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Friday, October 11, 2019

OxyContin maker Purdue begins showdown to halt opioid lawsuits

OxyContin maker Purdue Pharma LP will ask a U.S. Bankruptcy Judge on Friday to pause litigation against the company and its owners over the objections of U.S. states that allege the company is trying to protect the controlling Sackler family.

Purdue’s request promises to be one of the most contentious of the company’s Chapter 11 bankruptcy case, which was filed in September to try to implement a settlement proposal it values at more than $10 billion.
Privately-held Purdue said last month it needed to pause more than 2,600 lawsuits so the company can reduce legal costs and try to win over more plaintiffs to its proposed deal.
The lawsuits accuse Purdue and the Sacklers of fueling a public health crisis by aggressively marketing opioids while downplaying their overdose risks, contributing to some 400,000 deaths from 1999 to 2017, according to U.S. statistics.
The company said it has the support of a majority of the local governments that brought the bulk of the lawsuits, although at least 24 states oppose the deal.
Massachusetts Attorney General Maura Healey, a settlement opponent, has accused Purdue of protecting the billionaire Sacklers.
The family has not filed for bankruptcy protection, which generally automatically pauses litigation but also imposes obligations to open financial records. The family has pledged to contribute at least $3 billion to the settlement and will relinquish ownership of Purdue to the plaintiffs.
States opposed to the settlement disclosed in a court filing last week that Purdue steered about $12 billion in profits to the Sacklers.
At a Thursday court hearing, a lawyer for Purdue challenged that characterization and said it covered a period dating back to 1995, and was disclosed to plaintiffs a year ago. “The $12 billion figure is in fact not new at all,” said Marshall Huebner, a Davis Polk & Wardwell lawyer who represents Purdue.
Among other things, Purdue will have to convince U.S. Bankruptcy Judge Robert Drain in White Plains, New York, that pausing litigation is in the public interest.
Holdout states said their cases are aimed in part at uncovering the extent of the company’s misconduct.
“This court should not strip the states of their core function to enforce their own regulatory laws in their own courts and administrative bodies,” said a filing last week by the states opposed to the deal.

https://www.marketscreener.com/news/OxyContin-maker-Purdue-begins-showdown-to-halt-opioid-lawsuits–29366729/?countview=0

‘Historically cheap’ J&J a buy – Bernstein

Legal overhangs on the share price are overdone, says analyst Lee Hambright, noting a 13% decline from the 52-week high.
Settlements in the $50B range are a worst-case scenario, he says, yet are already priced in. A more likely range is $10B-$12B, he argues – $5B for opioids, $5B for talc, and $800M for Risperdal.
As for valuation, J&J (NYSE:JNJ) is trading at a 17% discount vs. a 12% premium to the S&P 500 at the end of last year – that’s almost two standard deviations below the long-term average.
He upgrades to Outperform and boosts his price target to $155 from $148. Shares are up 1.5% early to $131.
The Seeking Alpha Authors average rating is Bullish and the Quant Rating Neutral.
https://seekingalpha.com/news/3505267-historically-cheap-j-and-j-buy-bernstein

Vir Bio prices IPO at $20

Vir Biotechnology (VIR) has priced its initial public offering of 7,142,858 common shares at $20.00/share, for expected gross proceeds of ~$142.9M.
Underwriters over-allotment is an additional 1,071,428 shares.
The shares are expected to begin trading on Nasdaq today.
Net proceeds will be used  to complete and advance clinical trials, for working capital and other general corporate purposes.
Closing date is October 16.
https://seekingalpha.com/news/3505190-vir-bio-prices-ipo-20

Gilead and Galapagos’ filgotinib shows durable effect in late-stage RA studies

Gilead Sciences (NASDAQ:GILD) and licensor Galapagos NV (NASDAQ:GLPG) announce long-term results from Phase 3 clinical trials, FINCH 1 and FINCH 2, evaluating JAK1 inhibitor filgotinib in patients with moderately-to-severely active rheumatoid arthritis (RA).
Data at week 52 are consistent with the safety, tolerability and efficacy results observed at weeks 12 and 24. Detailed results will be presented at a future medical conference.
Marketing applications are currently under review in Europe and Japan. Gilead plans to file an NDA in the U.S. later this quarter.
GILD is up 1% and GLPG is up 2% premarket, both on light volume.
https://seekingalpha.com/news/3505212-gilead-galapagos-filgotinib-shows-durable-effect-late-stage-ra-studies

IPO BioNTech up 11% premarket

New IPO BioNTech (NASDAQ:BNTX) is up 11% premarket on modest volume as it tries to recoup yesterday’s 5% dip from its $15 offering price in its first day of trading.
https://seekingalpha.com/news/3505220-ipo-biontech-11-percent-premarket

RedHill Bio up 7% premarket on positive data on RHB-104 in Crohn’s

Thinly traded micro cap RedHill Biopharma (NASDAQ:RDHL) is up 7% premarket on light volume in response to 52-week results from a Phase 3 clinical trial, MAP US, evaluating RHB-104 in patients with Crohn’s disease.
The study continued to meet the primary endpoint of clinical remission achieved at week 26, showing a rate of 22.4% compared to 36.7% at the earlier time point (p=0.0048). Key secondary endpoints were also sustained.
On the safety front, there was a cardiac abnormality, progressive prolongation of the QTcF interval (heart rhythm disorder that can lead to serious arrhythmias), observed at week 52 but none resulted in serious adverse cardiac events.
Results from an open-label extension study, MAP US2, in patients with persistently active Crohn’s, showed a clinical remission rate of 27.8% at week 16 and 22.2% at week 52.
https://seekingalpha.com/news/3505261-redhill-bio-7-percent-premarket-positive-data-rhbminus-104-crohns

Flight Attendants Union Asks FAA To Ban E-Cigarettes On Airplanes

At least 265 incidents in the air or at airports have involved lithium-ion batteries since 1991, according to the FAA.
Out of those 265, a minimum of 48 smoke or fire incidents were from lithium batteries in e-cigarettes, which is more than the number caused by cell phones, laptops, battery chargers, tablets or spare batteries.
The vaping devices often contain cheaper batteries that are more likely to fail and start a fire, and the nation’s largest flight attendant union is calling on the Federal Aviation Administration to ban all e-cigarettes from airplanes, according to CBS News.
“A lithium-ion battery fire on a plane can be catastrophic,” Sara Nelson, president of the Association of Flight Attendants, told CBS.
Flight attendants have turned into de facto firefighters, and this means the FAA needs to do more, she said.
Even though flight attendants are trained to take care of fires by placing flaming devices in special fire-resistant bags, Nelson said it would be better if they didn’t have to manage those situations at all.
“How about we just not have these e-cigarettes on the plane at all?”

Mark Millam of the Flight Safety Foundation told CBS that a ban requires more information.
“A ban could happen when there is the right information that’s understood about it,” he said.
The FAA responded that it has “clear regulations” on the safe transport of lithium-ion batteries, and said vape pens, e-cigarettes and spare batteries must be put in carry-on bags.
https://www.benzinga.com/markets/cannabis/19/10/14575157/flight-attendants-union-asks-faa-to-ban-e-cigarettes-on-airplanes