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Showing posts with label Coronavirus Vaccine Tracker. Show all posts
Showing posts with label Coronavirus Vaccine Tracker. Show all posts

Covid-19 Vaccine: Serum Institute will apply for emergency authorisation in next 2 weeks

 University of Oxford and AstraZeneca on Monday said that their Covid-19 vaccine was up to 90 per cent effective in late-stage clinical trials.

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World News/Covid-19 Vaccine Tracker : The Serum Institute of India (SII) will apply for emergency license of Covid-19 vaccine within the next fortnight , said chief executive officer Adar Poonawalla on Saturday.

Speaking to reporters through virtual press conference minutes after Prime Minister Narendra Modi’s visit to SII’s facility in Pune on Saturday, Poonawalla said, the vaccine, post-authorization, will initially be distributed in India then to African countries.

“We are in process of applying for emergency licensing in the next two weeks. we will have to wait and see when we get the authorisation,” said Poonawalla while responding to an issue on Covishield vaccine’s distribution within the country.

“The vaccine will be distributed initially in India and then we will look at COVAX countries which are mainly in Africa. The united kingdom and European markets are being taken care of by AstraZeneca and Oxford. If they need our help for scaling up production capacity, we are always there to support them.”

The SII, the world’s largest vaccine maker, has signed an agreement to manufacture the vaccine developed by the Jenner Institute of Oxford University together with British-Swedish pharma company AstraZeneca.

University of Oxford and AstraZeneca on Monday said that their Covid-19 vaccine was up to 90 per cent effective in late-stage clinical trials, raising hopes for the arrival of shots in India by the end of the year.

According to Poonawalla, the Covishiled vaccine has proved effective during trials. “What we found in Covishield during trials globally was that there was zero hospitalisation and 60 per cent reduction in sterilizing immunity.”

Poonawala said during PM Modi’s visit to the manufacturing facility at SII, various issues about pricing and logistics also as pros and cons of other vaccine candidates were discussed.

The SII is currently producing 50-60 million doses per month and plans to proportion to 100 million doses by January next year.

“We are producing 50 to 60 million doses per month and post-January, it will be scaled up to 100 million doses a month. we have built the largest pandemic-level facility in Pune and our new campus in Mandri. That was also showcased to the PM with a tour around the facility and a lot of detailed discussions,” Poonawalla further mentioned.

On signing any deal with the govt of India, Poonawalla said there has been no contract signed with centre yet.

“As of now, we don’t have anything in writing on how many doses they will purchase but as indicated by the health ministry, they would need 300-400 million doses by July 2021,” said the SII CEO.

Poonawala also claimed the Oxford drug will be transported easily at normal refrigerator temperatures, unlike a number of the other candidates which require extreme cold storage.


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US Plans to Starts Covid vaccinations by 11 December: Official

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World News/Covid-19 Vaccine traker: The united states hopes to start a sweeping program of Covid vaccinations in early December, the head of the govt coronavirus vaccine effort said Sunday.

"Our plan is to be able to ship vaccines to the immunization sites within 24 hours of approval" by the US Food and Drug Administration, Moncef Slaoui told CNN.

"So I expect maybe on Day Two of the approval, on the 11th or the 12th of December."

FDA vaccine advisors reportedly will meet december 8 to 10 to discuss approving vaccines which Pfizer and Moderna say are a minimum of 95 percent effective.

Two leading vaccine candidates -- one by Pfizer and German partner BioNTech and another by US firm Moderna -- have shown to be 95 percent effective and Pfizer already applied to emergency use approval from US health authorities.

Meanwhile, Pfizer Inc applied to US health regulators on Friday for emergency use authorization (EUA) of its COVID-19 vaccine, the first such application during a major step toward providing protection against the new coronavirus.

The application to the U.S. Food and Drug Administration (FDA) comes just days after Pfizer and German partner BioNTech SE reported final trial results that showed the vaccine was 95% effective in preventing COVID-19 with no major safety concerns.

Pfizer Chief executive officer Albert Bourla confirmed the application had been made in a video posted on the company's website on Friday afternoon.

The FDA said on Friday it might hold a meeting of the advisory committee on December 10 at which members would discuss the vaccine.

Slaoui estimated that 20 million people across the US may be vaccinated in December, with 30 million per month after that.

US drug regulators on Saturday already gave emergency approval to a Covid-19 antibody therapy -- one used by US President Donald Trump -- and G20 nations were pushing for global "equitable" access to vaccines with worries poorer nations will be left behind.

The US, which recorded 177,552 new infections on Saturday, is now averaging almost 110,000 more daily cases than a month ago. Recently, US FDA approved an antibody cocktail from Regeneron Pharmaceuticals Inc. for coronavirus treatment.


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India’s Serum says produced 40 million doses of AstraZeneca COVID-19 vaccine

 India’s Serum Institute has said it's made 40 million doses of AstraZeneca's potential Covid-19 vaccine. The ICMR will pursue "early availability" of the shot in India, it added.

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Latest News/Covid-19 Vaccine/Corona Virus Vaccine Update: Serum Institute of India, the world's largest vaccine producer, has said it's made 40 million doses of AstraZeneca's potential Covid-19 vaccine, and can soon begin making Novavax's rival shot, as they both seek regulatory approval.

Serum on Thursday said it had enrolled 1,600 participants in India for late-stage trials of AstraZeneca's candidate, and also plans to seek regulatory approval to run late-stage trials for the Novavax vaccine.

The AstraZeneca vaccine, co-developed by Oxford University , is that the most advanced in human testing in India, Serum said, adding that the company and therefore the Indian Council of Medical Research (ICMR) will pursue "early availability" of the shot in India.

Representatives for both Serum and therefore the ICMR declined to comment on whether the 40 million doses of the AstraZeneca vaccine were meant for supply only in India. 

The ICMR, a federal government body, had funded the clinical trial site fees for the AstraZeneca vaccine, Serum said. The company and therefore the ICMR are currently conducting mid-stage clinical trials of the shot at 15 centres across India.

The news came as coronavirus infections in India, the world's second-worst hit country, reached 8.68 million on Thursday and therefore the death toll increased to over 128,000.

India also has at least two home-grown Covid-19 vaccine candidates in development, while local drugmaker Dr Reddy's Labs is carrying out a trial within the country for Russia's vaccine candidate.

Earlier in the week , Pfizer and its partner BioNTech said their vaccine candidate had proven over 90% effective based on initial trial results. Pfizer said it had been committed to advancing its engagement with India's government to supply its potential vaccine within the country.


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Pfizer says COVID-19 vaccine over 90% effective

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Coronavirus Vaccine Tracker/ World News: Pfizer Inc's (PFE.N) experimental COVID-19 vaccine is more than 90% effective based on initial trial results, the drugmaker said on Monday, a major victory in the war against a virus that has killed over a million people and battered the world's economy.

Experts welcomed the first successful interim data from a large-scale clinical test as a watershed moment that showed vaccines could help halt the pandemic, although mass roll-outs, which needs regulatory approval, will not happen this year.

Pfizer and German partner BioNTech SE (22UAy.F) said they had found no serious safety concerns yet and expected to seek U.S. authorization this month for emergency use of the vaccine, raising the chance of a regulatory decision as soon as December.

If granted, the companies estimate they can roll out up to 50 million doses this year, enough to protect 25 million people, and then produce up to 1.3 billion doses in 2021.

"Today is a great day for science and humanity," said Pfizer Chief Executive Albert Bourla.

"We are reaching this critical milestone in our vaccine development program at a time when the world needs it most with infection rates setting new records, hospitals nearing over-capacity and economies struggling to reopen," he said.

Experts said they still wanted to see the full trial data, which have yet to be peer-reviewed or published in a medical journal, but the preliminary results looked encouraging.

"This news made me smile from ear to ear. It is a relief to see such positive results on this vaccine and bodes well for COVID-19 vaccines in general," said Peter Horby, professor of emerging infectious diseases at the University of Oxford.

There are still many questions, such as how effective the vaccine is by ethnicity or age, and how long it will provide immunity, with the "new normal" of social distancing and face covering set to remain for the foreseeable future.

Pfizer expects to seek U.S. emergency use authorization for people aged 16 to 85. To do so, it will need two months of safety data from about half the study's 44,000 participants, which is expected in the third week of November.

U.S. Health and Human Services Secretary Alex Azar said it would take several weeks for U.S. regulators to receive and process data on the vaccine before the government could potentially approve it.


MARKETS SURGE

The prospect of a vaccine electrified world markets with the S&P 500 and Dow hitting record highs as shares of banks, oil companies and travel companies soared. Shares in companies that have thrived during lockdowns, such as conferencing platform Zoom Video (ZM.O) and online retailers, tumbled.

Pfizer shares jumped more than 11% to their highest since July last year, while BioNTech's stock hit a record high.

Shares of other vaccine developers in the final stage of testing also rose with Johnson & Johnson (JNJ.N) up 4% and Moderna Inc (MRNA.O), whose vaccine uses a similar technology as the Pfizer shot, up 8%. Britain's AstraZeneca (AZN.L), however, fell 2%. Moderna is expected to report results from its large-scale trial later this month.

"The efficacy data are really impressive. This is better than most of us anticipated," said William Schaffner, infectious diseases expert at Vanderbilt University School of Medicine in Nashville, Tennessee. "The study isn't completed yet, but nonetheless the data look very solid."

U.S. President Donald Trump welcomed the test results, and the market boost: "STOCK MARKET UP BIG, VACCINE COMING SOON. REPORT 90% EFFECTIVE. SUCH GREAT NEWS!" he tweeted.

President-elect Joe Biden said the news was excellent but did not change the fact that face masks, social distancing and other health measures would be needed well into next year.

The World Health Organization said the results were very positive, but warned there was a funding gap of $4.5 billion that could slow access to tests, medicines and vaccines in low- and middle-income countries.


'NEAR ECSTATIC'

"I'm near ecstatic," Bill Gruber, one of Pfizer's top vaccine scientists, said in an interview. "This is a great day for public health and for the potential to get us all out of the circumstances we're now in."

Between 55% and 65% of the population will need to be vaccinated to break the dynamic of the spread of COVID-19, said Germany's health minister Jens Spahn, adding that he did not expect a shot to be available before the first quarter of 2021.

The European Union said on Monday it would soon sign a contract for up to 300 million doses of the Pfizer and BioNTech COVID-19 vaccine.

The companies have a $1.95 billion contract with the U.S. government to deliver 100 million vaccine doses beginning this year. They did not receive research funding from the Trump administration's Operation Warp Speed vaccine program.

The drugmakers have also reached supply agreements with the United Kingdom, Canada and Japan.

Pfizer said the interim analysis, conducted after 94 participants in the trial developed COVID-19, examined how many had received the vaccine versus a placebo.

Pfizer did not break down how many of those who fell ill received the vaccine. Still, over 90% effectiveness implies that no more than 8 of the 94 had been given the vaccine, which was administered in two shots about three weeks apart.

The efficacy rate, which could drop once full results are available, is well above the 50% effectiveness required by the U.S. Food and Drug Administration for a coronavirus vaccine.

Shortly after Pfizer's announcement, Russia said its Sputnik V vaccine was also more than 90% effective, based on data collated from inoculations of the public. Its preliminary Phase III trial data is due to be published this month.

MORE DATA NEEDED

To confirm the efficacy rate, Pfizer said it would continue its trial until there were 164 COVID-19 cases among volunteers. Bourla told CNBC on Monday that based on rising infection rates, the trial could be completed before the end of November.

Pfizer said its data would be peer reviewed once it has results from the entire trial.

"These are interesting first signals, but again they are only communicated in press releases," said Marylyn Addo, head of tropical medicine at the University Medical Center Hamburg-Eppendorf in Germany.

Dozens of drugmakers and research groups around the globe have been racing to develop vaccines against COVID-19, which on Sunday exceeded 50 million cases since the new coronavirus first emerged late last year in China.

The Pfizer and BioNTech vaccine uses messenger RNA (mRNA) technology, which relies on synthetic genes that can be generated and manufactured in weeks, and produced at scale more rapidly than conventional vaccines. The technology is designed to trigger an immune response without using pathogens, such as actual virus particles.

The Trump administration has said it will have enough vaccine doses for all of the 330 million U.S. residents who want it by the middle of 2021.

News source: Reuters


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Covid-19: China gives ‘unproven’ vaccine to thousands of people, makes them sign ‘secrecy’ agreement

 Thousands of Chinese have already been inoculated by Covid-19 vaccines which are still under trial. China has said WHO gave them a go-ahead.

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Little is known about China’s Covid-19 vaccination programme. (REUTERS)

China is injecting thousands of its people with Covid-19 vaccine shots, which are still under trial and hence their efficacy unproven, reports said. people who are getting these vaccine shots are made to sign a “nondisclosure agreement”, according to which they can’t talk about it to the news media.

High-risk population, including staff of state-owned companies, government officials, vaccine company staff, teachers are being inoculated on an emergency basis. Global heath experts are raising questions whether their consent has are being taken or not.


In its defence, China has said that the world Health Organization supported China’s experimental coronavirus vaccine programme, which started in July. China informed WHO in June, Zheng Zhongwei, a National Health Commission official, told Reuters.


WHO chief scientist Soumya Swaminathan has said countries can approve use of medical products within their own jurisdiction in the current emergency situation but only as a “temporary solution”.


China currently has 11 vaccines in clinical trials and four in Phrase 3 trials.Among these. two are developed by state-backed China National Biotec Group and one by Sinovac Biotech. Another experimental vaccine was developed by CanSino Biologics, which was approved to be used in the Chinese military in June.


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When covid vaccines will be ready? Govt reviews progress of trials

 

Prime Minister Narendra Modi in his Independence Day speech on Saturday said India has prepared a roadmap to make sure that a COVID-19 vaccine reaches everyone within the shortest possible time

The Indian government on Monday reviewed the progress of the covid vaccines undergoing clinical trials within the country. The domestic pharma giants presented the present status of varied candidate vaccines for COVID-19 to the central government. The National Expert Group on Covid-19 Vaccine Administration on Monday met leading domestic vaccine manufacturers: Serum Institute of India, Pune; Bharat Biotech, Hyderabad; Zydus Cadila, Ahmedabad; Gennova Biopharmaceuticals, Pune; and Biological E, Hyderabad.


The meeting was mutually beneficial and productive, the health ministry said.


"It provided the National Expert Group with inputs about the present stage of various candidate vaccines being developed by the indigenous manufacturers as well as their expectations from the Union government."


Three Covid vaccine candidates in India are in several phases of clinical study.

The first is that the inactivated virus vaccine which is that the Bharat Biotech Vaccine being developed together with Indian Council of Medical Research (ICMR).


Similarly, the second is that the DNA vaccine of pharma giant Zydus Cadila.


The third, may be a recombinant Oxford University vaccine manufactured by Serum Institute of India (SII) which got approval from DCGI to conduct phase 2, 3 clinical study within the nation.

The central government has constituted a committee under the chairmanship of Dr VK Paul, member (health) at Niti Aayog, on covid vaccine administration.


The terms of reference of this expert committee are to streamline suitable vaccine selection, how procurement of vaccine are going to be done, how vaccine would be delivered, prioritising groups to whom vaccine has got to be administered.


Prime Minister Narendra Modi in his Independence Day speech on Saturday said India has prepared a roadmap to make sure that a COVID-19 vaccine reaches everyone within the shortest possible time.

He said three vaccine candidates are in several stages of trials within the country.


The prime minister said whenever there's talk about COVID-19, the question that involves everyone's mind is - when will a vaccine be ready.


"I want to tell people, the talent of our scientists is like that of 'rishi munis' and they are working very hard in laboratories. Three vaccines are in various stages of testing. When scientists will give us the green signal, it will be produced on a mass scale and all preparations have been made for it," PM Modi said in address.

Keyword : Coronavirus Vaccine Tracker

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