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Novavax鈥檚 Effort to Vaccinate the World, From Zero to Not Quite Warp Speed

[UPDATED on July 20]

On a sweltering June morning, Novavax CEO and covid vaccine maker Stanley Erck stood on a stage unmasked and did something that would have been unthinkable six months ago: He shook hands with Maryland鈥檚 governor.

Erck was with Gov. Larry Hogan to announce Novavax鈥檚 global vaccine headquarters 鈥 a campus expected to house laboratories and more than 800 employees. Hogan called Novavax鈥檚 future 鈥渂right鈥 and marveled that more than 71% of the state鈥檚 adults had received at least one shot.

None of those was a Novavax vaccine, which is still unavailable for the American public due to delayed clinical trial results and other difficulties. Hogan, for his part, vaccine dose 鈥 made by fellow biotech upstart Moderna 鈥 in January.

鈥淎s you can imagine, we鈥檙e eager to receive our own,鈥 said John Trizzino, Novavax鈥檚 chief commercial officer and interim chief financial officer. Its two-dose covid vaccine, which showed overall in key U.S. and Mexico trials, has yet to be authorized. 鈥淚n the meantime,鈥 Trizzino said, 鈥渨e鈥檝e had to use one of the existing licensed vaccines and we look forward to the booster鈥 made by Novavax.

Looking forward has kept Novavax afloat for decades 鈥 along with its deep ties to grant makers and federal agencies. With its focus on developing vaccines, including for the and MERS pandemics, Erck argues Novavax is 鈥渂uilt for this moment.鈥 Still, the 34-year-old startup has never brought one to market.

Novavax鈥檚 quest to scale up operations underscores how difficult it can be to launch a vaccine 鈥 even with the formula and technology in hand. So what happened? It has had the financial backing of the U.S. government and full faith of international agencies. Everything took longer than expected: hiring necessary researchers and scientists, getting supplies and transferring its vaccine technology. It didn鈥檛 move at warp speed.

America is awash with vaccine options, and Novavax does not plan to file for regulatory authorizations until late July at the earliest. The delay could have dire consequences for people across the globe awaiting a vaccine.

鈥淲e鈥檙e not making aspirin,鈥 Trizzino said. 鈥淲e鈥檙e making a very complicated biological.鈥

A Moonshot Goal

A year before the covid pandemic hit, Novavax had a failed late-stage trial on a potential respiratory virus vaccine, after which it cut its workforce and sold off all its manufacturing capabilities. So, when more than $2 billion in federal and international funding landed at its doorstep, Novavax found itself developing both 鈥渁 vaccine and a company鈥 in 12 months, said Dr. Gregory Glenn, president of research and development.

Novavax鈥檚 proprietary secret ingredient is Matrix-M, an immune booster. Executives say the additive 鈥 derived from Chilean soapbark trees 鈥 works so well that less of an antibody-producing antigen would be needed with it in a vaccine. One said Matrix-M 鈥渉as the potential to be of immense value.鈥

Equipped with its recombinant nanoparticle vaccine mixed with Matrix-M, Novavax deployed a core team of employees, dubbed 鈥淪uperNOVAs,鈥 to crisscross the globe. They assembled a manufacturing network and shared vaccine technology in India, South Korea, Spain, Japan and the Czech Republic as well as in the United States 鈥 about 20 contract manufacturing and test sites in all.

鈥淭his takes time and expertise,鈥 Trizzino said. 鈥淵ou just simply can鈥檛 hand over the recipe and then walk away from it and expect you鈥檙e going to have a high-quality product.鈥

Novavax is contracted to form the backbone of the COVAX initiative, having promised 1.1 billion doses starting this year for developing countries. And while President Joe Biden the U.S. would donate 500 million doses of the Pfizer-BioNTech vaccine abroad, Novavax is still seen as vital to urgent efforts to battle the virus and its variants.

Novavax鈥檚 moonshot goal of producing increasingly looks like a pipe dream for 2021. 鈥淚t is very hard to accept that they will make 2 billion doses as they had originally committed. I鈥檓 very skeptical,鈥 said Prashant Yadav, a health care supply chain expert and senior fellow at the Center for Global Development.

One of Novavax鈥檚 biggest challenges, Yadav said, is relying on 鈥渟o many sites鈥 that aren鈥檛 fully under its control, while other manufacturers own their plants. The more places Novavax produces the vaccine, the more challenging it is to make sure the vaccine and its elements are comparable in every place.

When Novavax executives announced another delay in May, the company鈥檚 stock plummeted to $121 a share 鈥 down 62% from a high of about $319 in February. As the company鈥檚 fortunes rose last year, Novavax executives cashed out tens of millions of dollars in common stock, . Last year, after the company benefited from grants and government contracts, CEO Erck sold $9.3 million in company shares, Glenn sold $14 million, and Trizzino sold $11.3 million.

Those top executives continued selling in 2021. Erck sold more than $22.5 million worth of common stock in early July.

Novavax executives use trading plans, and the sales often appear at the same time each month. In June, after Novavax announced its long-awaited U.S. and Mexico clinical trial results, Glenn sold more than 8,000 shares for $1.5 million. As a measure of the company鈥檚 spectacular rise in the pandemic, Glenn purchased 1,000 shares of stock in December 2016 for the price tag of just $1,446.

Novavax spokesperson Amy Speak said the company has programs in place to ensure best practices on stock sales. 鈥淢ost people, including our executives, sell stock for a wide variety of reasons,鈥 she said, adding that Novavax鈥檚 executives have 鈥済enerally sold a fraction of their overall holdings in the company.鈥

Charles Duncan, a biotechnology research analyst at Cantor Fitzgerald, called Novavax a 鈥渟how me鈥 investment in May. 鈥淚t鈥檚 one thing to have a place to make it,鈥 he said. 鈥淚t鈥檚 another thing to be able to make it there and get it certified.鈥

(Left to right) Dr. Gregory Glenn, Novavax鈥檚 president of research and development, and Dr. Robert Redfield, former director of the Centers for Disease Control and Prevention, stand with Maryland Gov. Larry Hogan and Novavax CEO Stanley Erck in front of the company鈥檚 soon-to-be global headquarters in Gaithersburg, Maryland. (Sarah Jane Tribble/KHN)

鈥楬adn鈥檛 Heard of Covid-19鈥

John Kutney, Novavax鈥檚 senior director of manufacturing, joined a in December, in an effort to recruit urgently needed talent. Kutney described the technology transfer as taking a recipe and teaching it to others. With that mission, he has traveled to the Czech Republic, Spain and the United Kingdom as well as Texas, North Carolina and New England.

When Novavax began work on its vaccine in January 2020, 鈥渕ost of us hadn鈥檛 heard of covid-19 and we were only beginning to become aware of what was happening in China,鈥 Kutney said. Novavax adapted its established vaccine platform to the new virus and then had to scale and transfer it to larger manufacturing sites, build a global supply chain and develop a regulatory strategy for emergency use.

鈥淭hese steps would normally take years,鈥 he said.

The key step of transferring Novavax鈥檚 vaccine technology can take three to six months, depending on the quality of the partner鈥檚 team. Once equipment and raw materials are secured, the teams start with small batches 鈥 first with a 50-liter bioreactor, then a 200-liter and eventually a 2,000-liter bioreactor, checking to make sure the partner operators know the process every step of the way.

鈥淲hat we鈥檙e trying to do here is not easy,鈥 said Fred Shemer, Novavax鈥檚 vice president of quality systems and compliance, in the video: 鈥淚t鈥檚 a challenging situation.鈥

In March 2020, Novavax received the first $4 million of nearly $400 million pledged by the Coalition for Epidemic Preparedness Innovations. CEPI is a global alliance backed by the Bill and Melinda Gates Foundation, which previously supported Novavax with for a vaccine for a common respiratory virus.

CEPI鈥檚 investment jump-started Novavax鈥檚 technology transfer to plants across Europe and Asia. It helped Novavax partner with in South Korea and paid for ramping up production at Praha Vaccines, which Novavax eventually bought, in the Czech Republic. It also supported scaling up production of Matrix-M at facilities in Sweden and Denmark.

Operation Warp Speed awarded $1.6 billion in July 2020 to Novavax so it would produce 100 million doses 鈥 one of the largest awards from the Trump administration鈥檚 vaccine incubator. It was 鈥渒ind of a stunning number for us,鈥 Trizzino said. In December, officials bumped the total to $1.74 billion with no changes to the previous contract. Novavax also has a $60 million contract with the Department of Defense for 10 million doses.

Paul Mango, a former senior official at the Department of Health and Human Services, said it wasn鈥檛 a 鈥渂ig concern鈥 for the Trump administration that Novavax had no successful vaccine. After all, that was also true for Moderna, which went on to launch its wildly successful mRNA vaccine.

Operation Warp Speed鈥檚 personnel resources and financial support would help carry the day. 鈥淲e thought we could do it,鈥 Mango said.

At the time, Trump officials invested in several vaccine platforms to hedge bets because it wasn鈥檛 known what would work, if any. 鈥淲e didn鈥檛 want to put all our eggs in mRNA,鈥 he said. 鈥淲e didn鈥檛 want to put all our eggs in viral vector,鈥 the platform used by Johnson & Johnson and AstraZeneca. Novavax鈥檚 technology uses a more established process with a baculovirus grown inside insect cells in a bioreactor.

鈥淚t was very important to have that array of technologies,鈥 Mango said. 鈥淲e had to pick the ones that had the best early results and the ones we thought could go through clinical trials before the spring of 2021.鈥

Novavax scientists have spent years collaborating with officials at federal agencies such as the National Institutes of Health, National Institute of Standards and Technology, and Walter Reed National Military Center 鈥 sometimes hiring from their ranks. In 2011, Novavax signed a to develop a seasonal and pandemic influenza vaccine with BARDA, the Biomedical Advanced Research and Development Authority.

As concerns about covid-19 rose, Novavax and BARDA began another negotiation, but Operation Warp Speed officials 鈥渟tepped over the top,鈥 Trizzino said. They asked Novavax what it would take to ramp up large-scale manufacturing, run a 30,000-subject clinical trial and the follow-on trials, and produce millions of doses.

鈥淭hey said, 鈥楧o all these things in parallel paths. You don鈥檛 worry about the funding risk. You do the work and we鈥檒l pay for those activities,鈥欌 Trizzino recalled.

Troubles in Texas

It was a tall order. Novavax had worked with Emergent BioSolutions and signed a for manufacturing in early 2020, but BARDA pushed Novavax to partner instead with Fujifilm Diosynth Biotechnologies and its plants in North Carolina, Texas and the U.K.

In retrospect, Trizzino said, Novavax 鈥渄odged a bullet.鈥 Production problems at Emergent鈥檚 Baltimore plant led to contamination or suspected contamination of millions of Johnson & Johnson and AstraZeneca doses, and in June federal regulators 60 million J&J doses unusable, The New York Times first .

Fujifilm鈥檚 Texas site, like Emergent鈥檚 plant in Baltimore, was set up in the aftermath of the to better prepare federal officials for the next one. It received $265 million last July to quickly boost manufacturing capacity, according to a federal contract.

The site began production in January but had to slow the cadence of its manufacturing lines for 鈥渢roubleshooting鈥 during Novavax鈥檚 technology transfer process, Fujifilm spokesperson Christine Jackman said. The plant is producing the Novavax vaccine and another undisclosed covid vaccine.

Trizzino said Fujifilm鈥檚 site in North Carolina was up and running quickly, but Texas didn鈥檛 have as much experience so 鈥渋t鈥檚 taken us a bit longer to ramp that up.鈥 A March inspection by the Food and Drug Administration found overcrowded and unorganized storage areas, a failure to consistently follow cleaning procedures and questions about why there was a backlog of batches, according to documents obtained by KHN in response to a public records request. The backup formed because bulk drug substance was being made faster than the facility could review produced batches, Fujifilm鈥檚 Jackman said.

FDA inspectors called Fujifilm鈥檚 operations 鈥渟ub optimal quality,鈥 according to an April response memo written by Gerry Farrell, Fujifilm鈥檚 chief operating officer for the facility. He said the criticism resonated and promised a thorough review with fixes completed in April and May.

Novavax and Fujifilm work closely to ensure all batches are reviewed and inspected by both companies鈥 quality control teams, said Speak, the Novavax spokesperson. The number of doses produced in Texas to date have not met projections. However, responding to federal inspections in Texas has not delayed Novavax鈥檚 vaccine development because Fujifilm鈥檚 North Carolina plant is the primary supplier of vaccine doses for the initial federal approval, Speak said.

Novavax鈥檚 manufacturing process is complicated because the vaccine is made in steps in different places. One plant makes the protein antigen, and another makes the adjuvant. Then the two components go to a final fill-and-finish facility where they are combined into 10-dose vials.

Its Matrix-M relies on quillaja extract from soapbark trees. The extract is also an additive in root beer and Slurpees. Novavax warned investors in its December 2020 financial filings that an inability to secure enough of the extract could delay production and prevent it from meeting 鈥渙bligations under our various collaborations and supply agreements.鈥 Still, Trizzino said that supply is 鈥渘ot an obstacle to total number of doses.鈥

Supply shortages have plagued the industry. For Novavax, those supplies included 2,000-liter bioreactor bags, used to culture cells; depth filters for the purification process; and the growth media, which is used to feed the cells.

Not having raw materials forced Novavax to trim the number of test batches that manufacturing lines could run. It has also taken longer to create quality control tests, known as assays, to ensure that vaccines are consistent and establish a standard quality for all subsequent batches. Those delays slowed the company鈥檚 ability to properly train operators, Trizzino said.

Novavax is working to reach 鈥渁 level of comfort that we鈥檙e able to produce these batches and then go to full capacity,鈥 Trizzino said. Novavax is working to complete the final phases of validating those tests.

Novavax鈥檚 global headquarters in Gaithersburg, Maryland, is now a 鈥渂lank canvas鈥 but is expected to house research and development, manufacturing and business operations. (Sarah Jane Tribble/KHN)

Too Late?

At the headquarters event, Glenn acknowledged that Novavax is late to the game. But the global demand is still enormous, he stressed.

鈥淲e know that 2 billion people worldwide have received at least one shot,鈥 he said, 鈥渂ut there are 6 billion people that need to be inoculated.鈥

The company is working to prove its vaccine will be useful even after the pandemic is contained. With its Matrix-M adjuvant, Novavax is testing a combined flu and covid vaccine, which is showing strong results in ferrets and hamsters. Novavax is also focused on booster shots.

Novavax joined trials this spring in the U.K. to test whether its vaccine works when paired with Moderna, Pfizer or AstraZeneca鈥檚 vaccines. Glenn said the results, so far, have been promising that 鈥渨e鈥檙e going to be able to use our vaccine after other licensed vaccines.鈥

First, though, 鈥渢he world has to collectively, as one, really stymie this global pandemic,鈥 said Dr. Dawd Siraj, a University of Wisconsin professor specializing in infectious diseases.

Siraj said Novavax鈥檚 delays shouldn鈥檛 cast doubt on the quality of the vaccine itself, given the positive trial results it has reported globally.

The shot is a 鈥渧ery good vaccine,鈥 he said, that could help turn the tide in developing countries unable to support their own vaccine development.

鈥淟et us never miss the most important point here,鈥 Siraj added. 鈥淎nyone who is getting a vaccine that is approved, the chances of dying, the chances of requiring ICU care, the chances of requiring a ventilator and high-flow oxygen, they almost disappear.鈥

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