MA-PATHAI
21.5.2024 09:01:26 CEST | Business Wire | Press release
PathAI, a global leader in AI-powered pathology, today announced a new Early Access Program (EAP) to drive adoption of its AISightTM Image Management System (IMS) in Mainland Europe.1 Earlier in 2023, PathAI announced a similar program for laboratories in the United States, which attracted over 50 laboratories with many exploring long-term use of PathAI’s AISight Image Management System and broad menu of AI Products.
As part of the EAP, AP Laboratories in Europe can trial AISight, a modern and cloud-based digital pathology solution compliant with GDPR, as well as conduct and publish real-world validation studies of PathAI’s AI Products such as ArtifactDetect, TumorDetect, AIM-TumorCellularity, AIM-PD-L1, and AIM-HER2.2
“We are thrilled to commence a more dedicated focus to bring AISight Image Management System to labs in Europe. We have continued to make improvements on the platform with input from our first set of commercial customers in the U.S. We are excited to partner with European labs in democratizing access to digital pathology, enhancing pathologist experience, and ultimately improving patient outcomes,” said Nick Brown, Chief Growth Officer at PathAI.
AISight is a cloud-based platform that enables efficient end-to-end digital pathology workflows. AISight provides best-in-class caseload balancing and assignment, caselist prioritization, image ingestion, image viewing, collaboration tools, and image and case management. Via AISight Link, AISight can also be integrated bidirectionally with laboratory information systems for streamlined workflows. Anatomic pathology laboratories of all sizes and specialties – including health systems, university hospitals, and reference laboratories – may utilize AISight.
“PathAI has been an excellent thought partner for helping our institution think through what it means to create a modern, next-generation digital pathology workflow that spans versatile use cases like research, clinical trials, and diagnostics,” said Prof. Dr. Jan Budczies, Head of Medical Bioinformatics at the University of Heidelberg. “We are excited to partner with PathAI on this Early Access Program and look forward to taking advantage of their growing portfolio of features and algorithms on AISight, starting with our Molecular Pathology Department where we are especially interested in understanding the feasibility of estimating tumor cell content and characterizing immune cell infiltrates more precisely by leveraging digital pathology and artificial intelligence.”
AISight enables pathologists with seamless access to a broad array of algorithms to drive workflow optimization, standardized biomarker quantitation, and next-generation case prioritization including ArtifactDetect, TumorDetect, AIM-TumorCellularity, AIM-PD-L1 (NSCLC, HNSCC, Melanoma, Urothelial), and AIM-HER2 Breast Cancer and will also host third-party algorithms on request.
“We have trialed AISight at our department for several months now. At our Molecular Pathology Unit we are especially interested in understanding the feasibility of estimating tumor cell content through image analysis. PathAI’s AIM-TumorCellularity can be a tool that will change time to treatment for patients in need of molecular testing,” said Prof. Dr. Holger Moch, Director of Pathology at the University of Zurich and PathAI Advisor. “PathAI has been responsive to our unique needs and a valuable thought partner in helping us think through how to pick the most modern and innovative digital pathology solution on the market. We are excited about our partnership with PathAI and look forward to taking advantage of their growing portfolio of algorithms and feature improvements on AISight.”
“We have been leveraging the AIM-PD-L1 NSCLC and AIM-TumorCellularity NSCLC Algorithms over the past few months at our institution as part of a large research cohort,” said Dr. Jose Palacios, Director of Pathology at Ramon y Cajal Hospital in Madrid, Spain. “Given the success we’ve seen at our own institution, there has been increasing demand from across Spain to leverage these algorithms and we are working with more than 10+ hospitals across Spain to implement these tools.”
PathAI expects IVDR Certification of AISight Dx for primary diagnosis by Q3 2024. Early Access Program Participants will be the first to receive access to this platform. To learn more about AISight, visit our website. PathAI’s team will also be at upcoming conferences including the European Congress of Digital Pathology in Vilnius, Lithuania (June 5-8), European Congress of Pathology in Florence, Italy (September 7-11), and the DP/AI Congress in London, United Kingdom (December 7-8).
Footnotes
1 AISight™ is for research use only. Not for use in diagnostic procedures.
2 ArtifactDetect™, TumorDetect™, AIM-TumorCellularity™, AIM-PD-L1™ and AIM-HER2™ are research use only. Not for use in diagnostic procedures.
About PathAI
PathAI is the only AI-focused technology company to provide comprehensive precision pathology solutions from wet lab services to algorithm deployment for clinical trials and laboratory use. Rigorously trained and validated with data from more than 15 million annotations, its AI-powered models can be leveraged to optimize the analysis of pathology samples to improve efficiency and accuracy of pathology interpretation, as well as to better gauge therapeutic efficacy and accelerate drug development for complex diseases.
PathAI is headquartered in Boston, MA. For more information, please visit www.pathai.com.
To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.
View source version on businesswire.com: https://www.businesswire.com/news/home/20240521660078/en/
About Business Wire
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Datavault AI Announces Board of Directors Has Requested Management’s Complete Plan for Dividend Spin-Out of Acoustic Sciences Division into Stand-Alone Public Company7.5.2026 15:07:00 CEST | Press release
Initial planning calls for Data Sciences Division to focus efforts in cyber secure infrastructure with dedication in fintech and patented Information Data Exchange® (IDE®) Management will harness its API Media acquisition, robust patent portfolio, ADIO® Inaudible Tones, WiSA® and Dolby® partnerships to establish worldwide acoustic industry standards in high-definition wireless transmission, spatial-audio control and interoperability Plan includes API media’s stand-alone and renewed execution of WiSA semiconductor and software modules strategy with an R&D effort targeted to new robotic and drone applications Datavault AI Inc. (“Datavault AI” or the “Company”) (NASDAQ:DVLT), a pioneering technology licensing company seeking to redefine data valuation, monetization, and secure Web 3.0 experiences, today announced that Company management has commenced its evaluation of a potential dividend spin-out of the Company’s Acoustic Sciences division which includes its ADIO®, WiSA®, Event Citadel™,
Incyte Announces 24-Week Long-Term Data from Phase 3 TRuE-AD4 Trial of Opzelura® (ruxolitinib) Cream in Adults with Moderate Atopic Dermatitis7.5.2026 14:50:00 CEST | Press release
First presentation of Week 24 results from TRuE-AD4 study in adults with moderate atopic dermatitis (AD) who had an inadequate response, intolerance or contraindication to topical corticosteroids (TCSs) and topical calcineurin inhibitors (TCIs)at the 2026 EADV SymposiumThe vast majority of patients achieving EASI50 at Week 8 and continuing double-blind, as needed treatment with Opzelura® (ruxolitinib) cream through Week 24 demonstrated disease control, with 84.3% achieving EASI75 (a ≥75% improvement in the Eczema Area and Severity Index score from baseline) and 70.6% achieving IGA-TS (Investigator’s Global Assessment Treatment Success)Data support Type-II variation application submitted for ruxolitinib cream 1.5% for the treatment of adults with moderate AD in the European Union (EU), feedback expected in 1H 2026 Incyte (Nasdaq:INCY) today announced final 24-week data from the Phase 3 TRuE-AD4 study evaluating the efficacy and safety of Opzelura® (ruxolitinib) cream in adults with mode
Rapid Medical™’s TIGERTRIEVER™ 13 Demonstrates Promising 90-Day Outcomes in DISTALS Trial, Reinforcing Pivotal Safety and Efficacy Findings7.5.2026 14:03:00 CEST | Press release
Full data presented at ESOC 2026 further strengthen the clinical evidence supporting TIGERTRIEVER™ 13 for the treatment of distal vessel occlusion stroke — a segment representing nearly half of all ischemic strokes Rapid Medical™, a leading developer of advanced stroke treatment devices, today announced full results from the DISTALS randomized clinical trial, presented at the 11th European Stroke Organisation Conference (ESOC) in Maastricht, Netherlands, showing that TIGERTRIEVER™ 13 can safely restore blood flow to the brain and may improve clinical outcomes in patients with distal and medium vessel occlusion (DMVO) stroke. These findings build on earlier results showing a threefold improvement in restoring blood flow compared with medical management alone (p<0.0001), with no cases of serious brain bleeding observed in the treatment group. “These results show we can now safely restore blood flow and suggest this will make a meaningful difference for the right patients,” said Jeffrey L
2 Million Downloads in Six Months: Tabelog’s Multilingual App Solves Critical Dining Pain Points for Travelers to Japan7.5.2026 14:00:00 CEST | Press release
“Eat Where Locals Eat” Making authentic Japanese dining experiences accessible to global travelers through instant reservations at over 70,000 restaurants nationwide. Tabelog (https://tabelog.com/en/), one of Japan’s largest (*1) restaurant search and reservation services operated by Kakaku.com, Inc., has announced that its multilingual smartphone app (iOS/Android) for travelers visiting Japan has reached 2 million downloads (*2). This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260507560248/en/ 2M+ Downloads in 6 Months. The app also ranked #1 in downloads among Restaurant Search Apps in Japan for International Travelers (*3) in Taiwan, Hong Kong, South Korea, and the U.S., reflecting its immense popularity among global visitors. Download URL: https://tabelog-tourists.onelink.me/3eEh/iqkkho9r The Trusted Choice for Global Travelers: Solving Two Major Dining Pain Points in Japan For years, international visitors to Japan have
Altasciences and Certara Announce Strategic Partnership to Accelerate Early Drug Development7.5.2026 14:00:00 CEST | Press release
Altasciences, a fully integrated drug development solution company, andCertara (Nasdaq: CERT), a global leader in model-informed drug development (MIDD), today announced a strategic partnership to accelerate early-phase development programs. Fewer than half of preclinical drug candidates successfully reach first-in-human trials. Failures are driven by toxicity, poor pharmacokinetics, lack of efficacy, and challenges translating results from animals to humans. Many of these risks can be mitigated through a fully integrated model-informed drug development approach. Building on Altasciences’ Acceleration Platform, the integration of Certara’s strategic drug development services and biosimulation technology enables sponsors to establish proof of mechanism earlier, design more efficient studies, and make informed go/no-go decisions with greater confidence. By embedding modeling insights and digital workflows directly into development execution, study designs are optimized, dosing strategies
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom
