DOJ Subpoenas Documents from Alnylam Over Marketing of Onpattro

After a trial that started in mid-June, jurors reached their conclusion Tuesday and awarded Ivie $2.4 million.

Ivie is in line to receive $1.87 million in damages plus another $510,423 for wages lost. She lost her job in 2019 after 19 years with the company.

Why would she change her name or want to work again? She received $2.4 million dollars.
 


















After a trial that started in mid-June, jurors reached their conclusion Tuesday and awarded Ivie $2.4 million.

Ivie is in line to receive $1.87 million in damages plus another $510,423 for wages lost. She lost her job in 2019 after 19 years with the company.

Why would she change her name or want to work again? She received $2.4 million dollars.

She got nothing except a reputation that will never leave her. Good luck with that.

“AstraZeneca Pharmaceuticals LP was correct that a former employee who an Oregon jury awarded $2.4 million after finding she was fired for blowing the whistle on an executive’s marketing drugs for unapproved uses failed to show a nexus to the state and can’t keep the award, a federal judge ruled.”
 












Federal prosecutors launch Alnylam marketing probe, demanding Onpattro documents
April 13, 2021 Eric Sagonowsky

Busy launching several new drugs, RNA biotech Alnylam posted a big revenue increase in 2020—and it expects more growth in 2021, partly thanks to its top-selling Onpattro drug. But now the U.S. Department of Justice is investigating its marketing practices for that very product.

The U.S. Department of Justice subpoenaed the biotech last week, demanding documents that detail its Onpattro marketing in the U.S., Alnylam said in a Monday SEC filing.

“The company is preparing a response to the subpoena and cooperating with the government,” Alnylam said in the filing. The biotech has retained “experienced outside legal counsel” to help handle the probe.

The company “takes matters like this very seriously, and we are cooperating fully with the government,” a spokeswoman said. … “Operating with integrity, honesty and transparency will always be core to our organization and are key parts of our core values and our goals. As a part of that, we believe our business conduct and in particular our interactions with healthcare providers must he held to the highest ethical standards.”

Onpattro, approved in August 2018 to treat polyneuropathy caused by hereditary transthyretin-mediated amyloidosis, generated more than $300 million last year.

The medicine was Alnylam’s first marketed drug, but now the biotech has a growing suite of RNA medicines on the market.

Alnylam scored FDA approval in November 2019 for Givlari to treat acute hepatic porphyria. And in November 2020, the FDA granted a green light to Oxlumo, which treats primary hyperoxaluria type 1, or PH1, a severe rare disease that causes patients to suffer from recurrent kidney stones and often forces patients into organ transplants.

In all last year, Alnylam generated more than $361 million from the three drugs, more than double the $166 million haul it posted in 2019. Onpattro contributed the lion’s share with more than $306 million in 2020. For 2021, Alnylam expects between $610 million and $660 million for the three drugs.

When the company released its 2021 guidance, Cantor Fitzgerald analyst Alethia Young wrote that the number “looks conservative.” Her team projects $687 million in sales for the company this year.

Aside from those three offerings, Alnylam’s partner Novartis late last year scored an approval in Europe for Leqvio to treat hypercholesterolemia. Alnylam picked up a $15 million milestone payment for the regulatory win. Alnylam discovered the drug and licensed it to The Medicines Company before that drugmaker’s buyout by Novartis.

Alnylam seeks to join the top 5 biotechs by market cap by 2025, CEO John Maraganore said earlier this year. To get there, the company will need six or more products and half a million patients on its therapies, plus aggressive revenue growth.

DOJ Subpoenas Documents from Alnylam Over Marketing of Onpattro - Global Genes

How much was the fine?
 












Allergan Agrees to Plead Guilty and Pay $600 Million to Resolve Allegations of Off-Label Promotion of Botox®

WASHINGTON – American pharmaceutical manufacturer Allergan Inc. has agreed to plead guilty and pay $600 million to resolve its criminal and civil liability arising from the company’s unlawful promotion of its biological product, Botox® Therapeutic, for uses not approved as safe and effective by the Food and Drug Administration (FDA), the Justice Department announced today. The resolution includes a criminal fine and forfeiture totaling $375 million and a civil settlement with the federal government and the states of $225 million.

Under the Food, Drug and Cosmetic Act (FDCA), a company in its application to the FDA must specify each intended use of a biological product. After the FDA approves the product as safe and effective for a specified use, any promotion by the manufacturer for other uses – known as “off-label” uses – renders the product misbranded.

Tony West, Assistant Attorney General for the Civil Division of the Department of Justice, and Sally Quillian Yates, U.S. Attorney for the Northern District of Georgia, today announced the filing of a criminal information against Allergan for promoting Botox® for headache, pain, spasticity and juvenile cerebral palsy – none of which were approved by the FDA. According to the criminal information, Allergan made it a top corporate priority to maximize sales of Botox® for such off-label uses.
 






Are the posts about the subpoenas rumors or for real? Are there also rumors of settlement like the recent post above??
Don’t want to apply for open roles if things are about to get weird as indicated by all these posts!
 































Item 8.01. Other Information.

On or about April 9, 2021, Alnylam Pharmaceuticals, Inc. (the “Company”) received a subpoena from the U.S. Department of Justice, U.S. Attorney’s Office for the District of Massachusetts, requiring production of documents pertaining to its marketing and promotion of ONPATTRO® (patisiran) in the United States. The Company is preparing a response to the subpoena and cooperating with the government. Experienced outside legal counsel has been retained to assist with this matter.


It's been over a year...when will it be over?