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Tuesday, May 15, 2018

3 Ways Amazon Could Transform Health Care

Amazon.com, Inc. AMZN 1.59% was reported last week to be building out a health and wellness team within its Alexa division to better integrate the assistant in health care.
Loup Ventures considers this program just the start of a broader, three-pronged invasion of the $3.3 trillion industry.
“Companies across the entire healthcare industry are quickly discovering that AI will be used in everything from operations to enhancing quality of life for patients,” Loup Ventures managing partner Andrew Murphy wrote in a note.

PBM Shakeups

The firm could transform logistics in the $453 billion pharmacy benefit management industry.
“Rising drug prices and rising drug demand has driven considerable backlash recently among American consumers,” Murphy wrote. “We feel this could be a golden ticket for disruption to a cost-conscious, logistics expert like Amazon.”

Provider Interactions

Alexa and Amazon’s artificial intelligence could support telehealth care programs and streamline paperwork to improve time spent with patients. At the same time, it could remind patients to take medicine, help manage care for diabetics or alert staff of emergencies.
“Imagine the safety, information, connectivity, and entertainment that an Alexa near every hospital bed could offer patients,” Murphy wrote.

Patient Data Networks

Amazon Web Services can provide storage, analytics and management tools for electronic health record systems. Cerner Corporation CERN 1.27% already leverages Amazon’s data analytics to coordinate care.

Gilead Sets CAR-T Manufacturing Toehold in Europe Ahead of EMA Decision

In anticipation of marketing approval in Europe, Gilead Sciences has leased a 117,000 square-foot facility in The Netherlands to manufacture and deliver Yescarta, its CAR-T product, to patients across Europe.
The new facility, located in Hoofddorp near the Amsterdam Airport, will engineer and produce Yescarta, which is currently under review by the European Medicines Agency. Yescarta was approved in the United States last year, the second CAR-T therapy given the green light by the U.S. Food and Drug Administration. When the site is fully operational by 2020, Gilead, the parent company of Kite Pharmaceuticals, said the facility will employ approximately 300 people. In Europe Gilead is seeking approval of Yescarta as a treatment for patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL), transformed follicular lymphoma (TFL), and primary mediastinal B-cell lymphoma (PMBCL) who are ineligible for autologous stem cell transplant.
John F. Milligan, Gilead’s president and chief executive officer, said the company was pleased to be “leading a new frontier of cancer innovation.”
This new European manufacturing facility will enable personalized cell therapies to be manufactured in closer geographic proximity to the patients who will receive them, potentially shortening the turnaround time for people who urgently need care,” Milligan said in a statement.
If Yescarta is approved in Europe it will be essential to have a CAR-T manufacturing facility on the continent in order to develop the personalized medicines within a short period of time and return them to the patients for treatment. Being close to the airport will be critical for the logistics needed to ensure safe manufacturing and delivery of the treatment.
Gilead acquired Kite in August 2017 ahead of the FDA’s October approval of Yescarta, a treatment for adult patients with relapsed or refractory large B-cell lymphoma. In the U.S. Gilead manufactures Yescarta n El Segundo, Calif., about 10 miles from the Los Angeles International Airport.
In addition to the Netherlands site, Gilead and Kite said it has also done acquired more space in the United States to expand its clinical manufacturing capabilities. Gilead purchased a new building space in Santa Monica, Calif. that was previously owned by Astellas Pharma Inc. Gilead said it will be used for cell therapy research, development and the expansion of clinical manufacturing capabilities. The company also leased a 26,000 square-foot facility in Gaithersburg, Md. to support the work of a new Cooperative Research and Development Agreement (CRADA) with the National Cancer Institute (NCI) to develop adoptive cell therapies targeting patient-specific tumor neoantigens. Neoantigens are mutations found on the surface of cancer cells that are unique to each person and tumor, offering the potential for more targeted antitumor activity. The company did not provide information at this time as to how many people could be employed at the two new U.S. sites.
Alessandro Riva, Gilead’s head of Oncology Therapeutics and head of cell therapy, said the three new facilities and the expanded CRADA with our research collaborators at the NCI will “help us bring cell therapies to more people with cancer around the world.”

In early test, Inovio HIV vax delivered immune responses lasting > 6 months

Aiming at one of the biggest targets in vaccine development, Inovio reported that its HIV vaccine, Pennvax-GP, induced immune responses that lasted at least six months after vaccination in a phase 1 study.
Dubbed HVTN 098, the study tested the shot in combo with an immune activator IL-12 in 94 participants, 84 of whom received the vaccine combo. Nine participants received a placebo injection.
Last year, the biotech reported that 71 of 76 (93%) of vaccinated subjects showed a T-cell immune response—CD4+ or CD8+—and that 62 of 66 showed antibody responses. No placebo recipients showed an immune response.
This week, the company said “immune responses were maintained in most subjects” six months after vaccination. The percentage of participants who showed CD8+ T cell responses “stayed the same or even increased slightly,” according to the biotech. In a statement, Inovio CEO Dr. J. Joseph Kim said the company looks forward to advancing its shot into later-stage testing.
Inovio is developing the vaccine as part of a collaboration with the National Institute of Allergy and Infectious Diseases that started with a $25 million contract in 2009. Since then, NIAID awarded another $16 million grant. The HIV Vaccine Trials Network is also involved in the work.
Aside from HIV, the biotech is researching vaccines against Ebola, MERS and Zika, plus a later-stage program designed to treat cancers caused by HPV.
HIV vaccines are one of the biggest targets in vaccine development, and the field has attracted some top global players in recent years.
Johnson & Johnson’s Janssen and partners reported last year that a “mosaic” HIV vaccine was well-tolerated and elicited HIV-1 antibody responses in a phase 1/2a study in 400 patients across the U.S, Rwanda, Uganda, South Africa and Thailand. The team designed the vaccine to protect against HIV subtypes all over the world, whereas past vaccines would have been limited to certain regions, the lead investigator said at the time.
Inovio, for its part, says its vaccine consists of four antigens to elicit cell and antibody responses, and to protect against HIV types across the globe.
Since the early-stage results from J&J, the team kicked off a first efficacy study late last year, planning to test the vaccine in 2,600 sexually active women between the ages of 18 and 35 in five southern African countries. At the time, Hanneke Schuitemaker, Janssen’s head of viral vaccines discovery and translational medicine, told FiercePharma that in order to develop a “global vaccine,” other efficacy tests would be needed.
But before J&J and that team advanced to efficacy testing, the NIH touted the start of a “historic” 2b/3 study in South Africa in late 2016. The regimen incorporates one experimental vaccine each supplied by Sanofi Pasteur and GlaxoSmithKline, combined with a GSK-supplied adjuvant called MF59. Results from the trial are expected in 2020.
Plenty of other HIV vaccines are in the works, including at GeoVax and Aelix Therapeutics.

Feds join claims Insys used strip clubs, super-doses, more to up Subsys sales

Prosecutors have already charged Insys founder John Kapoor and won guilty pleas from two characters in an ongoing kickbacks probe. Now, the Justice Department has escalated the case by joining in with whistleblowers who’ve detailed a stunning range of techniques the company allegedly used to push its powerful opioid painkiller.
The DOJ is allying with a half-dozen whistleblowers—among them former Insys employees and workers at a pharmacy benefits manager—who allege the company violated the federal False Claims Act by marketing Subsys for unapproved uses and using free dinners and entertainment to persuade doctors to prescribe more of its fentanyl nasal spray.
Six states also joined the litigation, according to the government’s filing. The action comes just two months after the DOJ charged five New York doctors with participating in the alleged kickback scheme and revealed that two former Insys employees pleaded guilty and are now cooperating with the government. The DOJ has requested that the False Claims litigation be held until the criminal cases against Insys are completed.
Insys released a statement Tuesday saying it is engaged in an ongoing dialog with the DOJ. When the company’s founder, John Kapoor, was charged with racketeering back in October, he issued a statement saying he was confident he would be vindicated. The company had previously told investors it may have to spend $150 million to settle charges against it, and its discussion with the DOJ “has not resulted in information that would cause the company to revise this estimate,” according to Tuesday’s statement.
Insys has undergone a management overhaul, and said in the statement that it is now “a completely transformed organization, with a promising pipeline, a strong commitment to serving patients as well as an organizational culture of high ethical standards.”
The government’s newly unmasked case alleged that starting in 2012, Insys operated a “sham” speaking program, paying physicians to talk about Subsys to healthcare professionals. In reality, the suit alleges, the speeches didn’t include “substantive” information about the drug.
“Many of these speeches have been attended only by the prescriber’s own office staff, by close friends who attended multiple presentations, or by people who were not medical professionals and had no legitimate reason for attending,” the suit reads.
The court document goes on to lay out the types of kickbacks Insys allegedly provided, including visits to strip clubs, “lavish” dining and entertainment outings and jobs for relatives and friends of people who prescribed Subsys. It details the actions of more than 19 prescribers and Insys sales representatives, including some who have been convicted for their roles in the company’s alleged kickback schemes.
They include Heather Alfonso, a nurse from Connecticut, and Natalie Levine, an Insys sales representative, both of whom pleaded guilty to violating antikickback statutes. Alfonso took $83,000 in speaking fees from Insys for more than 70 dinner speeches, according to the lawsuit, resulting in charges to Medicare of more than $1.2 million for Subsys prescriptions.
Many of the prescribers described in the DOJ’s suit were pain-management specialists whom Insys paid to speak at events typically attended only by the prescribers’ employees. A Pennsylvania doctor, for example, was paid $100,000 for 40 speeches, and the doctor’s daughter got a job as an Insys sales representative shortly after graduating college, the lawsuit stated. Medicare paid $4 million for Subsys prescribed by that doctor, the government alleged.

The case against Insys revolves around allegations that the company marketed Subsys to treat many types of pain, though it was only FDA-approved for cancer pain. The DOJ’s lawsuit offers examples of Insys training sales representatives to pitch the product for those off-label uses.
“When a patient’s in pain and it’s a severe pain … is it different they have cancer pain … or is it different they got, like, back pain … That’s the whole point, pain is pain,’” one executive said during a sales meeting, according to the suit.
Most of the patients who received Subsys prescriptions weren’t cancer patients, the lawsuit alleged. The government is seeking reimbursement for Medicare spending on scripts for patients who shouldn’t have been covered, as well as “recovery of all monies by which Insys has been unjustly enriched.”
The unsealed DOJ lawsuit reveals that the first whistleblower case against Insys was filed in 2013 by Maria Guzman, a former Insys employee. Her suit, which was simultaneously unsealed, alleged that in addition to paying speaking fees to prescribers, Insys encouraged physicians to prescribe Subsys doses as high as 800 micrograms—eight times the dosage recommended by the FDA.
In 2012, Guzman alleged, Insys created a new marketing campaign some dubbed “the kiss of death message.” Insys representatives were told to advise doctors that 100 micrograms of Subsys was not enough to relieve pain. Managers sent emails to sales reps daily reporting prescriptions below 400 mcg.
One employee who persuaded a doctor to switch a patient from a competing drug to Subsys at a dose of 1,200 micrograms received a congratulatory email—“Cha Ching again!” That was a reference to the $40,320 Insys would reap from that single prescription, Guzman’s whistleblower suit alleged.
In a single week in 2013, the lawsuit claims, 12 new patients went on Subsys for the first time, each at an average starting dose of 600 micrograms. Only one was prescribed the FDA-recommended dose of 100 micrograms.

Zymeworks could get up to $485M in expanded Daiichi immuno-oncology deal

When Zymeworks and Daiichi Sankyo initially teamed up on bispecific antibodies in 2016, they kept the financial details under wraps. Now, the pair is entering a new license agreement that could potentially be worth $484.7 million.
Under the original deal, Zymeworks licensed its Azymetric and Efect platforms to Daiichi Sankyo to develop a bispecific antibody therapy, for which Zymeworks is eligible to pick up milestone payments and royalties. It also received a license to certain immuno-oncology antibodies from Daiichi with the right to research, develop and market multiple bispecific products in exchange for royalties.
The new agreement sees the Vancouver-based biotech granting the Japanese pharma two more licenses for an upfront technology access fee of $18 million. It stands to receive up to $466.7 in clinical, regulatory and commercial milestones, with tiered royalties also up for grabs.

“Expanding our relationship with a leading global pharmaceutical partner like Daiichi Sankyo is extremely satisfying as it underscores the power, versatility and attractiveness of our technology platforms,” said Ali Tehrani, Ph.D., president and CEO of Zymeworks. “Having already used our platforms to discover one bispecific antibody, Daiichi Sankyo now has increased access to our technology to create additional therapeutic candidates. We are pleased to be working with a healthcare pioneer with a proven track record of over 100 years of innovation leading to major breakthroughs in patient care.”
The Azymetric technology works by doubling up on a drug’s potential target, offering a complementary approach to the Efect platform, a library of antibody Fc modifications that can be used to orchestrate an immune response: either turning it up or tamping it down.
Zymeworks has been on a dealmaking roll over the past few years. This includes an agreement with Janssen last November around six bispecific antibodies that saw it pick up $50 million up front, with another potential $282 million in development milestones and up to $1.12 billion in sales payments. Also in 2017, Zymeworks inked an R&D pact with The University of Victoria and BC Cancer Agency to develop engineered cytokine and cytokine receptor pairs.

Tactile Systems Technology outlook

Tactile Systems Technology Inc:
* FOR 2018, COMPANY NOW EXPECTS REVENUES IN RANGE OF $132 MILLION TO $134 MILLION
* TACTILE SYSTEMS TECHNOLOGY – QTRLY LOSS PER SHARE $0.00
* REVENUES FOR Q1 2018 INCREASED $7.0 MILLION, OR 35%, TO $26.8 MILLION, COMPARED TO $19.9 MILLION FOR QUARTER ENDED MARCH 31, 2017
* Q1 REVENUE VIEW $23.7 MILLION — THOMSON REUTERS I/B/E/S

Jazz estimates, target upped by Wells Fargo

Jazz Pharmaceuticals price target raised to $182 from $176 at Wells Fargo. Wells Fargo analyst David Maris maintained an Outperform rating on Jazz Pharmaceuticals and raised his price target to $182 from $176 on Jazz shares. The analyst also raised his 2018 EPS estimate to $13.00 from $12.91 after Jazz’s beat and raise quarter, and raised his outer year Xyrem growth forecasts from 8% to 10% in 2019, from 6% to 8% in 2020 and from 4% to 5% in 2021, based on Xyrem’s return to stronger growth in Q1. Maris concluded that he liked ” the conservative balance sheet and potential for strategic deals, the current sales trends, and the focus on pipeline progress.”