MedPath

CX-038839 Omicron (XBB.1.5)

Generic Name
CX-038839 Omicron (XBB.1.5)
Brand Names
Spikevax
Drug Type
Biotech
Chemical Formula
-
CAS Number
2918977-08-7
Unique Ingredient Identifier
4F9QRS7ZV2
Associated Conditions
-
Associated Therapies
-
foxnews.com
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New COVID vaccines get FDA approval for 2024-2025 season

The FDA approved updated COVID-19 vaccines from Moderna and Pfizer for 2024-2025, targeting the Omicron KP.2 strain. Approved for ages 12+ and authorized for 6 months-11 years, these vaccines aim to enhance protection against current variants. Vaccination is emphasized as key to COVID-19 prevention, with recommendations for high-risk groups and all individuals 6 months and older.
finance.yahoo.com
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Biotech Stock Roundup: MRNA's Q4 Results, RAPT Down on Study Results & Other Updates

Moderna reported Q4 2023 earnings of 55 cents per share, surpassing expectations, with $2.8 billion in revenue, mainly from COVID-19 Vaccine Spikevax sales. It expects RSV vaccine approvals in 2024. RAPT Therapeutics faced a clinical hold on zelnecirnon trials due to a liver failure case, halting dosing and new enrollments. Iovance Biotherapeutics' stock surged after FDA accelerated approval of Amtagvi for melanoma treatment, based on phase II study results showing effective responses.

Impact of extended-course oral nirmatrelvir/ritonavir on Long COVID outcomes

A case series of 13 individuals with Long COVID treated with extended courses of nirmatrelvir/ritonavir showed variable outcomes. Some reported significant symptom improvement, while others experienced temporary relief or no change. The findings suggest potential benefits of prolonged antiviral therapy for Long COVID, warranting further clinical trials to establish efficacy and safety.
gov.uk
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Coronavirus vaccine - summary of Yellow Card reporting

The MHRA updated the Yellow Card reporting format to focus on COVID-19 vaccines from the Autumn 2022 booster campaign, including safety monitoring. Vaccination is key to reducing COVID-19 deaths and severe illness. Common vaccine reactions are mild, like fever and fatigue. Bivalent vaccines targeting Omicron BA.1 and original strains were approved. The MHRA monitors vaccine safety, ensuring benefits outweigh risks. Yellow Card reports help identify new safety concerns, with most reactions being mild and temporary.
ema.europa.eu
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COVID-19 vaccines: key facts

COVID-19 vaccines are safe and effective, with most side effects being mild and short-lived. EMA emphasizes consulting reliable sources for vaccine information and addresses common misconceptions. Vaccines reduce virus transmission and are updated to combat new variants. Continuous safety monitoring ensures public health protection.
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