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Thursday, June 7, 2018

Superbug infections rising among injection drug users


One type of superbug bacteria is increasingly spreading among people who inject drugs, according to a new government report.
Users of heroin and other injection drugs were 16 times more likely than other people to develop severe illnesses from MRSA, said the report published Thursday.
“Drug use has crept up and now accounts for a substantial proportion of these very serious infections,” said Dr. William Schaffner of Vanderbilt University, one of the study’s authors.
The U.S. is in the midst of its deadliest drug epidemic ever. While overdose deaths have been the main concern, some studies have noted HIV and hepatitis C infections are spreading among drug users. The authors say the new report is one of the first — and the largest — to highlight how superbug bacterial infections are spreading, too.
MRSA, or methicillin-resistant Staphylococcus aureus bacteria, often live on the skin without causing symptoms. But they can become more dangerous if they enter the bloodstream, destroying heart valves or causing other damage. Health officials have tied MRSA to as many as 11,000 U.S. deaths a year.
Public health efforts have focused on MRSA’s spread in hospitals and nursing homes, and infection-control campaigns have been credited for recent drops in MRSA infections at health care facilities.
But as that success story has unfolded, MRSA infections tied to illicit drug use have risen.
The opioid epidemic began with abuse of prescription pain pills, but in recent years has shifted to heroin and other injectable drugs.
MRSA “is on the skin, and as the needle goes into the skin it brings the bacteria with it,” explained Dr. Isaac See of the Centers for Disease Control and Prevention, another of the study’s authors.
The proportion of invasive, bloodstream-infecting MRSA cases that occurred among injection drug users more than doubled in five years, the study found. In 2011, 4 percent of those MRSA cases involved injection drug users; in 2016, the proportion was 9 percent.
The report is based on infections diagnosed at hospitals across Connecticut and in parts of California, Georgia, Minnesota, New York and Tennessee. Data were collected from 2005 through 2016.
About 39,000 invasive MRSA cases were reported, including about 2,100 among people who inject drugs.

Insurer denials for hepatitis C treatment remain high


Despite the availability of certain hepatitis C drugs able to cure most patients, public and private health insurers denied treatment for more than a third of patients whose doctors prescribed the drugs between 2016 and April 2017, according to a study.
Insurance denials were high across all types of insurance plans despite efforts by policymakers and patient advocates to remove reimbursement restrictions, but treatment for commercially-insured patients was denied more often than patients enrolled in Medicaid or Medicare, the study published Thursday in the Open Forum Infectious Diseases journal found.
“I think much of it is a consequence of the cost of the drugs, which are anywhere from $35,000 to $100,000 for the treatment course,” said Dr. Vincent Lo Re, the study’s senior author and an associate professor of infectious disease and epidemiology at the University of Pennsylvania’s Perelman School of Medicine.
The hepatitis C drugs, known as direct-acting antiviral drugs, first became available in 2014 and cure about 95% of people with chronic hepatitis C, a viral liver disease that can cause liver failure or death. It affects about 3.5 million people and kills 19,000 a year, according to the Centers for Disease Control and Prevention.
Examples of the drugs include Harvoni, Sovaldi, Epclusa and Mavyret. The American Association for the Study of Liver Diseases and the Infectious Diseases Society of America recommend these direct-acting antiviral therapies for the treatment of hepatitis C. But the drugs come with high price tags. Harvoni, for example, costs $94,500 for a 12-week course.
Researchers expected denials would have decreased as public health officials gave the disease a vast amount of attention and many new treatments have come to market in recent years.
Researchers analyzed the prevalence of insurance denials among 9,025 patients in 45 states who were prescribed the hepatitis C treatment between January 2016 and April 2017. The data came from Diplomat Pharmacy, one of the largest specialty pharmacies, which was chosen for the study because of its national footprint.
Of the patients prescribed treatment, 3,200 patients, or 35.5%, received a denial from their insurer. Insurers’ requests for alternative oral drug treatments because of formulary restrictions were not counted as denials.
Insurers’ denials increased over the length of study period from a rate of 27.7% in the first quarter to 43.8% in the final quarter of the study.
Commercially insured patients, meaning those who were covered by employer-sponsored insurance or bought coverage on the individual market, received a denial for treatment more than half the time at 52.4%. Insurers denied treatment for 34.5% of Medicaid beneficiaries and 14.7% for Medicare enrollees.
Insurance industry lobbying group America’s Health Insurance Plans said thestudy “paints a misleading and inconclusive picture of coverage of antiviraltherapy for patients suffering from hepatitis C” because it doesn’t reflect whetherprescriptions were later approved after an appeal, and relies on the data of onespecialty pharmacy with claims concentrated in a handful of states. AHIP alsosaid that because the study didn’t look at the reasons for insurer denials,researchers do not know which claims for hepatitis C treatment were clinicallyappropriate or inappropriate. 
Researchers noted that the study was limited by their inability to analyze specificreasons that insurers denied coverage for treatment. That’s because whileinsurers may tell patients why they denied coverage, they don’t tell the specialtypharmacies, so that data was unavailable.
Denials also have increased compared with the rate of denials found by two prior studies published in 2016, the study found. Many insurers restrict reimbursement to only the sickest patients, those who are sober, or those who have seen a specialist. It’s likely that patients who receive denials didn’t have severe enough liver damage, or were active alcohol or drug users, the study notes.
Denials may have also increased over the years because physicians are seeing patients with less severe liver damage more often. When the new hepatitis C drugs first came out, physicians treated patients with very advanced liver fibrosis and cirrhosis who had been waiting years for treatment, Lo Re said. But now that those patients have been treated, doctors are often seeing patients with less damage, he said.
Insurers place reimbursement restrictions on the drugs to save money, but Lo Re said the hepatitis C drug treatments help to eliminate downstream costs.
“Studies show even at minimal stages of liver fibrosis you are saving enormous healthcare dollars by avoiding all the downstream costs of things like liver transplants, hospitalizations to manage end-stage liver disease, and liver cancer,” he said.
The CMS in late 2015 warned states that restricting access to the drugs based on saving costs could violate federal law. After that, class action lawsuits and other litigation against state Medicaid programs sprung up, prompting changes to Medicaid reimbursement of the drugs. But less is known about commercial and Medicare reimbursement.
The rate of denials among commercially insured patients is likely the highest because most attention for hepatitis C drug reimbursement has been directed toward public programs, Lo Re said.
“It warrants greater attention from public health sector, policymakers and advocates to continue to draw attention to access to these drugs, because if we are going to achieve the elimination of hepatitis C as a public health problem…we need to treat a sufficient enough people with chronic hepatitis C to be able to eliminate it,” Lo Re said.

New fed law may spur Medicare Advantage plans to avoid sick enrollees


Insurance companies may decline to offer additional benefits outlined in a new federal law in an effort to dissuade frail seniors from joining their Medicare Advantage programs, according to a new analysis published Wednesday.
The Chronic Care Act, which passed earlier this year, allows insurance companies offering MA plans to pay for non-medical services like installation of raised toilet seats and grab bars in bathrooms or provision of hearing aids, scooters or personal care services. Experts have predicted that covering these services would reduce emergency department use and readmissions.
The law’s goal was to integrate coverage and access to both medical and non-medical services. Under the statute, Medicare Advantage plans can offer these new benefits starting in 2020.
But insurance companies may decline to offer the expanded coverage to stop severely ill seniors who need costly care from joining their plans, according to the analysis in the New England Journal of Medicine. The piece was co-authored by a professor at University of Maryland School of Public Health and a scientist at Johns Hopkins Bloomberg School of Public Health.
There are significant Medicare spending differences for beneficiaries with functional impairment and those without such impairment, according to the co-authors..
To avoid this disincentive from offering new benefits, lawmakers should require fee-for-service Medicare to cover non-medical services too, according to David Lipschutz, senior policy attorney at the Center for Medicare Advocacy.
“It’s a matter of basic equity and its leaving the majority of Medicare patients without access to the new services,” Lipschutz said.
But insurance companies said the concerns highlighted in the analysis were overblown.
“The argument being made by these authors is speculative and does not recognize some of the important realities of the Medicare Advantage program,” said Cathryn Donaldson, a spokeswoman for AHIP.
Average spending on Medicare Advantage is roughly equivalent to Medicare fee-for-service and plans regularly work to direct resources to enroll more complex, chronically ill individuals, she added.
In addition, the analysis seems to ignore the existence of Medicare Advantage Dual Eligible Special Need Plans (D-SNPs), according to Dr. Cheryl Phillips, President and CEO SNP Alliance, a trade organization. These plans already enroll and coordinate care for some of the most chronically ill Medicare beneficiaries.
“This article seems to imply that MA plans will avoid high risk and high-cost beneficiaries, yet, that is the very population that SNPs serve,” Phillips said.

Biogen Options Stroke Drug from TMS in Deal That Could Hit $357M


Biogenheadquartered in Cambridge, Massachusetts, signed an exclusive option deal with Tokyo-based TMS for TMS-007 and backup compounds.
TMS-007 is a plasminogen activator associated with the breakdown of blood clots. It is also believed to inhibit local inflammation at the site of thrombosis. The combination gives the drug a shot at being best-in-class for treatment of acute ischemic stroke (AIS). The drug has shown an acceptable safety profile in a Phase I clinical trial and also reduced infarct volume, the among of dead tissue caused by the failure of blood supply, in rodent and primate models. It is currently being evaluated in a double-blind, placebo-controlled Phase II trial in Japan.
Biogen is paying $4 million upfront with an additional $18 million if Biogen exercises its option. TMS will be eligible for up to $335 million in development and commercialization milestones in addition to tiered royalties.
“Stroke represents a compelling opportunity that takes advantage of our deep expertise and capabilities in neuroscience as we seek to make a meaningful difference in patients’ lives,” said Michael Ehlers, Biogen’s executive vice president, Research and Development, in a statement. “Stroke impacts millions of people every year, and is a leading cause of death and long-term disability worldwide. TMS-007 complements our broader efforts in stroke, including our Phase III ready asset BIIB093 (intravenous glibenclamide), which targets prevention and treatment of edema in large hemispheric infarction, one of the most severe types of stroke. By growing our acute neurology portfolio, we aim to make new advances in a disease that in the past decades has seen limited therapeutic innovation.”
While much of the focus on Biogen has been about its ongoing Phase III clinical trial of aducanumab for Alzheimer’s disease, the company has been making a number of smaller investments such as this one to build up its neurology pipeline. It recently expanded an alliance with Ionis Pharmaceuticals to develop RNA-based drugs for brain diseases. It bought glibenclamide when it acquired New York-based Remedy Pharmaceuticals in 2017 for $120 million.
In March, Biogen bought PF-04958242 from Pfizer, a Phase IIb-ready AMPA receptor potentiator for cognitive impairment associated with schizophrenia. In November 2018, Biogen inked a global license and collaboration deal with Alkermes to develop and commercialize ALKS 8700, a novel, oral, monomethyl fumarate small drug molecule in Phase III to treat relapsing forms of multiple sclerosis (MS). In October 2017, Biogen and Japan-based Eisai Co expanded an existing deal to jointly develop and commercialize aducanumab for Alzheimer’s.
And in April 2017, the company licensed BMS-986168, a Phase II-ready drug for Alzheimer’s and progressive supranuclear palsy (PSP) from Bristol-Myers Squibb.
For some time, investors and analysts have wanted Biogen to make a large transformative deal, ranging from buying Ionis to acquiring Acadia. This is largely because much of the company’s revenues come from its drugs for MS, which are facing stiff competition. However, the company seems content, so far, of staying focused on marketing its MS drugs and Spinraza for spinal muscular atrophy (SMA), which went on the market in 2017, leaning heavily on its aducanumab program, and building up its pipeline for other neurological disorders.

Pfizer started at buy by Cantor

Cantor analyst Louise Chen initiated Pfizer with an Overweight and $45 price target.

Genetech gets FDA OK for Rituxan for 4th autoimmune indication


Genentech, a member of the Roche Group, announced that the U.S. Food and Drug Administration has approved Rituxan for the treatment of adults with moderate to severe pemphigus vulgaris, a rare, serious, potentially life-threatening condition characterized by progressive painful blistering of the skin and mucous membranes. Rituxan is the first biologic therapy approved by the FDA for PV and the first major advancement in the treatment of the disease in more than 60 years. The FDA previously granted Priority Review, Breakthrough Therapy Designation and Orphan Drug Designation to Rituxan for the treatment of PV. With today’s FDA decision, Rituxan is now approved to treat four autoimmune diseases.

Ionis Pharma closes on collaboration with Biogen to develop neurological drugs


Ionis Pharmaceuticals, Inc. announced that it closed its expanded strategic collaboration with Biogen to discover and develop novel antisense drugs for a broad range of neurological diseases following receipt of clearance under the Hart-Scott-Rodino (HSR) Antitrust Improvements Act of 1976. Biogen paid Ionis $1 billion in cash, which included $625 million for the purchase of 11,501,153 shares of Ionis common stock at a price of $54.34 per share and a $375 million upfront payment.
On April 20, 2018, Ionis and Biogen announced they would expand their strategic collaboration to develop novel antisense drugs for a broad range of neurological diseases through a new ten-year collaboration. This collaboration capitalizes on Ionis’ leadership in RNA-targeted therapies as well as Ionis and Biogen’s joint expertise in neuroscience research and drug development. It builds upon a productive collaboration that produced Spinraza (nusinersen), the first and only approved treatment for patients with spinal muscular atrophy.
The companies plan to advance programs for a broad range of neurological diseases for which few treatment options exist today. Disease areas include dementia, neuromuscular diseases, movement disorders, ophthalmology, diseases of the inner ear, and neuropsychiatry.
Ionis will be responsible for the identification of antisense drug candidates based on selected targets, while Biogen will have the option to license therapies arising out of this collaboration and will be responsible for and pay for non-clinical studies, clinical development, manufacturing, and commercialization. In addition, Biogen may pay milestone payments, license fees and royalties on net sales.
Ionis is the leading company in RNA-targeted drug discovery and development focused on developing drugs for patients who have the highest unmet medical needs, such as those patients with severe and rare diseases.