
DataBee®, a Comcast Company, Adds AI-Powered Network Detection and Response to Its Suite of Cybersecurity Products
PHILADELPHIA--(BUSINESS WIRE)-- DataBee ®, a Comcast Company, today announced the addition of BluVector®, an AI-powered network detection and response (NDR) platform, to its suite of cybersecurity products, which also includes DataBee, an award-winning security data fabric platform. DataBee BluVector provides an on-premise cybersecurity solution that leverages AI/ML and network visibility to help organizations detect network evidence of ransomware, in-memory malware, zero-day exploits, and other cyber threats so organizations can more rapidly initiate cybersecurity investigations and disrupt attacks.
DataBee BluVector's patented machine learning engine can detect zero-day malware, file-less attacks and polymorphic threats without prior signatures by analyzing file content for malicious traits. Purpose-built for high performance, DataBee BluVector can inspect millions of packets per second at line speed (scales beyond 10 Gbps) for real-time threat detection. Its adaptive AI/ML capabilities learn from an organization's unique environment, to continuously customize threat detection over time. Comcast acquired BluVector Inc. in 2019 and has since deployed the BluVector NDR platform throughout its vast environment, using it to prioritize and enrich threat hunting with detection and intelligence sources; leverage AI-powered detections for file-based malware and zero-day attacks; and help reduce costly log intake.
'DataBee BluVector is a powerhouse, working behind the scenes at Comcast to provide advanced threat detection, including the ability to detect and contain AI-based malware and zero-day threats as early as possible,' said Noopur Davis, Executive Vice President, Chief Information Security and Product Privacy Officer, Comcast Corporation and Comcast Cable. 'As part of the community of global CISOs, it feels great to be able to share highly effective tools and technologies with my industry peers through our DataBee business, and BluVector is certainly one of those.'
"With DataBee BluVector, we've gained valuable insights that identified previously unknown external and insider risks. Additionally, DataBee BluVector detects and identifies misconfigured devices, and aids in troubleshooting network issues, which helped solve critical compliance and operational challenges,' said Jesse Whaley, Vice President and Chief Information Security Officer for Amtrak. 'Noopur is right; DataBee BluVector is a highly effective NDR solution that is easy and quick to deploy and delivers immediate results."
DataBee Builds on Success with New Platform Enhancements
DataBee continues to enhance its offering to better meet the complex needs of cybersecurity teams. The DataBee security data fabric platform now supports all leading cloud storage options, as well as the ability to use on-premise storage. This gives customers the ability to use their existing cloud environments, such as AWS S3 and Azure Blob, to store and analyze their security data; customers do not have to invest in additional data infrastructure to benefit from the data transformations and insights that the DataBee platform delivers.
DataBee leverages Apache Iceberg ™, the open table format (OTF) for analytic datasets, as its data storage format, providing platform independence and flexibility, and eliminating the need for specific business intelligence tools or platforms.
'We want to make security data easily accessible and actionable within the parameters of our customers' existing technology choices and investments. Supporting cloud and on-prem storage options enables us to do just that,' said Nicole Bucala, General Manager of DataBee. 'Our security data fabric platform can help CISOs quickly get and act on data insights, while DataBee BluVector can provide critical network protection and visibility into even the most stealthy of attacks. Comcast's own results with these solutions are a tribute to the value they can bring to large enterprise security programs.'
As a testament to the strength of DataBee's offering and it's continuous enhancements, DataBee received the Data Breakthrough Award for ' Data Management Solution of the Year,' recognizing 'the breakthrough innovation of DataBee's cloud-native security, risk and compliance data fabric platform.' DataBee was also named a finalist for 'Best Compliance Solution' in the 2025 SC Awards, and was selected by industry analyst and consulting firm EMA for its annual ' Vendor Vision report ', which 'showcased twelve standout cybersecurity companies recognized for their innovation and leadership 1 '.
DataBee is a Platinum sponsor of the Gartner Security and Risk Management Summit taking place from June 9-11 in National Harbor, MD and can be found in booth 868.
For more information or to request a demo of the DataBee security data fabric platform and DataBee BluVector, visit https://www.databee.ai/.
1 Press release, ' EMA Unveils Top Security Innovators in Annual Vendor Vision Report Ahead of the 2025 RSA Conference,' April 16, 2025
About Comcast Corporation
Comcast Corporation (Nasdaq: CMCSA) is a global media and technology company. From the connectivity and platforms we provide, to the content and experiences we create, our businesses reach hundreds of millions of customers, viewers, and guests worldwide. We deliver world-class broadband, wireless, and video through Xfinity, Comcast Business, and Sky; produce, distribute, and stream leading entertainment, sports, and news through brands including NBC, Telemundo, Universal, Peacock, and Sky; and bring incredible theme parks and attractions to life through Universal Destinations & Experiences. Visit www.comcastcorporation.com for more information.
For more information on DataBee, visit databee.ai.
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Share The studies evaluated the safety and efficacy of INCA033989 in patients with ET as measured by hematologic response and reduction in mutCALR variant allele frequency (VAF). Results as of April 4, 2025, showed rapid and durable normalization of platelet counts across all dose levels, with a trend toward improved responses in higher doses (>400 mg), in patients with ET treated with INCA033989. Notably, 86% of patients at doses 400 mg and above achieved a complete or partial hematologic response, with the majority (82%) of patients achieving complete response. Eighty-nine (89) percent of evaluable patients (34/38) showed a reduction in mutCALR VAF from baseline. A partial molecular response (>50% VAF reduction) was observed in 21% of evaluable patients (8/38) after only 3 cycles of treatment. An exploratory study using single-cell DNA (scDNA) sequencing showed that INCA033989 directly targets and reduces cells carrying mutCALR. 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'These findings, and the further development of INCA033989, offer the potential to significantly transform the treatment of patients with CALR-mutant myeloproliferative neoplasms (MPNs).' The results (N=49) showed that INCA033989 was well tolerated across all dose cohorts (24 to 2,500 mg), with no dose-limiting toxicities observed. Only one (1) patient discontinued treatment, and only one (1) dose reduction due to treatment-emergent adverse events (TEAEs) was observed. No infusion interruptions due to TEAEs were reported, and a maximum tolerated dose was not reached. Forty-two (42) patients across the dose cohorts reported a TEAE. The most common TEAEs were fatigue (26.5%) and upper respiratory tract infection (20.4%), all of which were Grade ≤2. Thirteen (13) patients had Grade >3 TEAEs, with transient asymptomatic lipase increase as the most common (6%). 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More information regarding the EHA2025 Congress and the data from Incyte's hematology/oncology portfolio being featured at the meeting can be found on the EHA website: Incyte Conference Call and Webcast Incyte will host an in-person analyst and investor event on Sunday, June 15, 2025, from 6:00 - 7:30 a.m. ET (12:00 - 1:30 p.m. CEST) to discuss key mutCALR data presented at EHA. The event will be webcasted and can be accessed via the Events and Presentations tab of the Investor section of and it will be available for replay for 30 days. About Myeloproliferative Neoplasms Myeloproliferative neoplasms (MPNs) are a closely related group of blood cancers in which the bone marrow functions abnormally. The bone marrow is where the body's blood cells are made. MPNs are progressive blood cancers that can strike anyone at any age, but they are more common in older adults. Estimates of the prevalence of MPNs vary, but analysis of claims data suggests there may be as many as 200,000 people in the U.S. living with the most prevalent MPNs: myelofibrosis, polycythemia vera or essential thrombocythemia (ET). 1 About Mutations in Calreticulin (mutCALR) Calreticulin (CALR) is a protein involved in the regulation of cellular calcium levels and normal protein folding. Somatic, or non-inherited, DNA mutations in the CALR gene (mutCALR) can result in abnormal protein function and lead to the development of myeloproliferative neoplasms (MPNs), 2 a closely related group of clonal blood cancers in which the bone marrow functions abnormally, overproducing blood cells. 3,4 Among two types of MPNs, essential thrombocythemia (ET) and myelofibrosis (MF), mutCALR drives 25-35% of all cases. 2,3 There are approximately 60,000 patients in the U.S. and Europe with mutCALR positive ET. 5 Incyte is at the forefront of developing novel therapies for patients with mutCALR ET or MF that target only malignant cells, sparing normal cells, including INCA033989, a first-in-class, mutCALR-specific therapy. About the INCA033989 Trial Program The clinical trial program for INCA033989 includes two multicenter, open-label Phase 1 studies, INCA33989-101 (NCT05936359) and INCA33989-102 (NCT06034002), enrolling ~225 patients outside of the U.S. and ~140 patients in the U.S., respectively. The studies are evaluating the safety, tolerability, dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDE) of INCA033989 administered as a monotherapy or in combination with ruxolitinib in patients with myeloproliferative neoplasms (MPNs), including essential thrombocythemia (ET) and myelofibrosis (MF). The intent of Part 1A (dose escalation) is to identify the MTD and/or the RDE of INCA033989 among patients with MF and ET. In Part 1A INCA033989 is administered intravenously every two weeks at a protocol defined dose ranging from 24 mg. to 2,500 mg. In Part 1B (dose expansion), INCA033989 is administered at the RDE(s) identified during Part 1A. The primary endpoint of the studies focuses on safety and tolerability as measured by: the number of participants with DLTs up to 28 days, the number of participants with treatment-emergent adverse events (TEAEs) up to 3 years and 60 days, and the number of participants with TEAEs leading to dose modification or discontinuation up to 3 years and 60 days. Secondary endpoints include response rates, mean change of ET total symptom score from baseline, percentage of MF patients achieving spleen volume reduction, MF patient anemia response, mean change in disease-related allele burden and various pharmacokinetics measures up to 3 years and 60 days. For more information on the study, please visit: and About Incyte A global biopharmaceutical company on a mission to Solve On., Incyte follows the science to find solutions for patients with unmet medical needs. Through the discovery, development and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Oncology and Inflammation & Autoimmunity. Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe and Asia. For additional information on Incyte, please visit or follow us on social media: LinkedIn, X, Instagram, Facebook, YouTube. Forward-Looking Statements Except for the historical information set forth herein, the matters set forth in this press release, including statements regarding the presentation of data for Incyte's anti-mutCALR monoclonal antibody (INCA033989), the potential this monoclonal antibody offers for patients, and expectations regarding ongoing and future clinical trials contain predictions, estimates, and other forward-looking statements. These forward-looking statements are based on Incyte's current expectations and subject to risks and uncertainties that may cause actual results to differ materially, including unanticipated developments in and risks related to: further research and development and the results of clinical trials possibly being unsuccessful or insufficient to meet applicable regulatory standards or warrant continued development; the ability to enroll sufficient numbers of subjects in clinical trials and the ability to enroll subjects in accordance with planned schedules; determinations made by the FDA, EMA and other regulatory agencies; Incyte's dependence on its relationships with and changes in the plans of its collaboration partners; the efficacy or safety of Incyte's products and the products of Incyte's collaboration partners; the acceptance of Incyte's products and the products of Incyte's collaboration partners in the marketplace; market competition; unexpected variations in the demand for Incyte's products and the products of Incyte's collaboration partners; the effects of announced or unexpected price regulation or limitations on reimbursement or coverage for Incyte's products and the products of Incyte's collaboration partners; sales, marketing, manufacturing and distribution requirements, including Incyte's and its collaboration partners' ability to successfully commercialize and build commercial infrastructure for newly approved products and any additional products that become approved; greater than expected expenses, including expenses relating to litigation or strategic activities; variations in foreign currency exchange rates; and other risks detailed in Incyte's reports filed with the Securities and Exchange Commission, including its annual report on form 10-K and our quarterly report on Form 10-Q for the quarter ended March 31, 2025. Incyte disclaims any intent or obligation to update these forward-looking statements.