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Monday, May 2, 2022

Poland has no 'rationale to invoke force majeure in Pfizer vaccine deal -EU official

 Poland has no "coherent rationale" to invoke force majeure in an existing contract in order to stop paying for more COVID-19 vaccines from Pfizer , a European Commission official told Reuters.

In April Poland's health minister Adam Niedzielski said Warsaw had informed the European Commission and Pfizer that it would no longer take or pay for COVID-19 vaccines under a supply contract co-negotiated by the EU, acknowledging this would trigger a legal conflict.

Poland invoked the force majeaure clause in the contract with Pfizer in the wake of the war in Ukraine which saw an influx of about 3 million Ukrainian refugees into the country.

"There is no coherent rationale to claim force majeure," the European Commission official said, declining to be named because of the sensitivity of the matter.

"The war in Ukraine did nothing to change Poland's vaccination needs, if anything it now needs to vaccinate refugees."

The European Commission declined to comment.

In April a spokesman for the EU executive told journalists that member states were bound by contractual obligations, but Brussels was trying to facilitate a "pragmatic solution".

Pfizer declined to comment on whether it intended to start legal action, but a spokesman said: "Being cognisant of local needs, we are seeking to provide pragmatic solutions to requests whenever possible".

LAW FIRMS INVOLVED

"In the case of Pfizer, we are working with two law firms from Belgium," Wojciech Andrusiewicz, Polish health ministry spokesman, told Reuters on Monday, but said a legal dispute had not formally begun.

"Unfortunately, we cannot see solidarity on the part of the European Commission yet. On the other hand, four other EU countries are interested in negotiations on making contracts more flexible, and they too will start talks soon," Andrusiewicz added, without elaborating.

He said that similar talks with Moderna, which also supplies EU countries with COVID-19 vaccines, were "very good".

Moderna has so far not commented on the matter.

The EU has signed three contracts with Pfizer for the supply of the COVID-19 vaccine it developed with German biotech firm BioNTech. It has also two contracts with Moderna.

Pfizer, by far the main supplier to the EU, agreed last May with EU states the largest supply deal ever signed during the pandemic, guaranteeing up to 1.8 billion vaccines for up to 35 billion euros ($36.8 billion).

EU countries agreed to buy a share of vaccines that was roughly proportionate to their population.

The deal came after the EU had already secured a big volume of vaccines for its population. However, it reckoned more shots were needed after it experienced supply disruptions at the start of the vaccination campaign.

Poland has said the supply under that contract would cost the country over 6 billion zlotys ($1.4 billion) until 2023.

About 60% of the Polish population of 38 million has been inoculated with two doses of COVID-19 vaccines and about one-third has also received a booster shot. This is below the EU average of over 70% fully vaccinated, with half of the population who also got a booster.

https://www.marketscreener.com/quote/stock/MODERNA-INC-47437573/news/Poland-has-no-rationale-to-invoke-force-majeure-in-Pfizer-vaccine-deal-EU-official-40243563/

Coherus, Junshi Biosciences Receive Complete Response Letter from U.S. FDA

 Shanghai Junshi Biosciences Co., Ltd. (“Junshi Biosciences”, “Junshi”, HKEX: 1877; SSE: 688180) and Coherus BioSciences, Inc. (“Coherus”, Nasdaq: CHRS) announced today that the U.S. Food and Drug Administration (“FDA”, “the Agency”) has issued a complete response letter (“CRL”) for the Biologics License Application (“BLA”) for toripalimab in combination with gemcitabine and cisplatin in the first-line treatment of patients with advanced recurrent or metastatic nasopharyngeal carcinoma (“NPC”) and for toripalimab monotherapy in the second-line or later treatment of recurrent or metastatic NPC after platinum-containing chemotherapy.

The CRL requests a quality process change that Coherus and Junshi Biosciences believe is readily addressable. Coherus and Junshi Biosciences plan to meet with the FDA directly and expect to resubmit the BLA by mid-summer 2022. The Agency also communicated in the CRL that the review timeline for the BLA resubmission would be six months, as required onsite inspections have been hindered by travel restrictions related to the COVID-19 pandemic in China.

https://finance.yahoo.com/news/coherus-junshi-biosciences-receive-complete-110000485.html

Neuromuscular disease biotech PepGen prices $115 million IPO

 PepGen, a Phase 1 biotech developing oligonucleotide therapies for neuromuscular diseases, filed on Friday with the SEC to raise up to $115 million in an initial public offering.


PepGen is generating a pipeline of oligonucleotide therapeutic candidates for the treatment of severe neuromuscular and neurologic diseases using its Enhanced Delivery Oligonucleotide (EDO) platform, which was initially developed through a collaboration between researchers at the University of Oxford and the Medical Research Council of United Kingdom Research and Innovation. Its lead candidate, PGN-EDO51, is being developed for Duchenne muscular dystrophy (DMD) and recently entered a Phase 1 trial in healthy normal volunteers, with topline data anticipated by the end of 2022.

The Cambridge, MA-based company was founded in 2018 and plans to list on the Nasdaq under the symbol PEPG. PepGen filed confidentially on October 1, 2021. BofA Securities, SVB Leerink, Stifel, and Wedbush Securities are the joint bookrunners on the deal. No pricing terms were disclosed.

Sage, Biogen Start Rolling Submission of New Drug Application for Depression Med

 Sage Therapeutics, Inc. (Nasdaq: SAGE) and Biogen Inc. (Nasdaq: BIIB) initiated a rolling submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for zuranolone in the treatment of major depressive disorder (MDD). Zuranolone is an investigational two-week, once-daily oral drug being developed for MDD and postpartum depression (PPD). The companies have submitted the nonclinical module of the NDA to the FDA and plan to submit the remaining components for the MDD filing in the second half of 2022.

Data from the completed studies of zuranolone in the LANDSCAPE and NEST clinical development programs, including data from the ongoing open-label SHORELINE Study in MDD, as well as data from the completed clinical pharmacology studies, will comprise the full submission package. The rolling submission process allows completed sections of an NDA to be submitted to the FDA for review on an ongoing basis.

https://finance.yahoo.com/news/sage-therapeutics-biogen-initiate-rolling-103000084.html

U.S. likely to find out about next COVID booster by summer -Fauci

 Scientists and health officials by this summer should have a better sense of what type of COVID-19 booster will be needed to deal with the next phase of the pandemic and when it should be administered, top U.S. infectious disease expert Dr. Anthony Fauci said on Friday.

The National Institutes of Health, where Fauci serves as director of the National Institute of Allergy and Infectious Diseases, is conducting clinical studies to determine if the next COVID booster should be specific to a particular variant of the coronavirus or designed to address more than one variant, known as a bivalent vaccine, ahead of the fall season, he said.

"We likely will know over the summer when we'll be able to, and what we'll be able to, boost people with," Fauci said at a virtual event hosted by the National Press Club in Washington.

Fauci also said health experts are looking carefully into anecdotal reports that some people after taking a five-day course Pfizer Inc's oral antiviral treatment Paxlovid have tested positive for the coronavirus or experienced mild symptoms.

The government has been encouraging people at risk of severe disease who experience COVID symptoms to get a Paxlovid prescription as soon as possible.

While health officials look into whether a viral rebound after Paxlovid is a real phenomenon, Fauci said: "The drug is still clearly very effective in preventing you from progressing to requiring hospitalization, the 90% efficacy seems to be holding strong."

Fauci also said it will be very difficult for the U.S. population to reach classical herd immunity against this virus due to several factors. They include its ability to evolve and mutate into diverse variants, waning immunity from infections and vaccines, and an anti-vaccine movement that has kept millions of people from seeking protection.

It is unlikely the United States will ever eliminate COVID-19, he said, but the nation should strive to control the virus and get out of the acute pandemic phase.

"When I said we are no longer in that fulminant acute phase, that does not mean that the pandemic is over," he reiterated. "By no means is it over. We still are experiencing a global pandemic."

https://finance.yahoo.com/news/1-u-likely-next-covid-172435513.html

Africa CDC warns COVID-19 vaccine production could cease

 A lack of demand could jeopardise manufacturing of the Johnson & Johnson vaccine in South Africa. Paul Adepoju reports.

Global inequities in access to COVID-19 vaccines, diagnostics, and therapeutics have prompted a huge push to expand local manufacture of health technologies in Africa. In March, the Africa Centres for Disease Control and Prevention (CDC) warned that less than 1% of vaccines administered on the continent are manufactured locally, reducing countries’ ability to respond to pandemics and other health crises. A new plan aims to enable Africa to locally manufacture 60% of its vaccine needs by 2040. However, this plan could be undercut by a lack of demand.
An agreement to bolster manufacturing of Johnson & Johnson's single-dose vaccine was secured by South Africa-based Aspen Pharmacare in December, 2021. At a press briefing on April 14, the Africa CDC's Director John Nkengasong told journalists that countries are not ordering the vaccine. He added that if this situation continues “the risk is very, very high that the company [Aspen] may actually stop producing the J&J COVID vaccines”. Nkengasong noted that countries are reluctant to pay for Aspen's vaccine doses because hundreds of millions of free doses are now widely available—with some now struggling to quickly roll out the shots before they expire. As of April 25, 16% of the African population had been fully vaccinated. Of the 760 million total doses the continent has received, nearly 507 million have been administered. He described such reluctance as short-sighted.
Under the agreement, Aspen can fill vials with vaccine supplied by Johnson & Johnson, package the vaccine doses, and sell the finished form in Africa. Strive Masiyiwa, African Union special envoy on COVID-19 and head of the African Vaccine Acquisition Trust, which brokered the agreement with Johnson & Johnson, said the contract is for 400 million doses. “It gets us one step closer to securing Africa's future vaccine production and ensures that the gross vaccine inequality we witnessed in the early part of the pandemic is not repeated”, Masiyiwa said in November, 2021. However, no African countries have so far bought doses from Aspen.
Johnson & Johnson did not comment on a potential halt to production of COVID-19 vaccines, but said that it is aware of the challenges that vaccine manufacturers are experiencing as demand for COVID-19 vaccines evolves globally. Aspen Pharmacare declined to comment.
Nkengasong said that discussions have begun with Gavi, The Vaccine Alliance, and COVAX on the possibility of ordering COVID-19 vaccine doses from Aspen Pharmacare to ensure that the facility does not suspend its COVID-19 vaccine production line. Gavi, as a co-lead of COVAX, said it “proactively supports the expansion of regional manufacturing efforts as a fundamental cornerstone of future pandemic preparedness”.
Nigerian public health analyst Ifeanyi Nsofor told The Lancet that African countries’ reluctance to buy locally produced vaccine raises concerns regarding the fate of several other COVID-19 vaccine manufacturing initiatives in Africa. “African countries have to ramp up vaccination efforts to clear these backlogs to prevent expiry of vaccines before purchasing more doses. The African Union must encourage the participation of the private sector in Africa in efforts to manufacture vaccines on the continent, and should coordinate through the African Medical Supplies Platform”, Nsofor told The Lancet.
WHO and its partners established the first COVID-19 mRNA vaccine technology transfer hub in South Africa. Moderna plans to set up its first African mRNA vaccine manufacturing facility in Kenya. BioNTech is also setting up modular mRNA manufacturing facilities in Senegal, Rwanda, and South Africa. In Egypt, the production of the Sinovac COVID-19 vaccine is already underway, with the country's health ministry announcing plans to produce more than 1 billion doses annually. These plans are still going ahead.
Shu-Shu Tekle-Haimanot, senior advisor at The Global Fund to Fight AIDS, Tuberculosis and Malaria, noted that among the African countries that will be involved in vaccine manufacturing for COVID-19 and other diseases, there is the need to “understand economy of scale and to also create the markets for them”. She said the availability of and access to aid, including access to free vaccines, might have made many African countries complacent.
For Africa's vaccine manufacturing to thrive, Nkengasong said, countries should spend more on health and not rely heavily on aid. He expects that the African epidemic fund initiative, which was endorsed at an African Union Summit in February, 2022, will help the continent to speed up this process and increase access to essential tools such as locally produced vaccines for COVID-19 and other diseases.
“It will allow for pooling of resources to respond in a timely manner when we have these outbreaks. That may not be in the billions [of dollars], but it will be something that will kickstart an emergency response once we’re challenged with epidemics or outbreaks”, he told The Lancet.

Testing power of machine learning to unravel long Covid’s mysteries

 Long Covid, with its constellation of symptoms, is proving a challenging moving target for researchers trying to conduct large studies of the syndrome. As they take aim, they’re debating how to responsibly use growing piles of real-world data — drawing from the full experiences of long Covid patients, not just their participation in stewarded clinical trials.

“People have to really think carefully about what does this mean,” said Zack Strasser, an internist at Massachusetts General Hospital who has used existing patient records to study the characteristics of long Covid. “Is this true? Is this not some artifact that’s just happening because of the people that we’re looking at within the electronic health record? Because there are biases.”

One of the largest sources of real-world data on long Covid is a first-of-its-kind centralized federal database of electronic health records called the National Covid Cohort Collaborative, or N3C. Kickstarted as part of a $25 million National Institutes of Health award early in the pandemic, N3C now includes deidentified patient data from 72 sites around the country, representing 13 million patients and nearly 5 million Covid cases.

“If we are able to identify these sort of constellations of symptoms that make up these potential long Covid subtypes then, first of all, we might find out that long Covid is not one disease, but it’s five diseases or 10 diseases,” said Emily Pfaff, who co-leads the long Covid working group at N3C. The real-world data effort has garnered additional funding as part of RECOVER, the four-year NIH initiative to study long Covid, to more precisely characterize the syndrome.

That work has started to trace a clearer image of long Covid, most recently describing co-occurring clusters of cardiopulmonary, neurological, and metabolic diagnoses. But a firmer definition of the syndrome could also potentially support recruitment efforts for critical long Covid trials, some of which have been slow to make progress.

“There’s a concern that trials relating to long Covid are going to not be that successful,” said Melissa Haendel, a health informatics researcher at the University of Colorado Anschutz Medical Campus and co-lead of N3C, because its definition is still so diffuse.

Supporting more targeted recruitment is what Pfaff calls the project’s “sweet spot.” She and her colleagues hope that machine learning models could help identify potential participants who would otherwise be missed or underrepresented in prospective research. And by using algorithmic approaches to narrow down a cohort of people who are more likely to have long Covid, said Pfaff, “a research coordinator who’s making calls to potential participants is making calls from a list of 200 patients, rather than 2 million patients.”

That effort is still a work in progress. The team’s first stab at building an algorithm that could identify long Covid patients, released in a preprint now accepted at the Lancet Digital Health, had its limitations. At that point, “there was literally no structured way for a physician to enter ‘I think this patient has long Covid’ in their EHR,” said Pfaff. “We had to get creative and find a proxy.” They settled on records from about 500 patients who showed up at three long Covid specialty clinics.

The model performed decently when tested on records from a fourth clinic, differentiating between long Covid clinic patients and non-patients with a 0.82 area under the curve, a measure of accuracy used by machine learning researchers. But it was still based on a small number of patients that could be demographically skewed. And Pfaff pointed out the data might overrepresent long Covid patients with respiratory symptoms, because two of the clinics used for model training were based in pulmonary departments.

Since that round of work, medicine has found better awareness, if not necessarily a better understanding, of long Covid. In October, providers were finally able to track long Covid patients with a dedicated diagnostic code that “will be very important for recruitment,” said Lorna Thorpe, a co-investigator for RECOVER’s Clinical Science Core at NYU Langone Health. It can both provide a straightforward way to identify long Covid patients — there are 16,000 with the code in N3C so far — and help to develop a clearer definition of the syndrome.

“Eventually, the idea is to characterize the subtypes of long Covid that health care providers should expect to see in their clinics,” said Charisse Madlock-Brown, a health informatician at the University of Tennessee Health Science Center and co-lead for N3C’s social determinants of health team.

But the code could also be used to refine the next generation of N3C’s models, by teaching algorithms what to look for in electronic health records that could suggest a patient has long Covid — even if the code isn’t used.

“So much of getting a diagnosis of long Covid appears to have a lot to do with your access to care, as well as finding a doctor who even knows what long Covid is and is able to treat you,” said Pfaff. An algorithmic approach to recruitment could potentially help include patients who don’t have that access.

So now, the team is training models that learn from both clinic patients and those whose doctors have checked off the new diagnostic code, in the hopes of defining a “best of breed” classifier. When the group applied the latest version to N3C’s records, it turned up 158,000 potential long Covid patients, Pfaff said.

That’s not to say the model can or should be turned to patient recruitment immediately. Researchers both within N3C and the larger RECOVER initiative emphasize that algorithmic approaches are no silver bullet, and they’ll always need to be used in combination with human vetting to build study cohorts.

That’s because any skews in the data used to train a long Covid model could result in inaccurate predictions. And while N3C’s records have been cleaned up so they’re ready for analysis, “there are caveats to these data,” said Leonie Misquitta, whose clinical innovation team at the NIH’s National Center for Advancing Translational Sciences stewards the data platform. There are almost twice as many female patients with long Covid codes in the system than male patients — which could be a result of patient behaviors, coding practices, biological realities, or all the above. In a more egregious example, a clustering algorithm initially identified sexual activity as a comorbidity of long Covid because of the way one site documented its patients.

“I think this is an important approach. I’m super supportive of it, and we’re communicating that to NIH,” said Thorpe. “But it won’t be the perfect solution. Let’s be realistic. Recruitment’s going to increase, it’s going to get incrementally better, with all the different strategies that are applied.”

The N3C team will continue refining their models as more real-world data emerges. In particular, they’re interested in building a machine learning classifier that could identify long Covid patients with subtypes of the disease, like those suffering from new onset diabetes or certain types of kidney disease. “It may be easier to find people with the more common phenotypes,” said Jasmin Divers, another leader for RECOVER’s real-world data efforts at NYU Langone. “But if you wanted to fill a specific subset that you’re not seeing as often, then having that enriched pool to pull and recruit from could be beneficial.”

And critically, they’ll aim to test their predictions on new datasets as they roll in, seeing whether the results hold up across different health systems. “In medicine, the stakes are always high,” said Strasser. “I always err on the side of making sure things work correctly before and that things are really validated before we go ahead with using a technology like this.”

But while they acknowledge the limitations of real-world datasets and the algorithms trained on them, N3C researchers argue that using such models to identify trial cohorts is relatively low risk. “If somebody from a university were to be running a long Covid trial and asked me if I felt comfortable applying this model to help them make a potential recruitment list,” said Pfaff, “I would unequivocally say yes.” They could present certain recruitment sites with lists to follow up with, using a third party intermediary to protect personally identifiable information, or give them the code to run on their records internally to identify potential participants.

N3C leaders said the platform has been primed to support recruitment. Integrating the group’s EHR resources with clinical cohort identification was part of N3C’s initial proposals for RECOVER funding, but so far the NIH hasn’t funded that use of the tool. “The sort of framing initially of the work of the EHR cohorts was more a rapid strike: Let’s understand [post-acute sequelae of SARS-CoV-2 infection], let’s characterize it. It wasn’t in their contract with the NIH to do that,” said Thorpe.

“We have to wait for NIH to say yes, these are the things that we want you to prioritize and here’s the budget for those things,” said Haendel. “The recruitment sites and the data engineering team and N3C are ready to do such things, but there have to be resources and coordination.”

https://www.statnews.com/2022/04/29/long-covid-machine-learning-n3c/