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Monday, July 9, 2018

FDA Grants Eagle 7 Year Orphan Drug Exclusivity for Lead Med


Eagle Pharmaceuticals, Inc. (Nasdaq: EGRX) (“Eagle” or the “Company”) announced today that the U.S. Food and Drug Administration (FDA) has granted seven years of orphan drug exclusivity (ODE) in the U.S., for BENDEKA™ (bendamustine hydrochloride injection, or bendamustine HCI), a liquid, low-volume (50 mL) and short-time 10-minute infusion formulation of bendamustine hydrochloride.
As a result, and consistent with the order issued by the U.S. District Court for the District of Columbia (the Court) on June 8, 2018, the FDA will not approve any drug applications referencing BENDEKA until the ODE expires in December 2022. Additionally, on July 7, 2018, the FDA filed a motion with the Court asking it to clarify that the order was not intended to affect applications referencing TREANDA®. Eagle continues to believe that an appropriate application of ODE would first allow generic TREANDA entrants in December 2022, rather than November 2019, and expects to vigorously defend the scope of its exclusivity grant.

BD Acquires TVA Medical to Advance Solutions for Chronic Kidney Disease


BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today announced it has completed the acquisition of TVA Medical, Inc., a company that develops minimally invasive vascular access solutions for patients with chronic kidney disease requiring hemodialysis.
In the U.S. alone, there are more than 440,000 patients with End-Stage Renal Disease (ESRD) who are surviving on hemodialysisi. The addition of TVA Medical enables BD to offer the everlinQ™ endoAVF System, a new endovascular arteriovenous (AV) fistula creation technology that adds to the company’s ESRD portfolio of dialysis catheters, drug coated balloons, standard angioplasty balloons and endovascular stent graft products. This technology will further improve BD’s ability to serve physicians and their patients by providing a minimally invasive option for creating critical AV fistulas (joining arteries to veins to create a circuit) for hemodialysis procedures.
“The addition of TVA Medical allows BD to provide another innovative device to physicians who treat patients suffering from chronic kidney disease requiring hemodialysis,” said Steve Williamson, worldwide president of Peripheral Intervention at BD. “This technology is highly complementary to our Peripheral Intervention offerings, and we will continue to bring new technologies to market that improve our category-leading ESRD portfolio. This is a great example of our continued strategy to use tuck-in acquisitions to advance category leadership.”
Hemodialysis, a form of treatment for kidney failure patients, is a procedure that removes wastes, salts, and fluid from a patient’s blood when the kidneys can no longer perform these functions. Vascular access is considered a “lifeline” for hemodialysis patients. Options for vascular access include central venous catheters, AV grafts and surgical AV fistulas. Surgical fistulas are currently the preferred vascular access option for hemodialysis patients, resulting in lower mortality rates, fewer infections and lower cost of dialysis delivery compared to central venous cathetersii,iii,iv.
On June 22, the U.S. Food and Drug Administration (FDA) announced De Novo marketing authorization for the everlinQ endoAVF System. The system uses two, thin, flexible, magnetic catheters that are inserted into the ulnar artery and the ulnar vein in the arm through a small puncture. When placed close to each other, the magnets in each catheter attract, pulling the vessels together. After confirming alignment, an electrode from the venous catheter delivers radiofrequency energy to create the connection between the artery and vein. Embolization of the brachial vein is then recommended. The fistula is confirmed with an angiogram (X-ray image of the vascular system) to show that arterial blood is flowing to the low-pressure venous system. The procedure minimizes the amount of vessel and skin trauma compared to traditional fistula creation using open surgery. The everlinQ endoAVF System enables an additional AV fistula location for patients than what is typically done surgically. The device is already commercially available in Europe and Canada. For more information on the everlinQ endoAVF System, visit http://tvamedical.com/product/. The product name will be transitioned to WavelinQ™ EndoAVF System during integration.
“The FDA’s authorization and joining BD are the culmination of many years of hard work by a dedicated team of innovators at TVA Medical, and I’d like to thank them for their tireless efforts to get us to these important milestones,” said Adam L. Berman, co-founder of TVA Medical. “BD will enable us to deliver to physicians and patients what we believe is a highly-desirable and transformative endovascular technology as an integral part of a broader ESRD-focused portfolio of solutions. I look forward to the next chapter of our history as part of the BD family.”
This transaction is not expected to have a material impact on BD results for fiscal 2018 or 2019. Future results for TVA Medical will be reported under the Peripheral Intervention business within the Interventional Segment at BD. The company used cash on hand to finance the transaction. This transaction does not impact the company’s previously-communicated commitment to deleverage as part of the Bard acquisition. Terms of the transaction were not disclosed.

Guideline Care Fails to Boost Survival in Younger Rectal Cancer Patients


Patients with rectal cancer who are younger than 50 do not have an overall survival benefit from National Comprehensive Cancer Network (NCCN) guideline-driven care, researchers found.
The results suggest, the investigators said, that early-onset stages II and III rectal cancer in this younger group may differ in epidemiology, biology, and response to therapy compared with in older patients.
In the study, published online in Cancer, Andrew Kolarich of the University of Florida College of Medicine in Gainesville, and colleagues noted that because current NCCN guidelines for treating rectal cancer are based primarily on trials or databases with older patients, the team wanted to see how those treatment guidelines affected survival patterns in patients younger than 50.
As Conor Delaney, MD, PhD, chair of the Digestive Disease and Surgery Institute at the Cleveland Clinic, recently told MedPage Today, studies have shown that the incidence of colon and rectal cancer among younger patients has been increasing.
Kolarich et al performed a retrospective review of the National Cancer Data Base (NCDB), analyzing patients treated with curative-intent transabdominal resections with negative surgical margins for stages I to III rectal cancer between 2004 and 2014.
A total of 43,106 patients were included in the analysis, with outcomes and overall survival for patients under and over age 50 compared by subgroups based on NCCN guideline-driven care. About 21% of patients (9,126) were younger than 50, which is younger than the age at which the guidelines recommend screening should begin.
The researchers found that while patients younger than 50 showed a survival benefit from NCCN guideline-drive care for stage I disease, no such survival benefit was demonstrated when the guidelines were followed for stages II and III disease.
“These data may help to stimulate future trial proposals to investigate the possibility of the exclusion or selective use of adjuvant therapies for stage II and III disease in the younger cohort to help to decrease treatment toxicity,” Kolarich et al wrote.
They also found key differences between younger and older rectal cancer patients. For example, younger patients were more likely to be female, minorities, and uninsured. They were also more likely to be diagnosed at a higher stage and have poor tumor differentiation and other histological features associated with worse outcomes — data that could provide physicians with the ability to provide prognoses tailored to younger populations.
In an editorial accompanying the study, titled “Rectal Cancer in Young Patients: Time to Take Notice,” Matthew F. Kalady, MD, of the Cleveland Clinic, said the researchers should be applauded for continuing the conversation about young patients with rectal cancer.
“This article should open the eyes of physicians treating rectal cancer and of those making treatment guideline recommendations and screening policies,” he wrote. “The alarming trend of increased colorectal cancer in the young population should make us stand up and take notice. We need to evaluate why this is happening and explore the unique characteristics that define this population and potential differences in comparison with older age rectal cancers.”
Still, there are several limitations to studies based on data in large administrative data bases such as the NCDB, Kalady pointed out: For example, half of all patients with rectal cancer were excluded from the analysis by Kolarich et al because of missing data, and even for those patients included in the study, key variables such as tumor location, clinical circumferential margin, the number of lymph nodes evaluated, and the quality of the surgical specimen, were unavailable.
Delaney, who was not involved in the study, echoed Kalady in noting that the researchers focused on a population that in the past has not been well studied. “I think the most important thing about this paper is that it’s highlighting the frequency — and problems — in younger people getting rectal cancer,” Delaney said. “Overall we have done pretty well in the last couple of decades, and survival has improved for colorectal cancer. But it’s clear that the frequency of colorectal cancer in younger people is increasing.”
Delaney also pointed out that the American Cancer Society recently updated its colorectal screening guidelines to reflect the fact that the numbers are showing that new cases of colorectal cancer are occurring at an increasing rate among younger adults.
“[The thinking] used to be that screening should start with patients over 50 years of age. As a professional group we’ve made the recommendation that this age group should be dropped to 45. Screening now is recommended for all people over the age of 45, and [even younger if there is] a family history of colorectal cancer.
“That’s not enough – all of us who do a lot of this have many patients much younger than 45 who have rectal or colon cancer,” Delaney added. “The other important message for the public is to remind them that if they have symptoms, they have to be investigated.”
Kolarich reported having no conflicts of interest; one co-author reported financial relationships with Merck and Bayer for work outside of the study, as well as institutional research support from Incyte, Bristol-Myers Squibb, Bayer, Merck, NewLink, AstraZeneca/Med-Immune, and Tesaro.
Kalady reported having no conflicts of interest.

Azar Calls for Changes in 340B Drug Pricing Program


Health and Human Services Secretary Alex Azar continued his campaign against high drug prices on Monday, calling for more oversight of hospitals that get drug discounts under the federal 340B program because they serve many uninsured and low-income patients.
“By one estimate, discounted purchases under 340B totaled $16 billion in 2016 — a fourfold increase just since 2009,” Azar said at the annual meeting of 340B Health, a trade group for 340B hospitals. “Government programs can grow pretty fast, but they usually don’t grow that fast.”
“This growth has occurred without any increase in statutory oversight,” he continued. “HHS works hard within the powers we have to oversee the program. But a comprehensive system for reporting on the distribution and use of the program’s benefits does not exist … The current nature of 340B is such that it is quite possible for the program’s benefits to be diverted to unintended purposes, unrelated to supporting care for low-income patients.”
For example, Azar said, “the acquisition of outpatient clinics by 340B entities has meant that a Medicare patient could pay cost-sharing on the full price of a Part B drug administered in their doctor’s office, while the doctor’s office gets the drug at a large discount that will never be known to the patient, was never intended to support care for that kind of patient, and may not be used to support care for low-income patients at all. Indeed, the discount may be so steep that the patient’s cost-sharing is greater than the price their doctor paid for the drug.”
He called for two kinds of reforms for the 340B pricing program: “greater transparency surrounding how these discounts are being used, and reforms to reduce the gap between discounted prices and the reimbursement provided, particularly by government programs.”
“We believe changes along these lines are essential to the future of the 340B program,” Azar added. “Leaving a program as it is, within the rapidly changing context of healthcare, quickly renders it outdated.”
Maureen Testoni, 340B Health’s interim president and CEO, seemed taken aback by Azar’s remarks when she spoke after Azar left the lectern. “I credit the secretary with coming here,” she said. “It certainly gives me my marching orders going forward; we have a lot of work to do.”
“They came out with their blueprint and they are obviously concerned about an impact the 340B program may be having on the market and how the 340B dollars are being used,” Testoni told MedPage Today in a meeting with reporters afterward, with a media relations representative present. “Incumbent on us from the provider community to make that clear and educate the administration and members of Congress on how valuable the program is — the fact that they do so much more uncompensated care than other types of hospitals and see so many more Medicaid patients. We’re worried that is getting lost and we really need to make sure we get that out.”
“What’s not getting as much attention is all this publicly available data on how much uncompensated care 340 B hospitals provide,” said Testoni. “[If you compare] how much is being spent on [the 340B] discount compared to how much uncompensated care 340B hospitals provide, it’s just a fraction.”
Azar’s remarks came only a few days after a report from the Government Accountability Office (GAO) faulted the Health Resources and Services Administration (HRSA) for lax oversight of 340B contract pharmacies — mainly retail and independent pharmacies that 340B hospitals contract with to provide drugs to patients.
The GAO listed three main problems with HRSA’s work: lack of data on how many contract pharmacies are participating in the program; weaknesses in the audit process; and lack of specific guidance for the providers involved.
“As currently structured, weaknesses in HRSA’s oversight impede its ability to ensure compliance with 340B program requirements at contract pharmacies,” the report’s authors concluded. “As the 340B program continues to grow, it is essential that HRSA address these shortcomings.”
Azar didn’t just aim his remarks at 340B hospitals; he also repeated his criticism that pharmaceutical manufacturers weren’t taking seriously the administration’s call to lower their prices. “The drug companies that recently increased prices will be remembered for creating a tipping point in U.S. drug pricing policy. As you may have recently seen on Twitter, the President’s noticed, I’ve noticed, and, more importantly, the American people have noticed. Change is coming to prescription drug pricing, whether it’s painful or not for pharmaceutical companies.”
Azar was referring to a tweet from President Trump, which called out Pfizer and other companies for raising their prices. “Pfizer & others should be ashamed that they have raised drug prices for no reason,” Trump tweeted early Monday afternoon. “They are merely taking advantage of the poor & others unable to defend themselves, while at the same time giving bargain basement prices to other countries in Europe & elsewhere. We will respond!”
At the end of May, Trump predicted that “people will see for the first time ever in this country a major drop in the cost of prescription drugs … I think we’re going to have some big news … Some of the big drug companies are going to announce voluntary massive drops in prices.” No such decreases have yet occurred.

Strayer: Capella gets approval of change of ownership from regional accreditor


Strayer Education announced that Capella University received notice that its regional accreditor, the Higher Learning Commission, has approved the change of ownership of Capella University in connection with the merger between Capella University’s parent company, Capella Education Company, and Strayer Education, Inc., the parent company of Strayer University, which will change its name to Strategic Education, Inc. The merger is expected to close on or before August 1.

Celgene, Acceleron hit endpoints in Phase 3 blood disorder study


Celgene Corporation (CELG) and Acceleron Pharma (XLRN) announced results from a phase III, randomized, double-blind, multi-center clinical study. Luspatercept achieved a highly statistically significant improvement in the primary endpoint of erythroid response, which was defined as at least a 33 percent reduction from baseline in red blood cell transfusion burden with a reduction of at least 2 units during the protocol-defined period of 12 consecutive weeks, from week 13 to week 24, compared to placebo. BELIEVE evaluated the efficacy and safety of luspatercept plus best supportive care versus placebo plus best supportive care in adults with transfusion-dependent beta-thalassemia. In addition to achieving the primary endpoint of the study, luspatercept also met all key secondary endpoints of demonstrating statistically significant improvements in RBC transfusion burden from baseline of at least a 33 percent reduction during the period from week 37 to week 48, at least a 50 percent reduction during the period from week 13 to week 24, at least a 50 percent reduction during the period from week 37 to week 48, and a mean change in transfusion burden from week 13 to week 24. Adverse events observed in the study were generally consistent with previously reported data. The companies also recently announced that luspatercept met the primary and key secondary endpoints in the MEDALIST study, a phase III, randomized, double-blind, multi-center clinical trial evaluating the efficacy and safety of luspatercept versus placebo in patients with IPSS-R very low, low or intermediate risk myelodysplastic syndromes with chronic anemia and refractory to, intolerant of, or ineligible for treatment with an erythropoietin-stimulating agent, ring sideroblast-positive and require frequent RBC transfusions. Data from BELIEVE and MEDALIST will be submitted to a future medical meeting in 2018. The companies plan to submit regulatory applications for luspatercept in the United States and Europe in the first half of 2019. Luspatercept is not approved for any indication in any geography.

Pfizer responds to Trump, says list price ‘unchanged’ for majority of medicines


CNBC’s Meg Tirrell tweeted a statement from Pfizer in response to an earlier tweet sent from U.S. President Donald Trump about drug prices. “The list price remains unchanged for the majority of our medicines,” Pfizer said. “Our portfolio includes more than 400 medicines and vaccines; we are modifying prices for approximately 10% of these, including some instances where we’re decreasing the price. Importantly, list prices do not reflect what most patients or insurance companies pay. In the first quarter of 2018 the net selling price increase was 0% due to the growing amount of rebates paid back to stakeholders in the biopharmaceutical supply chain.”