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Friday, September 6, 2019

Opthea’s OPT-302 shows positive effect in mid-stage wet AMD study

Opthea Limited (OTCPK:CKDXYannounces additional data from a Phase 2b clinical trial evaluating the combination of OPT-302 and Roche’s (OTCQX:RHHBY) Lucentis (ranibizumab) compared to Lucentis alone in wet AMD patients. The results were presented at the European Society of Retina Specialists Congress in Paris.
Patients receiving the combination experienced superior vision gains versus sham + ranibizumab in addition to improved anatomical changes of retinal lesions and reduced subretinal fluid and intraretinal cysts.
OPT-302 is a soluble form of vascular endothelial growth factor receptor 3. It is a “Trap” molecule that blocks the activity of two proteins (VEGF-C and VEGF-D) that cause blood vessels to grow and leak.

Mednax cut to Underperform from Neutral by B of A

https://www.benzinga.com/stock/MD/ratings

Encompass Health upped to Buy from Neutral by B of A

https://www.benzinga.com/stock/EHC/ratings

For GW Pharma CEO Justin Gover, The CBD Trend Started 20 Years Ago

Remember the simpler times of the mid-2010s, when you could order a latte or cocktail in California without the option of adding CBD?
For Justin Gover, CEO of British drugmaker GW Pharmaceuticals (NASDAQ: GWPH), society’s sudden embrace of cannabidiol (CBD), the other active ingredient found in the cannabis plant, is a trip—though CBD won’t make you trip. That’s caused by THC, or tetrahydrocannabinol, the cannabis component responsible for most of marijuana’s psychoactive effects.
Businesses have been rapidly been building up around marijuana since states began legalizing its recreational use in 2012. More recently, CBD has been gaining in popularity as a potential treatment for health issues from seizures to inflammation, with businesses like GW cashing in. One study projected sales for the CBD market to reach $20 billion by 2024.
Founded in 1998 to develop medications from marijuana, GW is based in Cambridge, UK. In 2015, Gover relocated to California to open operations in the US. GW’s US subsidiary, called Greenwich Biosciences, is in Carlsbad, a city in North San Diego County. Today it houses more than 120 employees, or about 15 percent of the company’s 800-plus-person workforce. [Paragraph corrects founding year.]
Historically, financing cannabis companies has been difficult; US federal regulations treat marijuana as a controlled substance. But now investors are looking to cash in on the growing legal marijuana market. Earlier this month, Silver Spike Acquisition (NASDAQ: SSKU)—the third so-called blank-check company to launch this year targeting the cannabis industry—raised $250 million in an initial public offering, according to IPO research firm Renaissance Capital. Such companies, which have no operations, raise money from investors in an IPO and use the money to make acquisitions.
On the biotech side of the industry, it was only last summer that the FDA approved the first drug made from an active ingredient derived from marijuana: GW’s cannabidiol (Epidiolex), a treatment for seizures associated with two rare forms of epilepsy.
Many other CBD products are sold, both in retail stores and online, without similar regulatory oversight. While various benefits of CBD’s use have been reported, health officials and regulators have called for doctors and patients to learn more about use of the compound. GW is one of the few companies to study it extensively with three clinical trials that involved 516 patients, which helped lead to FDA approval.
Gover, who has led the company in raising more than $1 billion to fuel its growth over the past two decades, reflected last week on the company’s history, and the societal and regulatory changes that have taken place since it launched, at an event organized by the UK Department for International Trade and Biocom, the life sciences trade organization.
Here are five insights from the event, which took place at the Alexandria at Torrey Pines and featured Gover in a conversation with Biocom president and CEO Joe Panetta.
—Without patient advocates and the UK government’s acquiescence, GW may never have gotten off the ground.
“There started to emerge, at least in the UK, a significant patient voice—and, I’d say, particularly from the multiple sclerosis community—talking about uses of cannabis for symptom relief. … The British government, at the time, didn’t want to be ‘soft’ on marijuana, didn’t want to be seen to be legalizing cannabis. On the other hand, they were actually very supportive of the idea of doing real research,” Gover said.
GW spoke with the UK’s equivalent of the DEA and secured licenses to begin research, which began with an effort to standardize plant-based products and understanding the emerging pharmacology of the cannabis plant, he said.
—More than a decade after its founding, GW’s first drug, nabiximols (Sativex), the first approved cannabis-based drug in the world, was OK’d in the UK as a treatment for spasticity, a common symptom of multiple sclerosis—but the company was struggling.
“It was very hard to raise money … Regulators were very skeptical; I would say the medical community was largely very skeptical as well,” Gover said. But in 2012 there came a sea change, spurred by the family of Sam Vogelstein, a boy who has epilepsy, when they reached out to the company to learn more about its early research into CBD. (Read more about Vogelstein here.)
“They, like many families that have children with refractory epilepsy, had tried and failed multiple therapies and had started to pursue nonpharmaceutical options,” Gover said.
“At that point in time, in California, CBD preparations and oils were starting to become available, and they’d had some mixed success,” he said. “Sam had been given some CBD oils and had seen some pretty dramatic reductions in seizures and yet there were other CBD oil preparations where the seizures had not had any reduction or indeed got worse. The family was really hopeful and yet frustrated at the same time about this.”
Vogelstein and his family flew to the UK and the boy took a CBD preparation GW formulated for him. The day he arrived he had 68 seizures. Weeks later, the day he flew home, he had none, Gover said. This anecdotal show of the potential of the chemical compound accelerated the research underway at GW, which, eventually, led to Epidiolex’s 2018 approval in the US, Gover said.
“It’s remarkable to think that through this one boy’s experience, through the science that we generated that led his parents to finding us, to then developing this product through normal placebo-controlled trials and manufacturing this product, that Sam now has this medication prescription—and there are thousands around this country now … over 12,000 patients taking the medication today,” he said.
—Growing marijuana is easy. GW’s intellectual property is around how it turns the plant into a prescription product.
“One of the things we realized at the beginning was that if we were going to develop a standardized medicine from the cannabis plant, that actually there was no contracting organization that really could do that,” Gover said. “The size of the company that sits in the UK is a reflection of the fact that we do pretty much all of the key parts of R&D and manufacturing in-house. … The challenge, in terms of creating a medicine, really starts post-plant. The tens of millions in investment and the process, the technology, and the systems we have, are actually about taking that plant material and then going through various steps to end up with a pure product.”
—GW anticipates its drug for MS will be approved in the US and its drug for epilepsy in Europe—and that it, and other companies, will develop cannabis-based drugs to treat other conditions.
“For us as a company, I think we feel that the notion of cannabinoids as therapeutics in MS and in other areas … that era has now dawned,” Gover said. “I think we had to break down a number of obstacles, and some of it has taken 20 years to do that, but having done that, whether it’s ourselves or other companies in the room or around the country that want to develop FDA-approved medications from the cannabis plant, those doors are clearly open. … It’s a pretty interesting area now to be in, where I think—I hope—to see in another five to 10 years a whole range of these kind of medications.”
—The CBD craze, in a way, echoes the insight that prompted the company chairman, founder Geoffrey Guy, to start GW those 20 years ago.
“If you think about the cannabis plant as a plant that’s been in medicine—it’s a medicinal herb, only in the past few decades did it become a recreational drug—for three thousand years of medical use, and you hear that Queen Victoria was using it for this, and go back into ancient Egypt and China and all these different medical uses … In nature, the cannabis plant has more CBD than THC in it, and yet in the 1970s, ‘80s, and 90s, cannabis was essentially THC because it was bred for people to get high,” Gover said. “(Geoffrey Guy’s) insight was, well, if you think of three thousand years of experience, to explain all of that through THC because the plants wouldn’t have had much … His view, coupled with the science, was that CBD’s got to play a role.”

Global Blood could draw bid before sickle cell drug action – SunTrust

Global Blood Therapeutics (NASDAQ:GBT) is up another 3.4% after hours, adding on to today’s 10.9% gain fueled by FDA acceptance of a marketing application to apply voxelotor to sickle cell disease.
Earlier today, Wedbush raised its price target to $120 from $103 — now implying 128% upside from closing price of $52.66.
And SunTrust now adds that it wouldn’t be surprised to see Global Blood draw a takeover bid before any FDA action in February.
The agency’s not holding an advisory panel on the drug, analyst Joon Lee says, and management has said it’s been in “regular touch points” with big drugmakers.

Sumitomo Dainippon investing $3 billion in Swiss Roivant in overseas push

Japan’s Sumitomo Dainippon Pharma Co will pay $3 billion for a 10% stake in Swiss drugmaker Roivant Sciences Ltd and interests in five of its biopharmaceutical businesses, the two companies said on Friday.

The deal, which will open up new drug lines for Sumitomo Dainippon, will also give it the option to acquire interests in an additional six businesses, as well as access to Roivant’s technology platforms, they said in a statement.
It comes as Sumitomo Dainippon’s schizophrenia treatment Latuda is due to lose its U.S. market exclusivity in 2023. The Japanese company will take ownership of Roivant units that develop treatments for prostate cancer, urinary diseases, paediatric illnesses and respiratory diseases, they said.
“We look forward to deepening our relationship with Roivant, which has a rich development pipeline, technology platforms, and distinctive talents,” Sumitomo Dainippon CEO Hiroshi Nomura said in the statement.
Like its rivals, Japan’s seventh-largest pharma company by revenue, is grappling with a declining population at home and a need to go abroad to find growth.
While the bulk of Japanese drug firms have been largely cautious about overseas acquisitions, there are signs of change. Takeda Pharmaceutical this year completed a $59 billion purchase of Shire Plc, catapulting it into the list of the world’s top 10 drugmakers by sales – a rarity for a Japanese pharma company.
A fifth Roivant business unit will also be transferred before the deal’s conclusion, the two companies said.
The 11 businesses include more than 25 clinical programs with multiple product launches expected between 2020 and 2022, they said.

Bayer Counters Accusations Involving Monsanto Weedkiller

Monsanto Co.’s public-relations tactics in Europe didn’t break the law, according to a report commissioned by Bayer AG, which continues to battle fallout from its acquisition of the U.S. agrochemical company.
The German chemicals and pharmaceuticals group said a law firm had examined allegations about Monsanto’s listing of critics of the main ingredient of its Roundup weedkillers and found no wrongdoing.
Bayer has been in crisis mode since closing the Monsanto deal in 2018, with its share price falling sharply. In the past year, it has lost three jury trials alleging that Roundup causes cancer. Bayer is also facing bans in Europe on glyphosate, the weedkiller’s main ingredient, due to perceived environmental risks.
A separate front opened in May after French prosecutors launched an investigation following local media reports that Monsanto and a public-relations firm had drawn up lists in 2016 of hundreds of influential French personalities, some of whom had raised concerns about possible risks posed by Monsanto’s products.
While compiling so-called stakeholder lists is common practice in public relations, the media reports said they included sensitive personal information that wasn’t publicly available — the storage of which without permission can be illegal in some European Union countries. However, Bayer said Thursday that law firm Sidley Austin LLP had examined the allegations and found no evidence that the lists were illegal.
Monsanto has long been a lightning rod for environmentalists in Europe, who see it as a symbol for practices they oppose, from the genetic engineering of crops to the intensive use of pesticide in agriculture.
Bayer, which inherited that reputational baggage, has appealed the Roundup court verdicts in the U.S., insisting the product is safe when used with proper precautions. It has also criticized bans on glyphosate in Germany and Austria as unscientific.
As part of its effort to clear its name, Bayer hired Matthias Berninger, a former Green Party politician in Germany, as its head of public affairs and sustainability.
People familiar with the matter said Mr. Berninger caused consternation among former Monsanto employees in the U.S. when he publicly apologized for the company’s stakeholder lists in May before it was established whether the practice was illegal.
Sidley Austin said it assessed over 2.4 million documents in relation to the lists, which included 1,500 people, mostly in the EU — from journalists to officials working in EU institutions — but also in the U.S.
In its 49-page report, the law firm said the lists were “detailed, methodical, and designed to strongly advocate Monsanto’s positions to stakeholders and to the public.” But the firm said it found no evidence of illegal surveillance of personal hobbies or leisure activities or information that went beyond what was in the public domain.
The German Council for Public Relations in July also concluded that there was no wrongdoing.
The French prosecutor’s office couldn’t be reached to comment on the status of its probe.
A Bayer spokesman said the French prosecutor’s investigations were ongoing. The company said it hasn’t been presented with formal allegations or charges from any data-protection authority or other body, either in France or elsewhere in the EU.