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Erster Kombi-Impfstoff gegen Corona und Grippe vor EU-Zulassung

Die endgültige Zulassung muss noch von der EU-Kommission genehmigt werden. Sie gilt jedoch als reine Formsache. Nach der Genehmigung entscheiden die einzelnen EU-Mitgliedstaaten selbst, ob sie den Impfstoff in ihre nationalen Impfprogramme aufnehmen.

Bisher mussten sich vor allem Risikogruppen jedes Jahr mit zwei getrennten Impfungen gegen Covid-19 und Grippe impfen lassen. Die neue Kombination soll die bisherigen getrennten Impfungen künftig vereinfachen. Ziel ist es, mit nur einer Injektion Schutz vor beiden Atemwegserkrankungen zu ermöglichen und zugleich das Gesundheitssystem zu entlasten.

Das Vakzin basiert auf mRNA-Technologie und enthält Bestandteile, die das Immunsystem vor dem Coronavirus und drei Influenza-Typen schützen sollen. Nach Angaben der EMA kombiniert das Vakzin zwei Wirkstoffe, die bereits seit mehreren Jahren zugelassen sind. Dadurch soll das Immunsystem frühzeitig Schutz vor möglichen Virusinfektionen aufbauen.

In einer großen klinischen Studie mit rund 8.000 Teilnehmern im Alter von 50 Jahren und älter zeigte der Kombi-Impfstoff eine Wirksamkeit, die mit der zweier getrennter Impfungen vergleichbar war. Nach Angaben der EMA erreichten die geimpften Personen einen ebenso hohen Schutz vor Covid-19 und Grippe wie die Vergleichsgruppe, die die gleichen Impfstoffe getrennt erhielt.

Auch bei der Kombi-Impfung können wie bei anderen Impfungen Nebenwirkungen auftreten. Zu den häufigsten Nebenwirkungen zählen Schmerzen an der Einstichstelle, Müdigkeit, Muskel- oder Kopfschmerzen, Übelkeit sowie Fieber. Diese Beschwerden klingen in der Regel nach zwei bis drei Tagen wieder ab. Insbesondere für ältere Menschen und Personen mit geschwächtem Immunsystem könnte die kombinierte Impfung künftig eine einfachere Möglichkeit bieten, sich vor schweren Verläufen von Atemwegserkrankungen zu schützen.

Erster Kombi-Impfstoff gegen Corona und Grippe vor EU-Zulassung Die endgültige Zulassung muss noch von der EU-Kommission genehmigt werden. Sie gilt jedoch als reine Formsache. Nach der Genehmigung entscheiden die einzelnen EU-Mitgliedstaaten selbst, ob sie den Impfstoff in ihre nationalen Impfprogramme aufnehmen. Bisher mussten sich vor allem Risikogruppen jedes Jahr mit zwei getrennten Impfungen gegen Covid-19 und Grippe impfen lassen. Die neue Kombination soll die bisherigen getrennten Impfungen künftig vereinfachen. Ziel ist es, mit nur einer Injektion Schutz vor beiden Atemwegserkrankungen zu ermöglichen und zugleich das Gesundheitssystem zu entlasten. Das Vakzin basiert auf mRNA-Technologie und enthält Bestandteile, die das Immunsystem vor dem Coronavirus und drei Influenza-Typen schützen sollen. Nach Angaben der EMA kombiniert das Vakzin zwei Wirkstoffe, die bereits seit mehreren Jahren zugelassen sind. Dadurch soll das Immunsystem frühzeitig Schutz vor möglichen Virusinfektionen aufbauen. In einer großen klinischen Studie mit rund 8.000 Teilnehmern im Alter von 50 Jahren und älter zeigte der Kombi-Impfstoff eine Wirksamkeit, die mit der zweier getrennter Impfungen vergleichbar war. Nach Angaben der EMA erreichten die geimpften Personen einen ebenso hohen Schutz vor Covid-19 und Grippe wie die Vergleichsgruppe, die die gleichen Impfstoffe getrennt erhielt. Auch bei der Kombi-Impfung können wie bei anderen Impfungen Nebenwirkungen auftreten. Zu den häufigsten Nebenwirkungen zählen Schmerzen an der Einstichstelle, Müdigkeit, Muskel- oder Kopfschmerzen, Übelkeit sowie Fieber. Diese Beschwerden klingen in der Regel nach zwei bis drei Tagen wieder ab. Insbesondere für ältere Menschen und Personen mit geschwächtem Immunsystem könnte die kombinierte Impfung künftig eine einfachere Möglichkeit bieten, sich vor schweren Verläufen von Atemwegserkrankungen zu schützen.

27. Februar 2026 – Die Europäische Arzneimittelagentur (EMA) hat erstmals grünes Licht für einen kombinierten Impfstoff gegen Covid-19 und Influenza gegeben. Das Präparat stammt vom US-Pharmakonzern Moderna und trägt den Namen „mCombriax“. #ComboVaccine #COVID #Flu #EUApproval #Medicine #Healthcare

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France Plans 130 Million Euro Vine Removal, Up to 32,500 Hectares Targeted Amid Wine Sector Crisis Political uncertainty and EU approval threaten emergency support for winegrowers as government faces key parliamentary votes next week

FYI: France Plans 130 Million Euro Vine Removal, Up to 32,500 Hectares Targeted Amid Wine Sector Crisis #WineCrisis #FranceWine #VineRemoval #Agriculture #EUApproval

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France Plans 130 Million Euro Vine Removal, Up to 32,500 Hectares Targeted Amid Wine Sector Crisis Political uncertainty and EU approval threaten emergency support for winegrowers as government faces key parliamentary votes next week

France Plans 130 Million Euro Vine Removal, Up to 32,500 Hectares Targeted Amid Wine Sector Crisis #WineCrisis #FranceWine #VineRemoval #WineIndustry #EUApproval

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🔗 Read more: bit.ly/ONCOnews18D-02

#ONCOnews #OncoAlert #OncEd #OncologyNews #EUApproval #FollicularLymphoma #Hematology

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Israel moves EU approval for diaspora bond to Luxembourg from Ireland amid Gaza protests DUBLIN (Reuters) -Israel has moved the process of securing EU approval for its diaspora bond prospectus to Luxembourg from Ireland amid increasing opposition in Dublin to its central bank’s role in approving the programme on behalf of the European Union. Irish lawmakers and pro-Palestine campaign groups have called on the central bank to stop facilitating the sale of the bonds over the last year due to Israel’s near two-year military campaign in Gaza that has killed more than 63,000 people, mostly civilians, according to Gaza health officials. Israel’s diaspora bonds are relatively small and sold mainly in Jewish communities around the world to help supplement the state’s bond sales that finance its budget deficit that has risen due to the war. Israel launched a diaspora bond campaign in October 2023 to raise money amid the conflict. Non-EU countries must choose one EU member state to apply to for approval of a prospectus where securities are traded in the EU and Ireland’s central bank had been asked to approve Israel’s diaspora bond programme each year since 2021. A joint committee of Irish lawmakers recommended in August that the government seek to amend EU regulations so as to allow each individual European central bank to refuse to act as the competent authority for such bond prospectuses. Protestors have also demonstrated outside the central bank’s offices. Ireland is one of the most pro-Palestinian EU member states. It officially recognised a Palestinian state last year and the government is drafting legislation on restricting trade with Israeli settlements in the occupied Palestinian territories. 3rd party Ad. Not an offer or recommendation by Investing.com. See disclosure here or remove ads. The Irish central bank had consistently said it is legally obliged to approve any prospectus once the relevant conditions are met. In a letter to a lawmaker published by the central bank, Governor Gabriel Makhlouf said the approval for Israel’s programme would be transferred to Luxembourg upon the expiry of the prior year’s prospectus on Monday. Israel’s finance ministry did not immediately comment on the reasons for moving its EU bond prospectus approval. AI computing powers are changing the stock market. Investing.com's ProPicks AI includes dozens of winning stock portfolios chosen by our advanced AI. Year to date, 3 out of 4 global portfolios are beating their benchmark indexes, with 98% in the green. Our flagship Tech Titans strategy doubled the S&P 500 within 18 months, including notable winners like Super Micro Computer (+185%) and AppLovin (+157%). Which stock will be the next to soar?

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Boeing seeks EU approval for Spirit deal BRUSSELS (Reuters) -Boeing is seeking EU approval to buy back Spirit AeroSystems, the world’s largest standalone aerostructures company, documents on the European Commission website show. Boeing said in July last year that it had agreed to buy its former subsidiary for $4.7 billion in shares while Airbus would take on the supplier’s loss-making Europe-focused activities. Britain’s competition regulator cleared the acquisition this month after deciding against an in-depth investigation into whether the deal would be anti-competitive. 3rd party Ad. Not an offer or recommendation by Investing.com. See disclosure here or remove ads. ProPicks AI analyzes thousands of stocks using 100+ institutional-grade financial metrics to identify the strongest opportunities. With 80+ strategies across global markets, you might be surprised where BA appears. Our flagship Tech Titans strategy doubled the S&P 500 within 18 months, including notable winners like Super Micro Computer (+185%) and AppLovin (+157%). Each strategy refreshes monthly with 10-20 high-conviction picks. Even if BA isn't currently featured, you'll discover similar opportunities in the same industry or theme—stocks the AI identifies before they breakout. Now up to 50% off while our Summer Sale lasts.

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Exclusive-Prosus set to win EU nod for $4.74 billion Just Eat deal, sources say By Foo Yun Chee BRUSSELS (Reuters) -Dutch technology investor Prosus (OTC:PROSF) is set to win EU antitrust approval for its 4.1 billion euro ($4.7 billion) bid for Just Eat Takeaway, after agreeing to sell down its stake in Delivery Hero, people with direct knowledge of the matter said. Amsterdam-headquartered Prosus, which is majority owned by South Africa’s Naspers, announced the deal in February, banking on its artificial intelligence capability to boost Just Eat Takeaway, Europe’s biggest meal delivery company. Prosus last month offered to incrementally sell down its 27.4% stake in Delivery Hero and to give up its board seat to address EU competition concerns, other people familiar with the matter had told Reuters. Delivery Hero and Just Eat Takeaway compete with each other in Austria, Bulgaria, Italy, Poland and Spain. The European Commission, which is now seeking market feedback to Prosus’ offer and will decide on the deal by August 11, declined to comment. Prosus also declined to comment. The deal would make Prosus the world’s fourth-largest food delivery company after Meituan, DoorDash (NASDAQ:DASH) and Uber (NYSE:UBER), according to ING analysts. Delivery Hero and its Spanish unit Glovo were fined 329 million euros by the EU antitrust watchdog in June for taking part in a cartel which included an agreement to divide up markets among themselves and not to poach each other’s employees. ($1 = 0.8658 euros) Before you buy stock in TKWY, consider this: ProPicks AI are 6 easy-to-follow model portfolios created by Investing.com for building wealth by identifying winning stocks and letting them run. Over 150,000 paying members trust ProPicks to find new stocks to buy – driven by AI. The ProPicks AI algorithm has just identified the best stocks for investors to buy now. The stocks that made the cut could produce enormous returns in the coming years. Is TKWY one of them?

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Sanofi’s Sarclisa receives EU approval for newly diagnosed multiple myeloma Investing.com -- Sanofi SA (EPA:SASY) announced Friday that its drug Sarclisa has received approval in the European Union for the treatment of transplant-eligible newly diagnosed multiple myeloma. The approval extends Sarclisa’s use across all therapy lines in the EU, marking an important expansion of the drug’s treatment scope. According to the French pharmaceutical company, Sarclisa-VRD demonstrated a significant benefit in minimal residual disease (MRD) negativity, an important measure of treatment effectiveness in multiple myeloma patients. This regulatory milestone adds to Sarclisa’s existing approvals, now making it available for multiple myeloma patients at various stages of their treatment journey within the European Union. This article was generated with the support of AI and reviewed by an editor. For more information see our T&C. With valuations skyrocketing in 2024, many investors are uneasy putting more money into stocks. Sure, there are always opportunities in the stock market – but finding them feels more difficult now than a year ago. Unsure where to invest next? One of the best ways to discover new high-potential opportunities is to look at the top performing portfolios this year. ProPicks AI offers 6 model portfolios from Investing.com which identify the best stocks for investors to buy right now. For example, ProPicks AI found 9 overlooked stocks that jumped over 25% this year alone. The new stocks that made the monthly cut could yield enormous returns in the coming years. Is SASY one of them?

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Bulgaria set to join euro zone in 2026 after EU ministers’ approval Investing.com -- Bulgaria is set to become the 21st member of the euro zone on January 1, 2026, after European Union finance ministers formally supported the country’s adoption of the euro currency on Friday. The ministers’ backing follows positive assessments from both the European Commission and the European Central Bank regarding Bulgaria’s readiness to join the currency union. EU leaders are expected to endorse this decision at their upcoming summit in Brussels on June 27. The exchange rate for converting the Bulgarian lev to the euro will be determined by EU finance ministers at their meeting in early July. This will give Bulgaria a six-month preparation period for the technical transition before the start of 2026. Bulgaria has been working toward euro adoption since joining the European Union in 2007. Despite this long-standing goal, public sentiment in Bulgaria has shifted over time. According to a Eurobarometer poll conducted in May, 50% of Bulgarians now express skepticism about the euro, with some citizens concerned that the currency switch might lead to price increases. This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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Imfinzi gets EU recommendation for bladder cancer treatment Blog Mobile Portfolio Widgets About Us Advertise Help & Support Authors Risk Disclosure: Trading in financial instruments and/or cryptocurrencies involves high risks including the risk of losing some, or all, of your investment amount, and may not be suitable for all investors. Prices of cryptocurrencies are extremely volatile and may be affected by external factors such as financial, regulatory or political events. Trading on margin increases the financial risks. Before deciding to trade in financial instrument or cryptocurrencies you should be fully informed of the risks and costs associated with trading the financial markets, carefully consider your investment objectives, level of experience, and risk appetite, and seek professional advice where needed. Fusion Media would like to remind you that the data contained in this website is not necessarily real-time nor accurate. The data and prices on the website are not necessarily provided by any market or exchange, but may be provided by market makers, and so prices may not be accurate and may differ from the actual price at any given market, meaning prices are indicative and not appropriate for trading purposes. Fusion Media and any provider of the data contained in this website will not accept liability for any loss or damage as a result of your trading, or your reliance on the information contained within this website. It is prohibited to use, store, reproduce, display, modify, transmit or distribute the data contained in this website without the explicit prior written permission of Fusion Media and/or the data provider. All intellectual property rights are reserved by the providers and/or the exchange providing the data contained in this website. Fusion Media may be compensated by the advertisers that appear on the website, based on your interaction with the advertisements or advertisers.

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Bayer secures EU nod for 6 month Eylea treatment, shares rise Investing,com -- Bayer (OTC:BAYRY) shares rose over 2% on Friday after the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) recommended a label extension for Eylea 8 mg, allowing for longer treatment intervals for patients with two major retinal diseases. The CHMP opinion supports expanded dosing intervals of up to six months for aflibercept 8 mg, a treatment for neovascular (wet) age-related macular degeneration (nAMD) and diabetic macular edema (DME). The extension is contingent on a final decision from the European Commission, which is expected in the coming weeks. If approved, Eylea 8 mg would become the only anti-vascular endothelial growth factor (anti-VEGF) treatment in the EU authorized for six-month intervals for both nAMD and DME, according to Bayer’s statement Friday. “Following approval of the European Commission, extended treatment intervals with Eylea 8 mg of up to 6 months can significantly reduce the frequency of injections and visits to the clinic for patients,” said Christine Roth, executive vice president, Global Product Strategy and Commercialization at Bayer. The CHMP recommendation is based on three-year data from the PULSAR and PHOTON clinical trials. In these open-label extension studies, 24% of nAMD patients and 28% of DME patients who started with Eylea 8 mg at baseline were on six-month treatment intervals by the end of year three. Eylea 8 mg maintained the patients’ vision and anatomic outcomes over the study period, Bayer said. The safety profile remained consistent with that of the already-approved 2 mg dose, with no new safety signals reported. Eylea 8 mg is already approved in more than 50 markets, and further regulatory submissions are under review in additional countries. In the EU and U.K., Eylea 8 mg is the only anti-VEGF treatment currently approved for up to five-month intervals after three initial monthly injections.

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The EU approves Synopsys’ $35B acquisition of Ansys, following commitments to divest parts of their businesses. US and China approvals still pending. A major step for the tech industry’s consolidation. #Synopsys #Ansys #EUApproval #TechAcquisition #MergersAndAcquisitions #GlobalBusiness

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