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Bug-eyed telescope ready to find Earth-smashing asteroids

Bug-eyed telescope ready to find Earth-smashing asteroids

Yahoo05-06-2025

It's only a matter of time before a catastrophically sized asteroid barrels towards Earth again. Until very recently in human history, there was no way of knowing if one was hurtling towards us, much less do anything to alter its path. Now, international space agencies and disaster preparedness experts have powerful tools to keep watch over the skies—and the newest aide just opened its bug-inspired compound 'eye.'
According to the European Space Agency, the Flyeye-1 telescope recently completed its 'first light' test at the Italian Space Agency's Space Geodesy Center, located about 160 miles east of Naples. Soon, it and as many as three other similar installations around the world will work in tandem to provide comprehensive, automated surveys of space every night to scan for cosmic threats.
'The earlier we spot potentially hazardous asteroids, the more time we have to assess them and, if necessary, prepare a response,' explains Richard Moissl, Head of ESA's Planetary Defence Office. 'ESA's Flyeye telescopes will be an early-warning system, and their discoveries will be shared with the global planetary defence community.'
Similar to an insect's vision (hence its name), Flyeye captures incoming light through its 3.3-foot-wide primary mirror. That light is divided into 16 independent channels, all equipped with their own secondary lens and detector cameras designed to flag extremely faint objects. Flyeye's automated observation schedule is designed to factor in variables such as lunar brightness along with other survey telescopes like NASA's ATLAS, the Zwicky Transient Facility, and the forthcoming Vera Rubin Telescope.
So what happens if Flyeye spies a suspicious space rock out there in deep space? The plan is for experts at ESA's Near-Earth Object Coordination Center (NEOCC) to review and verify any potential concerns. If the situation warrants further investigation, the NEOCC will then forward their report to the Minor Planet Center, a global hub for asteroid data. Subsequent research will lead to international contingency planning, which could involve any number of solutions, such as smacking the asteroid off course with a targeted spacecraft launch.
Before that can happen, Flyeye needed to demonstrate its up to the task. For its first light test, Flyeye focused on multiple known asteroids, including 2025 KQ. Astronomers discovered the space rock only two days earlier, offering direct proof that the telescope is already capable of rapid follow-up observations.
'These images of the sky above the ancient stone hills of Matera, Italy, are more than just a test—they are proof that Flyeye is ready to begin its mission,' ESA said in its announcement.
Flyeye-1 is now on its way for installation on Monte Mulfara in Sicily. If all goes according to plan, the telescope's first sibling will be up and running sometime in 2028.

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It turns out weather on other planets is a lot like on Earth
It turns out weather on other planets is a lot like on Earth

Boston Globe

timea day ago

  • Boston Globe

It turns out weather on other planets is a lot like on Earth

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ESA's Solar Orbiter Should Solve Mystery Of Sun's Outermost Atmosphere
ESA's Solar Orbiter Should Solve Mystery Of Sun's Outermost Atmosphere

Forbes

time2 days ago

  • Forbes

ESA's Solar Orbiter Should Solve Mystery Of Sun's Outermost Atmosphere

ESA's Solar Orbiter mission will face the Sun from within the orbit of Mercury at its closest ... More approach. The European Space Agency's Solar Orbiter mission recently stunned the world with the first-ever full images of our Sun's South pole, proving that this was going to be a mission like no other. Using an orbital gravity assist from the planet Venus, the Solar Orbiter mission spacecraft was able to maneuver into an orbit that has taken it to an angle 17 degrees below the Sun's equator. Over the coming years, the spacecraft will tilt its orbit even further, so the best views are yet to come, says ESA. The 1.2-billion-euro Solar Orbiter mission, with NASA participation, should finally help us understand the origin of the Sun's solar winds as well as our understanding of the Sun's poles. And arguably most importantly, it should solve the puzzle of why our star's outermost atmosphere, or corona, is heated to millions of degrees Kelvin and is thus so much hotter than the Sun's own surface. By contrast, our Sun's visible photosphere, or surface, averages only 5,500 degrees K. With Solar Orbiter, we are clearly seeing energy releases on the nano-flare scale, Daniel Mueller, a solar physicist and ESA project scientist for both ESA's SOHO and Solar Orbiter missions to the Sun, tells me in his office in The Netherlands. But the question is, would these nano-flares continue like that infinitely, or is there a certain lower limit to the production of these nano-flares, Mueller wonders. The puzzle is whether these nano-flares are enough to heat up the Sun's corona to the temperatures with which it is routinely measured. 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Novo Nordisk's subcutaneous and oral amycretin data published in The Lancet and presented at ADA 2025
Novo Nordisk's subcutaneous and oral amycretin data published in The Lancet and presented at ADA 2025

Business Upturn

time2 days ago

  • Business Upturn

Novo Nordisk's subcutaneous and oral amycretin data published in The Lancet and presented at ADA 2025

By GlobeNewswire Published on June 21, 2025, 04:34 IST Subcutaneous amycretin phase 1b/2a data on the safety, tolerability and weight loss potential in people with overweight or obesity was published in The Lancet and presented at the American Diabetes Association (ADA) Scientific Sessions. 1,2 and presented at the American Diabetes Association (ADA) Scientific Sessions. Oral amycretin phase 1 data on the safety, tolerability and weight loss potential in people with overweight or obesity was also published in The Lancet. 3 Findings from the clinical trials indicate amycretin appeared tolerable with a safety profile consistent with other GLP-1 and amylin receptor agonists.1,2,3 Bagsværd, Denmark, 20 June 2025 – Novo Nordisk announces subcutaneous amycretin data being presented at the American Diabetes Association (ADA) 85 th Scientific Sessions in Chicago, US.1 Full results of two clinical trials evaluating the safety, tolerability and weight loss potential of subcutaneous and oral amycretin in people with overweight or obesity were published today in The Lancet medical journal.1,3 Amycretin is the first treatment that combines GLP-1 and amylin receptor agonism biology in a single molecule. The published and presented results from the once-weekly subcutaneous amycretin phase 1b/2a clinical trial showed that participants who received the treatment demonstrated significantly greater weight loss across the full range of doses investigated compared to placebo. Data being presented at ADA were collected from two parts of the trial; dose escalation (amycretin 60 mg), and dose escalation and maintenance (amycretin 20 mg, 5 mg and 1.25 mg).1,2 No plateauing in weight reduction was observed at the end of treatment (ranging from 20 to 36 weeks) with all tested doses, suggesting that a longer treatment duration may potentially contribute to additional weight loss.1,2 Estimated mean change in body weight from baseline with once-weekly subcutaneous (SC) amycretin: 1,2 * Dose Treatment % Weight change % Weight change duration (SC amycretin) (placebo) 60 mg 36 weeks -24.3% -1.1%20 mg** 36 weeks -22.0% 1.9%5 mg** 28 weeks -16.2% 2.3% 1.25 mg** 20 weeks -9.7% 2.0% * If all people adhered to treatment i.e. if all people followed the planned dosing schedule for the full trial period without any treatment discontinuations. ** Administered during a 12-week maintenance period. Once-weekly subcutaneous amycretin treatment escalated up to 60 mg appeared tolerable with a safety profile consistent with other GLP-1 and amylin receptor agonists.1,2 The number of treatment-emergent adverse events (TEAEs) increased in a dose-dependent manner, were mostly gastrointestinal, and were comparable to the rate and profile of TEAEs reported in early-phase studies of GLP-1 receptor, GLP-1 receptor/gastric inhibitory polypeptide (GIP) receptor, and amylin receptor agonists.1,2 The majority of TEAEs were mild to moderate in severity and resolved by the end of the study period.1,2 Of the participants who discontinued the trial, the majority were due to non-TEAE reasons.1,2 'As pioneers in obesity innovation, we are exploring multiple biological pathways to develop potentially transformative medicines that support the individual needs and preferences of people with obesity on their weight loss journey towards overall improved health,' said Martin Holst Lange, executive vice president for Development at Novo Nordisk . 'Amycretin is the first investigational treatment that combines GLP-1 and amylin receptor agonism biology in one molecule, working on distinct pathways and offering complementary effects on appetite control. The findings published and presented today are encouraging. We are excited to advance the clinical development of subcutaneous and oral amycretin into phase 3 to assess its potential as a therapeutic option for weight management.' The published once-daily oral amycretin phase 1 clinical trial data showed that participants receiving amycretin achieved greater weight loss compared to placebo.3 After 12 weeks of treatment with amycretin up to 50 mg and up to 2 times 50 mg, participants achieved a mean change in body weight of -10.4% and -13.1% respectively, compared to -1.2% with placebo.3 There were no apparent signs of weight loss plateauing within the 12 weeks of treatment in either of these amycretin-treated groups.3 Once-daily oral amycretin appeared to have an acceptable safety profile and was tolerable in all tested doses, with TEAEs in line with what was expected from targeting GLP-1 and amylin receptors.3 All reported TEAEs occurred in a dose-proportional manner, were mild to moderate in severity, and mostly gastrointestinal. No new safety signals appeared during the study.3 Based on the findings from the oral and subcutaneous amycretin trials, Novo Nordisk recently announced it will advance amycretin into phase 3 trials to further investigate the treatment as a potential new therapeutic option for weight management.4 About amycretin Amycretin is a unimolecular long-acting GLP-1 and amylin receptor agonist under development by Novo Nordisk, to provide an efficacious and convenient treatment for adults with overweight or obesity and for adults with type 2 diabetes. Amycretin is developed for subcutaneous and oral administration. Oral amycretin Phase 1 trial – The trial evaluated the single-ascending dose and multiple ascending doses for oral amycretin, up to 2 times 50 mg, in 144 people with overweight or obesity, with a total treatment duration of up to 12 weeks. Subcutaneous amycretin Phase 1b/2a trial – The trial investigated the safety, tolerability, pharmacokinetics, and proof-of-concept of once-weekly subcutaneous amycretin in 125 people with overweight or obesity. The trial was a combined single ascending dose, multiple ascending dose and dose-response trial investigating three different maintenance doses with a total treatment duration of up to 36 weeks. About Novo Nordisk Novo Nordisk is a leading global healthcare company founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 77,400 people in 80 countries and markets its products in around 170 countries. For more information, visit , Facebook , Instagram , X , LinkedIn and YouTube . Contacts for further information _______________________ References The Lancet: Dahl K, Toubro, S, Dey S, et al. Amycretin, a novel, unimolecular GLP-1 and amylin receptor agonist administered subcutaneously: Results of a randomised, controlled, phase 1b/2a study. Dahl, K, et al. (2025). Amycretin, a Novel, Unimolecular GLP-1 and Amylin Receptor Agonist: Results of a Phase 1b/2a Clinical Trial. Poster 2002-LB. American Diabetes Association (ADA) 85th Scientific Sessions, Chicago, US, June 20 – 23, 2025. The Lancet: Gasiorek A, Heydorn A, Gabery S, et al. Safety, tolerability, pharmacokinetics, and pharmacodynamics of the first-in-class GLP-1 and amylin receptor agonist, amycretin: a first-in-human, phase 1, randomised, placebo-controlled study. Novo Nordisk Company Announcement. Novo Nordisk to advance subcutaneous and oral amycretin for weight management into phase 3 clinical development. Available at: Attachment Disclaimer: The above press release comes to you under an arrangement with GlobeNewswire. Business Upturn takes no editorial responsibility for the same. Ahmedabad Plane Crash GlobeNewswire provides press release distribution services globally, with substantial operations in North America and Europe.

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