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Tuesday, February 4, 2025

Regeneron Pharma Q4 Earnings Crush Estimates, Initiates Dividend And Additional Stock Buyback

 On Tuesday, Regeneron Pharmaceuticals Inc (NASDAQ:REGN) reported fourth-quarter adjusted EPS of $12.07, up 2% year-over-year, beating the consensus of $11.29.

The company reported sales of $3.79 billion, up 10%, beating the consensus of $3.75 billion.

“Regeneron’s financial and commercial strength allows for continued investment in our industry-leading R&D pipeline, while simultaneously returning capital to our shareholders through our newly initiated dividend program and increased share repurchase capacity,” said Leonard S. Schleifer, Board co-Chair, President and CEO of Regeneron.

“In 2025, we will continue to focus on our four blockbuster medicines as we progress our approximately 40 investigational candidates covering dozens of disease states with expansive market potential.”


Fourth quarter 2024 U.S. net sales for Eylea HD and Eylea increased 2% year-over-year to $1.49 billion, including $305 million from Eylea HD.

A lower net selling price impacted the net product sales of Eylea HD and Eylea in the fourth quarter and full year 2024 compared to the same periods of 2023. LLibtayo’s global net sales increased by 50% to $367 million.

Sanofi collaboration revenue increased in the fourth quarter and full year 2024, compared to the same periods of 2023, due to an increase in the company’s share of profits from the commercialization of antibodies, which were $1.043 billion and $886 million in the fourth quarter of 2024 and 2023, respectively, and $3.924 billion and $3.137 billion for full-year 2024 and 2023, respectively.

Dividend: Regeneron approved initiating a quarterly cash dividend program and declared a cash dividend of $0.88 per share, payable on March 20, 2025, to shareholders of record as of February 20, 2025.

The company intends to pay a cash dividend every quarter.

The company’s board of directors also authorized an additional $3.0 billion share repurchase program, bringing the current capacity to approximately $4.5 billion.


https://finance.yahoo.com/news/regeneron-pharma-q4-earnings-crush-170240506.html

Novartis upped to Buy by Deutsche Bank

 From Hold

https://finviz.com/quote.ashx?t=NVS&ty=c&ta=1&p=d

'Centene sets itself up for ‘equilibrium’ in 2025'

 

  • On Tuesday, Centene touted healthy membership growth in Affordable Care Act plans, while arguing that Medicaid and Medicare — businesses that proved rocky last year — will stabilize in 2025.

  • Already the largest marketplace carrier, Centene now has upwards of 5 million ACA members paying premiums, executives told investors during a call to discuss its fourth-quarter results. That’s compared to 4.8 million members at the end of 2024.

  • Growth in ACA members was a major contributor to Centene’s $3.3 million in profit last year, according to the company. However, Centene expects enrollment to peak in the first quarter before sliding back down over the year, in part from efforts to improve program integrity, CEO Sarah London said.


Overall, Centene beat Wall Street expectations for earnings and revenue in the fourth quarter with a topline of $40.8 billion, up 3% year over year.

The St. Louis-based insurer’s profit was $283 million — more than six times larger than in the fourth quarter of 2023, when it was hit with higher taxes on premiums.

Centene’s bottom-line growth came despite elevated medical costs. The insurer reported a medical loss ratio, an important marker of spending on patient care, of 89.6% in the quarter, up slightly from 89.5% same time last year.

Centene chalked the increase up to higher acuity in Medicaid as the insurer continues to struggle with states’ payment rates not matching patients’ health needs in the safety-net insurance program.

The problem stems from Medicaid unwinding, a process in which states reviewed the eligibility of tens of millions of Americans for the safety-net program starting in spring 2023. Millions of people lost Medicaid coverage as a result, and individuals who remained in the program tended to be sicker and therefore more expensive for insurers that contract with states to manage Medicaid to cover.

Top insurance executives have said for months that they’re working with states to hike their rates. States are — Centene cited higher Medicaid rates as one driver of increasing revenue — but not as quickly or as dramatically as insurers may have hoped.


https://finance.yahoo.com/news/centene-sets-itself-equilibrium-2025-071937842.html

Pfizer Eyes Deals up to $15B, With ‘Fruitful’ China Discussions Ongoing

 

With just one asset in weight loss moving through the clinic, Pfizer targets the space for potential dealmaking, as well as bringing assets over from China.

As Pfizer beat analyst expectations for 2024 with revenue of $63.6 billion, all eyes turned to the pipeline and the pharma’s obesity strategy for future growth.

Analysts have been eagerly awaiting news on Pfizer’s next-gen GLP-1 weight loss candidate danuglipron, which has a dose-optimization study expected to read out in the first quarter of the year. The earnings release passed without that data, with newly minted Chief Scientific Officer Chris Boshoff declining to speculate on whether the asset could be on the chopping block if it doesn’t meet expectations.

Boshoff did say that actual weight loss numbers will be a secondary endpoint. The focus of this readout will be on pharmacokinetics and nailing down a once-daily dose for the oral candidate. While the data may include weight loss, Boshoff cautioned that it’s a small trial and the numbers may not be reliable.

Without news still to come about that asset’s potential, analysts wondered if Pfizer might be looking to some deals or partnerships to build out a more robust obesity pipeline. Andrew Baum, chief strategy and innovation officer, agreed that “obesity is heterogeneous and [will] likely require a set of tools encompassing both different modalities and different delivery devices in order to manage.”

“These assets do exist. Some are scattered. Some have portfolios,” Baum said. “But you could imagine that, of course, we are looking at all the opportunities and trying to understand what delivers the most value to patients and obviously to Pfizer shareholders.”

As for business development more broadly, Pfizer could also follow its peers to China for potential new assets, according to Baum. “It has not escaped our attention, of course, the innovation from China across multiple therapeutic areas.”

The region previously was a leader in oncology but now that innovation has opened up. Baum said Pfizer continues to have “very fruitful discussions” regarding a potential deal in China.

CEO Albert Bourla said that the company will be strategic in any dealmaking. Over 2024, business development activity was restricted as planned as the company worked to absorb Seagen, which the pharma company bought in 2023 for $43 billion. CFO Dave Denton said the company will look for deals in the ballpark of $10 billion to $15 billion.

“Everything we do will be due for a strategic lens of building around our core competencies, or building competences in the areas that maybe we have not been in previously,” Baum said of potential dealmaking.

Strong Footing

The New York pharma reported the 7% increase in revenue for the full year and earnings per share of $1.41, according to a fourth quarter earnings release issued Tuesday morning. For the fourth quarter, the company saw revenue of $17.8 billion, a 21% year-over-year increase. The beat was driven by strong performance across Pfizer’s commercial operations, particularly from the COVID franchise which has proven to be a “predictable and durable” contributor to earnings, according to Bourla.

R&D expenses increased 8% as Pfizer funneled more money into developing candidates from theSeagen acquisition. The change was offset by a decrease in spending on the vaccine program and the cost alignment program. Pfizer kicked off about a dozen clinical trials in 2024, including eight key Phase III studies, according to Bourla.

Pfizer also reorganized its R&D leadership last year, welcoming Boshoff in November 2024 to replace Mikael Dolsten, who led the R&D organization through the COVID-19 pandemic. Boshoff had previously served as Pfizer’s chief oncology officer.

“The good news with Chris is that he knew really the Pfizer organization, and I’m very impressed with the speed and thoughtfulness that he’s deploying his changes already,” Bourla said. In his short time in the role, Boshoff has selected a number of new leaders for the R&D organization and aided in efforts to refocus the pipeline.

Boshoff said that the changes have allowed for more efficient handoff of candidates between early to late-stage development. Bourla said that Pfizer has a higher success rate of molecules, hitting about 17% compared to the industry average of 10–11%. The company has also been faster, moving assets to the market in five to six years compared to eight for the industry average. But Pfizer could have done better actually choosing the molecules to focus the R&D organization on, according to the CEO.

“So historically, when you look back, there’s no shortage of first in class breakthrough molecules that we’ve successfully shepherded through development,” said Baum. “However, some of those really have not delivered in terms of financial revenues and therefore to shareholders. And the key issue is really ensuring that we have successful portfolio prioritization, bringing that commercial lens to much earlier during the process.”

Pfizer also reported $2.9 billion in impairment charges in the fourth quarter, including $1 billion specifically for Seagen asset felmetatug vedotin. Pfizer has discontinued a Phase I trial of the antibody-drug conjugate in solid tumors.

Pfizer has been cutting costs for the past few quarters, realizing $4 billion in savings. That target has been revised to $4.5 billion by the end of 2025.

“Importantly, we believe the steps taken to right size our cost base will put us on a strong footing towards increased operational efficiency and support our goal to return to pre-pandemic operating margins,” Denton said.

https://www.biospace.com/business/pfizer-eyes-deals-up-to-15b-with-fruitful-china-discussions-ongoing

Merck sinks as company halts Gardasil shipments to China, weighing on outlook

 Merck &Company Inc (NYSE:MRK) shares tumbled more than 10% Tuesday after reporting mixed fourth-quarter results, with earnings falling short of expectations, revenue surpassing estimates and full-year guidance coming in below analyst projections.

Merck (NSE:PROR) posted adjusted earnings per share (EPS) of $1.72 for Q4, missing the analyst consensus of $1.81 by $0.09. However, revenue for the quarter came in at $15.6 billion, beating the expected $15.47 billion. Compared to the same quarter last year, revenue increased 7%, or 9% excluding foreign exchange impacts.

The company forecasts full-year 2025 adjusted EPS of $8.88 to $9.03, below the consensus estimate of $9.21. Revenue is projected to be between $64.1 billion and $65.6 billion, also lower than the $67.36 billion analysts were expecting.

For the full year 2024, Merck reported worldwide sales of $64.2 billion, up 7% YoY or 10% excluding foreign exchange effects. The company's blockbuster cancer drug KEYTRUDA continued to drive growth, with sales rising 18% to $29.5 billion for the year.

"We delivered strong growth in 2024, reflecting demand for our innovative portfolio, including for KEYTRUDA, which continues to benefit more patients with cancer globally, the successful launch of WINREVAIR and strong performance of our Animal Health business," said Robert M. Davis, chairman and CEO of Merck.

Merck also said it has temporarily paused shipments of Gardasil to China beginning February 2025 through at least mid-year, which is reflected in the guidance.

The company has also withdrawn its previous $11 billion sales target for Gardasil by 2030, citing uncertainty around the timing of China's economic recovery, with growth expectations for the vaccine remaining unchanged in other markets.


https://finance.yahoo.com/news/merck-shares-tumble-q4-earnings-122223132.html

Robinhood halts rollout of Super Bowl betting contracts after CFTC request

Robinhood said on Tuesday it is rolling back the event contracts that would let users bet on the result of the Super Bowl clash this weekend, after the online brokerage received a request from the U.S. Commodity Futures Trading Commission.

The halt comes just a day after the launch of the product. Robinhood said it was "disappointed by the outcome."

"We are heeding their directive to cease offering these contracts despite the fact that the CFTC has not deemed Kalshi's football championship contracts illegal," said Lucas Moskowitz, Robinhood's general counsel.

Representatives for Kalshi and the CFTC did not immediately respond to Reuters' requests for comment.

The products would have allowed the company to tap into the betting mania around one of the most iconic sporting events in the country, as Robinhood looks to expand into segments that are gaining traction with retail investors.

The company had rolled out the contracts to 1% of its customers. Those who already placed the trades will get the option to close their positions or take them to resolution, Robinhood said.

Event derivatives trading involves buying and selling contracts that let traders speculate on the outcomes of specific events, including elections, economic data releases and policy decisions.

"Prediction markets and event contracts can be subject to complex regulatory landscapes," said Michael Ashley Schulman, partner and chief investment officer at Running Point Capital Advisors.

"The CFTC may be concerned that this could be perceived as an active retail betting platform disguised under an investment umbrella, especially since sporting events are much more frequent than presidential elections."

These products have enjoyed a warm reception, despite being relatively new and widely seen as high-risk, especially after a U.S. court struck down the CFTC's efforts to block KalshiEX's election betting contracts.

Robinhood's derivatives arm is planning to launch a "more comprehensive" event contracts platform later this year.


https://finance.yahoo.com/news/robinhood-receives-us-cftc-request-173527139.html

Quantum Biopharma Announces the Success of unbuzzd™ Clinical Trial

 

Trial Confirms unbuzzd™ Dramatically Accelerates Alcohol Metabolism, Speeds the Reduction of Blood Alcohol Concentration, and Reduces Symptoms of Intoxication, Impairment and Hangover

Quantum BioPharma Ltd. (NASDAQ: QNTM) (CSE: QNTM) (FRA: 0K91) (Upstream: QNTM) (“Quantum BioPharma” or the “Company”), a biopharmaceutical company dedicated to building a portfolio of innovative assets and biotech solutions, today announced that it has completed a double-blind, randomized, placebo-controlled crossover design clinical trial (NCT06505239) of its dietary supplement product unbuzzd™, investigating its effects on alcohol intoxication and alcohol metabolism.

Results of data analysis show definitively that unbuzzd™ accelerated the rate at which Blood Alcohol Concentration (“BAC”) was reduced in study subjects, while simultaneously reducing the symptoms of intoxication and hangover. All these results were statistically significant compared to placebo. Study participants were both male and female and between the ages of 21 and 43, with weights ranging from 119 to 232 pounds.

The positive effects of unbuzzd™ were rapidly apparent, occurring within 30 minutes after consumption of the dissolved powder. unbuzzd™ was well-tolerated and safe, with no reported product-related adverse effects.

https://www.globenewswire.com/news-release/2025/02/04/3020150/0/en/Quantum-Biopharma-Announces-the-Success-of-unbuzzd-Clinical-Trial.html