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Tuesday, April 6, 2021

Amarin launches Vascepa in all-important Europe as it slowly bleeds share to U.S. generic

 A drug’s EU launch seldom becomes more important than its U.S. rollout from a market opportunity perspective, but that’s exactly what’s happening to Amarin’s fish oil-derived heart drug Vascepa.

Amarin has started prepping sales reps in Germany for the planned launch of Vascepa—to be sold under the brand Vazkepa in Europe—before the end of September, the company said Tuesday. By mid-second quarter, it expects to have about 150 marketing staffers in place for product and disease awareness programs.

As Vascepa’s already facing a generic made by Hikma in the U.S. after losing a patent defense in an appeals court, industry watchers have pinned a large part of the drug’s commercial potential on the EU market. In an investor note on Tuesday, Cantor Fitzgerald analyst Louise Chen pegged the European opportunity at $1.1 billion in 2029, out of a total of $1.6 billion for Amarin that year.

Vazkepa won its official EU go-ahead a week ago. By SVB Leerink analyst Ami Fadia’s estimates, the drug’s EU label is broader than expected; the EU total addressable market could be 105% that of the U.S., she wrote in a note in February, when drug reviewers at the European Medicines Agency backed the drug’s approval.

In Europe, the drug can be used to reduce the risk of cardiovascular events in high-risk, statin-treated patients who have elevated blood fat and either established heart disease or diabetes plus at least one additional cardiovascular risk factor. In the U.S., the latter part of the indication requires patients to have diabetes and at least two additional risk factors.


During a recent SVB Leerink event, Amarin management also noted a higher prevalence of statin use as well as heart disease death rate in the EU, highlighting the EU opportunity for Vascepa to be “as large, or larger than in the U.S.,” Fadia wrote in a February note.

As the European market grows more important for Amarin with a broader-than-expected label, the company’s increasing its staffing plan there to about 300 people by the end of 2021, up from the 200 it had previously outlined.

Amarin plans to launch in the EU on a country-by-country basis and will tailor the price to each country based on the addressable patient population, Fadia noted. Now, the company’s targeting 10 countries, with Germany being the first, and will be filing reimbursement documents for those markets in the coming months.

A lot of work awaits Amarin, as no other product on the market has Vazkepa's indication, and awareness in the region among healthcare professionals is relatively low, the company noted. “Amarin believes that increasing awareness of Vazkepa in Germany and illuminating the patient population that can benefit from this new drug are important to Vazkepa’s early launch success,” it said in a statement Tuesday.


The 150-strong sales team will utilize digital outreach and “omnichannel engagement” with doctors. Its educational programs will target cardiologists, diabetologists and general practitioners.

“We are taking a thoughtful and proactive approach to leveraging the vast global experience of our team, while incorporating the learnings from other product launches made during the COVID-19 era,” Karim Mikhail, Amarin’s European commercial head, said in a statement.

The EU became more important for Amarin after it lost a patent fight against U.S. generic challengers last fall, and Hikma launched its copycat in November.

Not all is lost for Vascepa in the U.S., though. The Hikma drug only has the originator’s old label, which is meant to reduce blood fat in patients with very high triglyceride levels of at least 500 mg/dL. Vascepa added the key CV reduction indication in December 2019. According to Amarin, that first indication only accounts for about 7% of the brand drug’s use.

Hikma said at the launch that it would be “releasing limited quantities to ensure a consistent supply for customers,” suggesting a constrained supply at least during the early days.

According to data compiled by Cantor’s Chen, the Hikma generic had only been able to take up to around 12% of new-to-brand share as of March. The net pricing of the generic also tends to be higher than the brand for many patients and providers even though its wholesale acquisition price is 12% below Vascepa's, suggesting Amarin’s offering high rebates to payers, SVB Leerink’s Porges noted.

https://www.fiercepharma.com/marketing/amarin-launches-vascepa-all-important-europe-as-blockbuster-to-be-heart-drug-slowly

Graham Urges Fauci Assess If Biden Border Policies Create COVID 'Super-Spreader'

 Sen. Lindsey Graham (R-S.C.) on Monday once again urged infectious disease expert Dr. Anthony Fauci to visit the U.S.-Mexico border to determine whether Biden administration policies are undercutting the nation’s herculean efforts to control the spread of COVID-19.

Graham published his letter to U.S. National Institute of Allergy and Infectious Diseases (NIAID) director Fauci on Twitter, saying that he hopes Biden’s chief medical adviser will travel to the Southern border to survey what many consider to be a public health crisis related to the surge of migration from Central America.

“Is the Biden Administration undermining the work to stop the spread of COVID-19 with the current policies and procedures in place? I think so, but you [Dr. Fauci] are the expert,” Graham said in his letter.

It comes as the United States faces a surge in illegal border crossings in recent weeks. More than 100,000 apprehensions of illegal crossers were made in February—President Joe Biden’s first month in office—and another 26,000 people evaded capture, according to internal data reviewed by The Epoch Times.

Border Patrol agents detained more than 150,000 immigrants in March, former Customs and Border Protection Commissioner Mark Morgan said on March 30, citing internal data he was provided by sources.

While the Biden administration has said that the border isn’t open, Biden reversed or altered a number of key Trump-era provisions, which contributed to the surge, experts have told The Epoch Times.

Graham in his letter noted that as many as one in 10 migrants crossing the border have tested positive for COVID-19, the disease caused by the CCP (Chinese Communist Party) virus, and that some of the Customs and Border Protection facilities where they are housed are “sometimes 800-900 percent over capacity.”

“Given the dire overcrowding situation, the Biden administration has decided to quickly release migrants from these facilities. In many cases, the American taxpayer is paying to transport them thousands of miles from the U.S.-Mexico border,” Graham wrote.

The Republican senator said that he believes the “current setup” and procedures being used by the Biden administration are “creating a COVID super-spreader” event.

“However, your expert opinion could confirm or alleviate these concerns,” Graham wrote, adding that if his concerns are valid, “we need to find ways to stop it.”

“Let’s make sure the policies and procedures at the U.S.-Mexico border are protecting Americans from the spread of COVID-19, not accelerating its spread,” he concluded.

Graham’s letter comes just days after Fauci said that he’s too busy to visit the border, in response to growing Republican criticism that he has been silent on the matter.

Fauci told Fox News’ Neil Cavuto on Friday that it’s not his role to travel to the U.S.-Mexico border, calling Graham’s previous remarks “a little bit bizarre.”

When asked by Cavuto about whether he believes there could be a super-spreader event at the border, Fauci said that “it is a very difficult situation,” and that he believes the Biden administration is doing its best to alleviate the problem.

“Having me down at the border—that’s really not what I do,” Fauci responded.

“I develop vaccines, I develop countermeasures. I mean, having me at the border, I don’t know why they’re saying I should be at the border.”

People crossing the southern border “are tested to the extent possible,” Fauci told Cavuto.

“If they’re positive, they’re quarantined. That’s what I know about it. No one is denying that it’s not a difficult problem at the border.”

Sens. Chuck Grassley (R-Iowa), the ranking member of the Senate Judiciary Committee, and John Cornyn (R-Texas), the top Republican on the Senate Immigration Subcommittee, have called for Democrats to hold a public hearing on the border crisis and question Homeland Security Secretary Alejandro Mayorkas.

https://www.zerohedge.com/political/graham-urges-fauci-assess-if-biden-border-policies-are-creating-covid-super-spreader

New data push Scholar Rock's muscle disease drug closer to key test

 

  • Scholar Rock, a biopharmaceutical company based in Cambridge, Massachusetts, plans to sometime this year test its most important experimental drug in a clinical trial that could provide the evidence needed to ask for approval.
  • The drug, called apitegromab, is being studied as a potential treatment for spinal muscular atrophy, a rare, genetic disease that causes muscles to weaken and diminish. Scholar Rock on Tuesday announced results from a trial of almost 60 patients, showing those who were given apitegromab generally seemed to improve on certain scales used to measure the severity of the disease.
  • While Scholar Rock claims these results show its drug works, there are still important unanswered questions. For example, almost all patients in the trial were receiving apitegromab along with an approved SMA therapy known as Spinraza. It's therefore not yet clear what type of benefit Scholar Rock's drug provides on its own, and how long any benefit will last.
The treatment of SMA has advanced dramatically over the last five years. Before, there were no medicines to slow the disease's progression. But that changed in 2016 with the approval of Biogen's Spinraza, which works by boosting production of a protein critical to many cellular and body functions.

Since then, two more options have become available in Zolgensma, a gene therapy approved in 2019, and Evrysdi, an oral drug approved last year. Like Spinraza, Zolgensma and Evrysdi spur the body to make more of that critical protein, called survival motor neuron or SMN. All three of these treatments have been show to slow or even stabilize disease, although their price tags make them among the most expensive therapies on the market.

For drug developers, the next big advance would be to find ways to further improve SMA patients' motor function. Scholar Rock is betting apitegromab can do just that, and is using the data released Tuesday to make its case.

Apitegromab doesn't work like the currently marked SMA therapies. Instead, it targets a protein known to inhibit muscle cell growth. Scholar Rock's trial tested the drug across three groups of SMA patients who differed based on age, the severity of their disease and when they first started receiving treatment.

In the first group, patients were 5 to 21 years of age, able to walk and had the most mild form of SMA, known as Type 3. These patients were given apitegromab either by itself, or in conjunction with Spinraza. Scholar Rock noted that while the collective group ended up having a 0.3-point average decline on an SMA severity scale, the majority of the patients maintained or improved their motor function.

The second group were 5 to 21 years of age as well, but they could not walk and had the more moderate, Type 2 form of disease. These patients had started treatment with Spinraza at five years old or older. In the study, the group demonstrated an average 0.6-point improvement on a different scale used to measure SMA severity.

The last group were at least 2 years old, had Type 2 SMA, and began Spinraza treatment before they turned 5. Using the same scale as the second group, these patients demonstrated an average 7.1-point improvement when treated with a 20 milligram per kilogram dose of apitegromab and a 5.3-point improvement when given a lower, 2 milligram per kilogram dose.

Speaking with investors Tuesday, Scholar Rock executives said these results support the idea that apitegromab could provide an "additive therapeutic benefit" for a variety of SMA patients. They also believe the drug could have applications in other neuromuscular diseases, including Duchenne muscular dystrophy and Becker muscular dystrophy.

The company said it's planning a "proof-of-concept" clinical trial in Becker's that it aims to launch in 2022.

"As progress is made in the development of next generation, disease-stabilizing therapies, we believe apitegromab could have potential as an add-on to help improve motor function, and we remain committed to exploring this potential in the near term," said Ted Miles, Scholar Rock's chief financial officer, on the Tuesday call.

Investors don't appear sold on the fresh data or Scholar Rock's strategy, it seems, as the company's share price was down by about 15% Tuesday morning.

https://www.biopharmadive.com/news/new-data-push-a-biotechs-muscle-disease-drug-closer-to-a-key-test/597874/

Galectin Launches NAVIGATEnash.com Resource for Physicians, Patients

  Galectin Therapeutics Inc. (NASDAQ:GALT), the leading developer of therapeutics that target galectin proteins, today announced the launch of NAVIGATEnash.com, its dedicated trial website. The new website intends to educate patients and physicians about liver cirrhosis resulting from non-alcoholic steatohepatitis (NASH) as well as support NAVIGATE, the Company’s innovative, seamless adaptive Phase 2b/3 study in NASH cirrhosis.

There is currently no treatment to stop the progression and more serious complications of NASH cirrhosis. The NAVIGATE Study is offering patients and their families an opportunity to contribute to the development of the first potential therapy targeted specifically at NASH cirrhosis and designed to improve clinical outcomes.

“Discussions in our broad community tend to focus on investment and intervention in early stages of NASH, with little attention given to patients who have progressed to NASH cirrhosis. However, since assuming my role in September, I have been moved by the determination of this overlooked patient community and the physicians who treat them. Both deserve dedication and investment in finding a meaningful treatment,” said Joel Lewis, Chief Executive Officer and President of Galectin Therapeutics. “NAVIGATEnash.com is not only meant to engage this important community – who may be looking to participate in NAVIGATE – and inform others about NASH cirrhosis, it is intended to send a message to a much broader community that we are willing to overcome the largest challenge in this space.”

“NASH is quickly becoming the number one cause of liver cirrhosis. Unfortunately, the only treatment option for patients who progress to NASH cirrhosis is a liver transplant, something we, at Galectin Therapeutics, hope to change,” said Pol F. Boudes M.D., Chief Medical Officer of Galectin Therapeutics. “We want to provide the necessary information to patients and physicians about our study, since, unlike other clinical trials in NASH, NAVIGATE specifically targets the prevention of a potentially life-threatening manifestation of NASH cirrhosis.”

Oxford-AZ child vaccine trial paused over possible clot link

 Oxford-AZ vaccine trial on children paused while UK regulator investigates possible link to rare blood clots in adults.

https://www.bbc.com/news/health-56656356

Research letter: Moderna COVID-19 vaccine may have efficacy past 6 months

 Shares of Moderna Inc. MRNA, +3.88% gained 5.9% in trading on Tuesday after research correspondence published in The New England Journal of Medicine indicates that the company's COVID-19 vaccine generated antibodies that extend at least six months after the second dose among a small group of study participants. This is based on tracking COVID-19 antibodies in 33 participants in the Phase 1 clinical trial, which is still ongoing. This is a similar finding to data recently released about immune response to BioNTech SE BNTX, +0.39% and Pfizer Inc.'s PFE, -0.22% mRNA vaccine. "Our data show antibody persistence," the researchers wrote in the letter, which published Tuesday. At this time it is unknown how long the vaccines protect people who have been immunized. Shares of Moderna have gained 17.5% since the start of the year, while the broader S&P 500 SPX, -0.03% is up 8.6%.

https://www.marketwatch.com/story/research-letter-indicates-that-modernas-covid-19-vaccine-has-efficacy-past-6-months-2021-04-06


Greenwich LifeSciences Could See Another Spike in Stock in Early April

 On December 8, 2020, Greenwich LifeSciences (NASDAQ: GLSI) share price closed at $5.20 per share. Greenwich LifeSciences published its 5-year breast cancer data from a Phase IIb trial at the San Antonio Breast Cancer Symposium conference on December 9, which showed 0% breast cancer recurrences over 5 years of follow-up. On that day, the company's stock spiked to $158 per share and closed at $57 per share, surging the next day to $128 per share and closing at $72 per share.

The company experienced another spike in share price on March 8, 2021, opening at $23 per share, spiking at $53 per share, and closing at $37 per share. On March 8, Greenwich announced that Dr. Jaye Thompson would be brought on full time to lead the GP2 Phase III trial in the fight against breast cancer.

Greenwich could see a third one when it announces more GP2 data on April 9-10 at the AACR (American Association for Cancer Research) annual meeting, when the company will release the final 5-year immune response results from its Phase IIb trial.

https://finance.yahoo.com/news/greenwich-lifesciences-could-see-another-163143119.html