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Key communications tech firm liquidates in Chapter 11 bankruptcy

A leading provider solutions for wireless, cable and fixed broadband networks seeks bankruptcy court approvals to sell all of its assets.

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Financial distress in the telecommunications industry continues to grow in 2024 after several firms filed for bankruptcy protection last year.

Chapter 11 filings in 2023 included data center colocation, interconnection services and digital infrastructure provider Cyxtera Technologies, 5G wireless and telecom solutions provider QualTek Services, cloud-based data center provider Internap Holding, and licensed fixed wireless technology developer  and internet service provider Starry Group.

Related: Troubled wireless technology pioneer files Chapter 11 bankruptcy

Bankruptcy filings are also ramping up in 2024, as Airspan Networks Holdings MIMO on March 31 filed for a prepackaged Chapter 11 bankruptcy in the U.S. Bankruptcy Court for the District of Delaware with a plan to hand majority ownership to its senior secured prepetition lender Fortress Investment Group.

The debtor in the latest telecom bankruptcy, however, might not be as lucky as Airspan.

Casa Systems files bankruptcy to sell all of its assets

Casa Systems  (CASA) , a leading provider of physical and cloud-native infrastructure technology solutions for wireless, cable and fixed broadband networks, on April 3 filed for Chapter 11 bankruptcy protection in the U.S. Bankruptcy Court for the District of Delaware, seeking approval of sales of its assets and a plan of liquidation to wind down the company's operations. 

The Andover, Mass.-based communications technology company reached a restructuring support agreement with the ad hoc group of holders of the debtor's superpriority term loan claims and sub term loan claims. The debtor also entered into an asset purchase agreement to sell its 5G Mobile Core and RAN businesses, which include its Axyom Cloud Native 5G core software and RAN assets, to Lumine Group, the company said in an April 3 statement.

Lumine Group is a global acquirer of communications and media software businesses.

Casa Systems additionally entered into a stalking-horse asset purchase agreement to sell its cable business to an affiliate of Vecima Networks  (VNWTF) , a global leader in delivering scalable software, services, and integrated technology platforms for broadband access and content delivery. The deadline for bids for an auction of the cable assets is May 13, with an auction to be held May 15 if necessary. A sale hearing will be held May 31 to approve a sale with the deal proposed to close June. 6.

Checking apps on a smartphone screen including Whatsapp Facebook, Twitter, Instagram, Quora, Facebook Messenger and Snapchat on March 16, 2023. (Photo by Matt Cardy/Getty Images)

Matt Cardy/Getty Images

Lenders unwilling to provide DIP loan

The debtor's prepetition lenders were unwilling to provide debtor-in-possession financing to fund the Chapter 11 case and also unwilling to allow the debtor to seek DIP financing from a third-party. The Ad Hoc group, however, agreed to allow the debtor to use its cash collateral to fund its Chapter 11 case.

The debtor listed $262.5 million in assets and $315.9 million in total debts in its petition.

Casa Systems faced financial distress caused by shifting market dynamics, customer spending delays, customer losses, the Covid pandemic, substantial debt and the company's inability to meet a liquidity covenant under its superpriority credit agreement in June 2023, forcing it to file bankruptcy, according to a declaration by CFO Edward Durkin filed on April 3.

“Like many in our sector, Casa has experienced a significant decline in revenue and profits due in large part to industry-wide downward capital investment and procurement trends in the cable and telco markets," CEO Michael Glickman said in a statement. "We also have incurred significant investments to bring our 5G Mobile Core and RAN products to market. We believe the sales of our businesses through a Chapter 11 process will maximize value, preserve jobs and minimize disruption for our customers.”

Related: Veteran fund manager picks favorite stocks for 2024

 

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Yields Are Correct To Assume Jobs Market Has Not Yet Cracked

Yields Are Correct To Assume Jobs Market Has Not Yet Cracked

Authored by Simon White, Bloomberg macro strategist,

The widening gap between…

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Yields Are Correct To Assume Jobs Market Has Not Yet Cracked

Authored by Simon White, Bloomberg macro strategist,

The widening gap between household employment and payrolls is causing concern the weaker message from the household survey is the more accurate. However, the reality probably lies somewhere in between, and the jobs market is not yet weak enough to justify significantly lower yields.

Jobs day has come round again and focus will be on the mounting difference between the number of jobs recorded by the household survey and the establishment survey, i.e. payrolls. The household data is looking increasingly weak, prompting speculation we are on the precipice of a jobs market that’s about to crack.

But there are reasons to think the household survey may be stronger than the data currently suggest, and also that payrolls may be weaker. Overall, that would mean the “true” state of the jobs market is somewhere in between the two surveys, i.e. this is a slowing jobs market, but not one that is going to trigger an imminent recession, nor corner the Federal Reserve into making near-term rate cuts.

1) The household survey may not be properly accounting for increased immigration. A recent Brookings paper posits that the survey may be using too a low an estimate for the civilian population. That would bias employment growth lower, and unemployment rates (both national and state) too high if the estimate of the size the workforce is too low.

2) The BLS adjusts the household data to take account of the differences between the two surveys (orange line in the chart above). This series is also showing weakness, leading to speculation that even payrolls data is inherently soft. But the very jobs taken out of the payrolls survey to make the adjustment (agriculture, the unincorporated self-employed, unpaid family workers in family-owned businesses) are among those that are predisposed to having a bias towards immigrants.

3) On the other hand, payrolls – as it tracks jobs rather than employees as with the household survey – is doing more double counting. The number of multiple job holders is at a 30-year high. Payrolls could thus fall more quickly than household employment when the labor-market decisively turns.

4) The birth-death adjustment for payrolls, to account for new and closed businesses, is making an unusually large contribution to the data, adding 2.8 million jobs since March 2022. That has happened at the same time as survey response rates have dropped notably since the pandemic. It’s conceivable the adjustment is flattering payrolls, and it will eventually be revised away.

Today’s data will shed some light (and probably some heat too), but we would need to see a decisive weakening in both surveys to justify a significant turn lower in yields.

Tyler Durden Fri, 04/05/2024 - 08:10

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Pfizer’s Own Study Confirms Paxlovid Sucks

Pfizer’s Own Study Confirms Paxlovid Sucks

A Pfizer-funded, peer-reviewed paper authored by Pfizer scientists reveals that the company’s antiviral…

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Pfizer's Own Study Confirms Paxlovid Sucks

A Pfizer-funded, peer-reviewed paper authored by Pfizer scientists reveals that the company's antiviral COVID medication Paxlovid completely sucks, confirming what everyone's known since it came out.

In a randomized phase 2-3 trial of the drug conducted between Aug. 25, 2021 through July 25, 2022, 654 out of 1,296 patients were dosed with at least one 300mg dose of Paxlovid + 100mg of protease inhibitor ritonavir vs. a placebo group. The results showed that the median time until COVID-19 symptoms ended through day 28 was 12 days in the treatment group vs. 13 days in the placebo group.

According to the authors, the result of the drug, which is also known as nirmatrelvir, "was not significant."

"Similar results were observed in the high-risk subgroup (i.e., participants who had been vaccinated and had at least one risk factor for severe illness) and in the standard-risk subgroup (i.e., those who had no risk factors for severe illness and had never been vaccinated or had not been vaccinated within the previous 12 months)," the authors added.

And while 0.8% of the Paxlovid group suffered 'hospitalization or death' vs. 1.6% of placebo recipients, the authors also concluded that it was not statistically significant, however placebo recipients had longer average hospital stays and were more likely to be admitted to intensive care units.

According to the authors, "the usefulness of nirmatrelvir–ritonavir in patients who are not at high risk for severe COVID-19 has not been established."

The trial included adults who had tested positive for COVID-19 and shown at least one symptom, had previously received the COVID-19 vaccine, and had at least one risk factor - such as being a cigarette smoker.

Pfizer had previously announced that they were halting enrollment in the trial over "a very low rate of hospitalization or death observed in the standard-risk patient population."

Paxlovid was previously found not to reduce the risk of long COVID either.

As the Epoch Times notes, Dr. Vinay Prasad, an epidemiology professor at the University of California, San Francisco, who was not involved with the research, said on social media platform X that the trial showed Paxlovid "doesn’t work in vaccinated people."

"It was embarrassing to watch the administration and many ID doctors recommend this without any credible data," he continued - criticizing the government for spending upwards of $12 billion for Paxlovid "without much trial data."

A previous Pfizer trial, which was run to assess Paxlovid’s efficacy and safety among the unvaccinated, found that Paxlovid shortened the time to sustained symptoms alleviation and reduced the severity of COVID-19 symptoms. The trial enrolled people with COVID-19, with symptoms, and who had a risk factor for progression to severe disease or were 60 years of age or older.

Based on the results from that trial, the U.S. Food and Drug Administration in 2023 authorized the drug for both unvaccinated and vaccinated adults with mild to moderate COVID-19 who were deemed at high risk for progression to severe COVID-19. -Epoch Times

"The benefit observed among unvaccinated high-risk persons does not extend to those at lower risk for severe COVID-19," wrote Drs. Rajesh Gandhi and Martin Hirsch in an editorial about the new paper. That said, they also concluded that "it still appears reasonable to recommend the drug to older people and people with substantial underlying conditions."

What?

Tyler Durden Thu, 04/04/2024 - 23:20

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Judge offers early win for Arbutus as Moderna vaccine patent spat heats up

A Delaware federal judge has sided with Arbutus’ interpretation of three patent claim terms in its case against Moderna, giving the biotech a small win…

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A Delaware federal judge has sided with Arbutus’ interpretation of three patent claim terms in its case against Moderna, giving the biotech a small win in a drawn-out patent dispute.

Arbutus and Genevant filed suit against Moderna in 2022, alleging the company’s historic mRNA vaccine used lipid nanoparticle (LNP) technology developed and patented by Arbutus. While plaintiffs agreed that the Covid-19 pandemic would have been “immeasurably worse” without the widespread availability of Moderna’s vaccine, they argued that the achievement was made possible by Arbutus’ discoveries around LNPs.

LNPs are bubbles of fat that protect and escort mRNA into cells. Arbutus said its technology was “developed with great effort and at great expense,” and is now seeking royalties on Moderna’s Spikevax sales. The vaccine generated $6.7 billion last year alone.

Judge Mitchell Goldberg, who rejected Moderna’s effort to toss the case last year, issued an opinion Wednesday on arguments around the interpretation of several patent claims. The judge sided mostly with plaintiffs, giving Arbutus a potential advantage in the overall case. Goldberg sided with Moderna on one of the terms. Arbutus’ stock $ABUS rose nearly 16% on Wednesday.

Michael McElhaugh

“We are pleased with how the Court construed the disputed claim terms,” Arbutus interim president and CEO Michael McElhaugh said in a news release. “We remain committed to protecting and defending our intellectual property and look forward to the next steps in the litigation.”

Jefferies analysts said Wednesday that the opinion bodes well for Arbutus, and “should help derisk” a trial coming next year.

Moderna denied infringement of Arbutus patents in a statement to Endpoints News on Thursday, adding that its LNP system is “the result of our independent research and development.”

“We are confident in our position and look forward to presenting our case at trial next year,” the spokesperson said.

Arbutus and Genevant filed similar claims against Pfizer and BioNTech last April. That case is ongoing.

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