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Monday, January 27, 2020

Select Medical sees FY 2020 revenues as high as $5.675B

Select Medical Holdings (NYSE:SEM) announces its business outlook for calendar year 2020.
Net operating revenues FY 2020 is expected in the range of $5.575B to $5.675B.
Adjusted EBITDA for FY 2020 is expected in the range of $725M to $760M.
FY 2020 EPS in the range of $1.27 to $1.46.
The company will release it Q4 and FY 2019 on Thursday, February 20, 2020 after the market closes.
https://seekingalpha.com/news/3534649-select-medical-sees-fy-2020-revenues-high-5_675b

Liquidia files U.S. application for inhaled formulation for hypertension

Under the abbreviated 505(b)(2) pathway, Liquidia Technologies (NASDAQ:LQDT) has submitted a marketing application to the FDA seeking approval for an inhaled dry powder formulation of treprostinil for the treatment of pulmonary arterial hypertension.
Treprostinil, administered intravenously or subcutaneously, is marketed under the brand name Remodulin by United Therapeutics. It markets an inhalable solution formulation under the brand name Tyvaso.
Shares down 6% premarket on light volume.
https://seekingalpha.com/news/3534651-liquidia-files-u-s-application-for-inhaled-formulation-of-treprostinil

Coronavirus in China could threaten pharma’s ingredient sourcing

As a novel coronavirus spreads through China and rattles the rest of the world, the pharmaceutical industry is on guard over the adequacy of its global supply chain.
Over the past decade, China has become a bigger player in the market for active pharmaceutical ingredients, which are the building blocks found in each drug. China is now home to 13% of all facilities that make ingredients for medicines that are sold in the U.S., according to the Food and Drug Administration. By comparison, 28% of such facilities are in the U.S. and 26% are in the European Union.
Most ingredient production is concentrated in Zhejiang province, which is something of a manufacturing hub that lies along the East China Sea, far from the city of Wuhan, where the outbreak began, explained a source familiar with the Chinese pharmaceutical market but who asked not to be named.
But as the virus proliferates, illnesses and deaths mount, and the Chinese government increasingly locks down portions of the country, there are likely to be mounting questions about adequate production and supplies of active ingredients going forward, as well as the extent to which shipments can be made if transit hubs are out of commission.
“The time to worry is now,” said Steven Lynn, a former director of the FDA Office of Pharmaceutical Quality, who subsequently worked in global quality compliance for both Novartis and Mylan before leaving to start his own consulting firm.
“I would be asking my supply chain folks what do we have coming from China, what’s our inventory, and if we don’t have enough, can we get as much as fast possible? And remember, this isn’t just a U.S. problem. It’s a global problem if China starts shutting down its borders.”
Of course, the situation can vary.
Generally, most drug makers have more than one ingredients supplier available for each medicine. A GlaxoSmithKline (GSK) spokeswoman, for instance, wrote us that the company maps out reliable supplies by stockpiling inventory and “dual sourcing” ingredients, as well as conducting risk assessments.
For large, brand-name companies, this can help explain why adequate supplies may be less of a concern, according to Martin VanTrieste, a former chief quality officer at Amgen, who now heads Civica Rx, a nonprofit that is working with hospitals and health plans to supply lower-cost generics in the U.S. market.
Although data are hard to come by, he estimated brand-name drug makers obtain only a small fraction of their active ingredients from China, given apprehension over quality issues. “If the virus stays contained, the problem won’t be that big on the branded industry,” he said. “But if it isn’t contained, it could be a serious problem.”
Roughly 80% of active ingredients used by commercial sources to produce finished medicines come from China.
Christopher Priest, deputy assistant director, U.S. Defense Health Agency
For the moment, an FDA spokesman wrote us, the agency has not received any shortage notifications from manufacturers that make products for the U.S. market due to the current coronavirus outbreak.
On a wider scale, though, there may already be reason for concern.
Roughly 80% of active ingredients used by commercial sources to produce finished medicines come from China,  Christopher Priest, deputy assistant director at the U.S. Defense Health Agency, said in testimony given last July to the U.S.-China Economic and Security Review Commission.
This view reflects the fact that the overall market for prescription drugs consists of brand-name and generic medicines. Again, data is lacking on the volume of ingredients from China that reach the U.S. But a growing number of Indian generic makers purchase ingredients from China. In fact, the Indian government is trying to find ways for its domestic industry to become less reliant on Chinese suppliers.
There are implications here for consumers elsewhere — and the possibilities can be seen by playing connect the dots. In the U.S., for instance, medicines imported from India account for 40% of all generics used. And roughly 90% of all prescriptions written in the U.S. are for generics. The upshot: An untold amount of ingredients made in China are finding their way to U.S. medicine cabinets.

A spokeswoman for the Association for Accessible Medicines, which represents generic drug makers in the U.S., wrote us that “most of our members have a second source for all active pharmaceutical ingredients. In addition, they don’t order per batch. Rather, each order is for two to five years of manufacturing needs.”
But the reliance on ingredients from China is already worrisome, said Rosemary Gibson, a health care and patient safety expert at The Hastings Center, a bioethics nonprofit, and co-author of “China Rx: Exposing the Risks of America’s Dependence on China for Medicine,” a book that examines the growing clout that China has a global ingredients supplier.
She pointed out that 85% of medicines in the U.S. strategic national stockpile depend on some component coming from China, whether it is an active ingredient, the chemical intermediates used to make ingredients, or raw materials. And the novel coronavirus may exacerbate the issue if China keeps supplies for itself or stops export of certain medicines to stockpile on a large scale for their own health care system.
“When you think about it, though, all it takes is for one ingredient plant to cause a problem in the near term. The production of some medicines depends on one (ingredient) supplier,” she explained. “This is why long supply chains for critical products should be rethought.
“We need a government entity that monitors global supply and demand — and events like this outbreak — to understand our vulnerabilities, predict possibilities and have a plan to prepare, rather than scramble. We track food supplies around the world. We do this for energy supplies. We need to do the same thing for medicines.”
‘The time to worry is now’: The coronavirus in China could threaten pharma’s ingredient sourcing

J&J CEO to testify at trial for first time on Baby Powder risks

Johnson & Johnson Chief Executive Officer Alex Gorsky was set to be called as a witness on Monday in what would be his first appearance in a jury trial over allegations that the company’s Baby Powder causes cancer.

Lawyers for three men and one woman who sued J&J subpoenaed Gorsky in a trial playing out in a state courtroom in New Brunswick, New Jersey near the company’s headquarters.
All four have mesothelioma, a rare and incurable cancer that they said was caused by their exposure to asbestos in Baby Powder applied when they were diapered as infants.
During an earlier phase of the trial, the jury held J&J liable for the plaintiffs’ cancers and awarded them $37.2 million in compensation. Now their lawyers are seeking to persuade a second jury that J&J’s behavior was so reckless that punitive damages are warranted.
J&J fought the subpoena of Gorsky, arguing that he had no first-hand knowledge about the safety of its powders and that the case involves corporate conduct that occurred long before he joined the company in 2012. Compelling his testimony, J&J said in a motion, would set a precedent that could result in other chief executives being hauled to court and “would serve no purpose other than to harass Mr. Gorsky and divert him from his executive responsibilities.”
Last week, the New Jersey Supreme Court turned down the company’s request to suspend the subpoena, clearing the way for Gorsky to be called to testify.
The stakes are high. J&J faces more than 16,000 lawsuits. They assert that J&J sold powders contaminated with asbestos, a known carcinogen, and failed to warn users. J&J also faces a federal criminal investigation into how forthright it has been about the products’ safety.
In October, J&J disclosed that a contract lab for the U.S. Food and Drug Administration had found asbestos in a bottle of Baby Powder produced in 2018. The company questioned the finding and commissioned tests on samples from the same bottle and talc from the same lot. Less than two weeks later, J&J announced those tests had found no contamination, other than some asbestos it attributed to an air conditioner in the lab.
In December 2018, a Reuters report based on J&J documents produced in litigation showed that the company knew small amounts of asbestos had been found in its talc on occasion since 1971. J&J dismissed the Reuters’ report as “an absurd conspiracy theory.”
Gorsky’s road to court began in the days following the publication of that report when he took the lead in company efforts to rebut it. The chief executive attested to the safety and purity of Johnson’s Baby Powder in a video posted on the company’s website and in an appearance on CNBC’s “Mad Money.”
“We unequivocally believe that our talc, our Baby Powder, does not contain asbestos,” Gorsky told the investment show’s host Jim Cramer.

https://www.marketscreener.com/JOHNSON-JOHNSON-4832/news/J-J-CEO-to-testify-at-trial-for-first-time-on-Baby-Powder-risks-29895567/?countview=0

Genentech submits U.S. marketing application for Tecentriq + Avastin

Roche (OTCQX:RHHBY) unit Genentech has completed a supplemental Biologics License Application (sBLA) submission to the FDA for Tecentriq (atezolizumab) in combination with Avastin (bevacizumab) for the treatment of people with unresectable hepatocellular carcinoma (HCC) who have not received prior systemic therapy.
The FDA is reviewing the application under the Real-Time Oncology Review pilot program.
https://seekingalpha.com/news/3534561-genentech-submits-u-s-marketing-application-for-tecentriq-avastin

Anavex Life completes enrollment in mid-stage blarcamesine study

Anavex Life Sciences (NASDAQ:AVXL) has met its enrollment target for the ANAVEX2-73 (blarcamesine) Phase 2 study in Parkinson’s Disease Dementia (PDD).
Topline results are expected by mid-2020.
The study enrolling over 120 patients measures efficacy, tolerability, and safety of two different oral ANAVEX2-73 doses or placebo.
Primary and secondary endpoints will assess cognition and Parkinsonian motor symptoms and sleep function during the 14-week study.
Shares are up 5% premarket.
https://seekingalpha.com/news/3534606-anavex-life-completes-enrollment-in-mid-stage-blarcamesine-study-shares-up-5-premarket

Lilly and Incyte’s Olumiant shows mixed results in late-stage dermatitis study

Incyte (NASDAQ:INCY) and licensee Eli Lilly (NYSE:LLY) announce results from a Phase 3 clinical trial, BREEZE-AD4, evaluating Olumiant (baricitinib) in adults with moderate to severe atopic dermatitis (AD) who were inadequate responders to, intolerant of or contraindicated for cyclosporine.
The study met the primary endpoint of a statistically significant proportion of patients achieving at least a 75% improvement in AD (EASI 75) from baseline at week 16 compared to placebo at the highest dose (4 mg), but did not for the 1 mg and 2 mg doses.
No new safety signals were observed.
Complete results will be submitted for presentation at future medical conferences and publication.
The FDA approved the JAK inhibitor in June 2018 for rheumatoid arthritis at a recommended dose of 2 mg once daily.
Lilly’s recently submitted its marketing application for AD in Europe and plans to file applications in the U.S. and Japan this year.
https://seekingalpha.com/news/3534611-lilly-and-incytes-olumiant-shows-mixed-results-in-late-stage-dermatitis-study