Neue Novavax: Anstieg nach 1:20 Re-Split
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Danke, aber mein Sonntag ist trotz des aufkommenden Gewitters erhellt.
…The Aug. 8 study concluded that the vaccine was only 42 percent effective against the virus in July when Delta was the dominant variant. This is a significant drop in protection for a vaccine whose efficacy was 95 percent in clinical trials. "If that's not a wakeup call, I don't know what is," a senior Biden official told Axios.
The study set out to compare the effectiveness of the two mRNA vaccines, Pfizer and Moderna. The data was compiled via the Mayo Clinic Health System through the months of January to July. Initially, the study found that the Moderna vaccine was 86 percent effective against infection while Pfizer was 76 percent effective against infection. And the vaccines were more protective against hospitalization and severe disease. Moderna's vaccine was 92 percent effective against hospitalization, and Pfizer's was 85 percent effective.
But both vaccines saw a significant drop in effectiveness when the Delta variant became more prevalent in July. During that month, Moderna was 76 percent effective against infection, while Pfizer was only 42 percent effective. "Based on the data that we have so far, it is a combination of [two] factors," study lead author Venky Soundararajan, PhD, told Axios. "The Moderna vaccine is likely—very likely—more effective than the Pfizer vaccine in areas where Delta is the dominant strain, and the Pfizer vaccine appears to have a lower durability of effectiveness."
https://www.yahoo.com/lifestyle/...O8kesxtRpPbjRBgK6HsiqxH51f0uK4f4Ao
Moderna wird schon der Tesla unter den COVID Vaccines genannt.
https://www.finanzen.at/nachrichten/aktien/...ich-zu-tesla-1030744919
von Biontech. Das kann nur Novavax sein. Wenn er uns damit ein Paar Prozentpunkte mehr
beschert, soll’s mir recht sein.
Blöd, dass ich heute morgen eingestiegen bin. 5% an ersten Tag ins minus zu rutschen ist schon ärgerlich. Aber bin optimistisch, sonst wäre ich nicht rein.
…“It’s all very uncertain”
Speaking to Reuters on condition of anonymity, an EU official familiar with the process said “we expect data around October but it’s all very uncertain – we are not sure about the precise timing.” They added that, though further delays were possible, “vaccine approval is still possible this year.”
The setbacks are due to a change in production strategy which has complicated the approval of Novavax’s manufacturing sites by regulators. The vaccine’s clinical data has been under rolling review by the EMA since February.
Under pressure to set a date, Novavax said in its latest earnings announcement that data would be submitted to the EU “within weeks” of its filing to British regulators. A spokesperson set a likely timeline between late September and early October, according to Reuters.
https://cphpost.dk/?p=127328
…Funded by the UK government's Vaccines Taskforce and the UK Research and Innovation (UKRI), the study is being led by the University of Glasgow and University of Birmingham. It is a follow-on to OCTAVE (Observational Cohort Trial -T-cells Antibodies and Vaccine Efficacy in SARS-CoV-2), which evaluated the immune response to COVID-19 vaccines in participants with impaired immune systems due to cancer, inflammatory arthritis, kidney or liver diseases, or a stem cell transplant.
As part of OCTAVE-DUO, 320 participants with lymphoid malignancies from OCTAVE and similar studies who demonstrated low or no response to two doses of a primary COVID-19 vaccine regimen will be randomly assigned to receive a third vaccine dose from one of three manufacturers at least 14 days after completing the initial 2-dose regime. The individuals may receive the same vaccine as the first two doses or one from another manufacturer. Of these participants, one third will be administered Novavax' recombinant nanoparticle protein-based COVID-19 vaccine, NVX-CoV2373.
"We expect the results of this study to be particularly helpful to better understanding how our vaccine might work as a heterologous third dose in immunocompromised individuals," said Gregory M. Glenn, M.D., President of Research and Development, Novavax. "As the pandemic continues to surge, the ability to have a flexible approach to vaccine regimens will be important for both medically vulnerable individuals as well as to achieving population-wide coverage."
Participants will be evaluated for changes in vaccine-specific immune responses and any adverse events, with findings expected later in 2021. The Medicines and Healthcare products Regulatory Agency (MHRA) and Joint Committee on Vaccination and Immunization (JCVI) will review the results to further inform the use of vaccination in immunocompromised populations.
https://ir.novavax.com/...b_qMFbDNte-6SdjTEBtr1L-pqKHX7mhZehdSdrYyDWQ
https://asia.nikkei.com/Spotlight/Coronavirus/...n-over-contamination
die wurden einfach auf hohem nivoue abverkauft von us seite , die amis stehen auf und sehen die Biotech werte sind um 5-7 % in europa gestiegen und beginnen kasse zu machen mehr nicht
short käufe löse doch keine kurzstürze aus junge
im gegenteil wenn die kurse steigen und die short eindeckungen dann aufgelöst werden dann kommt es meistens zu einem weiteren anstieg short squez genannt
https://www.wbtv.com/video/2021/08/24/...y-isnt-novavax-available-us/
Gefunden in der Beschreibung zum Einreiseformular für Griechenland -> https://travel.gov.gr/#/
Wird irgendwo schon Novavax's Impfstoff verimpft oder ist das nur "weise" Voraussicht?
Key Points:
•Novavax has more significant catalysts on the way than Moderna does.
•Novavax's valuation is much more attractive than Moderna's.
•Novavax has more potential wild cards that could work to its advantage than Moderna does.
https://www.fool.com/investing/2021/08/29/...amp;utm_campaign=article
Ein letztes Mal nachgelegt. Von mir aus darf sich der Kurs jetzt verdreifachen :0))
…The CDC guidance states that participants in the Novavax PREVENT-19 Phase 3 clinical trial meet the criteria to be considered fully vaccinated two weeks after they have completed the vaccine series.
https://ir.novavax.com/...9-Clinical-Trial-Participants?sf150361986=1
Die Fragen die ich mir stelle:
1. ist es ein Hinweis auf eine baldige Zulassen?
oder
2. wissen die jetzt schon das sie die Probleme nicht in den Griff bekommen und es zu weiteren Verzögerungen kommt? Somit wären aber die jetzt schon mit NVX-CoV2373 geimpften nicht im Nachteil.
Ich glaube weiterhin es ist ein Geduldsspiel für das man gute Nerven braucht, allerdings wähne ich uns kurz vor dem Ziel :0)