Welcome to our dedicated page for Moderna news (Ticker: MRNA), a resource for investors and traders seeking the latest updates and insights on Moderna stock.
Moderna, Inc. reports developments in mRNA medicines, including commercial vaccines, investigational respiratory vaccines, oncology programs and rare-disease candidates. News commonly covers regulatory authorizations and agency interactions for products such as Spikevax, mRESVIA, mNEXSPIKE and mCOMBRIAX, as well as clinical data for seasonal influenza, pandemic influenza and cancer immunotherapy programs including intismeran autogene and mRNA-4359.
Company updates also include quarterly financial results, revenue mix, expense actions, strategic partnerships, scientific meeting presentations and intellectual-property matters tied to Moderna's infectious disease portfolio and broader mRNA technology platform.
Moderna (Nasdaq: MRNA) announced in vitro neutralization data for its COVID-19 Vaccine against emerging variants B.1.1.7 and B.1.351. The vaccine demonstrated strong neutralizing titers against B.1.1.7, with no significant decline. However, a six-fold reduction was observed against B.1.351, although levels remained protective. The company plans to conduct a Phase 1 trial for an emerging variant booster candidate, mRNA-1273.351. CEO Stéphane Bancel emphasized the importance of being proactive against evolving virus strains.
Moderna Inc (Nasdaq: MRNA) has initiated a Phase 1/2 clinical trial for its COVID-19 vaccine candidate (mRNA-1273 or TAK-919) in Japan, in partnership with Takeda Pharmaceutical Co. The study will involve 200 healthy adults and will assess the vaccine's safety and immunogenicity. Participants will receive two vaccinations 28 days apart. Pending licensure, Takeda plans to import and distribute 50 million doses starting in the first half of 2021. This represents Moderna's first clinical trial in Japan, aiming to enhance the country's COVID-19 vaccination efforts.
Moderna (Nasdaq: MRNA) and Uber (NYSE: UBER) have announced a partnership to enhance COVID-19 vaccine uptake. The collaboration will begin with providing vaccine safety information through Uber's app and will explore options like in-app ride scheduling for immunization appointments. Uber previously committed to offering 10 million free or discounted rides to facilitate access to vaccines, especially in underserved communities. Both companies aim to expand this initiative globally, reinforcing vaccine education and accessibility efforts.
Moderna (Nasdaq: MRNA) has appointed José M. Vega, M.D. as its new Chief Safety Officer as of January 11, 2021. Dr. Vega, who brings extensive experience from Merck and Amgen, will oversee safety and pharmacovigilance to ensure high standards of patient safety. His previous roles included leading a global team at Merck and holding significant positions at Amgen. This strategic hire is expected to support Moderna's growth and its commitment to delivering transformative mRNA medicines.
Moderna, Inc. (Nasdaq: MRNA) has received authorization from Swissmedic for its COVID-19 Vaccine in Switzerland. This milestone follows a rigorous examination of data from its Phase 3 clinical study. The Swiss Federal Government has ordered 7.5 million doses, with initial deliveries expected soon. Moderna's COVID-19 vaccine is already authorized in numerous countries, including the U.S. and EU, with ongoing applications under review globally. This approval marks a significant step in Moderna's efforts to combat the COVID-19 pandemic.
Moderna (Nasdaq: MRNA) is actively expanding its innovative vaccine pipeline following the success of its COVID-19 vaccine. The company has announced three new mRNA vaccine candidates targeting seasonal flu, HIV, and the Nipah virus. Additionally, it is broadening its respiratory syncytial virus (RSV) vaccine program to include older adults. CEO Stéphane Bancel highlighted the achievements of 2020 as a pivotal moment for Moderna, boosting confidence in pursuing more ambitious vaccine programs. With 24 mRNA candidates across five therapeutic areas, 13 are currently in clinical stages.
Moderna (Nasdaq: MRNA) received approval from the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) for its COVID-19 vaccine under Regulation 174. This temporary authorization is based on recommendations from the UK Commission on Human Medicines, allowing supply in Great Britain. The UK government has confirmed an additional purchase of 10 million doses, totaling 17 million doses. This marks the fifth jurisdiction to authorize the vaccine, and the first deliveries are expected early in 2021.
Moderna, Inc. (Nasdaq: MRNA) announces the appointment of Corinne Le Goff as Chief Commercial Officer, effective January 19, 2021. Le Goff, a seasoned executive from Amgen, will join Moderna's Executive Committee and report to CEO Stéphane Bancel. Her extensive experience includes leadership roles at Amgen, Roche, Sanofi, and Pfizer. Bancel emphasized Le Goff's strategic importance as Moderna shifts to a commercial organization, particularly during the launch of its COVID-19 vaccine and its upcoming CMV vaccine study. Moderna is advancing mRNA science for transformative medicines.
Moderna, Inc. (Nasdaq: MRNA) has received a conditional marketing authorization from the European Commission for its COVID-19 vaccine, allowing widespread vaccination in the EU. This follows recommendations from the European Medicines Agency (EMA) and marks the fourth authorization for the vaccine globally, after the U.S., Canada, and Israel. The EU's confirmed order commitment has increased to 160 million doses. Initial deliveries are expected to commence next week. Moderna highlights its role in tackling the pandemic through its innovative mRNA technology.
Moderna (Nasdaq: MRNA) announced that Israel’s Ministry of Health has authorized the import of its COVID-19 Vaccine. This marks the vaccine's third regulatory approval, following the U.S. and Canada. Moderna has secured a contract to supply 6 million doses, with deliveries expected to start soon. The decision is based on comprehensive scientific evidence, including data from its Phase 3 clinical study. The vaccine is currently under review for additional authorizations in various countries, including the EU and the UK.