Federal multidistrict litigation tracker
MDL 3094 Update — Ozempic / GLP-1 Lawsuit
In re: Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAs) Products Liability Litigation. Counts are monthly JPML snapshots and can change between reports.
Lawsuit status — October 2026
Ozempic / GLP-1 Lawsuit
Verified October 23, 2026
- MDL
- MDL-3094
- Court
- E.D. Pa.
- Judge
- Judge Karen Spencer Marston
- Current phase
- Rule 702 closing arguments set for October 13, 2026; no ruling yet
- Settlement status
- No public settlement program identified
- Latest development
- The public MDL-3094 orders page, checked October 23, lists the October 8 scheduling order for Rule 702 closing arguments on Cross Cutting Issues 2 and 3 but no ruling on those motions.
- Next major event
- No future public court date is currently verified in this record.
What changed this month?
- ●The public MDL-3094 orders page, checked October 23, lists the October 8 scheduling order for Rule 702 closing arguments on Cross Cutting Issues 2 and 3 but no ruling on those motions. Source
- ●An October 8 scheduling order sets closing arguments on the pending Rule 702 motions for Cross Cutting Issues 2 and 3 for October 13, 2026. The public orders page reviewed October 11 shows no Rule 702 ruling, bellwether trial date or settlement program. Source
- ●JPML reports 4,025 pending actions in MDL-3094 on October 1, 2026, up 3 from 4,022 on September 1; 4,139 total historical actions are reported separately. Source
- ●The separate MDL-3163 has 247 pending actions as of October 1, 2026, compared with 216 on September 1. Source
- ●JPML reports 4,022 pending actions on September 1, 2026, compared with 3,928 on August 3; 4,056 total historical actions are reported separately. Source
MDL details
- Created
- February 2, 2024
- Pending
- 4,025
- Total actions filed
- 4,139
- Monthly change
- +3
Defendants named in the tracked record
Novo Nordisk (Ozempic, Wegovy, Rybelsus, Saxenda); Eli Lilly (Mounjaro, Zepbound, Trulicity). Defendants dispute the allegations.
Historical case counts
| Report | Pending | Total filed |
|---|---|---|
| October 1, 2026 | 4,025 | 4,139 |
| September 1, 2026 | 4,022 | 4,056 |
| August 3, 2026 | 3,928 | 3,962 |
What the litigation alleges
The tracked claims concern prescription drug injury claim (federal mdl), including gastroparesis and severe gastrointestinal injuries. These are allegations; defendants dispute liability and causation.
Stage and bellwether status
The court held the Rule 702 evidentiary hearing on September 14–18, 2026. An October 8 scheduling order sets closing arguments on the pending Rule 702 motions for Cross Cutting Issues 2 and 3 for October 13, 2026, in place of that day's status conference. No Rule 702 ruling appears on the public orders page reviewed October 11. This is an expert-evidence proceeding, not a bellwether trial, and NAION vision-loss claims are coordinated separately in MDL-3163.
Settlement status
The Eastern District of Pennsylvania public MDL orders reviewed October 11, 2026 do not announce a GLP-1 injury settlement program or official payout amounts. The Rule 702 proceeding concerns expert evidence, not settlement eligibility or an individual award.
Individual claims: The Eastern District of Pennsylvania public MDL orders reviewed October 11, 2026 do not announce a GLP-1 injury settlement program or official payout amounts. The Rule 702 proceeding concerns expert evidence, not settlement eligibility or an individual award.
Official sources
- JPML — October 1, 2026 pending and historical actions
- JPML — September 1, 2026 pending and historical actions
- October 8, 2026 scheduling order: Rule 702 closing arguments on October 13
- JPML — August 3, 2026 pending and historical actions
- JPML — September 1, 2026 assignments and transfer dates
- Official court case orders
- An August 28 order rescheduled the Rule 702 evidentiary hearing to September 14–18, 2026. It is not a jury trial.
- JPML — Pending MDL Dockets (monthly statistics)
- CMO No. 32 — Fifth Amended Scheduling Order (Apr 30, 2026)
- FDA — Ozempic (semaglutide) approval and label information