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AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI

 
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AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
(September 29, 2018) Vaccitech licenses MERS rights to Oxford University
CEPI (the Coalition for Epidemic Preparedness Innovations) today announced a collaboration with The Jenner Institute
at the University of Oxford and Janssen Vaccines & Prevention B.V.—part of the Janssen Pharmaceutical Companies of Johnson & Johnson
—through which they will receive funding to advance the development and manufacture of a vaccine against Middle East Respiratory Syndrome Coronavirus (MERS-CoV).
Oxford has already initiated clinical development of the MERS-CoV vaccine,
with funding from the UK Department of Health and Social Care, and a phase 1 clinical trial of the vaccine is underway in the UK.
Under the terms of the Framework Partnering Agreement for the collaboration, Oxford and Janssen will receive $14.6 million from CEPI
to support manufacturing of a phase 2 batch and preparation for stockpiling of a MERS-CoV vaccine candidate.
Oxford will undertake phase 2 testing of the vaccine, in partnership with the King Abdullah International Medical Research Centre (KAIMRC) in Riyadh,
Kingdom of Saudi Arabia, and the Kenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme at Kilifi, Kenya.
[link to www.vaccitech.co.uk (secure)]

(July 4, 2019) Machine Learning is Transforming Drug Discovery at AstraZeneca
AstraZeneca has been experimenting with machine learning across all stages of research and development, and most recently in pathology
to speed up the review of tissue samples. AstraZeneca uses Amazon SageMaker Ground Truth
—a machine learning-powered, human-in-the-loop data labeling and annotation service—to automate
some of the most tedious portions of this work, resulting in reduction of time spent cataloging samples by 50 percent.
“We want to unlock all the hidden potential in the data and research we’re already doing,” says Goodwin.
“It’s the start of a broad change in our business—using all of this imaging and molecular data along with AI to develop a holistic approach,
one that lets our scientists interact and interpret the data in ways that have never been possible.”
[link to www.wired.com (secure)]

(April 30, 2020) AstraZeneca Joins U. of Oxford and Spinout to Develop COVID-19 Vaccine
AstraZeneca will oversee global development, manufacturing, and distribution of the COVID-19 vaccine
candidate that was created by researchers at University of Oxford, and is now being studied in a human clinical trial
launched last week, the partners said today. AstraZeneca, the University, and its spinout company Vaccitech
which has joint rights to the platform technology behind the vaccine candidate, ChAdOx1 nCoV-19—said
they will start work immediately while hammering out final terms of their collaboration agreement.
According to AstraZeneca, vaccines made from the ChAdOx1 virus
have been given to more than 320 people to date and have been shown
to be safe and well tolerated—although they can cause temporary side effects
such as a temperature, flu-like symptoms, headache or sore arm, the company acknowledged.
[link to www.genengnews.com (secure)]

(May 21, 2020) U.S. Raises Ante in Vaccine Race With $1.2 Billion for Astra
The U.S. threw its weight behind one of the fastest-moving experimental solutions
to the coronavirus pandemic, pledging as much as $1.2 billion to AstraZeneca Plc
to help make the University of Oxford’s Covid vaccine.
The U.K. drugmaker received the money from the U.S. Biomedical Advanced Research and Development Authority (BARDA)
and said it has secured capacity to make 1 billion doses. Astra has identified supply chains in the U.S. and U.K., according to Soriot.
Soriot said Astra is working with groups including the World Health Organization,
the Coalition for Epidemic Preparedness Innovations(CEPI) and Gavi, the Vaccine Alliance,
on making sure the vaccine is allocated fairly so that poorer countries have access.
The company has supply agreements for 400 million doses.
[link to www.bloomberg.com (secure)]

(May 28, 2020) AstraZeneca locks up COVID-19 vaccine supply with Oxford BioMedica production deal
AstraZeneca is on the hook for millions of doses of the University of Oxford's front-runner COVID-19 vaccine candidate,
assuming it proves effective. To fill those orders, the British drugmaker has agreed to a short-term manufacturing deal
that will help it bridge the gap. AstraZeneca and Oxford BioMedica inked a one-year deal covering "multiple batches" of the University of Oxford's adenovirus-based
COVID-19 vaccine candidate, AZD1222 (ChAdOx1 nCoV-19), as part of a consortium aimed at speeding production of the shot.
The vaccine, developed by the University of Oxford’s Jenner Institute, contains the genetic material of the SARS-CoV-2 spike protein.
[link to www.fiercepharma.com (secure)]

(June 7, 2020) AstraZeneca Approaches Gilead About Potential Merger
AstraZeneca Plc has made a preliminary approach to rival drugmaker Gilead Sciences Inc. about a potential merger,
according to people familiar with the matter, in what would be the biggest health-care deal on record.
The U.K.-based firm informally contacted Gilead last month to gauge its interest in a possible tie-up,
the people said, asking not to be identified because the details are private.
AstraZeneca didn’t specify terms for any transaction, they said.
AstraZeneca, valued at $140 billion, is the U.K.’s biggest drugmaker by market capitalization
and has developed treatments for conditions from cancer to cardiovascular disease.
Gilead, worth $96 billion at Friday’s close, is the creator of a drug (remdesivir)
that’s received U.S. approval for use with coronavirus patients.
[link to www.bloomberg.com (secure)]

(June 11, 2020) Emergent BioSolutions signs deal to make AstraZeneca COVID-19 vaccine
Emergent BioSolutions Inc said on Thursday it signed an $87 million deal to make AstraZeneca Plc's experimental COVID-19 vaccine
in the United States, boosting the British drugmaker's efforts to bring a vaccine to the market.
The deal comes weeks after the United States pledged up to $1.2 billion to secure 300 million doses
of AstraZeneca's vaccine, which is among the first to move into mid-stage trials.
Emergent, which has also signed a deal with Johnson & Johnson
to make its COVID-19 vaccine, said it would reserve some of its large-scale manufacturing
capacity through 2020 for AstraZeneca.
[link to www.jpost.com (secure)]
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(June 13, 2020) AstraZeneca to deliver 400M vaccine doses to Europe once approved
AstraZeneca announced Saturday that it has reached an agreement with the Inclusive Vaccines Alliance of Europe
to supply as many as 400 million doses of the University of Oxford's COVID-19 vaccine, with deliveries beginning at the end of the calendar year.
"This agreement will ensure that hundreds of millions of Europeans have access to Oxford University's vaccine following approval," said Pascal Soriot,
AstraZeneca's chief executive officer, in a press statement. "With our European supply chain due to begin production soon,
we hope to make the vaccine available widely and rapidly. I would like to thank the governments of Germany, France, Italy and the Netherlands
for their commitment and swift response."
"AstraZeneca recognises that the vaccine may not work but is committed to progressing the clinical programme
with speed and scaling up manufacturing at risk," the company's statement said.
[link to www.upi.com (secure)]
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
(June 16, 2020) Cobra Biologics signs supply agreement with AstraZeneca for manufacture of COVID-19 vaccine candidate
Cobra Biologics (Cobra), part of the Cognate BioServices family, an international CDMO for biologics and pharmaceuticals,
today announced it has signed a supply agreement with AstraZeneca UK Ltd. ("AstraZeneca") to provide GMP manufacture of the adenovirus vector-based COVID-19 vaccine candidate AZD1222,
previously known as ChAdOx1 n-CoV-19. The production agreement is part of AstraZeneca's recently announced in-licensed programme with the University of Oxford
to ensure broad and equitable supply of the vaccine throughout the world, at no profit during the COVID-19 pandemic.
Cobra, along with other consortium members, will be manufacturing the vaccine with first deliveries to begin in the UK in September 2020.
Cobra is supported by leading shareholder EW Healthcare Partners, as well as Medivate Partners, a Middle Eastern Sovereign Wealth Fund and Blackrock,
who continue supporting the business and its expansion activities.
[link to www.prnewswire.com (secure)]

(June 16, 2020) AstraZeneca CEO Soriot says fast-tracked COVID-19 shot will protect for just one year
AstraZeneca, advancing a COVID-19 vaccine from the University of Oxford,
is among global frontrunners in the worldwide hunt for a viable vaccine.
Now, the drugmaker’s CEO says the vaccine is expected to provide protection for one year.
“We think that it will protect for about a year,” AstraZeneca CEO Pascal Soriot said on a Belgian radio station, according to reports.
After that protection runs out, it isn’t clear whether recipients would be instructed
to get another dose, or another vaccine, or rely on COVID-19 treatments if they're approved.
So far, Gilead's remdesivir is the only treatment with an emergency use authorization, but research is underway on many other options.
On Tuesday, researchers in the United Kingdom reported that the inexpensive steroid dexamethasone cut deaths by a third for patients on ventilation.
Numerous governments have already signed deals with the drugmaker to order doses,
including an agreement over the weekend from Italy, France, Germany and the Netherlands worth $843 million for 300 million doses.
Before that deal, AstraZeneca agreed to provide doses to the United Kingdom and inked a $1.2 billion agreement with the U.S. government for hundreds of millions of doses.
The company has also struck deals with CEPI and Gavi, the Vaccine alliance—plus the Serum Institute of India—to allow for access in low- and middle-income countries.
[link to www.fiercepharma.com (secure)]
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(July 17, 2020) AstraZeneca and R-Pharm announce agreement to manufacture and export COVID-19 vaccine
AstraZeneca and R-Pharm announce a collaboration for the manufacturing of COVID-19 vaccine, AZD1222
aimed at preventing infection from the SARS-CoV-2 virus in Russia.
Under the agreement, R-Pharm will provide technological capabilities for the implementation of the project.
The vaccine vector was transferred to Russia, it is planned to produce the finished dosage form.
At the same time Russia will become one of the hubs for the production and supply of vaccines to international markets.
AstraZeneca is confident that, together with R-Pharm, will be able to provide millions of people with the vaccine in the most efficient way.
AstraZeneca recognises that the vaccine may not work but is committed to progressing the clinical programme with speed and scaling up manufacturing at risk.
[link to gmpnews.net (secure)]

(July 27, 2020) AstraZeneca pledges $174M to ramp up coronavirus vaccine supply deal with Emergent
With a $174 million manufacturing pact signed Monday, Maryland-based Emergent BioSolutions
will help produce bulk drug substance for AstraZeneca and Oxford's adenovirus-based COVID-19 shot starting this year.
The agreement follows a separate $87 million deal the companies inked in early June
to reserve space at Emergent's Baltimore Bayview facility for three years of commercial production.
The partnership now totals $261 million through 2021, with an option to expand in future years, Emergent said in a release.
AstraZeneca and Emergent's original deal in June reserved large-scale manufacturing capacity for Oxford's shot, dubbed AZD1222,
through at least 2020 with the possibility for more based on a "flexible capacity deployment model."
[link to www.fiercepharma.com (secure)]
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
I like the cut of your jib, Billy
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
I like the cut of your jib, Billy
 Quoting: Anonymous Coward 79129227


hf
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
(July 27, 2020) AstraZeneca to Be Exempt From Coronavirus Vaccine Liability Claims in Most Countries
"This is a unique situation where we as a company simply cannot take the risk if in ... four years the vaccine is showing side effects," Ruud Dobber,
a member of Astra's senior executive team, told Reuters. "In the contracts we have in place, we are asking for indemnification.
For most countries it is acceptable to take that risk on their shoulders because it is in their national interest,"
he said, adding that Astra and regulators were making safety and tolerability a top priority. Dobber would not name the countries.
EU officials told Reuters this week product liability was among contentious points in European
efforts to secure supply deals for potential COVID-19 vaccines from Pfizer, Sanofi and Johnson & Johnson.
The United States, however, already has a law to exclude tort claims from products that help control a public-
health crises in the form of the 2005 Public Readiness and Emergency Preparedness, or PREP Act.
[link to www.nytimes.com (secure)]
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
(July 30, 2020) AstraZeneca to Be Exempt From Coronavirus Vaccine Liability Claims in Most Countries
"This is a unique situation where we as a company simply cannot take the risk if in ... four years the vaccine is showing side effects," Ruud Dobber,
a member of Astra's senior executive team, told Reuters. "In the contracts we have in place, we are asking for indemnification.
For most countries it is acceptable to take that risk on their shoulders because it is in their national interest,"
he said, adding that Astra and regulators were making safety and tolerability a top priority. Dobber would not name the countries.
EU officials told Reuters this week product liability was among contentious points in European
efforts to secure supply deals for potential COVID-19 vaccines from Pfizer, Sanofi and Johnson & Johnson.
The United States, however, already has a law to exclude tort claims from products that help control a public-
health crises in the form of the 2005 Public Readiness and Emergency Preparedness, or PREP Act.
[link to www.nytimes.com (secure)]

(August 6, 2020) AstraZeneca takes COVID-19 vaccine to China with BioKangtai deal for 200M-dose capacity by 2021
AstraZeneca reached a licensing deal with Chinese firm BioKangtai
to help provide its adenovirus vector-based COVID-19 vaccine candidate, created by the University of Oxford, to China,
AstraZeneca said (Chinese) in a social media post on Thursday. The pair will also explore the possibility of producing the vaccine for other markets.
Under the pact, AZ grants exclusive clinical development, production and commercialization rights
to the vaccine in China to BioKangtai, which will in return reserve enough capacity to make at least 100 million doses
of the shot by the end of 2020 and expand to 200 million doses per year
by the end of 2021. Financial terms were not disclosed.
AZ’s shot is only the third foreign COVID-19 vaccine candidate to have looped in China.
Fosun Pharma holds China rights to BioNTech’s mRNA program through a licensing agreement worth up to $135 million.
The pair just kicked off a phase 1 trial in China with the goal to enroll 144 healthy volunteers.
Outside of China, BioNTech and its partner Pfizer launched their 30,000-subject phase 3 efficacy trial last week.
In addition, Inovio previously teamed up with Beijing Advaccine Biotechnology for work on its DNA vaccine candidate, INO-4800.
[link to www.fiercepharma.com (secure)]
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
(August 8, 2020) Brazilian billionaire Jorge Lemann leads initiative to build Covid-19 vaccine factory
Brazilian billionaire Jorge Lemann’s foundation and other business interests will fund the building of factory
to produce the COVID-19 vaccine being developed by Oxford University and pharmaceutical company AstraZeneca PLC.
The Lemann Foundation said in a statement on Friday that the 100 million reais ($18 million) factory
will be donated to Brazil’s premier biomedical research and development lab, the Oswaldo Cruz Foundation, or Fiocruz.
It said the factory will be ready to produce 30 million doses of the vaccine per month as of the beginning of 2021.
The Oxford/AstraZeneca vaccine is being tested on Brazilian volunteers in a study led by the Federal University of São Paulo that is also funded by the Lemann Foundation.
Other donors to the initiative to ensure Brazil can absorb the technology
to produce the potential vaccine include Brazilian brewer Ambev SA, Itaú Unibanco, the Votorantim Institute and the Behring Family Foundation.
[link to www.hindustantimes.com (secure)]
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(August 11, 2020) AstraZeneca bumps up vaccine deal with Brazil to $360M with more doses, licensing rights
Brazilian President Jair Bolsonaro ordered $360 million set aside last week for a supply and licensing deal with AstraZeneca for at least 100 million doses
of the University of Oxford's adenovirus-based COVID-19 vaccine.
An AstraZeneca spokesman said the new agreement "builds on" the drugmaker's earlier deal
with Brazil in June to supply around 30 million unfinished doses of the vaccine at a price tag of $127 million.
Brazil also committed to produce an additional 70 million doses, with AstraZeneca supplying the unfinished vaccine at no cost.
The vaccine doses were set to be finished and filled at Fiocruz
as AstraZeneca does not have a vaccine production suite at its Brazilian manufacturing facility.
The expanded Brazil deal comes as AstraZeneca looks to lock up manufacturing capacity to reach its stated goal of 2 billion doses produced annually.
[link to www.fiercepharma.com (secure)]
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(August 15, 2020) AstraZeneca concludes agreement with European Commission for supply of up to 400 million doses of AZD1222 COVID-19 vaccine
AstraZeneca has concluded an agreement with the European Commission (EC) to supply up to 400 million doses of the AZD1222 COVID-19 vaccine.
Pascal Soriot, chief executive officer, said: “This first vaccine agreement with the European Commission will ensure that millions of Europeans have access to the AZD1222 vaccine
following its approval. With production in our European supply chain soon to be started, we hope to make the vaccine available widely and rapidly,
with the first doses to be delivered by the end of 2020.
AZD1222 was co-invented by the University of Oxford and its spin-out company, Vaccitech.
It uses a replication-deficient chimpanzee viral vector based on a weakened version of a common cold virus (adenovirus)
that causes infections in chimpanzees and contains the genetic material of the SARS-CoV-2 virus spike protein.
After vaccination, the surface spike protein is produced,
priming the immune system to attack the SARS-CoV-2 virus if it later infects the body.
[link to www.pharmabiz.com]
deplorable scottfree

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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
Summary?
J 17:15: "I pray not that Thou shouldst take them out of the world, but that Thou shouldst keep them from the evil.

Truth, beauty and virtue ... all the things that THEY hate. All the things God loves.
Gorgol

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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
No coincidence that the 2 Dutch ministers that are handling the Covid narrative in the Netherlands both have a brother inside Astra-Zeneca

Marien de jonge is the brother of Corona-minister Hugo de Jonge
Marien de Jonge - [link to www.radboudumc.nl (secure)]

Hans Sijbesma is THE DIRECTOR of ASTRA-ZENECA GERMANY

[link to www.commonsensetv.nl (secure)]

He is also the brother of the other Dutch Covid minister Feike Sijbesma

Needless to say, both ministers say that the "covid crisis" can only end when there is a vaccine

Follow the fucking money

Fuckin'scam, Theft, Fraud, Mass Murder and High Treason

Last Edited by Gorgol on 08/15/2020 04:50 PM
Gorgol -No Jab, No Jitter
Too Dark Park™ Two

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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
bump
Bless my fuck



"It’s in my interest, in ours perhaps, or maybe the interests of the greater good, for me to smoke a joint, and calm down.”
— Hunter S. Thompson



"I've got the spirit, but lose the feeling!"



:rockon:
Gorgol

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Big wall of text scared everyone away?
Gorgol -No Jab, No Jitter
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Re: AstraZeneca, Oxford Jenner Institute, vaccine, AZD1222 (ChAdOx1 nCoV-19), CEPI, BARDA, GAVI
(August 19, 2020) CSIRO welcomes Australian agreement with AstraZeneca to provide access to Oxford’s COVID-19 vaccine
CSIRO welcomes the Australian Government’s agreement with pharmaceutical company AstraZeneca,
to give Australians access to the University of Oxford’s COVID-19 vaccine,
should it prove successful, safe and effective. CSIRO also welcomes the news that the Australian Government is working with CSL and AstraZeneca
to assess whether it is possible to provide local manufacturing support for the vaccine,
should it prove successful. As Australia’s national science agency, CSIRO is playing a critical role
in the global efforts to develop a COVID-19 vaccine. In March this year, the Coalition for Epidemic Preparedness Innovations (CEPI) engaged CSIRO
to undertake a preclinical trial of Oxford’s vaccine candidate at the Australian Centre for Disease Preparedness (ACDP).
ACDP is CSIRO’s high-containment biosecurity facility, the only lab of its kind in the southern hemisphere.
CSIRO has shared early data from the preclinical trial with CEPI and Oxford University,
which enabled the vaccine candidate to progress on to phase 3 clinical (human) trials.
[link to www.scimex.org (secure)]
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(August 21, 2020) Coronavirus: Belgian experts ‘shocked’ as AstraZeneca seeks liability waiver for vaccine
“In the US it is common for firms to cover for themselves in this way, but, in Europe, it is exceptional,”
Stefaan Callens, university professor of medical law at KU Leuven, told HLN.
Thierry Vansweevelt, professor of medical law at the University of Antwerp called the request “very exceptional” and even “slightly shocking,”
in light of existing EU regulations on companies’ liability for what they put on the market.
“There is a European directive on product liability,”
Vansweevelt said. “Any producer who places a defective product on the market is responsible for that without exceptions.
You can’t escape that.” But, Ruud Dobber, an AstraZeneca executive, told Reuters that most countries with whom it had signed procurement deals
had already granted its request, but refused to name the countries in question.
Dobber said that AstraZeneca could “simply not take the risk” of being faced with liability claims if “in four years the vaccine is showing side effects.”
[link to www.brusselstimes.com (secure)]
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(August 21, 2020) Officials have no answers about legal liabilities for vaccine’s potential side-effects
Australian health officials and drug maker AstraZeneca have declined to comment
on whether the pharma company is seeking indemnification against potential liability
arising from any side effects of its vaccine candidate.
The government’s signing of a letter of intent with Britain’s AstraZeneca
to secure the Oxford University vaccine has raised questions over the exact nature of the agreement,
with finer details around numbers and rollout not yet announced.
The government said “a final formal agreement will include distribution, timing and price of the vaccine”
but those details are not yet ironed out.
[link to thenewdaily.com.au (secure)]
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technology is scary , until you need it.
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(May 22, 2019) AstraZeneca joins with BenevolentAI for drug discovery
Strategic partnership between AstraZeneca and BenevolentAI to use artificial intelligence and machine learning to identify new kidney and lung drugs.
Pharma giant AstraZeneca has announced a new long-term collaboration with artificial intelligence experts BenevolentAI.
The collaboration aims to combine AstraZeneca’s world-leading clinical data with BenevolentAI’s machine learning capabilities
and artificial intelligence to discover new drugs for chronic kidney disease (CKD) and idiopathic pulmonary fibrosis (IPF).
As a recent study in Respiration shows, CKD and IPF are two of the most fatal and prevalent age-associated diseases.
[link to www.longevity.technology (secure)]

(June 5, 2020) 2 billion doses of the Oxford coronavirus vaccine will be available after a new deal that included $750m from Bill Gates, AstraZeneca says
The global supply of a potential coronavirus vaccine being developed at Oxford University has been doubled to 2 billion
after a deal including $750 million from the Bill and Melinda Gates Foundation.
The vaccine is being produced by AstraZeneca British drug maker, drawing on work by researchers from Oxford University.
It announced Thursday that it had signed agreements with the Coalition for Epidemic Preparedness Innovations (CEPI) and Gavi
the Vaccine Alliance to boost its supplies. The company has committed to mass-producing the vaccine before it has been proved effective, an unusual
step designed to compress the long timeline of vaccine production.
CEPI and Gavi are both charities supported the Bill and Melinda Gates Foundation and the World Health Organization.
The $750 million agreement with CEPI and Gavi will support manufacturing, procurement and distribution for 300 million of the 2 billion doses.
The statement also said that AstraZeneca struck a licensing partnership with the Serum Institute of India (SII),
the world's largest manufacturer of vaccines by volume, for 1 billion doses of the vaccine earmarked for low- and middle-income countries.
[link to www.businessinsider.com (secure)]

(June 15, 2020) AstraZeneca taps Catalent for COVID-19 vaccine finishing, packaging at Italian plant
British drugmaker AstraZeneca is shooting for the moon with its plan to produce 2 billion doses per year of a potential COVID-19 vaccine.
To reach that lofty goal, AstraZeneca has reached a deal with New Jersey-based Catalent
to help with the final stages of the shot's manufacturing.
Catalent will be tasked with finishing and packaging duties for AstraZeneca and the University of Oxford's COVID-19 vaccine candidate, AZD1222,
at its 305,000-square-foot manufacturing facility in Anagni, Italy, the CDMO said Monday.
As part of their agreement, Catalent will help AstraZeneca produce "hundreds of millions of doses" beginning in August 2020
and potentially running through March 2022, if the vaccine receives full regulatory approval.
Last week, AstraZeneca and Emergent BioSolutions inked an $87 million deal to manufacture doses of Oxford's adenovirus-based COVID-19 shot for U.S. supply.
The accord was part of the Trump administration's Operation Warp Speed initiative
to develop and rapidly scale production of targeted vaccines before the end of 2020.
For its part, Catalent will also work with Johnson & Johnson to help produce its COVID-19 vaccine hopeful.
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(June 29, 2020) AstraZeneca reaches supply deal with Brazilian government to produce millions of doses of COVID-19 shot
AstraZeneca and the government of Brazil have inked a deal valued at $127 million
to produce doses of the University of Oxford's adenovirus-based COVID-19 vaccine candidate, AZD1222,
as the country combats a rising count of new infections.
Brazil—which trails only the U.S. in terms of total reported COVID-19 cases and deaths—will make available around 30 million finished doses
of the vaccine, with roughly half that amount available by December, AstraZeneca said. Brazil has also committed to produce an additional 70 million doses,
with AstraZeneca supplying the unfinished vaccine at no cost.
The vaccine doses will be finished in Brazil by the Oswaldo Cruz Foundation, also known as Fiocruz,
as AstraZeneca does not have a vaccine production suite at its Brazilian manufacturing facility, the drugmaker said.
On Friday, local Japanese drugmaker Daiichi Sankyo said it was piecing together a supply deal with AstraZeneca for Oxford's shot
after the Japanese government agreed to sit down at the negotiating table to discuss a possible deal.
Daiichi Sankyo Biotech, a subsidiary of the Japanese drugmaker, plans to receive Oxford's undiluted vaccine, which it will finish at its own facilities.
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(August 24, 2020) Catalent Signs Agreement with AstraZeneca to Expand Manufacturing Support for COVID-19 Vaccine AZD1222
SOMERSET, N.J.--(BUSINESS WIRE)--Catalent, Inc. (NYSE: CTLT), the leading global provider of advanced delivery technologies,
development, and manufacturing solutions for drugs, biologics, cell and gene therapies,
and consumer health products, today announced that Catalent Cell & Gene Therapy will provide drug substance manufacturing to AstraZeneca
for the University of Oxford’s adenovirus vector-based COVID-19 vaccine, AZD1222,
at Catalent’s commercial gene therapy manufacturing facility located in Harmans, Maryland.
Catalent will prepare the Harmans facility, close to Baltimore-Washington International (BWI) airport,
to enable multiple production trains to run in parallel to produce the vaccine candidate drug substance commencing late in the third quarter of 2020.
This agreement expands Catalent’s support of the AZD1222 program following the announcement in June
that Catalent’s facility in Anagni, Italy, will provide large-scale vial filling and packaging of AZD1222.
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(August 30, 2020) Australian Religious Leaders Criticize ‘Immoral’ COVID-19 Vaccine Deal
SYDNEY, AUSTRALA - A coronavirus deal signed by Australia with an international drug company is raising ethical concerns among prominent church leaders.
Australia has signed a deal with the pharmaceutical company AstraZeneca to produce and distribute a vaccine being developed by Britain's Oxford University...
if the treatment works. But three of Australia's most senior archbishops have written to Prime Minister Scott Morrison urging him to reconsider the agreement,
saying the use of "fetal tissue” in the research is “deeply immoral.”
“To use that tissue then for science is reprehensible,” said Glenn Davies, Anglican Archbishop of Sydney.
“Once I know something that is morally compromised, it is my job to speak out about it.”
The Oxford University study uses embryonic kidney cells harvested from a female fetus in the Netherlands in 1973.
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(September 3, 2020) AMRI Selected to Support AstraZeneca in Delivery of COVID-19 Vaccine
ALBANY, N.Y.--(BUSINESS WIRE)--Albany Molecular Research, Inc. (AMRI), a leading global provider of advanced drug development
and manufacturing solutions, today announced that it has signed a supply agreement with AstraZeneca
to support the manufacture of AstraZeneca’s COVID-19 vaccine candidate AZD1222, intended to protect against the SARS-CoV-2 novel coronavirus.
On May 21, 2020, AstraZeneca announced it had received more than $1B from the U.S. Biomedical Advanced Research and Development Authority (BARDA)
for the development, production and delivery of the COVID-19 vaccine it is developing in cooperation with University of Oxford.
AMRI has been chosen to contribute to the supply of the vaccine candidate through sterile fill/finish of AZD1222 at AMRI’s drug product manufacturing facility in Albuquerque, New Mexico.
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(September 3, 2020) AstraZeneca's COVID-19 vaccine to be tested at military sites
Five Department of Defense facilities will participate in the Phase 3 trial of a COVID-19 vaccine, the Pentagon announced Thursday.
According to the Department of Defense, researchers are still seeking volunteers
for the next phase of testing for AZD1222, a COVID-19 vaccine candidate under development by AstraZeneca.
The upcoming trial will take place at
- Naval Medical Center in San Diego,
- Joint Base San Antonio,
- Wilford Hall Ambulatory Surgical Center in San Diego,
- Walter Reed National Military Medical Center in Bethesda, Md.,
- and Fort Belvoir Community Hospital in Fort Belvoir, Virginia.

"The Department of Defense continues to play a key role in the development of a potential COVID-19 vaccine,"
Tom McCaffery, assistant secretary of defense for health affairs, said in a statement.
The vaccine is the result of a partnership between AstraZeneca and Oxford Vaccine Group,
with funding from the Biomedical Advanced Research and Development Authority,
a branch of the U.S. Department of Health and Human Services, as well as the British government.
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People don't ALL have time to finish 'walls of text'.

We come on here and enjoy the information given and

if it involves a little light reading, that's fine.

But these should be given a summary of some sort before

we get into all those posts.

You have 24 or more significant posts with links

on each and a paragraph for all.

Don't you think a summary would help???

Just asking...
Living has taught me one thing; nothing is certain...except salvation through Jesus Christ!
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09/05/2020 03:56 PM
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(January 16, 2018) Google invests in UK vaccine pioneer Vaccitech
Google has invested £20 million ($27.1m) in a biotech firm spun out of Oxford University
working on novel treatments which include a universal flu vaccine
and a therapeutic cancer vaccine. The tech giant’s GV division (formerly known as Google Ventures)
was the lead investor in Vaccitech in its Series A investment round, with Silicon Valley investor Sequoia Capital
and existing backer Oxford Sciences Innovation and Neptune Ventures also contributing.
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Anonymous Coward
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09/05/2020 04:02 PM
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People don't ALL have time to finish 'walls of text'.

We come on here and enjoy the information given and

if it involves a little light reading, that's fine.

But these should be given a summary of some sort before

we get into all those posts.

You have 24 or more significant posts with links

on each and a paragraph for all.

Don't you think a summary would help???

Just asking...
 Quoting: 1guynAz


Each individual will create an opinion based on information , knowledge and intuition,
in my opinion is important to stay vigilant and keep up the good work.
hf
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(September 9, 2020) AstraZeneca Vaccine Tests Face Delay After Patient Gets Ill
AstraZeneca Plc stopped giving shots of its experimental coronavirus vaccine after a person participating in one of the company’s studies got sick,
a potential adverse reaction that could delay or derail efforts to speed an immunization against Covid-19 for the world.
The pause stemmed from a standard review of the company’s vaccine trials after one person developed an unexplained illness (transverse myelitis, inflammation of the spinal cord)
AstraZeneca said in a statement. The move was intended to give researchers time to examine safety data
while maintaining the integrity of the trials, the company said.
Paul Offit, a pediatrician and vaccine expert at the Children’s Hospital of Philadelphia,
said the AstraZeneca shot involves giving large doses of a monkey adenovirus engineered
so it can’t replicate. It is therefore important for researchers to investigate
whether the adverse event wasn’t somehow being triggered by a reaction to that large viral dose, he said.
“When you have that kind of viral load, you can have side effects,” said Offit.
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(September 12, 2020) AstraZeneca Resumes Its COVID-19 Vaccine Trials In The U.K.
Drugmaker AstraZeneca announced Saturday that its COVID-19 vaccine studies have resumed in the United Kingdom,
though not yet in the United States. The vaccine trials had been placed on hold
around the world earlier in the week after a U.K. participant in one of the studies developed a neurological illness.
AstraZeneca said it cannot disclose further medical information because it is the study sponsor,
but added in its statement, "All trial investigators and participants will be updated with the relevant information,
and this will be disclosed on global clinical registries, according to the clinical trial and regulatory standards."
In late July, results of a preliminary safety and effectiveness study found that more than two-thirds
of the people who received the experimental vaccine reported fatigue and headache after inoculation.
Muscle aches and fever were also common. In May, the Trump administration awarded the AstraZeneca
effort up to $1.2 billion from the Biomedical Advanced Research and Development Authority as part of Operation Warp Speed,
the administration's push to have a widely available coronavirus vaccine by January.
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Thread: COVID-19 RELATED TIMELINE
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Human 2.0





GLP