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A Newly Discovered Comet is Dazzling Skygazers—Here's How to See It While You Can

A Newly Discovered Comet is Dazzling Skygazers—Here's How to See It While You Can

Yahoo14-04-2025

A newly discovered comet is currently visible in the morning sky using a small telescope or binoculars.
The comet, which was designated as C/2025 F2 (SWAN), was detected by SWAN, an instrument on the SOHO spacecraft.
C/2025 F2 (SWAN) will be visible from the Northern Hemisphere throughout April and is expected to reach perihelion on May 1.Skygazers are in for an exciting surprise throughout April—a new glowing green comet was recently discovered and is currently visible with a small telescope or binoculars.
The comet was detected by SWAN, an instrument on the European Space Agency's SOHO spacecraft, which was designed to study the sun. On April 8, the comet was designated as C/2025 F2 (SWAN) by the Minor Planet Center. It's also referred to by the nickname SWAN25F.
C/2025 F2 (SWAN) was discovered by Vladimir Bezugly from Ukraine and Michael Mattiazzo from Australia. Per EarthSky, both amateur astronomers detected the comet on March 29 by examining images taken by the SOHO spacecraft. Mattiazzo posted a photo of the glowing green comet to X.
The comet is currently visible with binoculars or a small telescope. To see it, look toward the northeastern horizon just before sunrise. In late April, the comet may be visible during evening hours as it approaches perihelion—its nearest point to the sun—which it is expected to reach on May 1. According to The Planetary Society, there will be a new moon on April 27, which may make seeing the comet easier.
SWAN25F has gotten notably brighter since it was initially discovered. If it continues to brighten, it may be visible to the naked eye. However, The Planetary Society notes that it is difficult to predict what comets will look like in advance.
By early May, the comet will no longer be visible from most of the Northern Hemisphere, so be sure to catch a glimpse of this rare phenomenon while you can. That said, those in the Southern Hemisphere will be able to see the comet in May just after sunset above the horizon.
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U.S. FDA Accepts New Drug Application Under Priority Review for sevabertinib (BAY 2927088) in HER2-Mutant Non-Small Cell Lung Cancer
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U.S. FDA Accepts New Drug Application Under Priority Review for sevabertinib (BAY 2927088) in HER2-Mutant Non-Small Cell Lung Cancer

Regulatory submission is based on positive results from the ongoing Phase I/II SOHO-01 trial in patients with advanced HER2-mutant non-small cell lung cancer (NSCLC). Investigational agent sevabertinib (BAY 2927088) is an oral, small molecule, tyrosine kinase inhibitor (TKI) being evaluated as a potential new targeted therapy for patients with NSCLC harboring HER2 activating mutations. The U.S. Food and Drug Administration (FDA) grants Priority Review designation for the evaluation of medicines that, if approved, would provide a significant improvement in the safety or effectiveness of the treatment, prevention, or diagnosis of a serious condition. 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The Bayer brand stands for trust, reliability and quality throughout the world. In fiscal 2024, the Group employed around 93,000 people and had sales of 46.6 billion euros. R&D expenses amounted to 6.2 billion euros. For more information, go to © 2025 BayerBAYER and the Bayer Cross are registered trademarks of Bayer. Find more information at Our online press service is just a click away: Follow us on Facebook: Follow us on X: Forward-Looking StatementsThis release may contain forward-looking statements based on current assumptions and forecasts made by Bayer management. Various known and unknown risks, uncertainties and other factors could lead to material differences between the actual future results, financial situation, development or performance of the company and the estimates given here. 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U.S. FDA Accepts New Drug Application Under Priority Review for sevabertinib (BAY 2927088) in HER2-Mutant Non-Small Cell Lung Cancer
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Results from patients with advanced NSCLC harboring a HER2-activating mutation, who experienced disease progression after ≥1 systemic therapies for advanced disease and were naïve to HER2-targeted therapy. 1 The FDA grants Priority Review designation for the evaluation of medicines that, if approved, would provide a significant improvement in the safety or effectiveness of the treatment, prevention, or diagnosis of a serious condition. 2 In 2024, the FDA granted sevabertinib Breakthrough Therapy designation for the treatment of adult patients with unresectable or metastatic NSCLC whose tumors have activating HER2 (ERBB2) mutations, and who have received a prior systemic therapy. The Breakthrough Therapy designation was supported by preliminary clinical evidence from the SOHO-01 trial. The FDA grants Breakthrough Therapy designation for the evaluation of investigational medicines that are intended to treat a serious condition, and preliminary clinical evidence indicates that the drug may demonstrate substantial improvement over available therapy on a clinically significant endpoint(s). 3 About sevabertinib (BAY 2927088) 4 Sevabertinib is an investigational agent and has not been approved by any health authority for use in any country, for any indication. It is currently being evaluated as a potential new targeted treatment option for patients with NSCLC harboring human epidermal growth factor receptors 2 (HER2) activating mutations. Sevabertinib is also being studied in patients with metastatic or unresectable solid tumors harboring HER2-activating mutations. Sevabertinib is an oral, reversible tyrosine kinase inhibitor (TKI) that potently inhibits mutant HER2, including HER2 exon 20 insertions and HER2 point mutations, as well as epidermal growth factor receptors (EGFR), with high selectivity for mutant vs wild-type EGFR. Investigational agent sevabertinib is derived from Bayer's strategic research alliance with the Broad Institute of MIT and Harvard in Cambridge, MA, USA. 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We have a wealth of expertise in areas including Tumor Cell Intrinsic Pathways, Targeted Radionuclide Therapies, and selective Next-Generation Immuno-Oncology. With our portfolio we are advancing cancer treatments from early to metastatic stage, with the goal of extending survival while limiting side effects for the cancer patients we serve. About Bayer Bayer is a global enterprise with core competencies in the life science fields of health care and nutrition. In line with its mission, 'Health for all, Hunger for none,' the company's products and services are designed to help people and the planet thrive by supporting efforts to master the major challenges presented by a growing and aging global population. Bayer is committed to driving sustainable development and generating a positive impact with its businesses. At the same time, the Group aims to increase its earning power and create value through innovation and growth. The Bayer brand stands for trust, reliability and quality throughout the world. In fiscal 2024, the Group employed around 93,000 people and had sales of 46.6 billion euros. R&D expenses amounted to 6.2 billion euros. For more information, go to © 2025 Bayer BAYER and the Bayer Cross are registered trademarks of Bayer. Find more information at Our online press service is just a click away: Follow us on Facebook: Follow us on X: Forward-Looking Statements This release may contain forward-looking statements based on current assumptions and forecasts made by Bayer management. Various known and unknown risks, uncertainties and other factors could lead to material differences between the actual future results, financial situation, development or performance of the company and the estimates given here. These factors include those discussed in Bayer's public reports which are available on the Bayer website at The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments. References Le X, et al. Safety and efficacy of BAY 2927088 in patients with HER2-mutant NSCLC: expansion cohort from the phase I/II SOHO-01 study. Presented at the 2024 IASLC World Conference on Lung Cancer; San Diego, CA, September 7-10, 2024. PL04.03. U.S. Food and Drug Administration. 'Priority Review.' Accessed April 21, 2025. U.S. Food and Drug Administration. 'Breakthrough Therapy.' Accessed April 21, 2025. First in Human Study of BAY2927088 in Participants Who Have Advanced Non-small Cell Lung Cancer (NSCLC) With Mutations in the Genes of Epidermal Growth Factor Receptor (EGFR) and/​or Human Epidermal Growth Factor Receptor 2 (HER2). Clinical trial registration No. NCT05099172. Accessed April 21, 2025. American Cancer Society. 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Sigenergy and Intertek Jointly Release White Paper to Advance Safety in Commercial and Industrial Energy Storage
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Sigenergy and Intertek Jointly Release White Paper to Advance Safety in Commercial and Industrial Energy Storage

SHANGHAI and LONDON, May 27, 2025 /CNW/ -- Sigenergy, a leading energy innovator, and Intertek, a leading Total Quality Assurance provider to industries worldwide, have officially released the white paper Comprehensive Safety Protection for C&I Energy Storage Systems, offering in-depth insights into safety strategies for commercial and industrial energy storage solutions. The white paper was initially previewed during a joint launch ceremony at Intersolar Europe 2025, attended by Samuel Zhang, Chief Technology Officer at Sigenergy, and Klaus Herrmann, Global Certifier at Intertek. Today's official release marks the full publication of their findings and reaffirms both companies' commitment to advancing safety standards across the energy storage industry. As the global energy transition accelerates, commercial and industrial (C&I) energy storage systems are playing a crucial role in improving energy efficiency and balancing power supply and demand. However, their rapid adoption has also brought safety concerns to the forefront, underscoring the urgent need for more rigorous standards and comprehensive safety solutions. In response, Intertek and Sigenergy have collaborated to release a White Paper that helps shape industry-wide benchmarks for the safe deployment and operation of C&I energy storage systems. The White Paper focuses on key safety challenges in C&I energy storage—such as thermal runaway, fire mitigation, and system complexity—and presents technical perspectives based on the evaluation of Sigenergy's SigenStack. With its modular and scalable architecture, SigenStack serves as a practical model for how future energy storage systems can balance safety, flexibility, and operational efficiency. According to the White Paper, SigenStack has undergone a full suite of internationally recognized and automotive-grade safety tests—including UL 9540A, IEC 62619, and GB/T 36276. Test results presented in the publication indicate that the system maintained structural integrity under extreme conditions and achieved operational efficiencies exceeding 95%. By sharing these findings, the White Paper aims to promote best practices and foster the long-term, sustainable development of the global energy storage industry. Samuel Zhang, Chief Technology Officer at Sigenergy, added: "At Sigenergy, we believe safety and innovation must go hand in hand. Through our collaboration with Intertek, we are proud to contribute to the development of high-integrity safety standards and help drive the global transition toward smarter and more sustainable energy systems." Klaus Herrmann, Global Certifier at Intertek commented: "The release of this White Paper marks a significant step in our shared commitment to advancing safety in the energy storage sector. As a global leader in quality assurance, Intertek remains dedicated to enabling innovation through rigorous testing and certification, helping companies meet evolving safety requirements and expand confidently into new markets." Download the Safety White Paper here. View original content to download multimedia: SOURCE Sigenergy Technology Co., Ltd. View original content to download multimedia: Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

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