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Monday, November 16, 2020

Indian drugmaker Biological E. starts human trials of COVID-19 vaccine candidate

India’s Biological E. Ltd has started human trials of its COVID-19 vaccine candidate and expects results by February, the drugmaker said on Monday.

The Hyderabad-based firm initiated phase I and phase II trials of its vaccine candidate - being developed with Baylor College of Medicine in Houston, Texas, and U.S.-based Dynavax Technologies Corp DVAX.O - after getting the green signal from the Drugs Controller General of India.

The trial will test two doses of the vaccine in about 360 healthy subjects aged 18 to 65 years, Biological E. said.

Separately, Bharat Biotech, a private company developing a vaccine candidate, COVAXIN, with the government-run Indian Council of Medical Research, said it was starting phase III trials on Monday.

India has reported 8.85 million confirmed cases of the virus - the second highest in the world, after the United States - but the number of new daily cases has fallen since a peak in mid-September.

Meanwhile, hopes for a vaccine got a fresh boost after U.S.-based Moderna Inc MRNA.O said on Monday its experimental vaccine was 94.5% effective in preventing COVID-19 based on interim data from a late-stage clinical trial.

Separately, Bharat Biotech, a private company developing a vaccine candidate, COVAXIN, with the government-run Indian Council of Medical Research, said it was starting phase III trials on Monday.

India has reported 8.85 million confirmed cases of the virus - the second highest in the world, after the United States - but the number of new daily cases has fallen since a peak in mid-September.

Meanwhile, hopes for a vaccine got a fresh boost after U.S.-based Moderna Inc MRNA.O said on Monday its experimental vaccine was 94.5% effective in preventing COVID-19 based on interim data from a late-stage clinical trial.

https://www.reuters.com/article/us-health-coronavirus-india-vaccine/indian-drugmaker-biological-e-starts-human-trials-of-covid-19-vaccine-candidate-idUSKBN27W1T4

Lonza aims to make ingredients for 400M doses of Moderna's COVID vaccine annually

Swiss contract drug manufacturer Lonza's LONN.S plants in the United States and Switzerland are due to make ingredients for 400 million doses of Moderna's MRNA.O COVID-19 vaccine annually, Lonza said on Monday.

Lonza, which in September began “large-scale production” in the United States and expects Swiss production to start this year, made the announcement after Moderna said its vaccine candidate showed 94.5% efficacy, according to interim data.

Moderna, whose vaccine requires two doses per person, has said it remains on track to produce between 500 million and 1 billion doses annually by 2021, while planning U.S. shipments of about 20 million doses already this year.

Basel-based Lonza is building four production lines -- one in Portsmouth, New Hampshire, and three in Visp deep in the Swiss Alps -- for $60-70 million each, with each line capable of producing 100 million doses. Moderna has its own production capacity, too.

Lonza has previously said it could potentially increase production capacity for Moderna’s vaccine, including at a site in Singapore or in Switzerland, although a spokesperson said on Monday the company is initially focused on completing the four production lines now in the works.

"With positive interim results from both Moderna's and Pfizer's PFE.N mRNA vaccine candidates, we are witnessing a major step forward in the evolution of vaccine technology, with the potential to change the way we manage infection and disease in the future," said Lonza Chief Executive Pierre-Alain Ruffieux in a statement.

https://www.reuters.com/article/us-health-coronavirus-lonza-moderna/lonza-aims-to-make-ingredients-for-400-million-doses-of-modernas-covid-vaccine-annually-idUSKBN27W1N0

New Jersey to set new Covid-19 restrictions

Vaccine development sends investors back into dine-in restaurant names

  • Investors are showing some confidence in dine-in restaurant stocks as today's Moderna vaccine news outweighs short-term concerns over new COVID-19 restrictions.
  • Moderna reported a 94.5% efficacy rate for its COVID-19 vaccine in a Phase 3 trial without any safety concerns.
  • Notable gainers in the premarket session include Brinker International (NYSE:EAT) +3.33%, Dave & Buster's Entertainment (NASDAQ:PLAY) +10.98%, Ruth's Hospitality Group (NASDAQ:RUTH) +8.33%, Bloomin' Brands (NASDAQ:BLMN) +5.25%, Cheesecake Factory +5.55%.
  • Papa John's International (NASDAQ:PZZA) and Domino's Pizza (NYSE:DPZ) are both down about 1.2% in the early session. Pandemic favorite Chipotle (NYSE:CMG) is off 0.35% and Wingstop (NASDAQ:WING) could see a drop when it starts trading.
  • https://seekingalpha.com/news/3636525-vaccine-development-sends-investors-back-dine-in-restaurant-names

Russia focuses on freeze-dried vaccine doses as transport fix

Russia expects to produce primarily freeze-dried Sputnik V coronavirus vaccine doses by the spring, a top official said, eliminating the need for transport at ultra-low temperatures as part of an ambitious plan to inoculate its population.

Vaccine developers globally are scrambling to work out how to ship and store their vials, some of which must be kept in specialised freezers at extremely low temperatures.

The logistical challenge was brought into sharp focus after promising interim trial data for the vaccine developed by BioNTech and Pfizer, a major breakthrough in the race to curb the pandemic.

This vaccine needs to be shipped and stored at minus 70 degrees Celsius, equivalent to an Antarctic winter, posing a challenge for even the most sophisticated hospitals in the United States.

It also puts it out of reach for the moment for many poor countries.

Transportation is a pressing issue for Russia, which has many extremely remote settlements and has already begun rolling out a programme of mass inoculation of frontline medical workers across the country, though human trials of Sputnik V are not yet complete.

Whether being trucked across Siberia or flown to the far reaches of the Arctic, its vials must be stored at minus 18 degrees Celsius or below, according to the Gamaleya Institute which developed the shot.

But Russia has also been testing a version that has undergone lyophilisation, turning the liquid vaccine into a dry, white mass that can be stored at normal fridge temperatures of 2 to 8 degrees Celsius (35.6-46.4°F). It is then diluted before injection.

Russia has not previously disclosed how many doses of freeze-dried vaccine it is planning to produce. But Kirill Dmitriev, head of the Russian Direct Investment Fund (RDIF), which is backing and marketing the vaccine, told Reuters it would soon be the main focus.

"We expect that, starting roughly from February, we will switch mainly to the lyophilised form," he said. "A large proportion of doses, if not a majority, will be specifically in this form.

"We have conducted trials that confirm that the immune response to the lyophilised form is the same as to the standard form of the vaccine."

Interim results for the vaccine in liquid form showed the shot to be 92% effective.

Lead scientist at the Gamaleya Institute, Alexander Gintsburg, said in an interview with Reuters earlier this year that freeze-drying was not yet a primary focus, as lyophilisate is more expensive and takes longer to produce.

However, Dmitriev said that the process was not significantly more expensive, and that the main limitation is the time needed to acquire additional equipment.

Russia plans to produce around 2 million doses of Sputnik V this year, ramping up to 15 million per month by the spring.

Contracts seen by Reuters in the state tender register show that the Gamaleya Institute placed an order for materials from laboratory supplier Dia-M to be used for packaging 2.9 million doses of the shot in liquid form, and 720,000 doses freeze-dried. The order must be fulfilled by Dec. 21.

The health ministry, which supervises the Gamaleya Institute, did not comment on the contracts. Dia-M also did not respond to a request for comment.

Freeze-drying, if applied widely, could give Russia an advantage in some export markets.

The health secretary of the Brazilian state of Bahia told Reuters he had ruled out buying the vaccine produced by Pfizer and BioNTech as they required ultra-cold freezers for transportation.

Bahia signed a deal with Russia for 50 million doses of Sputnik V in September.

Russia is not alone in looking at freeze-drying.

In Japan, Daiichi Sankyo Co is making a so-called messenger RNA (mRNA)-based candidate which it hopes will give it an edge for storing at higher temperatures. The technology uses a chemical messenger to instruct cells to make proteins that mimic the outer surface of the coronavirus, thereby creating immunity.

"We believe we can offer a much, much better condition (for storage)," said Masayuki Yabuta, head of the company's biologics division. "Freeze-dried is the best formulation."

VACCINE SPETSNAZ

The technique would be particularly useful for mRNA vaccines, such as the one developed by Pfizer and BioNTech, because of the ultra-low temperature storage needs, Anna Blakney, research fellow at Imperial College, said.

But it could also be used for other types of vaccines, including ones based on an adenovirus vector like in Russia.

"I think it just hasn't permeated into these big pharma companies yet," she said.

More testing may still be needed to check if freeze-drying affects a vaccine's efficacy.

"You have to show equivalency between the formulation. So someone that's vaccinated with the original formulation gets the same immune response as somebody vaccinated with the freeze-dried formulation," she said.

In late September, Russian authorities ran a test of the supply chain, sending small quantities of the vaccine in liquid form to every region of the country.

At the Moscow headquarters of logistics and courier firm Biocard, staff tracked the movements, receiving real-time updates on the temperature inside the special containers.

Containers are able to maintain a consistent temperature of minus 18.5 degrees for up to four days.

"The challenge is that ... you can't change the temperature by even half a degree, not even for a minute or a second," Oleg Baykov, Biocard director, said. "So you have very little time," Baykov said. "We're like the Spetsnaz (rapid deployment forces) of the world of medical distribution."

Outside temperatures can also affect how long the containers are able to function. Winter weather in remote Russian towns, many built around oil or gas deposits, mean Biocard is gearing up to use helicopters for transporting some doses.

Russia has so far exported the vaccine to four destinations: Belarus, Venezuela, India and the United Arab Emirates. The Venezuela delivery was handled by delivery firm DHL, Baykov said, which also placed an order with Biocard for its temperature-controlled containers for the trip.

https://www.marketscreener.com/quote/stock/DAIICHI-SANKYO-COMPANY-L-6498062/news/Exclusive-Russia-focuses-on-freeze-dried-vaccine-doses-as-transport-fix-31790618/

Inovio Pharma to begin mid-stage study of COVID-19 vaccine candidate

Inovio Pharmaceuticals Inc has received U.S. health regulator's clearance to begin a mid-stage study of its COVID-19 vaccine candidate, the vaccine maker said on Monday.

The trial for the vaccine, INO-4800, will be funded by the U.S. Department of Defense, the company said.

The U.S. Food and Drug Administration in September put Phase 3 of the mid-to-late stage trial on hold, as it sought more information, including details on a delivery device used to inject genetic material into cells.

INO-4800 is administered through a device called Cellectra, which sends out an electrical pulse to open pores in a cell so DNA molecules can enter.

Phase 3 portion of the trial will remain on partial clinical hold until Inovio has satisfactorily resolved FDA's remaining concerns, the company said.

In June, the U.S. defense department granted $71 million to Inovio to scale up production of Cellectra.

It has also agreed to provide additional funding for advanced clinical trials of the vaccine candidate, Inovio said.

https://www.marketscreener.com/quote/stock/INOVIO-PHARMACEUTICALS-I-17937428/news/Inovio-Pharmaceuticals-to-begin-mid-stage-study-of-COVID-19-vaccine-candidate-31791697/

EU regulator starts real-time review of Moderna's COVID-19 vaccine candidate

Europe's health regulator said on Monday it had launched a real-time review of U.S. drugmaker Moderna Inc's experimental COVID-19 vaccine, following similar such reviews of rival vaccines from AstraZeneca and Pfizer.

The European Medicines Agency's human medicines committee has started a "rolling review" of Moderna's mRNA-1273 vaccine candidate and is evaluating the first batch of data, the regulator said.

Rolling reviews allow drug companies to submit applications for COVID-19 medicinal products before development work is concluded and prior to the availability of complete supporting documentation, aimed at speeding up any approval process.

In October, Moderna had said it would apply for real-time reviews of its vaccine in Europe.

EMA's announcement comes a week after Switzerland began a real-time review of data from Moderna's vaccine candidate.

Moderna said earlier this month that it has enough data for a first interim analysis of its late-stage COVID-19 vaccine trial. 

https://www.marketscreener.com/quote/stock/ASTRAZENECA-PLC-4000930/news/EU-regulator-starts-real-time-review-of-Moderna-s-COVID-19-vaccine-candidate-31790954/