Judge Grants Defendants’ Motion for Summary Judgment in Diabetes Drug MDL, Excludes Plaintiffs’ Experts

Carolyn Casey, J.D.

Written by
— Updated on August 6, 2021

Judge Grants Defendants’ Motion for Summary Judgment in Diabetes Drug MDL, Excludes Plaintiffs’ Experts

On March 9, 2021, a U.S. District Court judge in the Southern District of California granted the defendants’ motion. The drug companies had filed a motion for summary judgment in a consolidated multidistrict litigation (MDL). The plaintiff claimed the defendants failed to warn about the risks of pancreatic cancer associated with their type-2 diabetes drugs. In Judge Anthony Battaglia’s decision for In re Incretin-Based Therapies Products Liability Litigation, the court found that federal law preempted the plaintiffs’ state failure-to-warn claims. Further, the ruling excluded the plaintiffs’ experts, denied the exclusion of defendants’ experts, and did not find general causation.

The Diabetes Drugs in Question

The diabetes drug MDL involved five type-2 diabetes drugs marketed and/or manufactured by a number of household-name drug giants. The defendants were AstraZeneca PLC’s Amylin Pharmaceuticals, Eli Lilly and Co, Merck & Co Inc, and Novo Nordisk Inc. The FDA generally classifies the diabetes medications in question as incretin mimetics or incretin-based therapies.

The Journey to the Recent Summary Judgement in Diabetes Drug MDL

Starting in 2013, 1,500 eventual MDL class members began to file cases with similar claims. The claims centered around pancreatic cancer risks and these type-2 diabetes drugs. The volume of cases eventually led to consolidation and the diabetes drug MDL ran its course. The cases had a litany of additions, motions, filings, and discovery issues.

On November 9, 2015, Judge Battaglia issued a summary judgment based on preemption in favor of the defendants. On appeal, the case was remanded to allow certain plaintiffs additional discovery, and to order the judge to consider “the materiality of Plaintiffs’ asserted new safety information, and reinstate the opinion of Plaintiffs’ expert, Dr. Fleming” in 2017. The appellate court did not rule on the preemption question.

After completion of the additional discovery, the defendants again asked the court for summary judgment saying, “it is impossible to comply with both the FDA’s regulatory scheme and state law failure-to-warn requirements, and because there is no genuine dispute of material fact as to general causation.” The plaintiffs asserted that preemption had not been established and that their experts could show a path to causation.

March 2021 Summary Judgment Ruling

The court recently ruled on these motions. In the ruling’s introduction, the court notes that the U.S. Food and Drug Agency (FDA) oversees new drug introductions, regulates the content of labeling, and enforces compliance with post-marketing compliance. The court also explains that product labeling responsibility lies in the hands of the manufacturers who have a duty to provide warnings of risks based on reasonable evidence.

Judge Battaglia disagreed with the plaintiffs that a Canada Health publication provided such reasonable evidence. The judge went on to granularly review FDA studies, publications, and a citizen petition to remove one of the drugs at issue from the market. Judge Battaglia found that there was no sound evidence of pancreatic cancer risks in incretin-based therapies. The defendant drug companies could not unilaterally change their labels without reasonable evidence. Because of this, Judge Battaglia found that there was a conflict between state warning laws and federal law. Thus, federal law preempts, resulting in the summary judgment for defendants.

Though saying it was unnecessary, the court also found that the defendants had established “clear evidence that the FDA would not approve a label change.” Both its own monitoring of incretin mimetics for pancreatic safety for decades and the defendants’ material reports to the FDA fully informed the federal agency. Therefore, the court reasoned, the FDA had essentially said it would not approve a pancreatic cancer warning on the label.

Plaintiff’s Experts Excluded in Diabetes Drug MDL

In this case, both sides sought to have the other’s experts excluded under Daubert. The judge analyzed the Daubert motions (central to general causation) to deny the plaintiffs’ expert exclusion motions. According to the judge, these motions were moot after granting the defendant’s motion to exclude plaintiffs’ experts.

Biostatistician Experts

Plaintiff offered two biostatistician experts. Judge Battaglia found the first expert’s analysis dated and based on a selective data review. This testimony would be “unreliable and not helpful to the jury.” The second expert opined that there is “strong evidence of a causal association between GLP-1 exposure and pancreatic cancer.” This opinion was based on favorable, cherry-picked data—not good science, according to the court.

Biological Plausibility Expert

The plaintiffs also proffered a biological plausibility expert. This expert theorized “that incretin-based therapies promote the development of pancreatic cancer because they activate GLP-1 signaling in certain pancreatic cells, causing those cells to proliferate, which in turn, causes cancer.” The expert also admitted that he “just didn’t have time” to compare the animal and human dosages. The court saw this and other gaps as indicators that he did not use the level of intellectual rigor expected of an expert in his field and his testimony was excluded.

Oncology Expert

The plaintiff’s oncology expert analyzed whether incretin-based therapies cause or contribute to pancreatic cancer. The expert’s latency opinion lacked foundation, said the court. “… [t]he literature from which he extrapolates his conclusion does not concern incretins, and he has not explained why such an extrapolation is scientifically sound.” The court also did not like that he failed to independently review the statisticians’ evidence and did not weigh all available evidence.

Chemical Toxicology Expert

The plaintiff’s chemical toxicology expert analyzed the existence of a viable mechanism “whereby incretin-based therapies could contribute to the development of pancreatic cancer.” The court booted this testimony because he did not “consider all available clinical trial data, observational studies, and other epidemiological literature on incretin-based therapies.”

Gastroenterology Expert

Next, a gastroenterology expert reviewed literature to opine on “whether incretin mimetics more likely than not increase the risk of pancreatic cancer.” This testimony was excluded in large measure. This happened because he admitted the plaintiffs’ counsel “first taught him about the alleged relationship between incretins and pancreatic cancer.”

Pathology Expert

Finally, the plaintiffs’ pathology expert examined non-human primate slides from two toxicology studies involving exenatide. Judge Battaglia said the record showed that this “methodology of applying the human PanIN classification system to non-human primates is not a reliable scientific method.” The testimony was thus ruled inadmissible.

Future MDL Impacts

A “new study” will not easily overcome years of FDA monitoring of the safety of drugs. This is important to know for plaintiffs planning to bring class actions relating to cancer risk warnings on drug labels. The plaintiff’s evidence demonstrating new information on risks must be based on rigorous science that goes beyond what the FDA already has established. This Ninth District Court, at least, is more than willing to painstakingly assess the FDA change in labeling process under legal precedent to find that with a conflict, federal law will preempt state drug warning laws.

Further, the importance of the quality of experts and their methodologies in these types of cases where general causation is not easily understood by laypeople can’t be overstated. The gaps in the experts’ evaluations in this case ultimately crushed any chance of proving general causation.

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