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LECTRA: First half 2025: stable revenues and limited decline in EBITDA in a context of increased volatility in Q2
Globenewswire· 2025-07-24 16:17
Core Insights - The company reported stable revenues of €261.3 million for the first half of 2025, with a slight decline of 1% compared to the previous year, while EBITDA before non-recurring items decreased by 4% to €40.4 million [5][12][13] - The global economic situation has deteriorated, leading to increased uncertainty and a wait-and-see attitude among customers, particularly in the fashion and automotive sectors [2][3][9] - The company’s net income for the first half of 2025 remained stable at €11.1 million, despite a reduction in tax expenses [10][14] Financial Performance - Q2 2025 revenues decreased by 4% on an actual basis and 2% on a like-for-like basis, with new system orders down 27% [9][10] - The EBITDA margin before non-recurring items for Q2 2025 was 15.2%, down 0.7 percentage points from the previous year [10][13] - The annual recurring revenue (ARR) as of June 30, 2025, was €90.9 million, reflecting a 6% increase on a like-for-like basis [12] Market Context - The indirect impacts of US tariff announcements have led to a pause in investment decisions among customers, who are adapting to the new economic landscape [3][4][5] - The company has taken measures to mitigate the impact of tariffs, including adjusting price lists and rerouting shipments [5][6] - The current economic and political uncertainty has rendered the company's annual objectives irrelevant, as there are no signs of significant improvement [18][19] Strategic Outlook - The company remains focused on its long-term vision and strategic roadmap, emphasizing the development of its SaaS business despite the challenging environment [16][19] - The turbulence in strategic markets presents medium- and long-term development opportunities, necessitating structural changes in supply chains [8][7] - The company’s balance sheet remains strong, with shareholders' equity at €343.8 million and net debt at €34.1 million, reflecting continued deleveraging [15]
LECTRA: Second Quarter and First Half 2025 financial report available
Globenewswire· 2025-07-24 16:15
Core Viewpoint - Lectra has released its Management Discussion and Analysis of Financial Condition and Results of Operations for the Second Quarter and First Half of 2025, which is available on its website and upon request at its headquarters [1][2]. Company Overview - Founded in 1973, Lectra specializes in industrial intelligence technology solutions, integrating SaaS software, cutting equipment, data, and associated services for the fashion, automotive, and furniture industries [3]. - The company emphasizes innovation and transformation, leveraging key technologies of Industry 4.0, including AI, big data, cloud, and the Internet of Things [3]. Operational Footprint - Lectra operates in over one hundred countries and has three production sites for cutting equipment located in France, China, and the United States [4]. - The company employs approximately 3,000 individuals who are guided by core values of open-mindedness, trust, and passion for innovation, with a strong focus on social responsibility [4]. Financial Performance - In 2024, Lectra reported revenues of €527 million, with €77 million derived from its SaaS offerings [5]. - The company is publicly listed on Euronext and is included in several indices, including CAC All Shares, CAC Technology, EN Tech Leaders, and ENT PEA-PME 150 [5].
Dr. Makary: “The FDA did fail” on OxyContin #shorts #oxycontin #fda #wallstreetweek
Bloomberg Television· 2025-07-11 23:18
FDA Oversight & Regulation - FDA aims to remove industry members from advisory committees where possible to preserve the scientific process [1] - FDA needs to monitor drugs and devices immediately after approval to detect safety signals early [2] - The industry should not wait 19 years after a drug's approval to learn about potentially fatal downstream effects, such as the alleged million deaths linked to Oxycontton [2] - FDA is eliminating the ability of a small group of bureaucrats to block safety epidemiology studies [3] - The safety team should work freely without barriers to evaluate drug safety [3] Potential Conflicts of Interest - There is a potential conflict of interest if the team that approved a drug is also responsible for evaluating its safety [4]