Actos Trial Resolved as Settlement Reached in Two Nevada Bladder Cancer Cases

After agreeing to pay $2.4 billion in Actos settlements to resolve thousands of claims brought by former users of the diabetes drug diagnosed with bladder cancer, Takeda Pharmaceuticals agreed to settle two more claims this week, resolving a two-month trial in Nevada state court.

A tentative agreement was reached to settle an on-going Actos trial involving claims brought by George Decou and the family of Maurice Iorio, who died of bladder cancer in November 2013.

The settlement ends a trial that began in late August in Las Vegas, alleging that Takeda Phamaceuticals failed to adequately warn consumers and the medical community about the risk that side effects of Actos may increase the risk of bladder cancer.

Did You Know?

Millions of Philips CPAP Machines Recalled

Philips DreamStation, CPAP and BiPAP machines sold in recent years may pose a risk of cancer, lung damage and other injuries.

Learn More

More than 8,000 similar claims have been filed in state and federal courts nationwide by former users of Actos diagnosed with bladder cancer, and the drug maker announced last month that the required threshold of 95% was met to allow a previously reached Actos settlement to move forward, in which plaintiffs will receive an average payment of about $296,000 per case.

Actos (pioglitazone) was one of the most widely used type 2 diabetes drugs in the United States, until concerns emerged in 2010 about the potential link between Actos and bladder cancer.

In June 2011, the FDA required Takeda Pharmaceuticals to update the Actos warning label to add information about the bladder cancer risk, informing consumers that they may face an increased risk the longer the drug is used.

In lawsuits filed in state and federal courts throughout the United States, plaintiffs allege that Takeda knew about the risk of bladder cancer from Actos, but actively withheld the information in an attempt to minimize the impact on sales of their blockbuster treatment.

Prior to reaching the global settlement, Takeda Pharmaceuticals was hit with a groundbreaking $9 billion verdict in the first federal Actos trial, which went before a jury in April 2014. While that verdict was later reduced to $37 million by the U.S. District Judge presiding over the federal litigation, the judge suggested that the evidence presented against Takeda raises questions about whether the U.S. Supreme Court needs to update rules on what is considered excessive in order to effectively deter large corporations from engaging in the type of bad behavior exhibited surrounding Actos.

Decou and Iorio were pursing more than $2 billion in damages at the trial, arguing that Takeda concealed what they knew about Actos risks and “destroyed evidence on a massive scale in an attempt to avoid responsibility.” Details of the settlement have not been disclosed

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

AT&T Data Breach Lawsuits Seek Damages for 70M Customers Whose Information Was Released
AT&T Data Breach Lawsuits Seek Damages for 70M Customers Whose Information Was Released (Posted today)

AT&T faces a growing number of data breach class action lawsuits, which plaintiffs say should be consolidated before one federal judge for coordinated pretrial proceedings.

Fairness of Philips CPAP Recall Settlement Being Evaluated By MDL Judge
Fairness of Philips CPAP Recall Settlement Being Evaluated By MDL Judge (Posted yesterday)

A federal judge has held a fairness hearing for a proposed Philips CPAP class action lawsuit settlement, which seeks to resolve claims that consumers suffered economic damages due to the massive recall over toxic sound abatement foam.