NuvaRing Settlement Plan To Be Discussed at MDL Hearing
Parties involved in the federal NuvaRing litigation are scheduled to meet with the Court later this month to discuss a possible plan to negotiate a resolution or settlement for lawsuits filed by women who allege that they suffered serious blood clot injuries from side effects of NuvaRing birth control.
All NuvaRing lawsuits filed in federal district courts throughout the United States are consolidated for pretrial proceedings as part of an MDL, or multidistrict litigation, which is centralized before U.S. District Judge Rodney W. Sippel in the U.S. District Court for the Eastern District of Missouri.
NuvaRing is a form of birth control that releases a combination of etonogestrel and ethinyl estradiol through a small ring that is inserted into the vagina once a month.
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Side effects of NuvaRing may increase risk of blood clots, pumonary embolism, DVT, death. Lawsuits pending.
The complaints all involve similar allegations that Merck and their Organon Pharmaceuticals subsidiary failed to properly research the birth control ring or adequately warn about the risk of blood clots from NuvaRing.
Plaintiffs claim that they have suffered a variety of serious injuries after taking NuvaRing birth control, including deep vein thrombosis (DVT), pulmonary embolism, heart attacks, strokes and other blood clot problems.
Following a status conference with Judge Sipple last week, the Court issued an Order that directed the parties to be prepared to discuss a preliminary plan for alternative dispute resolution at hearing set for February 28.
Last month, Judge Sipple ordered attorneys for plaintiffs and defendants to submit proposed plans for alternative dispute resolution, which would be designed to assist the parties in negotiating a potential NuvaRing settlement agreement. While attorneys for the plaintiffs submitted a plan that calls for the appointment of a special master to oversee the negotiations, attorneys for Merck and Organon have suggested that it is premature to consider such efforts.
In a document filed January 23, the drug maker indicated that the court should first rule on potentially dispositive motions they intend to file, such as challenges to the admissibility of certain expert testimony. In addition, the defendants suggested that before any attempts to settle NuvaRing cases can be meaningful, initial bellwether trials should be held.
The parties are currently preparing a handful of lawsuits, known as “bellwether” cases, for early trial dates. The cases are designed to help the parties gauge how juries are likely to respond to certain evidence that will be introduced throughout other cases in the litigation. In complex pharmaceutical litigation, the results of such trials often factor heavily into settlement negotiations.
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