Barron\'s - 02.09.2019

(Axel Boer) #1

20 BARRON’S September 2, 2019


the European Union by 2030.


The second drug in the company’s pipeline,


which will treat a liver disease called ornithine


transcarbamylase deficiency, would be the first


available drug to treat the underlying causes of


the disease. Yang forecasts 2030 sales in the EU


and the U.S. at $600 million, though safety trials


for the drug have yet to begin.


So will the science work?


Daniel Anderson, a professor of chemical engi-


neering at the Massachusetts Institute of


Technology who has been doing research for


Heartlein’s group for years, said that a major


validation of the technology came in August of


last year, when the FDA approved a drug


called Onpattro, made by Alnylam Pharma-


ceuticals (ALNY).


Onpattro, which treats a rare genetic disease


called hATTR amyloidosis, works by entering


liver cells and knocking out mRNA molecules.


To get into the cell, the drug uses a lipid nano-


particle—the same delivery device used by the


mRNA therapies.


“For everybody working on messenger RNA,


we can point to that and say look, you can do


it,” Anderson said. “It’s not exactly the same,


but it’s not some science-fiction story.”


Anderson, who looks a bit like Robert F.


Kennedy, is a lipid nanoparticle guru. He de-


signed the lipid nanoparticle that Translate is


using in its second treatment, which targets a


rare liver disease, in his lab at MIT’s Cam-


bridge campus. There, postdocs and graduate


students work at long tables amid bottles, pi-


pettes, high-tech liquid handlers, and old-fash-


ioned Schlenk lines.


At the lab, grad student Allen Jiang han-


dled a chunk of plastic with tiny channels


drilled through it. To make an experimental


mRNA drug, Jiang shot synthetic mRNA into


one hole and lipids into another. They combine


in the channel, the lipids wrapping themselves


around the mRNA to make a lipid nanoparti-


cle. Jiang and his colleagues experiment with


novel lipids to test new ways to deliver the


synthetic mRNA, and then dose mice to see if


it’s working.


“What you really want is to get the most effect


for the minimal amount of nanoparticle,” Ander-


son said. “We think if we can get the vehicle to


work great, it can be used for many diseases.”


The tests in mice are ongoing. Of course,


mice are a long way from people.


“There are a lot of really exciting data in a


range of different model systems that make us


think it is really going to work,” Anderson said.


“The human data we get over the next few


years will help us determine how broadly


mRNA technology can be used.”


Other experts say that the challenges of mak-


ing it work in people shouldn’t be underestimated:


“It sounds very promising. Why don’t we see


more?” asks Xiling Shen, a professor of biomed-


ical engineering at Duke University, who has


studied mRNA therapies but doesn’t focus on


the field.


The fact that an mRNA therapy would need


to be taken regularly, like a normal drug, could


make it safer than gene therapies. But it also


means that the risk of an unwanted and danger-


ous immune reaction is greater.


“If you repeatedly inject something foreign,


you can cause an immune response in the body,”


Shen said. He added that the transient nature


of the therapy makes delivery of the drug very


challenging. Can you get enough mRNA into


the body to produce enough proteins for a


human patient to experience an effect?


The answers are coming soon.


At Translate Bio’s lab in


Lexington, Mass., teams of


scientists and technicians


are working on curing


diseases with mRNA.


Tell Us What


You T hink


Would you take a


gamble on investing in


mRNA? And what do


you think the future of


biotech will be?


Write us at mail@


barrons.com and we


may publish your take.


Find out more at


barrons.com/mailbag.


Placing Bets


On Biotech


Disruption


For investors, there are a handful of ways to


get comfortable with a gamble on mRNA.


The strongest endorsement of Moderna


(ticker: MRNA) and Translate Bio (TBIO) may


have come from Big Pharma. AstraZeneca


(AZN) is among the largest shareholders of


Moderna, with a 7.7% stake, and has three


separate drug-development deals with the


company. Merck (MRK) has another two.


Translate has a drug-development deal with


Sanofi Pasteur. Takeda Pharmaceutical


(TAK) owns 13.9% of Translate; GlaxoSmith-


Kline (GSK) has another 6.3%.


One way to make hedged bets on mRNA is


through companies such as AstraZeneca and


Merck, which are set to profit if Moderna’s


technology begins to work out.


Two private German companies are also


major players. CureVac, based in Tübingen,


was focused on mRNA-powered prophylactic


vaccines until its new CEO, Dan Menichella,


took over last year and reoriented the com-


pany’s efforts toward oncology and rare dis-


eases. Mainz-based BioNTech, which develops


mRNA-powered personalized cancer vaccines,


raised $325 million in July, with an enormous


valuation that makes it the European version


of Moderna. Neither is expected to go public in


the near term, but both could be promising


opportunities if they do.


Another public company, Arcturus Ther-


apeutics Holdings (ARCT), is also pursuing


mRNA therapies. It is smaller than Translate,


with operating expenses of $10.7 million for


the most recent fiscal quarter, compared with


Translate’s $29.4 million.


Moderna’s broad approach to drug devel-


opment could give investors confidence; the


company doesn’t need to bat a thousand to


succeed. And the vaccine business may be


argument enough.


“There are only a couple of technologies


that can serve vaccine markets,” says Chris-


tian Koch, a member of the investment man-


agement team at BB Biotech, a Swiss biotech


investment company that holds Moderna. “One


is the classical approach....That has been en-


trenched in Big Pharma, due to the scale and


breadth of manufacturing and distribution.”


With the advantages offered by mRNA,


Moderna could handle the manufacturing, Koch


says. Distribution remains an issue, but he


says that the vaccines remain an investment


argument for his firm.


For other investors, the wisest bet may to


let the Big Pharma business-development de-


partments do the research for you, and be


ready to wait a good long while for profitabil-


ity. That points to Moderna, and perhaps to


Translate Bio—and to a lot of patience.


—JOSHNATHAN-KAZIS

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