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Thursday, April 27, 2023

Medicare's Policy on Alzheimer's Drugs Comes Under Fire at House Hearing

 House members on both sides of the aisle were in surprising agreement on a number of healthcare issues Wednesday, most notably the need for Medicare to reconsider its coverage decision on amyloid-inhibiting Alzheimer's drugs such as aducanumab (Aduhelm) and lecanemab (Leqembi).

"There's been a lot of attention to a decision by CMS [the Centers for Medicare & Medicaid Services] to severely restrict access to an entire class of FDA-approved Alzheimer's drug treatments," said Rep. Brett Guthrie (R-Ky.), chair of the House Energy & Commerce Health Subcommittee, at a hearing on legislative solutions to increase healthcare transparency and competitionopens in a new tab or window. "One thing I can say both sides absolutely agreed on is that we need to work on the Alzheimer's drug and make sure that people have access as we move forward."

"There's a huge concern here," Rep. Anna Eshoo (D-Calif.), the committee's ranking member, told CMS administrator Chiquita Brooks-LaSure, the hearing's first witness. "This is a progressive disease. We know that early intervention with progressive diseases is really essential. So I hope that you will leave this hearing with a new commitment and a new view of how to do this."

Accelerated Approval

The FDA approved both aducanumab and lecanemab under an accelerated approval process. However, a congressional investigation foundopens in a new tab or window that the agency broke with its own protocols in reviewing and subsequently approving aducanumab by inappropriately collaborating with drugmaker Biogen on briefing documents, holding unreported meetings, and failing to gain internal consensus before engaging in such collaborations. The agency also approved the drug despite it receiving a nearly unanimous thumbs downopens in a new tab or window from an FDA advisory committee.

CMS decided that Medicare would cover aducanumabopens in a new tab or window only when patients taking it were enrolled in clinical trials to further explore efficacy; a similar decision was later made for lecanemab. However, the coverage decision for aducanumab noted that this was in part because the drug's approval was based on a surrogate endpoint for efficacy: amyloid reduction. Future anti-amyloid drugs that showed clinical efficacy could also be covered if patients were enrolled in a drug registry or other type of trial, the agency said.

In contrast to CMS's decision, the Department of Veterans Affairs (VA) has approved coverage for lecanemab provided patients meet certain criteria, including being over 65 and having been diagnosed with early-stage Alzheimer's. Several committee members expressed concern about the conflicting decisions for the drug, which costs about $27,000 annually. "Let me describe to you two constituents: one is a grandfather and a veteran," said Eshoo. "He has coverage and has been diagnosed [with Alzheimer's]. His wife was also diagnosed; she's not a veteran [and isn't covered for the drug]. How do I -- or any of us -- explain that to our constituents?"

Brooks-LaSure said that part of the issue was the fact that both drugs were approved on an accelerated approval basis rather than full approval. "When FDA fully approves drugs, that means that the FDA has made a determination that it will affect the disease itself," she said. "And when FDA fully approves drugs for Alzheimer's disease, CMS will cover it more broadly."

Support for Physician-Owned Hospitals

Committee members also had other issues that concerned them. Rep. Michael Burgess, MD, (R-Texas) discussed a bill he is sponsoring to get rid of Medicare's prohibition on paying for services delivered at physician-owned hospitals. "It is just fundamentally wrong that because of an academic degree that I have, I am not able to engage in a lawful practice in this country," he said to Brooks-LaSure. "And yet, you brought up in your testimony that consolidation in healthcare allows hospitals to own doctors. This is nuts. Hospitals can own doctors, but doctors can't own hospitals. Why is that OK?"

He asked Brooks-LaSure if she'd be willing to work with him on the issue; she agreed to do so.

Pharmacy benefit management (PBM) companies also came in for scrutiny at the hearing. One bill under consideration calls for more transparency in the way PBMs determine how drugs get on their formularies. "This is a bipartisan issue; this is a nonpartisan issue," said Rep. Buddy Carter (R-Ga.), a pharmacist. "I never went to the counter and asked, 'Are you a Republican or a Democrat?' High drug prices impact everyone here in America, all Americans, that's why we have to do something about it." He noted that 45 independent retail pharmacies are going out of business every year, "largely because of policies of PBMs."

Kristin Bass, chief policy and external affairs officer at the Pharmaceutical Care Management Association, which represents PBMs, agreed that "the data people can use to lower costs can be transparent. Where we have a slight quibble is, for example, in federal bidding for contracts, you don't have bidders bid openly; you make them sealed bids so people will bid as low as possible to get the business ... That's what we have concerns about. Just with respect to competitors knowing what the best bid is, that would be the problem."

Site-Neutral Payment Spotlighted

The subcommittee is also considering a bill to institute "site-neutral payment," in which Medicare would pay the same amount for particular procedures regardless of whether they're performed in a physician's office or hospital outpatient department. "Hospitals are motivated to gobble up physician practices because they're able to bill Medicare roughly double the amount that private practices are," said Rep. Mariannette Miller-Meeks, MD, (R-Iowa). "For example, a level 2 nerve injection in 2023 done in a physician's office would result in a $226 payment for Medicare, but that same injection provided by a hospital outpatient department would result in a $741 payment."

Ashley Thompson, senior vice president of public policy analysis and development at the American Hospital Association, said there was "nothing neutral" about site-neutral payment policies and that there were reasons for giving hospital outpatient departments higher reimbursement. "Hospital outpatient departments treat patients who are often older, sicker, and with more complex conditions ... and they're required to maintain standby capacity, as well as deliver emergency care regardless of insurance status."

But Loren Adler, associate director of the USC-Brookings Schaeffer Initiative for Health Policy, said that hospitals buying up physician practices and then being able to charge more for the same service "unambiguously leads to high prices for consumers ... and lower quality of care."

"We need to stop digging the hole deeper," he said. "Medicare rates are intended to reflect the cost of providing services from efficient providers. As such, Medicare should not be paying more for services provided in hospital outpatient departments."

https://www.medpagetoday.com/practicemanagement/reimbursement/104216

New Contender in Diet Rankings Puts Kibosh on Some 'Heart Healthy' Diets

 The American Heart Association weighed in on how popular diets stack up against its healthy dietary pattern recommendations, giving a low ranking to several diets billed as good for the heart.

The organization issued a scientific statement scoring the top 10 dietary patterns on adherence to its 2021 dietary guidelinesopens in a new tab or window if the diets were followed as intended, rather than how people often actually eat when on the diets, noted Christopher Gardner, PhD, of Stanford University in California, who chaired the committee that wrote the statement published in Circulationopens in a new tab or window.

At the top of the list, with a perfect score on the 100-point scale, was the Dietary Approaches to Stop Hypertension (DASH) diet. Other diets in the top tier with scores above 85 were the Mediterranean, pescatarian, and vegetarian (including dairy, eggs, or both) diets.

Ranking at the bottom of the list were the paleolithic (paleo) and very low carbohydrate diets, such as the ketogenic (keto) and Atkins diets.

"There really isn't any way to follow [these] diets as intended and still be aligned with the American Heart Association's dietary guidance," Gardner said in a press release. "They are highly restrictive and difficult for most people to stick with long term. While there will likely be short-term benefits and substantial weight loss, it isn't sustainable. A diet that's effective at helping an individual maintain weight loss goals, from a practical perspective, needs to be sustainable."

The rankings match fairly closely with the U.S. News & World Reportopens in a new tab or window "Best Diets" rankings over the past several years, which have consistently put the Mediterranean and DASH diets in the top slots both overall and for heart health.

The Mediterranean diet ranked slightly below the DASH diet in the AHA statement because it doesn't explicitly address added salt and encourages moderate alcohol consumption, whereas guidelines suggest limiting alcohol intake and not starting to drink if one doesn't already.

A number of very low fat diets -- such as the Ornishopens in a new tab or windowEsselstynopens in a new tab or window, and Pritikinopens in a new tab or window diets -- are touted for their heart health, even claiming to reverse heart disease. However, these were ranked below average by the AHA, with a score of 72 out of 100. They were in the same tier as very low carbohydrate diets, such as the Zone, South Beach, and low-glycemic index diets.

"The additional avoidance of nuts and liquid plant oils in very low-fat patterns is out of alignment with AHA's emphasis on including healthy fats," Gardner's group wrote. "Similarly, low-carbohydrate patterns are problematic for limiting healthy grains, legumes, and some whole fruits, which are all AHA priority features."

Vegan and low-fat diets, both comprised of more than 10% fat, were ranked in the middle, with scores of 78 out of 100. While there's potential for both diets to support optimal cardiovascular health, they also present challenges in that regard, the AHA statement noted.

"A key challenge for the vegan pattern is its restrictive nature, making it infeasible and an impediment for long-term adherence for most patients," it said. "In addition, restricted intake of foods emphasized in the 2021 AHA dietary guidance, which was intended to help adults meet their nutrient needs through foods, places adults following vegan patterns at risk for macronutrient and micronutrient deficiencies, particularly vitamin B12 deficiency."

In addition, people often cut fat in their diet by increasing intake of less healthy carbohydrates, which tend to raise triglycerides and lower high-density lipoprotein cholesterol.

"For both patterns, the proliferation of highly processed foods that are low fat or vegan but sources of refined grains, added sugars, and sodium can often lead to implementation of the pattern not as intended but rather through higher consumption of unhealthy convenience foods," Gardner and colleagues noted.

They recommended that patients choosing a vegan or low-fat diet may require referral for more in-depth nutritional counseling.

Coming in at the bottom, with scores under 55 out of 100, were "patterns of strong concern": paleo, keto, and other very low carbohydrate diets. Even if followed optimally, these diets restrict food groups considered essential to a heart-healthy diet, such as legumes and whole grains, while allowing high saturated fat intake that is strongly discouraged by the AHA.

The statement acknowledged that each of the popular diets they ranked have healthier and less healthy ways to follow them and that nutrition misinformation is rampant, leading people to follow them in a way not as intended.

"Given the poor overall diet quality among U.S. adults, it is critical for healthcare professionals to query patients or consumers about how they implement a given pattern to identify potential misunderstanding and opportunities for modifications where room for improvement exists to better align with the AHA guidance features," the statement noted.

It suggested that providing patients resources like nutrition education may help them adopt healthy patterns as intended.

The rankings didn't consider any diets aimed specifically at managing gastrointestinal conditions or diseases, allergies, or intolerances, nor did it look at those designed to be followed short term (Whole 30) or with commercial programs (like Noom and Weight Watchers).

Disclosures

The guideline writing committee disclosed no financial relationships with industry.

Primary Source

Circulation

Source Reference: opens in a new tab or windowGardner CD, et al "Popular dietary patterns: alignment with American Heart Association 2021 dietary guidance: a scientific statement from the American Heart Association" Circulation 2023; DOI: 10.1161/CIR.0000000000001146.


https://www.medpagetoday.com/cardiology/prevention/104222

AbbVie closes cystic fibrosis chapter after combo ‘just did not work’

 AbbVie is discontinuing all work in cystic fibrosis after a phase 2 flop, while also scrapping another phase 2 program in immunology.

After analyzing data from a proof-of-concept study of the triple combination cystic fibrosis therapy, AbbVie decided that the interim results "did not meet our criteria" to continue development, Thomas Hudson, M.D., AbbVie’s SVP of R&D and chief scientific officer said on a quarter one earnings call today. 

The triplet program—a combination of one potentiator and two corrector molecules targeting the cystic fibrosis transmembrane regulator—“just did not work,” according to Hudson.

“This was not our first attempt at producing one and we do not have another backup, so we don't have another option other than to discontinue this program,” the CSO said about the cystic fibrosis program.

It’s déjà vu for the Big Pharma. Last spring, AbbVie discontinued cystic fibrosis medicine ABBV-119 after an interim analysis revealed that the therapy did nothing when added to a two-drug regimen of AbbVie’s C1 corrector and potentiator therapies. The discarded asset was a C2 corrector that had been licensed from Galapagos back in 2018. An interim analysis of a phase 2 trial didn’t meet AbbVie’s prespecified criteria to move the study forward, Hudson said at the time. 

The Chicago-based pharma ditched the Galapagos asset, but continued with its combo—that is, until now. The tossed program has put the pharma’s ongoing efforts to compete with Vertex’s Trikafta to rest.

AbbVie also announced that it is scrapping ABBV-154, an antibody drug conjugate that was being studied in polymyalgia rheumatica and Crohn's disease. The investigational immunology treatment, once thought of as a potential Humira successor, has been axed due to its risk profile. 

While the company reported efficacy results for the ADC, some changes in biomarkers consistent with systemic steroid exposure at higher doses were also observed, according to Hudson.

“The benefit risk does not sufficiently differentiate 154 from other available treatments,” Hudson said.

AbbVie continually clocks in with one of the lowest R&D budgets in Big Pharma. Long-time CEO Richard Gonzalez said the company continues to look to biotech for potential pipeline opportunities. Valuations for good assets are “pretty high,” though, he said. 

“I'd say the interest level in that engagement is similar to what has been for the last 12 to 24 months,” Gonzalez said, adding that an asset must show significant value to justify that kind of valuation in return.  

The leader also mentioned a potential search for his successor—one of the first times Gonzalez has publicly confirmed a potential transition in the near-decade since he took helm of the company. The CEO said the idea of a successor has been discussed with the board, but he wants the company to get through its Humira erosion phase, noting that no leadership switch-up would be occurring in 2023.

Since closing at $161.80 per share yesterday, AbbVie’s stock has sunk 8.7%, hitting $147.59 as of 11 a.m. ET today.

https://www.fiercebiotech.com/biotech/abbvie-closes-cystic-fibrosis-chapter-after-combo-just-did-not-work

Sanofi Q1 profit buoyed by better-than-expected Dupixent sales

 French drugmaker Sanofi on Thursday posted better-than-expected earnings for the first quarter as continued gains from anti-inflammatory drug Dupixent more than offset declining sales from an established multiple sclerosis drug.

It reported an 8.7% rise in quarterly business operating income, or adjusted earnings before interest and tax, to 3.33 billion euros ($3.7 billion), ahead of an average analyst estimate of 3.14 billion posted on the company's website.

Revenue from eczema and asthma drug Dupixent, jointly developed with Regeneron, surged more than 43% to 2.32 billion euros, above a consensus of 2.27 billion euros.

Quarterly sales of an older multiple sclerosis pill known as Aubagio dropped almost 17% to 419 million euros, after it was hit by cheap generic copies that came to U.S. markets in mid-March. In Europe, market exclusivity is expected to end in the fourth quarter.

The Paris-based drugmaker said on Thursday it still expected 2023 adjusted earnings per share to grow by a "low single digit" percentage, not taking into account an expected negative currency impact of between 5.5% and 6.5%.

It had previously flagged a negative currency impact of between 3.5% and 4.5%.

Dupixent was successfully tested last month to treat "smoker's lung" or chronic obstructive pulmonary disease (COPD), potentially adding billions to the Sanofi's growth prospects, but also underscoring a heavy reliance on the bestseller.

Finance chief Jean-Baptiste de Chatillon said in a media call that, for now, there would be no new annual peak sales estimate for the product, which Sanofi has put at more than 13 billion euros.

According to presentation slides, the details of the COPD study are scheduled to be published at a meeting of the American Thoracic Society in Washington DC on May 19-24.

Also last month, Sanofi struck a deal to acquire Provention Bio for $2.9 billion to bolster its work on an approved type 1 diabetes therapy and strengthen its drug pipeline following development setbacks. CFO de Chatillon said on Thursday the takeover was progressing as planned.

https://news.yahoo.com/sanofi-q1-profit-buoyed-better-053302370.html

UK Confirms Depleted Uranium Munitions Being Used Against Russians In Ukraine

 The British military has confirmed that thousands of depleted uranium rounds are now in Ukraine, despite prior vehement Russian warnings not to follow through with the transfer.

"We have sent thousands of rounds of Challenger 2 ammunition to Ukraine, including depleted uranium armour-piercing rounds," British Armed Forces Minister James Heappey said while fielding a question from Scottish MP Kenny MacAskill.

Heappey confirmed that the controversial munitions "are now under the control of the Armed Forces of Ukraine (AFU)" and that the UK Defense Ministry "does not monitor the locations from where DU rounds are fired by the AFU in Ukraine."

The defense chief was also grilled by MPs over whether the UK is tracking the rates of depleted uranium rounds are being used against Russian forces, to which he responded, "For operational security reasons, we will not comment on Ukrainian usage rates for the rounds provided."

As for the United States, the Bradley Fighting Vehicles which have already been sent to Kiev are capable of being outfitted with depleted uranium munitions, but the White House hasn't revealed whether or not they are equipped with them.

When it was first revealed in March that Britain would send the armor-piercing tank rounds for Challenger II tanks to Ukraine, the reports triggered a fierce reaction from the Kremlin, with a strong-worded statement emphasizing that such a weapon will be treated as tantamount to using a nuclear dirty bomb.

"Yugoslav scenario. These shells not only kill, but infect the environment and cause oncology in people living on these lands," Foreign Ministry spokeswoman Maria Zakharova said at the time, in reference to cancer and other deadly ailments. "By the way, it is naive to believe that only those against whom all this will be used will become victims. In Yugoslavia, NATO soldiers, in particular the Italians, were the first to suffer. Then they tried for a long time to get compensation from NATO for lost health. But their claims were denied," she said. Zakharova then added, "When will they wake up in Ukraine?… Their benefactors poison them."

During the US occupation of Iraq, use of depleted uranium by NATO allies was linked to cancer and birth defects among the Iraqi population.

Putin as a result of the UK move said that Russia announced he would deploy tactical nuclear weapons to Belarus.

https://www.zerohedge.com/geopolitical/uk-confirms-depleted-uranium-munitions-being-used-against-russians-ukraine

Quest Diagnostics beats profit estimates as routine testing demand returns

 Quest Diagnostics Inc posted first-quarter profit ahead of Wall Street estimates on Thursday as its base business helped offset a fall in COVID-19 test kits sales.

Demand for routine diagnostic tests has picked up as an increasing number of people return to the healthcare system for routine care after delaying care during the pandemic.

Healthcare giant Abbott Laboratories and hospital operator HCA Healthcare Inc last week sounded optimistic about demand for medical device procedures, routine diagnostic testing and consumer-based health products, as cases of COVID-19 infection decline.

Sales at Quest Diagnostics's base business excluding COVID-19 products rose 10% from a year earlier to $2.21 billion.

Global sales of its COVID-19 test kits slumped 80.2% to $119 million and the company lowered its annual COVID-19 sales forecast to between $150 million and $200 million from $175 million to $275 million, as the U.S. government plans to end the COVID-19 Public Health Emergency next month.

Separately, Quest said it would buy cancer test developer Haystack in an all-cash deal worth up to $450 million, which consists of $300 million on the deal's closure and up to $150 million in potential milestone payments.

The deal will bulk up Quest Diagnostic's advanced testing portfolio and is expected to be completed by the second quarter. It will be modestly dilutive to the company's profit over the next three years.

Excluding one-off items, Quest's profit was $2.04 per share for the quarter ended March 31, higher than analysts' average estimate of $1.97 cents per share, according to Refinitiv data.

The company revised its annual adjusted profit forecast to between $8.45 per share and $8.95 per share from $8.40 per share and $9 per share.

https://finance.yahoo.com/news/quest-diagnostics-beats-profit-estimates-132806571.html

West Pharmaceutical raises annual profit forecast on proprietary products strength

 Medical equipment supplier West Pharmaceutical Services Inc raised its annual profit outlook on Thursday after strong sales of proprietary and injection-related products helped top quarterly profit and revenue estimates.

However, the drug-packaging supplier reported a lower profit compared with a year earlier, as COVID-related sales declined.

During the pandemic, biotech and pharmaceutical firms benefited from surging demand for lab equipment, including COVID-19 testing tools.

Pharmaceutical companies have warned of a plunge in pandemic-related product sales this year as cases of COVID-19 infections decline.

Brokerage William Blair analyst Matt Larew said in a note he views this as a signal "that packaging remains a lone bright spot in the broader bioprocessing ecosystem."

West Pharmaceutical posted an adjusted profit of $1.98 per share for the quarter ended March 31, compared with estimates of $1.67 per share, according to Refinitiv data.

The company now expects to report a profit of $7.50 to $7.65 per share for the year, compared with its previous guidance of $7.25 to $7.40 per share.

The Pennsylvania-based firm cut its COVID-19 sales expectation for the year to $60 million from $85 million.

The company said its capital spending program remains on track and that it expects global capacity expansion projects to be completed throughout the rest of the year and in 2024.

https://finance.yahoo.com/news/west-pharmaceutical-raises-annual-profit-141002219.html