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Cytokinetics’ Phase III data sets up cardiomyopathy challenge to BMS

May 16 @ 2:17 am

Cytokinetics’ Phase III data sets up cardiomyopathy challenge to BMS

Published: May 14, 2024

By Tristan Manalac

BioSpace

Cytokinetics on Monday unveiled primary data from its highly anticipated Phase III SEQUOIA-HCM study, showing that its investigational cardiac myosin blocker aficamten significantly improved exercise capacity in patients with obstructive hypertrophic cardiomyopathy.

At 24 weeks, peak oxygen uptake increased by 1.8-mL/kg/min in patients treated with aficatmen, while placebo counterparts saw zero change in this metric. This effect was statistically significant, according to Cytokinetics, and aficamten’s therapeutic benefits were consistent across different subgroups, including age, sex and background use of beta-blockers.

The drug candidate also met its key secondary endpoints, significantly reducing symptom burden in treated patients versus placebo, as quantified by the Kansas City Cardiomyopathy Questionnaire Clinical Summary Score. At 24 weeks, aficamten substantially lowered the levels of NT-proBNP, an indicator of cardiac wall stress.

In terms of safety, SEQUIOA-HCM found that aficamten was well-tolerated and its adverse event profile was comparable to that of the placebo group. There were no instances of worsening heart failure and none of the patients had to stop treatment due to side effects. Cytokinetics also published these data on Monday in The New England Journal of Medicine.

Fady Malik, executive vice president of R&D at Cytokinetics, in a statement said these data from SEQUIOA-HCM show that “aficamten is associated with statistically significant, rapid and sustained improvements in exercise capacity, symptoms, cardiac function and cardiac biomarkers” in patients with obstructive hypertrophic cardiomyopathy (HCM).

These findings “are strongly supportive of the potential approval of aficamten,” Malik continued, adding that Cytokinetics currently plans to submit regulatory filings for the drug candidate in the U.S. and Europe later this year.

Monday’s readout brings Cytokinetics one step closer to a first approval and a positive ending to what has been a difficult road for the company. In February 2023, the FDA rejected Cytokinetics’s small molecule cardiac myosin activator omecamtiv mecarbil, which it proposed as a treatment for heart failure.

At the time, the FDA said that the Phase III data supporting omecamtiv mecarbil was not enough to establish its clinical benefit and requested another trial. However, Cytokinetics indicated that it had no plans to conduct an additional clinical trial for the candidate and about a month later the biotech announced that it was discontinuing the development of its amyotrophic lateral sclerosis candidate reldesemtiv after disappointing Phase III findings.

If approved, aficamten will compete with Bristol Myers Squibb and its oral drug Camzyos (mavacamten), which was approved in April 2022 for obstructive HCM patients of New York Heart Association Class II to III. Camzyos comes with a boxed warning for heart failure due to systolic dysfunction.

Source: BioSpace

US FDA declines to approve expanded use of Dynavax’s hepatitis B vaccine

May 16 @ 2:17 am

US FDA declines to approve expanded use of Dynavax’s hepatitis B vaccine

May 14 (Reuters) – Dynavax Technologies (DVAX.O) said on Tuesday the U.S. Food and Drug Administration (FDA) has declined to approve the expanded use of its hepatitis B vaccine in patients undergoing hemodialysis, citing insufficient safety and effectiveness data.
 
The FDA, in its so-called “complete response letter”, stated that the data was insufficient as a third-party clinical trial site operator had destroyed data source documents for about half of the subjects enrolled in the vaccine’s trial, according to the company.
 

Shares of the California-based company fell more than 7% in premarket trading.
 
Dynavax’s vaccine, Heplisav-B, was first approved by the FDA in 2017, having been rejected twice before in 2013 and 2016 over unresolved safety concerns.

 
 

Bayer cuts 1,500 jobs and lowers 2024 earnings guidance as Q1 sales dip

May 16 @ 2:17 am

Bayer cuts 1,500 jobs and lowers 2024 earnings guidance as Q1 sales dip

Published: May 14, 2024

By Tristan Manalac

BioSpace

Bayer released its first-quarter 2024 earnings on Tuesday announcing that it has reduced its headcount by approximately 1,500 jobs—mostly management positions—amid a slight decline in sales, while lowering its full-year earnings outlook.

“Approximately two-thirds of these were management jobs,” CEO Bill Anderson said in a Tuesday morning media call, referring to the workforce reductions which impacted its pharmaceuticals, crop science and consumer health divisions.

“Our senior leadership circle is already considerably smaller than it was a year ago,” Anderson noted, adding that the layoffs will help the company hit its target of €500 million ($540 million) of sustainable cost savings in 2024 and €2 billion ($2.16 billion) in 2026.

The reduction in workforce comes as Bayer logged more than $14.86 billion in sales, representing a 4.3% reported decline from the same period during the prior year. When adjusting for currency and portfolio effects, Bayer’s year-over-year decline slowed to 0.6%. Of its three divisions, only pharmaceuticals saw a boost in its Q1 sales.

Bayer’s pharma division performed well in the quarter, increasing nearly 4% to bring in more than $4 billion in sales on a currency- and portfolio-adjusted basis. The company attributed the growth to “significant gains” for its new products Nubeqa (darolutamide), indicated for specific types of prostate cancer, and Kerendia (finerenone), approved for chronic kidney disease in type 2 diabetes.

In Q1, Nubeqa sales grew 59%, reaching nearly $306 million, while Kerendia surged 63.5% bringing in $56 million.

Despite sustaining a slight dip in revenue, the anticoagulant Xarelto (rivaroxaban) and the eye treatment Eylea (aflibercept) remained Bayer’s best-selling assets in the quarter, generating approximately $1 billion and $844 million, respectively.

Looking ahead to the rest of the year, Bayer lowered its 2024 earnings-per-share guidance to a range of $5.19 to $5.62, down from the previously announced $5.35 to $5.78 EPS. The adjustment is due to the “negative impact from anticipated currency effects,” according to the company.

Since taking the helm at Bayer in June 2023, Anderson has tried to turn the company around from its disastrous $66 billion acquisition of agricultural giant Monsanto in 2016.

In January 2024, Anderson rolled out his new operating model designed to maximize operational efficiency and reduce bureaucracy and hierarchies in the company. The new model, dubbed Dynamic Shared Ownership, is a sweeping restructuring initiative that includes job cuts through 2025.

In March 2024, Bayer axed its executive roster which now only counts eight members, down from 14 previous positions.

Source: BioSpace

 

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Biopharmaceutical mega M&A deals surge by 71% YoY during Q1 2024

May 16 @ 2:17 am

Biopharmaceutical mega M&A deals surge by 71% YoY during Q1 2024

Mergers and acquisitions (M&As) in the biopharmaceutical industry have rebounded with a $76.9 billion increase in total deal value seen from 2022 to 2023. In Q1 2024 alone, biopharmaceutical M&A reached a total deal value of $43.5 billion, with a 71% year-on-year (YoY) increase of mega deals that were valued at $1 billion or more compared to Q1 2023, reveals GlobalData, a leading data and analytics company.

Alison Labya, Business Fundamentals Analyst at GlobalData, comments: “The recent upturn in biopharmaceutical M&A signals a return in dealmaking confidence, as big pharma companies also look to mitigate the challenges such as the Inflation Reduction Act and upcoming patent expirations.”

GlobalData’s recent The State of the Biopharmaceutical Industry 2024 report reveals that the surveyed healthcare industry professionals expected mega M&A deals to be one of the factors to have the greatest positive impact on the pharmaceutical industry in 2024.

The largest M&A deal reported in Q1 2024 was Novo Nordisk’s holding and investment company’s Novo Holdings’ $16.5 billion acquisition of US-based contract development and manufacturing organization (CDMO) Catalent, announced in February 2024. Another notable M&A deal was Gilead Sciences’ $4.3 billion acquisition of US-based company CymaBay Therapeutics, which was completed in March 2024.

Labya adds: “Companies developing antibody-drug conjugates (ADCs) and radiopharmaceuticals attracted high levels of M&A investment continuing into Q1 2024, as large pharmaceutical companies seek to replenish portfolios with those sought-after drug classes.”

Johnson & Johnson acquired US-based ADC company Ambrx Biopharma for $2 billion in March 2024, and AstraZeneca also announced in the same month to acquire US-based radiopharmaceutical company Fusion Pharmaceuticals for $2 billion.

Oncology was the top therapy area for M&A deals in Q1 2024, with a total deal value of $29 billion. However, immunology-focused M&As had the largest growth in deal activity compared to Q1 2023, with a 314% surge in deal value in Q1 2024 totalling to $14 billion.

Labya concludes: “Q1 2024 saw an increase in billion-dollar M&A transactions involving large biopharmaceutical companies, such as Gilead and Novartis. Given that the biopharmaceutical industry can overcome regulatory challenges set by the Federal Trade Commission, the remainder of 2024 is poised for continued M&A investment from large biopharmaceutical companies, which could accelerate R&D and the launch of innovative drugs.”

Note: Data in the chart includes all announced and completed M&A deals globally from 2021 to Q1 2024 where at least one drug is involved, as well as deals with and without a deal value disclosed in the public domain.

Source: GlobalData

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May 16, 2024
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Ambient data in clinical trials: the future of patient-reported outcomes

May 16 @ 2:17 am

Ambient data in clinical trials: the future of patient-reported outcomes

By Anthony Mikulaschek, IQVIA

Today, there are a variety of ways that technology is integrated into clinical trials, and as the trial landscape develops, so does the role of technology. Methods of capturing patient reported outcomes (PROs) have evolved over the years, as seen with the shift from paper to electronic assessments, and the next generation of data capture is here. The use of wearables and personal devices to capture patient data electronically has expanded as sponsors embrace decentralized clinical trial (DCT) elements within their trial design. Hybrid trial models, which include a mix of both on-site and DCT aspects, have become increasingly popular, especially as sponsors prioritize patient centric methods of data capture.

Collecting patient data through electronic PROs (ePROs) or electronic clinical outcome assessments (eCOAs) has been integral for patient centricity. These tools allow sponsors to meet patients where they are to gather real-time insights directly from the source, boosting patient retention and engagement. ePROs and eCOAs improve clinical trial outcomes with additional data points around a patient’s experience. However, the addition of consumer technologies that can collect ambient data points is poised to enhance outcomes even more, bringing treatments faster to those who need them most.

The future is bright

The next generation of technology for clinical trials is already intertwined into patients’ lives. Tools like home pods, smart assistants and smart watches can provide new types of ambient data to inform clinical trial progress.

Ambient data can identify new patterns and signals from the patient that cannot be captured through sporadic conversations. Things such as tone, inflection or emotion state can be identified to reflect the patient’s state and shed even more light into individual experience. Additionally, the location and impact of activities can be measured in real-time with personalized interactions through the capabilities of smart watches. The combination of the data accumulated, from both traditional ePROs/eCOAs and consumer technologies like home pods or smart assistance, may open the door for additional, otherwise unrecognizable signals or outcomes.

The goal of ePROs and eCOAs is to better inform clinical trials, ultimately helping to bring safer, more effective therapies to market faster. Ambient data collection can provide even further details around the patient experience to ramp up trial efficiency and sharpen insights.

How to get there

Consumer technology has the potential to be a major asset within clinical trials, but there are a few factors that impact the integration of these tools.

  • Trust Building trust between patients and the technology is critical. Without trust, the level of patient reliance on and confidence in the tool will diminish. It will take a collaborative effort between industry leaders as well as global health authorities to begin to foster a sense of trust and comfort. Regulatory bodies need to be engaged, and new use cases must be explored to provide the foundation of trust for consumer technology within trials.
  • Regulations – As the process of establishing regulations around technology that interacts with patients is lengthy, it is critical that regulatory bodies are engaged in the discussion. The use of innovative technology relies on the input of health authorities, to not only build trust but to showcase how ambient data can improve patient experience and clinical outcomes.
  • Use cases – New use cases that focus on the integration of ambient data capture within clinical trials will help build both the credibility and feasibility of these methods. The validation of use cases highlights that devices such as home pods or smart assistants can be an asset in gathering further insight into patient experience. Sponsors, regulatory bodies and patients alike will require proven applications of ambient data collection tools within clinical trials prior to integration.

While ambient data offers transformative potential for clinical trials, bridging the gap between its promise and the current readiness of the clinical trial infrastructure to leverage consumer technologies remains a critical challenge. Enhancing clinical trial outcomes and accelerating the delivery of superior treatments are key goals for the industry. Ambient data, with its deeper insights, can unveil unique opportunities for innovation.

Building trust with patients, engaging regulatory authorities and demonstrating the reliability of ambient data through concrete use cases are essential steps forward. The success of this integration depends on a collaborative effort across the industry, calling for unity among leaders, regulators and patients towards a common goal. Adopting these measures can transform ambient data into a pivotal element of clinical trial innovation, paving the way for a future where comprehensive patient data drives the development of safer, more effective therapies.

Anthony Mikulaschek, IQVIA As vice president of eCOA operations at IQVIA, Anthony Mikulaschek manages all operations, data management, quality management, training and eCOA project work associated with IQVIA eCOA. Anthony has extensive experience in validated system implementation, systems integration, business process reengineering, IT operations, and consulting. He has successfully led the development, delivery, and management of technology solutions for over 30 years including 26 years in the pharmaceutical sector.

Musk’s Neuralink has faced issues with its tiny wires for years, sources say

May 16 @ 2:17 am

May 15 (Reuters) – Neuralink’s disclosure last week that tiny wires inside the brain of its first patient had pulled out of position is an issue the Elon Musk company has known about for years, according to five people familiar with the matter.
 
The company knew from animal testing it had conducted ahead of its U.S. approval last year that the wires might retract, removing with them the sensitive electrodes that decode brain signals, three of the sources said. Neuralink deemed the risk low enough for a redesign not to be merited, the sources added.
 
Neuralink is testing its implant to give paralyzed patients the ability to use digital devices by thinking alone, a prospect that could help people with spinal cord injuries.
 
The company said last week that the implant’s tiny wires, which are thinner than a human hair, retracted from a patient’s brain in its first human trial, resulting in fewer electrodes that could measure brain signals.
 
The signals get translated into actions, such as moving a mouse cursor on a computer screen. The company said it managed to restore the implant’s ability to monitor its patient’s brain signals by making changes that included modifying its algorithm to be more sensitive.
 
The sources declined to be identified, citing confidentiality agreements they had signed with the company. Neuralink and its executives did not respond to calls and emails seeking comment.
 
 

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Eisai, Biogen launch rolling BLA for subcutaneous Alzheimer’s therapy Leqembi

May 16 @ 2:17 am

Eisai, Biogen launch rolling BLA for subcutaneous Alzheimer’s therapy Leqembi

Published: May 15, 2024

By Tristan Manalac

BioSpace

Eisai and Biogen on Tuesday announced that they have initiated a rolling Biologics License Application for a subcutaneous formulation of its anti-amyloid Alzheimer’s disease therapy Leqembi (lecanemab).

The partners are seeking approval for a weekly maintenance dose of Leqembi delivered by an autoinjector. If approved, the subcutaneous injection would be available for patients who complete a biweekly initiation phase with intravenous Leqembi and would allow patients to administer their maintenance doses at home, though they would still have the option of taking it at medical facilities.

Eisai and Biogen are supporting the rolling Biologics License Application (BLA) with data from the open-label extension phase of the Phase III Clarity AD study, as well as modeling results of observed data.

Designed to maintain effective levels of the drug in the body, Leqembi’s subcutaneous formulation is also easier to use and could reduce the need for patients to go to hospitals. “Subcutaneous maintenance dosing may be more convenient for patients and their care partners,” the companies said in Tuesday’s announcement.

Subcutaneous Leqembi could also sustain the clearance of toxic protofibrils, which otherwise contribute to nerve damage and cognitive problems as typically seen in Alzheimer’s patients. Protofibrils are the most toxic form of amyloid-beta proteins, according to the companies, and reducing them has the potential to slow disease progression.

In April 2024, Biogen and Eisai announced that they had missed their March 2024 target to file a BLA for the subcutaneous Leqembi injection. The companies initially planned to file the rolling BLA under Leqembi’s existing Fast Track and Breakthrough Designation, but the FDA clarified that they would need a separate Fast Track designation for the subcutaneous injection BLA.

Unable to start the rolling BLA for subcutaneous Leqembi, the partners instead filed a supplemental BLA for a monthly maintenance intravenous dosing regimen.

Leqembi is a humanized IgG1 monoclonal antibody that targets soluble and insoluble amyloid-beta plaques in the brain, tagging them for clearance from the brain and preventing the disruption of cognition. In January 2023, the FDA granted Leqembi accelerated approval based on biomarker data, which demonstrated that the antibody lowered amyloid-beta levels in the brain.

In July 2023, the regulator awarded Leqembi full approval making it the first anti-amyloid antibody to be traditionally approved for Alzheimer’s.

Despite full approval and broader CMS coverage, uptake of Leqembi has been slow with Eisai announcing in February 2024 that it would likely fall short of treating 10,000 patients by March 2024. However, Biogen revealed in its first-quarter earnings report in April 2024 that Leqembi sales have started to take off, generating $19 million in Q1.

Eisai projects Leqembi revenue to total approximately $360 million in fiscal year 2024, which runs April 2024 through March 2025. 

Source: BioSpace

FDA delays review by three months for Ascendis’ hypoparathyroidism therapy

May 16 @ 2:17 am

FDA delays review by three months for Ascendis’ hypoparathyroidism therapy

Published: May 15, 2024

By Tristan Manalac

BioSpace

Ascendis Pharma on Tuesday announced that the FDA has extended its review of the company’s investigational hypoparathyroidism treatment TransCon PTH (palopegteriparatide). The new target action date is Aug. 14, 2024.

The delay comes after Ascendis submitted additional information to support its New Drug Application (NDA), which the regulator considered a major amendment.

“We have responded to all requests received to date from FDA and will work with the agency as they continue their review of our NDA,” CEO Jan Mikkelsen said in a statement, adding that patients who are currently receiving TransCon PTH through clinical trials or Ascendis’ Expanded Access Program will still be able to get their treatment.

Tuesday’s delay adds to TransCon PTH’s regulatory woes. Ascendis first tried for an approval in 2022 but was rejected by the FDA in May 2023. At the time, the regulator did not identify problems with the candidate’s clinical or safety data but took issue with the biotech’s “manufacturing control strategy” for dose variabilities in the final drug-device product.

Ascendis filed its resubmission in November 2023, which the FDA accepted a month later and set a target action date of May 14, 2024. The regulator considered the resubmission a “complete, class 2 response,” according to the biotech.

TransCon PTH is approved in the European Union and in the U.K., where it carries the brand name Yorvipath.

Designed as a once-daily subcutaneous injection, TransCon PTH is a long-acting prodrug of the parathyroid hormone. It works by raising hormone levels to physiologic levels for 24 hours, which could help address hypoparathyroidism, a rare disorder characterized by low calcium and high phosphate concentrations linked to parathyroid hormone insufficiency.

Hypoparathyroidism manifests as weakness, headaches and muscle cramps. When left unchecked, the condition can lead to calcium deposits in the brain, kidneys and eyes. Hypoparathyroidism is currently managed through high-dose calcium and active vitamin therapy, though these do not adequately control the condition.

Results of the Phase III PaTHway trial, published online in January 2023 in the Journal of Bone Mineral Research, showed TransCon PTH met its composite primary endpoint, which included achieving normal levels of albumin-adjusted serum calcium, independence from conventional vitamin D therapy and no increase in the study drug over four weeks.

Source: BioSpace

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As sales of weight loss drugs skyrocket, the insulin market falters

May 16 @ 2:17 am

As sales of weight loss drugs skyrocket, the insulin market falters

Published: May 15, 2024

By Karen Fischer

BioSpace

When the Inflation Reduction Act rolled out in January 2023, a key tenet of the legislation was the associated Affordable Insulin Now Act, which caps the price of insulin products at $35 per month for Medicare Part D enrollees. Two months later, Novo Nordisk announced that in response, the firm was going to chop the cost of various insulin products by up to 75%. By November, however, Novo changed its tune: Instead of lowering insulin product Levemir by 65%, the firm announced that it was discontinuing the medication instead. Both FlexPens and vials will be completely off the market by the close of 2024.

“[Novo] can’t make a product they’re losing money on, which may be the case with some insulins, and at some point they need to be smart with capital,” BMO Capital Markets analyst Evan Seigerman told BioSpace.

Meanwhile, Q1 sales across the Novo portfolio increased 24% year-over-year with quarterly revenue of $9.37 billion due to the sky-high sales of GLP-1 drugs Ozempic and Wegovy, approved for type 2 diabetes and weight loss, respectively.

In a similar move, weight-loss competitor Eli Lilly also slashed the cost of insulin drug Humalog by 70% to cost patients approximately $25 per vial. Then in March, the company reported that it was facing Humalog manufacturing constraints and warned that it may be temporarily out of stock of the drug by early April, though so far no shortages have been reported.

Also like Novo, Lilly reported strong sales of its GLP-1 weight-loss drug, Zepbound, which was approved last November. In Q1 2024, Zepbound’s first full quarter on the U.S. market, sales of $517.4 million beat analysts’ expectations of $373 million. While below Wegovy’s $1.34 billion in Q1 sales, new Zepbound prescriptions now outpace Wegovy scripts. Lilly also saw continued strong sales of Mounjaro, its GLP-1 for type 2 diabetes.

With such strong sales of GLP-1 drugs, questions arise about how crackdowns on insulin pricing will influence pipeline strategies and if pharma firms have a social responsibility to produce insulin, even at a loss. Moreover, if GLP-1s prevent obesity and diabetes on a mass scale, will insulin stay in such high demand?

Does Levemir’s Withdrawal From Market Really Matter?

Novo decided to discontinue Levemir in the U.S. “due to a combination of factors,” according to comments emailed to BioSpace, “most notably global manufacturing constraints, significant insurance formulary losses impacting patient access effective in January 2024 . . . as well the availability of alternative options in the U.S. market.”

Manny Jurado, principal at the life sciences consulting Dedham Group who works with both biopharma and digital health clients in the GLP-1 and insulin space, added that the complexity of the American healthcare system also played a role. “In the U.S., we definitely live in a higher complexity healthcare ecosystem driven by factors like private insurance and . . . vertically integrated organizations like Cigna-ESI [and] Aetna-CVS, which pretty much touch every aspect of healthcare at this point,” Jurado told BioSpace.

Considerations like differing state and federal regulations, as well as socioeconomic diversity of patients, makes it challenging for any pharma company to successfully launch their product to the American masses, Jurado said. As for insulin as a product, he said that there are other long-lasting insulins on the market, such as Tresiba, Lantus and Toujeo, among others, so patients are not being left without any insulin at all.

However, with pricing caps, the availability of those existing insulins may also change in the future. “I believe manufacturers will continue to re-evaluate their strategic approaches to insulin as supply continues to be an issue,” Jurado said.

How Are the GLP-1 and Insulin Markets Connected?

Jurado said that few drugs have ever gripped the American public like GLP-1 weight-loss drugs. With all of that media noise and accompanying sales, critics of discontinuing Levemir have questioned whether sales of Novo’s Wegovy and Ozempic could have helped subsidize its production.

Seigerman said that when it comes to the strength of GLP-1 sales, there is more that meets the eye. “Yes, on a per-product basis, Wegovy, Ozempic, Mounjaro, and others are profitable,” he said. “[But] you have to remember to get to where these products are now, billions upon billions of dollars were invested. It takes time to recoup; it’s not just the cost of goods.”

For now, Seigerman sees the question of GLP-1 success as a completely separate equation from insulin pricing and supply. “Insulin is unique,” he told said. “These products cost money to make, and [Medicare paying] $35 a month is never going to be able to recoup the cost [of production].” If Levemir were reimbursed at a more appropriate rate for the investment, Seigerman argued, the drug may not have been discontinued.

Seigerman added that the price caps also discourage drugmakers from developing insulin biosimilars. He noted that there are no biosimilars for Levemir—and that, he said, is the real problem in discontinuing the drug. “There should be biosimilars for these [insulins], and that begs the question of why there’s not.”

Future Entanglement of GLP-1s and Insulin Sales

Seigerman predicted that the rise of GLP-1s in popularity may impact the rates of diabetes and thus the need for insulin products because there is a “big overlap” between the obese population and diabetes patients. However, he said that it’s too early to tell how these markets will influence each other, and it may take a decade-plus for any such interplay to come to fruition.

Jurado acknowledged the common links between obesity, diabetes and cardiovascular indications, along with other chronic conditions that GLP-1s address, but emphasized that it’s not enough to trigger a massive phase-out of insulin. “There will always be a strong need for insulin,” he said.

Jurado said that drug manufacturers have social responsibility to people with diabetes—and that most recognize this. “I think these insulin manufacturers acknowledge that these drugs are truly life-time chronic [ones] and are finding ways to continue to support these patients and keep up with supply, despite these manufacturing challenges,” he said.

As for the withdrawal of Levemir, Seigerman is of the firm belief that Novo was justified in its decision and not at fault for the lack of a biosimilar. “In the world of pharma, if you have products losing money with no strategic benefit, you have to look at your portfolio and say, is this how we want to use our limited resources? You have to make capital allocation decisions in R&D, manufacturing, and getting the appropriate products to the right patient every time.”

Source: BioSpace

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Novo acquires majority stake in Austrian life sciences tools company

May 16 @ 2:17 am

Published: May 15, 2024

By Tristan Manalac

BioSpace

Novo Holdings announced Wednesday that it is buying a majority stake in the Austrian life sciences tools company Single Use Support, a provider of fluid management services.

While Novo did not disclose specific financial terms of the transaction in its press release, a spokesperson told Reuters that the deal would be in the “high triple-digit million euros.” The Danish holdings firm, which is the parent company of pharmaceutical giant Novo Nordisk, will own around a 60% controlling stake in Single Use Support, while the Austrian company’s two founders will each retain 10% stakes.

The remaining 20% of Single Use Support will be owned by global life sciences and diagnostics company Danaher.

Johan Heuffer, senior partner of principal investments at Novo Holdings, in a statement called Wednesday’s acquisition an “important and complimentary addition to our fast-growing life science tools and diagnostics portfolio.” The investment will help Novo Holdings advance healthcare solutions and technologies, according to Heuffer.

The Single Use Support deal will also enable Novo Holdings to provide life sciences services to other pharmaceutical companies. The company does not currently use Single Use for its blockbuster weight-loss drug Wegovy (semaglutide), Hueffer told Reuters.

Novo Holdings and Single Use Support did not specify when they expect to close the deal but said that the transaction’s completion will depend on certain regulatory clearances.

Founded in 2017, Single Use Support is a solutions provider focused on fluid and cold-chain management for pharmaceutical substances. The company, headquartered in Austria and with a subsidiary in the U.S., helps drugmakers to safely and efficiently handle and transport their products including biologics, cell and gene therapies and mRNA vaccines.

Some of its products and services include sterile single-use consumables and assemblies, ultra-cold freezers, bioprocess containers and automated aliquoting systems, among others.

For Novo Holdings, Wednesday’s deal with Single Use Support comes as it looks to beef up its manufacturing capacities and supply chain in support of Novo Nordisk’s top-selling Wegovy and type 2 diabetes drug Ozempic (semaglutide).

In February 2024, Novo Holdings dropped $16.5 billion in an all-cash deal to buy CDMO giant Catalent. The acquisition has since hit several regulatory road bumps and has triggered concerns among Catalent’s other pharma clients including Novo’s competitor Eli Lilly.

In April 2024, Novo Nordisk Foundation withdrew and refiled its antitrust filing with the FTC, in effect delaying the deal by 30 days. Earlier this month, the merger was hit with another 30-day delay after the FTC requested additional information regarding the transaction.

In March 2024, Novo Holdings announced that it would pump around $556 million into its China footprint, enabling the construction of a sterile preparations facility. Late last year, Novo also unveiled a $6 billion investment in Denmark to bolster its manufacturing capabilities.

Source: BioSpace

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