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Wednesday, February 2, 2022

Biotech Investors: Mark Your Calendar For These Key February PDUFA Dates

 After a fairly robust 2021, the new year started on a mixed note as far as regulatory decisions are concerned.

About three new molecular entities, or NMEs, were approved during the month, including Immunocore Holdings plc's 

 Kimmtrak for certain patients with advanced eye melanoma and Pfizer, Inc.'s  atopic dermatitis treatment Cibinqo.

NME approval is an important indicator to measure innovation in drug research. NME approvals totaled 50 in 2021, almost equaling the numbers of the previous year.

Regeneron Pharmaceuticals, Inc. 

-Sanofi , however, failed to get the nod for expanding the Libtayo label to include cervical cancer. Pfizer also faced rejection for its pediatric growth hormone deficiency treatment Somatrogon.

A PDUFA date is the date/period by which the Food and Drug Administration is required to announce its verdict on a sponsor company's regulatory application. This will determine the fate of millions of dollars invested in developing the treatment from the preclinical-stage to clinical testing. Therefore, it is a key binary catalyst for a stock.

Click here to access Benzinga's FDA Calendar.

Here are the key PDUFA dates scheduled for February:

Agios Seeks Approval For Drug To Treat Rare, Inherited Disease That Leads to Accelerated Destruction Of RBCs

  • Company: Agios Pharmaceuticals, Inc. 
  • Type of Application: new drug application
  • Candidate: Mitapivat
  • Indication: pyruvate kinase deficiency
  • Date: Feb. 17

Mitapivat is Agios' most advanced drug candidate, and it is a pyruvate kinase R activator that is currently being evaluated for the treatment of three distinct hemolytic anemias. Pyruvate kinase deficiency is a rare, inherited disease that presents as chronic hemolytic anemia, which is the accelerated destruction of red blood cells.

Agios' application for Mitapivat was accepted for priority review by the FDA on Aug. 7.

Reata Hopes For A Miracle After Adcom Recommends Against Approving Kidney Disease Drug

  • Company: Reata Pharmaceuticals, Inc. 
  • Type of Application: NDA
  • Candidate: bardoxolone methyl
  • Indication: Alport syndrome
  • Date: Feb. 25

Bardoxolone is an investigational, once-daily, orally administered drug that is being evaluated as a treatment option for Alport syndrome is a rare, genetic form of chronic kidney disease caused by mutations in the genes.

The FDA's Cardiovascular And Renal Drugs Advisory Committee, which met on Dec. 8 to discuss the NDA, voted "no" on the question of whether the provided evidence demonstrated that bardoxolone is effective in slowing the progression of CKD in patients with Alport syndrome and that its benefits outweigh its risks.

Can Amryt's Rare Skin Disorder Drug Clear FDA Hurdle After 3-Month Delay

  • Company: Amryt Pharma plc 
  • Type of Application: NDA
  • Candidate: Filsuvez (Oleogel-S10)
  • Indication: epidermolysis bullosa
  • Date: Feb. 28

Filsuvez is a potential treatment for the cutaneous manifestations of junctional and dystrophic epidermolysis bullosa, a rare genetic skin disorder affecting young children and adults for which there is currently no approved treatment.

The initial PDUFA date of Nov. 30 was extended by three months to give the FDA time to review additional information provided by the company upon the regulator's request.

'No' or ‘No-Go' For Legend Biotech's T-Cell Therapy For Blood Cancer?

  • Company: Johnson & Johnson (JNJ)/Legend Biotech Corporation 
  • Type of Application: biologic license application
  • Candidate: ciltacabtagene autoleucel (Cilta-cel)
  • Indication: multiple myeloma
  • Date: Feb. 28

Cilta-cel is a B-cell maturation antigen CAR-T therapy that is being investigated for the treatment of adults with relapsed and/or refractory multiple myeloma. Legend Biotech entered into an exclusive worldwide license and collaboration agreement with J&J's Janssen unit in 2017 to develop and commercialize cilta-cel.

Legend Biotech began the rolling submission of the application in December 2020 and the application was granted priority review in May 2021, with the PDUFA date of Nov. 29. In late October, the FDA communicated a 3-month delay in the review.

Will Gilead's Long-Acting HIV Drug Clear The FDA Hurdle?

  • Company: Gilead Sciences, Inc. 
  • Type of Application: NDA
  • Candidate: Lenacapavir
  • Indication: HIV-1 infection
  • Date: Feb. 28

Gilead is seeking approval for lenacapavir, an investigational, long-acting HIV-1 capsid inhibitor, for the treatment of HIV-1 infection in heavily treatment-experienced people with multi-drug resistant HIV-1 infection.

CTI BioPharma's Rare Blood Cancer Drug Awaits FDA Nod

  • Company: CTI BioPharma Corp. 
  • Type of Application: NDA
  • Candidate: Pacritinib
  • Indication: myelofibrosis patients with severe thrombocytopenia
  • Date: Feb. 28

The FDA accepted the regulatory application for priority review on June 1 and announced a PDUFA date of Nov. 30. The decision date was later extended by three months to Feb. 28.

Pacrotinib, if approved, is expected to address the unmet medical need of myelofibrosis patients with severe thrombocytopenia.


Adcom Calendar

FDA's Oncologic Drugs Advisory Committee is scheduled to meet on Feb. 10 to discuss BLA for sintilimab injection, submitted by Eli Lilly & Company's 

 partner Innovent Biologics.

The proposed indication for this product is in combination with pemetrexed and platinum-based chemotherapy for the first-line treatment of patients with Stage IIIB, IIIC, or Stage IV non-squamous non-small cell lung cancer with no epidermal growth factor receptor or anaplastic lymphoma kinase genomic tumor aberrations.

A joint meeting of the Anesthetic and Analgesic Drug Products Advisory Committee and the Drug Safety and Risk Management Advisory Committee is tentatively scheduled for Feb. 15, to discuss Avenue Therapeutics, Inc.'s 

 NDA for intravenous tramadol for the U.S. market.

The NDA for the pain drug was shot down twice by the FDA and subsequently, the company filed a formal dispute resolution request with the FDA's Office of New Drugs in August. The OND has sought additional advisory committee inputs to resolve the dispute.

https://www.benzinga.com/general/biotech/22/02/25314646/attention-biotech-investors-mark-your-calendar-for-these-key-february-pdufa-dates

BA.2 Blitzes Through Households, Even More Than Original Omicron

 Omicron subvariant BA.2 was associated with higher susceptibility of infection among households, regardless of vaccination status, than the original BA.1 variant, Danish researchers found.

Compared with the original variant, BA.2 was linked with more than two times higher odds of infection among unvaccinated individuals (OR 2.19, 95% CI 1.58-3.04), vaccinated individuals (OR 2.45, 95% CI 1.77-3.40), and boosted individuals (OR 2.99, 95% CI 2.11-4.24), reported Frederik Plesner Lyngse, MD, of University of Copenhagen, and colleagues.

Indeed, unvaccinated primary cases in BA.2 households were associated with more than two times higher odds of transmission (OR 2.62, 95% CI 1.96-3.52) compared to BA.1 households, the authors wrote in a preprint on medRxiv.

Not surprisingly, the authors found lower transmissibility in both BA.1 and BA.2 households when the primary case was vaccinated with or without a booster.

While there was significantly increased transmissibility associated with BA.2 households versus BA.1 when the primary case was unvaccinated, it was non-significant when the primary case was vaccinated and non-boosted or boosted, according to the authors.

BA.2 has recently garnered media attention due to its higher transmissibility. Lyngse's group noted that the two variants "differ by approximately 40 mutations."

Lyngse's group said the increasing number of BA.2 cases led them to explore two issues through their study: "Is there a difference in the household transmission patterns between ... BA.1 and BA.2; and ... if there is a difference, is it due to a difference in susceptibility, transmissibility, or both, and could this indicate a difference in immune evasiveness between the subvariants?"

They used Danish registry data that included households with two to six members, from Dec. 20, 2021 to Jan, 11, 2022, with a 7-day follow-up period until Jan. 18, 2022.

Primary cases were identified via RT-PCR, followed by whole-genome sequencing to determine if the variant was BA.1 or BA.2. Households were identified as BA.1 or BA.2 depending on the sequencing of the primary case.

Overall, there were 2,122 BA.2 households, with a total of 4,587 potential secondary cases and, of those, 1,792 tested positive for an estimated secondary attack rate of 39%. There were 6,419 BA.1 households, with a total of 13,358 potential secondary cases and, of those, 3,910 tested positive for an estimated secondary attack rate of 29%.

Notably, a 14-day follow-up found similar patterns, with a secondary attack rate of 42% for BA.2 versus 36% for BA.1.

"A potential mechanism for the higher transmissibility of unvaccinated individuals infected with BA.2 compared to BA.1 could be a higher viral load," the authors wrote, adding because no such difference was found in vaccinated non-boosted or boosted individuals, this "could be a result of a lower viral load in vaccinated individuals with a breakthrough infection."

Limitations to the data include that it was collected over Christmas and New Year's, when families held communal gatherings, so some co-primary cases were most likely misclassified as secondary cases, the authors noted.


Disclosures

Lyngse disclosed support from the Independent Research Fund Denmark, Novo Nordisk Foundation, the Danish National Research Foundation through its grant to the Center for Economic Behavior and Inequality (CEBI) at the University of Copenhagen.

A co-author disclosed support from the Novo Nordisk Foundation.

Decades-old database became hugely profitable dossier on health of 270M in US

 To most Americans, the name MarketScan means nothing. But most Americans mean everything to MarketScan.

As a repository of sensitive patient information, the company’s databases churn silently behind the scenes of their medical care, scooping up their most guarded secrets: the diseases they have, the drugs they’re taking, the places their bodies are broken that they haven’t told anyone but their doctor. The family of databases that make up MarketScan now include the records of a stunning 270 million Americans, or 82% of the population.

The vast reach of MarketScan, and its immense value, is unmistakable. Last month, a private equity firm announced that it would pay $1 billion to buy the databases from IBM. It was by far the most valuable asset left for IBM as the technology behemoth cast off its foundering Watson Health business.

The financial trajectory of MarketScan was perhaps unimaginable in 1981, when a former insurance executive named Ernie Ludy founded the company. His idea was to simply collect patients’ data and parcel it out to big companies that were seeking to control costs by getting a more granular view of their employees’ health care use. The biggest companies were looking for savings from the data, not new ways to make money.

“Because we had a 360-degree view of our patients, you could absolutely sell it and get a view that Amazon or Google might love,” Ludy told STAT in a rare interview. “The industry wasn’t developed like that initially. I thought we were in sacred territory when we had this kind of data. ”

Today, a multibillion-dollar marketplace has formed around anonymized health information bought and sold without patients’ knowledge or explicit consent. No longer just for big companies, patient data have become far more valuable as they are fed into an exploding array of software and artificial intelligence tools whose financial returns enrich technology entrepreneurs and their investors, not patients whose medical problems are their secret ingredients.

Surveying the industry, Ludy is disturbed by what he sees.

As one of the first to understand the power of aggregated health data, his optimism for disruptive change is now colliding with discomfort over the way consumers are losing control over their own information and the ability to benefit — and not be harmed — by its use.

Since he founded MarketScan, sources and uses of data have changed dramatically. Google, Facebook and Twitter were formed, creating impossibly deep wells of ancillary demographic and health information from internet searches, geolocation tracking, and unguarded social media posts. Medical data mining companies have made a business of scraping the details of consumers’ daily lives into medical dossiers that, if combined with MarketScan’s de-identified information, could be used to re-identify the individuals within its databases.

“I don’t believe there’s nearly enough governance around how people can use personal information, whether it’s health care (data) or not,” Ludy said in the interview. He added that consumers are not only owed better transparency and disclosure, but a portion of the wealth — through royalties or another vehicle — that is generated from their data.

“That would mean some of the exponential value that technology companies are gaining by using this derivative information gets shared,” Ludy said.  “Without data, there is no AI. Without data, there is no machine learning.”

MarketScan, which has been sold four times now, may not be the only national database of sensitive patient information, but it is especially large and influential. And as a forerunner, its evolution and growth through multiple owners traces the arc of how Americans’ health data became an open secret in an industry that now treats their information as its hottest commodity.

When Ludy launched his company, he set forth a mission to build “the most trusted name in health care information,” a goal he enforced through layers of encryption, security protocols, and audits. But 40 years later, the walls he carefully constructed around the information are buckling under the weight of a new economic model.

“To me, the whole idea of an autonomous economy and autonomous society is much larger than health care, but health care data falls into that realm,” Ludy said. “I just don’t believe that anywhere there are the appropriate controls.”

MarketScan was never an attempt to build a dossier on patients that could be directly sold for profit. As a former executive at Blue Cross Blue Shield in western Pennsylvania, Ludy had a singular goal: disrupt an insurance industry whose ever-rising fees and premiums were exacting a tremendous financial toll on individuals, employers and the broader economy.

He started by reaching out to the biggest corporations. If they would agree to give him data on their employees’ paid medical claims, he would return to them an analysis of their cost drivers, benefit designs, and manageable risks that would give them leverage in negotiations with insurers. Armed with better information, the corporations could begin to slow the rise of their health costs for themselves and their employees.

His company, initially named Medstat, became the first example in health care of a now pervasive model known as software as a service — and its launch in 1981 opened a portal into highly sensitive medical data that had never before existed.

Ludy vividly remembers the core-rattling excitement of landing his first client. After years of developing its analytics capabilities, in early 1984, he signed a contract with Chevron. The massive energy company was the first in the nation to become self-insured under the federal employee benefit law known as ERISA, and its director of benefits needed help managing his risks and losses.

“Chevron was the door opener,” he said. “It was approved by the benefits committee of the board. That was an incredible day. It was a huge contract.”

Each deal, he said, ranged between $250,000 and $2 million a year, and many more followed. Ford and Hewlett Packard signed contracts, so did Federal Express, UPS, and Walmart. By far the biggest was General Electric, which became the company’s 17th client and was bigger than the first 16 combined. “They were so large we had to shut down sales for six months,” Ludy said. “GE proved we could do it at scale.”

From there, Medstat inked deals with Medicare, several state Medicaid plans, hundreds of hospitals, and two dozen commercial insurers all clamoring for the company’s insights. By late 1994, 1,400 clients were supplying Ludy’s company with data on patients’ medical encounters and costs. The company could see one of every two hospitalizations in the United States and had compiled several years of data on tens of millions of patients.

Not a single one of those patients had directly consented to their data being shared with Medstat.

Instead, their employers, insurers, and the hospitals that cared for them offered that consent, based on forms signed when employees were hired, received care, or changed their benefits. If an organization’s intent for sharing the information did not align perfectly with the wishes of a customer or employee, there was no way to get it back, opt out, or sue for some perceived loss of value.

“There are very few protections for individuals for health data that are de-identified,” said Kayte Spector-Bagdady, a lawyer and bioethics professor at the University of Michigan. The de-identification of the data means it is no longer protected under HIPAA or other federal regulations surrounding the use of health information.

Those rules apply only to the health entities that initially collected the data, not the commercial companies that compile and re-deploy it in search of profit. That hands-off approach means technology companies that in recent years have amassed the largest stockpiles of highly sensitive health data, such as IBM, Google and data aggregators such as Verana Health, Datavant, and IQVIA, face the fewest restrictions on its use.

“It’s reached the point where it’s much easier for researchers at academic medical centers or who are federally funded to just go buy your data from the private entities of the world.”

KAYTE SPECTOR-BAGDADY, LAWYER AND BIOETHICIST

“The federal government has allowed commercial and industry entities to run amok without almost any regulation whatsoever,” Spector-Bagdady said. “It’s reached the point where it’s much easier for researchers at academic medical centers or who are federally funded to just go buy their data from the private entities of the world.”

The implications of the data trade, and its privacy risks, become even harder to understand as ownership of patient information changes over time. MarketScan has been sold several times during its history — first from Medstat to Thomson Corp., which later combined with the media company Reuters, and then to a New York-based private equity firm named Veritas Capital. In June 2012, Veritas re-branded the company as Truven Health Analytics, and its executives promised to make the databases even bigger and more broadly sourced.

By 2015, thanks to its steady expansion by different owners, MarketScan held detailed medical data on more than 200 million patients nationwide from more than 8,000 clients. Its impressive size and scope made it an ideal target for technology companies with grand designs to disrupt the nation’s $3.5 trillion health care industry.

Chief among them was IBM.

IBM’s acquisition of Truven for $2.6 billion in early 2016 opened a new chapter in MarketScan’s history. The deal was based almost entirely on the potential to combine its sprawling databases with the power of IBM’s Watson artificial intelligence engine to “change the face of health care.

“This is going to be a goldmine of insights,” John Kelly, a senior vice president of cognitive solutions and research at IBM, told Forbes after announcing the deal.

His description underscored what MarketScan had become — a commodity to be traded among companies looking to monetize its sensitive medical data. IBM wanted to merge its contents with datasets of medical images and patient records obtained through other acquisitions. Watson, IBM promised, would use that data to give pharmaceutical companies a new way to discover drugs and help hospitals cut unnecessary costs while targeting patients in need of more care.

IBM saw it as a $200 billion market opportunity. By then, it had already formed partnerships with an array of other businesses that bought into the idea, including CVS Health, Johnson & Johnson, and the device maker Medtronic.

The level of interest generated tremendous buzz and positive headlines for IBM. But where some saw a chance to harness the power of big data, others saw encroachment by IBM and other data aggregators on the confidentiality of conversations between doctors and patients. The company’s possession of such detailed information on patients, whether de-identified or not, meant that it was being used for something far different than the reason it was originally disclosed.

“As a patient you may have confided in me secrets you may not have even told your spouse or your best friends because you’ve held on to it for so long, but the moment I document it in the medical record, I can’t tell you who’s going to be able to see that anymore,”  said Harlan Krumholz,  a cardiologist and director of the Center for Outcomes Research and Evaluation at Yale University.

“Monetizing my own sensitive health data in ways that may not be consonant with my preferences should be out of bounds,” he added. “It’s a business model gone awry.”

IBM’s efforts to use the repository to transform broad swaths of the health care system ultimately fizzled. The company struggled to create the cloud storage and computing infrastructure needed to combine all the data so it could be analyzed by its AI and analytics machinery.

As its business foundered, IBM ceded its first-mover advantage to an expanding ecosystem of digital health companies with novel strategies to link data and derive insights that could accomplish the kind of disruption IBM envisioned. Between 2014 and 2021, when IBM put its Watson Health division up for sale, the firms operating in that sector collectively raised more than $80 billion to bankroll their ambitions, according to Rock Health, a venture capital firm that tracks investments in digital health businesses. About one-third of that money was raised in the last year alone, including investments by the private equity firm that will soon own MarketScan.

Francisco Partners had previously purchased stakes in the telemedicine and drug coupon company GoodRx, the virtual appointment booking company ZocDoc, and Edifecs, a company that builds software to enable a more seamless exchange of data. The firm declined to comment on the acquisition or its plans for the MarketScan database.

To some, no matter how the firm decides to use the data, the deal is a disquieting reminder of the lack of controls over highly sensitive health information. But to Ludy, who agrees with those concerns, it dredged up a more complicated set of emotions. He now works as an executive partner for Ardan Equity Capital, a Florida-based private equity firm that also invests in the digital health sector. He said he has empathy for employees and managers of the company who have gone through so many destabilizing transitions. On another level, though, the sale was a reminder of what he had accomplished.

“It’s a remarkable (testament) to the sustainable asset value of MarketScan over its 40-year life cycle,” he said. “When you create something that lasts 40 years it makes you feel good.”

Ludy said he now expects MarketScan to become part of a broader effort to develop software that can generate faster and more meaningful insights from health data — and make medical services more targeted, effective, and valuable.

“That’s the opportunity — driving these new business models for capturing the digital dividend of automating so many of the transactions,” he said. “We’re accustomed to seeing this in other industries. It just hasn’t happened in health care.”

https://www.statnews.com/2022/02/01/ibm-watson-health-marketscan-data/

Unusual authorization plan for Covid vaccine for kids under 5 questioned

 The Food and Drug Administration’s willingness to consider authorizing a Covid-19 vaccine developed by Pfizer and BioNTech for children under the age of 5 — without evidence yet that it would be protective — is raising concerns among some vaccine experts who fear the plan could backfire and undermine vaccine uptake in this group.

Pfizer and BioNTech confirmed Tuesday that they had been asked by the FDA to submit an application for the use of a two-dose vaccine in children 6 months to 4 years old. Data on a third shot would be submitted to regulators once they became available in the spring — ostensibly clearing the way for the agency to authorize a three-shot regimen for the youngest children who can get vaccinated. 

If the two-dose series is authorized by the FDA and the Centers for Disease Control and Prevention, potentially sometime this month, parents who want to vaccinate children under 5 could begin to do so before Pfizer has proven that the vaccine is protective for this entire age group — something that doesn’t normally happen.

“It’s certainly a creative approach to trying to address the urgency that FDA and the White House is hearing from parents … for making these vaccines available for this younger age group,” said Jason Schwartz, an assistant professor of health policy at the Yale School of Public Health.

“But … the stakes are high and they’re never higher than for vaccines in this youngest age group, both for their effects on this vaccine and the effects on childhood vaccination and vaccine confidence generally.”

Pfizer announced before Christmas that in a clinical trial of children aged 2 to 4 years old, two doses of vaccine failed to generate antibody levels on par with those seen in people aged 16 to 25 after two shots. Paradoxically, two doses given to infants aged 6 months to 23 months did generate antibody levels similar to those seen in the 16- to 25-year-olds, levels that are deemed to equate with protection.

In both groups of little kids, the vaccines appeared to be safe and the side effect profile was tolerable. Side effects included fever and chills, which are not uncommon reactions to vaccines in early childhood. 

The companies decided to test whether adding a third dose would raise antibody levels to required levels. But the data from the modified trial aren’t expected until late March and the FDA appears to be unwilling to wait until then. A source told STAT that the agency’s independent vaccine expert panel, the Vaccines and Related Biological Products Advisory Committee, will meet Feb. 15 to review the data Pfizer is submitting with this application.

The idea of authorizing use of the first two doses while the third-dose data are pending is being framed as a way to allow parents eager to vaccinate children 4 and under to get a head start on the process, with a third dose to follow after review of the results of that part of the study.

None of the experts STAT spoke to for this article could recall a precedent for this approach. And several worried going down this path could erode willingness on the part of parents of young children to get them vaccinated. To date only about 20% of children aged 5 to 11 have received two doses of vaccine, according to CDC data.

“I don’t think authorizing two doses in children ages 2 to 4 years of age where effectiveness in this age group hasn’t been confirmed is going to convince the majority of parents to vaccinate their children,” said Norman Baylor, president and CEO of Biologics Consulting and a former head of the FDA’s Office of Vaccines. “If the vaccine in this age cohort is a three-dose vaccine, FDA should review the data from the three-dose series before authorizing the vaccine.”

In a poll released Monday by the Kaiser Family Foundation, 31% of parents of young children said they intend to have them vaccinated as soon as they are able. But 26% said they would not vaccinate children under the age of 5. A further 12% said they would only vaccinate their children if they were required to and 29% said they would take a “wait and see” approach.

Baylor said those results suggest following normal procedures would make more sense here. “The question is, where’s the fire?” he asked. “I think we can take a little time. If that third dose data is available in March, that’s not that long now.”

Schwartz has a vaccinated 8-year-old and a 2-year-old who was home from day care on Tuesday because a teacher tested positive for Covid. He suggested expediting the process for children 4 and younger will be welcomed by some parents, but won’t lead to a flood of vaccinated kids.

“To the extent that this is moving the clock ahead just by a few months, I think we should recognize that it will be a pretty limited number of families who will jump at this opportunity in the way that I have and in the way I probably would, depending on what the data look like,” he said.

Saad Omer, director of Yale University’s Institute for Global Health, said he understands concerns about what pursuing this plan could do to vaccine hesitancy among parents who aren’t convinced of the need to vaccinate children against Covid or the safety of the vaccines. But at this point, his expectations for vaccine uptake rates in children are not high.

“Childhood immunization coverage [for Covid] isn’t stellar anyway,” Omer said. “I don’t think this will particularly dent it.” 

Likewise, he wasn’t too concerned that this approach will provide ammunition to the burgeoning anti-vaccination movement. “The bottom line is contrarians will do what they do. That’s their schtick,” Omer said. “And anti-vaccine people will do what they always do.”

Malia Jones, an epidemiologist who teaches at the University of Wisconsin-Madison and who specializes in vaccine hesitancy, said it has been clear for a while that getting children vaccinated against Covid is going to be an uphill battle. She worries that the low level of confidence in Covid vaccines for children will erode parental support for other vaccines. “This is the thing that keeps me up at night,” she said.

“I think already it’s kind of a disaster for vaccine uptake in kids,” Jones said of the prospects for persuading parents to vaccinate their children against Covid and whether the FDA’s approach here will influence them. “Is it throwing gasoline on a dumpster fire? Maybe. But it was already a dumpster fire.”

https://www.statnews.com/2022/02/02/worry-vaccinating-under-5-could-backfire/

Biden once pledged to ‘cure cancer.’ His new approach is far more modest

 President Biden has been pledging to “cure” cancer for the past six years, beginning with his moonshot effort as vice president. He re-upped that pledge on the campaign trail, too, vowing again: “If I’m elected, we’re going to cure cancer.”

This time, though, Biden’s no longer promising a “cure.”

Instead, Biden will relaunch the White House Cancer Moonshot on Wednesday with an ambitious but noticeably more measured goal: Cutting the cancer death rate in half within 25 years. In substance and tone, the effort is modest when compared to 2016. Most notably, it doesn’t call for any new research funding — a key pillar of the Obama-era push.

Instead, the program will create a White House “Cancer Cabinet” geared toward expanding cancer screening and prevention, improving the experiences of cancer patients, survivors, and caregivers, and addressing racial disparities in cancer outcomes.

The effort represents Biden’s first attempt, as president, to tackle one of his signature issues. Since his son Beau Biden’s death in 2015 from glioblastoma, a form of brain tumor, cancer has been a deeply ingrained part of the president’s political identity.

But the Cancer Moonshot redux also illustrates the limitations of what the White House can do without a flood of new research money, and amid looming uncertainty about Biden’s ability to confirm new leaders for key federal research agencies. The president’s nominee to lead the Food and Drug Administration, the agency that oversees cancer clinical trials and the approval of new drugs, is stalled on Capitol Hill. The White House hasn’t announced a replacement for Francis Collins, the longtime director of the National Institutes of Health who stepped down in December.

Biden’s signature science proposal is languishing on Capitol Hill, too: The creation of ARPA-H, a new research agency that Biden has said could “end cancer as we know it.”

“There is great value in a president giving the populace hope that science can lead to cures,” said Jill O’Donnell-Tormey, the CEO of the Cancer Research Institute, a nonprofit focused on cancer immunotherapies. “But I would say without funding for a research component, you’re not going to get over the goalpost.”

While they welcomed the announcement, other cancer research advocates echoed calls for new research funding, and acknowledged that without progress on other fronts, the moonshot’s impact may be limited.

“We hope that today’s event at the White House will serve as a catalyst for the administration to appoint permanent leadership at the NIH, [National Cancer Institute], and FDA,” as well as provide funding boosts to those agencies, said Jon Retzlaff, the chief policy officer for the American Association for Cancer Research.

The new effort does contain a number of measures that the White House can pursue without help from Congress and without new funding, including a major personnel move: The appointment of Danielle Carnival as White House cancer coordinator.

Carnival, a neuroscientist who served as the original moonshot’s policy director, also worked as vice president of the Biden Cancer Initiative, the nonprofit Biden founded after leaving the White House in 2017, and later as CEO of the advocacy group I Am ALS, the driving force behind a $500 million research bill Congress passed late last year.

The new moonshot will also include a renewed call for Americans to receive cancer screenings. The White House estimated that approximately 9.5 million were missed thanks to the Covid-19 pandemic. It also will include efforts to expand HPV vaccinations, which help prevent cervical cancer, and the potential creation of diagnostics that can detect multiple cancers simultaneously, perhaps via an annual blood draw.

Perhaps most critically, it could once again galvanize the entire cancer research community, much like the 2016 effort and the more recent federal efforts surrounding Covid-19, said Elizabeth Jaffee, a physician and oncology professor at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins who advised the original Cancer Moonshot and sat on the Biden Cancer Initiative’s board.

When the pandemic began, she said, “we needed an organized group of researchers and an organized government coming together, and in nine months, we had a vaccine.”

“I don’t think in nine months, we’re going to have a cure for cancer,” she said. “I’m just trying to make the analogy: There’s a lot out there, but you have to mobilize it.”

https://www.statnews.com/2022/02/02/biden-once-pledged-to-cure-cancer-his-new-approach-is-far-more-modest/

Gilead antiviral Veklury blew past sales estimates in late 2021 as omicron surged, vaccinations lagged

 Just when it looked like Gilead’s COVID-19 medicine Veklury was destined to be crowded out of the market by antibody treatments and antiviral pills, the omicron variant helped spark a surge in sales.

In the fourth quarter of last year, with a late boost in demand in December, Veklury rang (PDF) up $1.4 billion in sales, far exceeding the Wall Street consensus estimate of $864 million.

Gilead reported the figure Tuesday when it presented its fourth quarter and 2021 earnings. The strong quarter brought Veklury sales up to $5.6 billion for the year and helped push Gilead’s revenue figure to $27.3 billion in 2021, an 11% increase from 2020 that the company attributed almost entirely to Veklury.

“In the December/January time frame we’ve really seen Veklury play a critical role,” Johanna Mercier, Gilead’s chief commercial officer, said during the company’s fourth quarter earnings conference call.

Mercier credited Veklury’s resurgence to the ineffectiveness of antibody drugs, such as those produced by Regeneron and Eli Lilly, against omicron. While omicron has generally produced a milder form of the virus, it still has landed more in the hospital, boosting demand for Gilead’s infused drug.

“We’ve seen that Veklury sales truly track to hospitalizations,” Mercier said. “We’ve seen that again with the omicron surge. Despite the fact that omicron seemed to have a less severe impact, unfortunately the number of cases were much greater—just the pure, absolute number of hospitalizations went up.”

Late last month, the FDA expanded Veklury's use to those with COVID-19 who are not in the hospital. The nod provides doctors with a much-needed additional tool with which to combat omicron.

One miscalculation made by the company, it said, was assuming that vaccination rates would increase, thereby decreasing hospitalizations. Instead, a stabilization of the vaccination rate between 60 and 65% in the U.S. has helped sustain Veklury’s demand.

Gilead believes that as the pandemic shifts into an endemic stage and as antiviral pills become more readily available that hospitalizations will decline, limiting the need for Veklury. Still, the company is projecting 2022 sales for the antiviral at $2 billion.

Gilead’s chief medical officer Merdad Parsey believes that oral antivirals will come to be used at an earlier stage of the virus while Veklury’s niche will be at a later stage.

“Many people may progress and/or not get treated early enough and end up in the hospital,” Parsey said. “I do think there will be a role for both of them.”

As for Gilead’s bread-and-butter HIV treatments, their total sales were up 7% for the fourth quarter over the same period in 2020. Biktarvy’s sales jumped in the quarter by 22%, year over year, while sales for Truvada and Atripia declined by 58% and 29% respectively, year over year in the quarter, owing to their loss of exclusivity in the U.S. in late 2020.

https://www.fiercepharma.com/pharma/gilead-credits-veklury-s-strong-sales-to-omicron-s-surge-antiviral-pulled-1-4-billion-q4