 a.m.-3:30 p.m. PST.
  • William Donnellan, MD, Director of Leukemia/Myelodysplastic Syndrome Research, Sarah Cannon Research Institute, will present on ˜Use of Venetoclax (VEN) and Hypomethylating Agents (HMA) in Newly Diagnosed Acute Myeloid Leukemia (AML) in the United States (US) “ Real World (RW) Response, Treatment Duration, Dose and Schedule Modifications on December 6 from 7 a.m.-3:30 p.m. PST.
  • Dr. Flinn will present on ˜Debulking Regimens Prior to Initiating Venetoclax Therapy in Untreated Patients with Chronic Lymphocytic Leukemia: Interim Results from a Phase 3b Study on December 7 from 7 a.m.-3:30 p.m. PST.
  • Henning Schade, MD, Assistant Member Physician, Colorado Blood Cancer Institute at Presbyterian/St. Lukes Medical Center “ HealthONE, will present on ˜HPN217-3001: A Phase 1/2 Open-Label, Multicenter, Dose Escalation and Dose Expansion Study of the Safety, Tolerability, and Pharmacokinetics of HPN217, a Bcma-Targeting T-Cell Engager, in Patients with Relapsed/Refractory Multiple Myeloma on December 5 from 7 a.m.-3:30 p.m. PST.

About The Sarah Cannon Blood Cancer Network

The Sarah Cannon Blood Cancer Network offers patients convenient, community-based access to complex blood cancer care including blood and marrow transplantation (BMT), clinical trials and innovative therapies such as CAR T-Cell Therapy. The Sarah Cannon Blood Cancer Network brings together physician-led blood cancer programs across the United States and United Kingdom and is one of the largest providers of BMT. In fact, it conducts more than 1,200 transplants annually through eight FACT/JACIE accredited transplant centers and has performed more than 14,000 transplants since inception of its first program. The Sarah Cannon Blood Cancer Network programs include Sarah Cannon Blood Cancer Center at St. Davids South Austin Medical Center in Austin, Texas, Medical City Dallas in Dallas, Colorado Blood Cancer Institute at Presbyterian/St. Lukes Medical Center- HealthONE in Denver, Sarah Cannon Blood Cancer Center at Research Medical Center in Kansas City, Mo., Sarah Cannon Center for Blood Cancer at TriStar Centennial Medical Center in Nashville, Tenn., Texas Transplant Institute at Methodist Hospital in San Antonio, HCA Healthcare UK at University College Hospital, Private Care (London), Private Care at Guys at London Bridge Hospital (London) and The Christie Private Care, part of HCA Healthcare UK (Manchester). For more information about the Network and Sarah Cannons full suite of oncology services, visit sarahcannon.com.

Becca Gelman

[email protected]

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Children’s Hospital Los Angeles Offers FREE Flu Vaccination Family Clinic

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Childrens Hospital Los Angeles:

WHAT:

Get your free flu shot at select CHLA Specialty Care Centers. No appointment needed. Available for the whole family. www.CHLA.org/events

 

 

 

 

WHY:

The American Academy of Pediatrics, the Centers for Disease Control and Prevention, and the Infectious Diseases Society of America recommends everyone over 6 months of age receive the flu vaccine every year. With COVID-19 numbers still at dangerous levels, its now more crucial than every to be vigilant about your familys health.

 

 

 

 

WHEN:

Saturday, December 5

 

 

Saturday, December 12

 

 

Saturday, December 19

 

 

 

 

 

9 a.m. “ 3 p.m.

 

 

 

 

WHERE:

Walk-up clinic

 

  • South Bay “ 3440 Torrance Blvd., Torrance, CA 90503 (in the main lobby)

Drive-up clinics

  • Arcadia “ 468 E. Santa Clara St., Arcadia, CA 91006
  • Encino “ 5363 Balboa Blvd., Encino, CA 91316
  • Valencia “ 23838 Valencia Blvd., Valencia, CA 91355

 

(PRESS ONLY)

Lauren Song, [email protected] or 323-203-6737

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Glancy Prongay & Murray LLP, a Leading Securities Fraud Law Firm, Announces the Filing of a Securities Class Action on Behalf of Fortress Biotech, Inc. (FBIO) Investors

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Glancy Prongay & Murray LLP (GPM), a leading national shareholder rights law firm, announces that a class action lawsuit has been filed on behalf of investors who purchased or otherwise acquired Fortress Biotech, Inc. (Fortress or the Company) (NASDAQ: FBIO) securities between December 11, 2019 and October 9, 2020 inclusive (the Class Period). Fortress investors have until January 26, 2021 to file a lead plaintiff motion.

If you suffered a loss on your Fortress investments or would like to inquire about potentially pursuing claims to recover your loss under the federal securities laws, you can submit your contact information at https://www.glancylaw.com/cases/fortress-biotech-inc/. You can also contact Charles H. Linehan, of GPM at 310-201-9150, Toll-Free at 888-773-9224, or via email at [email protected] to learn more about your rights.

Fortress develops and commercializes pharmaceutical and biotechnology products. In December 2019, the Company’s majority-controlled subsidiary, Avenue Therapeutics, Inc. (“Avenue”), submitted a New Drug Application (“NDA”) for its intravenous (“IV”) Tramadol product to the U.S. Food and Drug Administration (“FDA”) for the management of moderate to moderately severe pain in adults in a medically supervised health care setting.

On October 12, 2020, Avenue disclosed receipt of a Complete Response Letter (“CRL”) from the FDA regarding the NDA for its IV Tramadol product. Specifically, the FDA advised Avenue that “it cannot approve the application in its present form” because “IV tramadol, intended to treat patients in acute pain who require an opioid, is not safe for the intended patient population.” Specifically, the CRL stated: “[I]f a patient requires an analgesic between the first dose of IV tramadol and the onset of analgesia, a rescue analgesic would be needed. The likely choice would be another opioid, which would result in opioid ‘stacking’ and increase the likelihood of opioid-related adverse effects.”

On this news, Fortress’s stock price fell $1.00 per share, or 23.98%, to close at $3.17 per share on October 12, 2020, thereby injuring investors.

The complaint filed alleges that throughout the Class Period, Defendants made materially false and/or misleading statements, as well as failed to disclose material adverse facts about the Companys business, operations, and prospects. Specifically, Defendants failed to disclose to investors that: (1) IV Tramadol was not safe for the intended patient population; (2) as a result, it was foreseeable that the FDA would not approve the NDA for IV Tramadol; and (3) as a result, Defendants’ statements about its business, operations, and prospects, were materially false and misleading and/or lacked a reasonable basis at all relevant times.

Follow us for updates on LinkedIn, Twitter, or Facebook.

If you purchased or otherwise acquired Fortress securities during the Class Period, you may move the Court no later than January 26, 2021 to ask the Court to appoint you as lead plaintiff. To be a member of the Class you need not take any action at this time; you may retain counsel of your choice or take no action and remain an absent member of the Class. If you wish to¯learn more¯about this action, or if you have any questions concerning this announcement or your rights or interests with respect to these matters, please contact Charles Linehan, Esquire, of GPM, 1925 Century Park East, Suite 2100, Los Angeles California 90067 at 310-201-9150, Toll-Free at 888-773-9224, by email to [email protected], or visit our website at www.glancylaw.com. If you inquire by email please include your mailing address, telephone number and number of shares purchased.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethical rules.

Glancy Prongay & Murray LLP, Los Angeles

Charles H. Linehan, 310-201-9150 or 888-773-9224

1925 Century Park East, Suite 2100

Los Angeles, CA 90067

www.glancylaw.com

[email protected]

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