J&J Talc Verdicts Top $2.5B in 2025
Johnson & Johnson faced over $2.5 billion in talc-related jury verdicts in 2025, including the largest individual award in litigation history.
29 articles
Johnson & Johnson faced over $2.5 billion in talc-related jury verdicts in 2025, including the largest individual award in litigation history.
2025 saw major mesothelioma treatment advances including TEAD inhibitors, bispecific antibodies, and perioperative immunotherapy. Here's the full review.
A Baltimore jury awarded $1.56 billion to Cherie Craft, a Maryland woman who developed mesothelioma after 40+ years of using Johnson & Johnson baby powder.
A Minnesota jury awarded $65.5 million to a mother of three who developed mesothelioma after childhood exposure to Johnson & Johnson baby powder.
Los Angeles jury awards $40 million to two women who developed ovarian cancer after decades of using Johnson & Johnson talc-based body powders.
A Dutch trial found two drugs achieved a 60% response rate in mesothelioma patients whose cancer returned after immunotherapy.
FDA withdrew its rule requiring asbestos testing in cosmetic talc. Public health advocates warn of ongoing contamination risks.
Novartis halted its experimental mesothelioma drug IAG933, but a competitor's TEAD inhibitor shows strong results in clinical trials.
An Australian trial will test Cyncado's TT-4 A2B receptor antagonist in ~50 people with mesothelioma after first-line therapy.
Special master approves expert testimony in 67,500 J&J talc lawsuits, clearing the path for federal trials in ovarian cancer cases.
Despite banning asbestos in 2006, Japan sees 1,500+ mesothelioma deaths yearly. The country's experience shows why bans alone aren't enough.
A 2025 federal study found missile alert facility workers at Minot AFB have increased cancer risk from asbestos in Cold War-era underground bunkers.
Diagnosed with peritoneal mesothelioma at 21 while pregnant, Tamron Little shares her 18-year journey and the reality of long-term survivorship.
An LA jury awarded $966 million to the family of Mae Moore, an 88-year-old who died from mesothelioma after using Johnson & Johnson baby powder daily.
A Los Angeles jury awarded $966 million to the family of Mae Moore, 88, who died from mesothelioma after lifelong use of Johnson's Baby Powder.
September 26 is Mesothelioma Awareness Day. Learn about the history of awareness efforts, current statistics, and how to get involved.
Johns Hopkins phase 2 trial shows pre- and post-surgery immunotherapy is safe and effective for operable mesothelioma, with 28.6-month median survival.
Patients on VT3989 went 40 weeks without cancer progression. Vs. 15 weeks on standard chemo. FDA granted Fast Track status.
A Johns Hopkins trial found that immunotherapy before and after surgery extended median survival to 28.6 months, 10 months longer than average.
Baylor and Duke are testing immunotherapy before surgery for mesothelioma. Trial now enrolling operable patients.
The IMPALA trial in France is testing intrapleural photodynamic therapy combined with nivolumab for inoperable mesothelioma. Results expected mid-2026.
A New York appeals court upheld a $3.3M verdict against Ford after a former dealership worker was diagnosed with peritoneal mesothelioma from brake dust.
Paramount Studios faces lawsuits alleging asbestos exposure on film sets and soundstages. The entertainment industry has a hidden asbestos history.
A jury awarded $117M to a sheet metal worker exposed to asbestos at the original World Trade Center, the largest such verdict in New York history.
H.R.4247 would require sellers and landlords to disclose known asbestos hazards before completing sales or leases of residential properties.
BioNTech's dual-target immunotherapy achieved a 52% response rate in people with mesothelioma. Results presented at ASCO 2025.
UK government allocates £470 million for 656 schools and £750 million for NHS sites to address asbestos, crumbling infrastructure in 2025-2026.
Despite banning asbestos, Canada sees 472 mesothelioma deaths annually. Legacy asbestos in buildings and the disease's long latency explain the trend.
FDA approval of Opdivo Qvantig allows subcutaneous nivolumab delivery in under 5 minutes, compared to 30-minute IV infusions for people with mesothelioma.