Welcome to our dedicated page for Johnson & Johnson news (Ticker: JNJ), a resource for investors and traders seeking the latest updates and insights on Johnson & Johnson stock.
Johnson & Johnson (NYSE: JNJ) generates a steady flow of news across Innovative Medicine and MedTech, reflecting its role in pharmaceutical preparation manufacturing and medical technologies. On this news page, readers can follow company announcements on clinical trial results, regulatory milestones, strategic transactions, manufacturing investments and corporate actions.
Recent oncology news includes positive topline data from the Phase 3 MajesTEC-9 study of TECVAYLI (teclistamab-cqyv) monotherapy in relapsed or refractory multiple myeloma, where Johnson & Johnson reported a substantial reduction in the risk of disease progression or death versus standard of care in a population predominantly refractory to anti-CD38 therapy and lenalidomide. The company has also shared longer-term results from the OrigAMI-1 study of RYBREVANT (amivantamab-vmjw) plus chemotherapy in metastatic colorectal cancer, supporting further Phase 3 evaluation of amivantamab-based regimens in first- and second-line settings.
In neuroscience and mental health, Johnson & Johnson has highlighted new data on CAPLYTA (lumateperone), SPRAVATO (esketamine) and the investigational agent seltorexant at major scientific meetings, including analyses focused on remission in major depressive disorder, treatment-resistant depression and sleep-related symptoms. The company has also announced positive Phase 2b results for nipocalimab in systemic lupus erythematosus and plans to initiate a Phase 3 program, underscoring its activity in autoantibody-driven diseases.
MedTech news covers developments such as the FDA submission of the OTTAVA robotic surgical system for De Novo classification, supported by an IDE study in gastric bypass procedures, and an expanded indication for the TRUFILL n‑BCA Liquid Embolic System for chronic subdural hematoma. Corporate and financial updates, including quarterly dividend declarations, U.S. manufacturing investments and government agreements to improve access to medicines, also appear in Johnson & Johnson’s news flow. Investors, clinicians and observers can use this page to monitor how Johnson & Johnson’s clinical, regulatory and strategic decisions evolve over time.
Johnson & Johnson (NYSE: JNJ) received Emergency Use Authorization (EUA) from the FDA for its COVID-19 vaccine booster for adults aged 18 and older, effective two months after the initial vaccination. The booster dose will share the same formulation and dosage as the primary shot. The EUA is based on a favorable recommendation from the FDA's advisory committee, highlighting robust efficacy and safety data from clinical trials. Over 15.2 million doses of the vaccine have already been administered in the U.S., underscoring its significant role in combating the ongoing pandemic.
Johnson & Johnson (NYSE: JNJ) reported Q3 2021 results, showcasing a 10.7% increase in reported sales to $23.3 billion and a 3.2% rise in net earnings to $3.67 billion. Adjusted EPS surged 18.2% to $2.60. Pharmaceutical sales grew 13.8%, led by drugs like DARZALEX and STELARA. Medical Devices operations rose 7.6%, while Consumer Health increased 5.7%. CEO Alex Gorsky announced his transition to Joaquin Duato effective January 2022, underscoring ongoing investment in innovation amidst dynamic market conditions.
Johnson & Johnson (NYSE: JNJ) announced that the FDA's Vaccines Advisory Committee voted 19-0 in favor of Emergency Use Authorization (EUA) for a booster dose of its COVID-19 vaccine for adults at least two months post-initial vaccination. This decision is backed by results from the Phase 3 ENSEMBLE 2 trial showing 94% protection against symptomatic COVID-19 after two months and 100% against severe cases. The company's commitment to combat COVID-19 continues as it awaits further regulatory decisions both nationally and internationally.
On October 14, 2021, lawyers representing over 30,000 women filed lawsuits against Johnson & Johnson (JNJ) regarding cancer claims tied to its talc body powders. They criticize J&J's bankruptcy move to evade legal accountability as hypocritical and unjust, especially given the company's substantial profits. J&J’s new subsidiary, LTL Management LLC, has filed for bankruptcy to manage these claims, proposing a $2 billion settlement fund despite total liabilities estimated at over $25 billion. The legal battle raises concerns for pending trials and could prolong suffering for affected patients.
Johnson & Johnson (NYSE: JNJ) announced that LTL Management LLC, a newly formed subsidiary, has filed for voluntary Chapter 11 bankruptcy to manage claims related to cosmetic talc litigation. This bankruptcy aims to provide an equitable resolution for current and future claimants. JNJ will fund LTL with a $2 billion trust and royalty revenue streams worth over $350 million. The company maintains its stance on the safety of its talc products, citing favorable jury trial outcomes. All cosmetic talc litigation cases will be stayed pending the bankruptcy proceedings.
Johnson & Johnson (NYSE: JNJ) is set to host a Business Review for the investment community on November 18, 2021. The event will offer insights into the company's Pharmaceuticals business, highlighting its unique strategy and strong pipeline for growth. Participants can expect a detailed overview of six therapeutic areas, live sessions with executives, and Q&A opportunities. Registration opens on November 1. A replay of the event will be available after it concludes.
Johnson & Johnson (NYSE: JNJ) appointed Jessica Moore as Vice President of Investor Relations, effective November 1, 2021. Moore, with 20 years of financial experience, most recently served as CFO for the Janssen Pharmaceutical business in EMEA. She will report to Joseph Wolk, CFO, and is expected to enhance communication of JNJ's strategies to investors. Moore holds degrees in Finance and Accounting and an MBA. This leadership change aims to leverage her expertise to positively impact JNJ's financial narrative.
Johnson & Johnson (NYSE: JNJ) announced the retirement of Dr. Paul Stoffels, Vice Chairman and Chief Scientific Officer, effective December 31, 2021. Dr. Stoffels has been pivotal in enhancing the company's innovation pipeline, leading initiatives that delivered over 25 new medicines, some of which are on the WHO's Essential Medicines List. He also played a key role in developing the COVID-19 vaccine and in global health advocacy. Johnson & Johnson aims to continue his legacy of innovation and public health commitment under new leadership.
Johnson & Johnson (NYSE: JNJ) will participate virtually in the Credit Suisse 30th Annual Healthcare Conference on November 10, 2021. Ashley McEvoy, Executive Vice President and Worldwide Chairman of Medical Devices, will represent the company in a session at 11:20 a.m. ET. This event will be accessible to investors and interested parties via the Johnson & Johnson website. A webcast and podcast replay will be available about 48 hours post-event.
For more details, visit www.investor.jnj.com.
On October 6, 2021, Janssen Pharmaceutical Companies of Johnson & Johnson revealed groundbreaking preclinical data in Nature, showcasing a novel antiviral compound that may treat all dengue fever serotypes. The compound operates by obstructing key viral proteins, inhibiting replication, and demonstrating efficacy in both prevention and treatment settings. As dengue affects up to 400 million people annually, this advancement marks a significant step in addressing a critical public health issue. Janssen aims to escalate the compound's clinical development to deliver impactful solutions for at-risk communities.