2025-06-23 07:32 | UU:JNJ | | News Release200 | IMAAVY(TM) (nipocalimab-aahu) showed greater sustained disease control versus approved FcRn blockers for generalized myasthenia gravis (gMG) at multiple timepoints over 24 weeks in newly published indirect treatment comparison (ITC) |
2025-06-15 03:15 | UU:JNJ | | News Release200 | Investigational combination of first-in-class bispecifics TALVEY(TM) and TECVAYLI(TM) shows deep and durable responses in heavily pretreated multiple myeloma patients with extramedullary disease |
2025-06-13 11:00 | UU:JNJ | | News Release200 | Johnson & Johnson's dual-targeting CAR T-cell therapy shows encouraging first results in large B-cell lymphoma |
2025-06-12 11:00 | UU:JNJ | | News Release200 | New results for Johnson & Johnson's bleximenib demonstrate promising antileukemic activity in combination with venetoclax and azacitidine for acute myeloid leukemia |
2025-06-11 08:05 | UU:JNJ | | News Release200 | New data show TREMFYA(TM) (guselkumab) is the only IL-23 inhibitor proven to significantly inhibit progression of joint structural damage in active psoriatic arthritis |
2025-06-10 16:51 | UU:JNJ | | News Release200 | Johnson & Johnson Elects Daniel Pinto, President, JPMorganChase to its Board of Directors |
2025-06-03 10:45 | UU:JNJ | | News Release200 | Early results from Johnson & Johnson's trispecific antibody show promising response in heavily pretreated multiple myeloma patients |
2025-06-03 10:45 | UU:JNJ | | News Release200 | Single infusion of CARVYKTI(TM) (ciltacabtagene autoleucel) delivered lasting treatment-free remissions for at least five years in patients with relapsed or refractory multiple myeloma |
2025-06-03 10:45 | UU:JNJ | | News Release200 | DARZALEX FASPRO(TM) (daratumumab and hyaluronidase-fihj)-based regimen shows 95 percent progression-free survival at four years in transplant-eligible, newly diagnosed patients with multiple myeloma who achieved sustained MRD negativity |
2025-06-03 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson leads with first PARP inhibitor combo to improve efficacy in patients with HRR-altered mCSPC |
2025-05-28 16:43 | UU:JNJ | | News Release200 | Johnson & Johnson to Host Investor Conference Call on Second-Quarter Results |
2025-05-21 16:40 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the Bernstein's 41st Annual Strategic Decisions Conference |
2025-05-20 18:21 | UU:JNJ | | News Release200 | U.S. FDA Oncologic Drugs Advisory Committee votes in favor of the benefit-risk profile of DARZALEX FASPRO(TM) (daratumumab and hyaluronidase-fihj) for high-risk smoldering multiple myeloma |
2025-05-14 16:40 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the Goldman Sachs 46th Annual Global Healthcare Conference |
2025-05-09 08:05 | UU:JNJ | | News Release200 | Icotrokinra results show significant skin clearance in patients with difficult-to-treat scalp and genital psoriasis |
2025-05-08 08:12 | UU:JNJ | | News Release200 | Johnson & Johnson expands efforts to champion the nursing workforce globally |
2025-05-05 08:05 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) positioned to become the first and only IL-23 inhibitor to offer subcutaneous induction in ulcerative colitis as demonstrated in new data through 24 weeks |
2025-05-05 08:05 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) delivers sustained clinical and endoscopic remission in ulcerative colitis through two years |
2025-04-30 08:29 | UU:JNJ | | News Release200 | Johnson & Johnson receives FDA approval for IMAAVY(TM) (nipocalimab-aahu), a new FcRn blocker offering long-lasting disease control in the broadest population of people living with generalized myasthenia gravis (gMG) |
2025-04-28 16:22 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the Bernstein's 41st Annual Strategic Decisions Conference |
2025-04-26 14:00 | UU:JNJ | | News Release200 | Johnson & Johnson's TAR-200 monotherapy achieves high disease-free survival of more than 80 percent in BCG-unresponsive, high-risk papillary NMIBC |
2025-04-26 13:50 | UU:JNJ | | News Release200 | Johnson & Johnson's TAR-200 monotherapy demonstrates highest complete response rate with sustained clinical benefits in patients with certain types of bladder cancer |
2025-04-24 13:17 | UU:JNJ | | SEDAR Interim MD & A813 | SEDAR Interim MD & A |
2025-04-24 13:11 | UU:JNJ | | SEDAR Interim Financial Statements812 | SEDAR Interim Financial Statements |
2025-04-21 09:36 | UU:JNJ | | News Release200 | Johnson & Johnson unveils highly anticipated and potential practice-changing data in bladder cancer treatment at AUA |
2025-04-16 16:28 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the 2025 RBC Capital Markets Global Healthcare Conference |
2025-04-15 08:55 | UU:JNJ | | News Release200 | NYSE Content Advisory: Pre-Market update + Bank of America beats earnings estimates |
2025-04-15 08:55 | UU:JNJ | | News Release200 | NYSE Content Advisory: Pre-Market update + Bank of America beats earnings estimates |
2025-04-15 06:25 | UU:JNJ | | News Release200 | Johnson & Johnson Announces 63rd Consecutive Year of Dividend Increase; Raises Quarterly Dividend by 4.8% |
2025-04-15 06:20 | UU:JNJ | | News Release200 | Johnson & Johnson Reports Q1 2025 Results |
2025-04-10 08:05 | UU:JNJ | | News Release200 | Icotrokinra results show 75% of adolescents with plaque psoriasis achieved completely clear skin and demonstrate favorable safety profile in a once daily pill |
2025-04-08 03:00 | UU:JNJ | | News Release200 | Johnson & Johnson highlights new data that showcase the strength of nipocalimab, demonstrating long-term sustained disease control in adults living with generalized myasthenia gravis (gMG) |
2025-04-07 16:25 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the BofA Securities 2025 Healthcare Conference |
2025-04-04 08:05 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) is the first and only IL-23 inhibitor to significantly reduce both the signs and symptoms and the progression of structural damage in adults living with active psoriatic arthritis |
2025-04-02 08:44 | UU:JNJ | | News Release200 | Johnson & Johnson Closes Landmark Intra-Cellular Therapies, Inc. Acquisition to Solidify Neuroscience Leadership |
2025-04-01 16:06 | UU:JNJ | | News Release200 | Johnson & Johnson Announces Expected Closing Date for Intra-Cellular Acquisition |
2025-03-31 22:20 | UU:JNJ | | News Release200 | Johnson & Johnson to Return to Tort System to Defeat Meritless Talc Claims |
2025-03-26 11:45 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus LAZCLUZE(TM) (lazertinib) outperforms osimertinib with a significant and unprecedented overall survival benefit in patients with EGFR-mutated non-small cell lung cancer |
2025-03-26 08:03 | UU:JNJ | | News Release200 | New nipocalimab data and real-world research at AAN 2025 highlight positive Phase 3 results and commitment to people living with generalized myasthenia gravis (gMG) |
2025-03-21 06:00 | UU:JNJ | | News Release200 | Johnson & Johnson Increases U.S. Investment to More than $55 Billion Over the Next Four Years |
2025-03-20 18:12 | UU:JNJ | | News Release200 | U.S. FDA approves TREMFYA(TM) (guselkumab), the first and only IL-23 inhibitor offering both subcutaneous and intravenous induction options, for adult patients with moderately to severely active Crohn's disease |
2025-03-20 08:00 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus LAZCLUZE(TM) (lazertinib) significantly outperforms standard of care in first-line EGFR-mutated lung cancer with compelling new data at ELCC 2025 |
2025-03-18 08:03 | UU:JNJ | | News Release200 | Nipocalimab, the first and only investigational treatment to be granted U.S. FDA Breakthrough Therapy designation for the treatment of adults with moderate-to-severe Sjogren's disease, has now received Fast Track designation |
2025-03-10 08:00 | UU:JNJ | | News Release200 | Icotrokinra meets primary endpoint of clinical response in ulcerative colitis study and shows potential to transform the treatment paradigm for patients |
2025-03-08 09:00 | UU:JNJ | | News Release200 | Icotrokinra results show potential to set a new standard of treatment in plaque psoriasis |
2025-03-07 14:33 | UU:JNJ | | SEDAR MD & A815 | SEDAR Annual Report |
2025-03-07 14:27 | UU:JNJ | | SEDAR Audited Annual Financial Statements804 | SEDAR Audited Annual Financial Statements |
2025-03-05 16:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Host Investor Conference Call on First-Quarter Results |
2025-03-04 16:15 | UU:JNJ | | News Release200 | Johnson & Johnson Announces Darren Snellgrove as Vice President, Investor Relations |
2025-02-21 07:00 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) subcutaneous (SC) induction data support potential to be the first and only in its class to offer the option of both intravenous and SC induction therapy in ulcerative colitis |
2025-02-13 08:05 | UU:JNJ | | News Release200 | New nipocalimab data published in mAbs journal details differentiated molecular design, clinical profile and potential of nipocalimab to treat IgG-driven alloantibody and autoantibody diseases |
2025-02-03 16:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the 45th Annual TD Cowen Healthcare Conference |
2025-01-23 05:35 | UU:JNJ | | News Release200 | Findings from pivotal nipocalimab Phase 3 study in a broad antibody positive population of people living with generalized myasthenia gravis (gMG) published in The Lancet Neurology |
2025-01-22 06:20 | UU:JNJ | | News Release200 | Johnson & Johnson Reports Q4 and Full-Year 2024 Results |
2025-01-21 08:00 | UU:JNJ | | News Release200 | SPRAVATO(TM) (esketamine) approved in the U.S. as the first and only monotherapy for adults with treatment-resistant depression |
2025-01-15 08:00 | UU:JNJ | | News Release200 | New Drug Application initiated with U.S. FDA for TAR-200, the first and only intravesical drug releasing system for patients with BCG-unresponsive high-risk non-muscle-invasive bladder cancer |
2025-01-13 06:32 | UU:JNJ | | News Release200 | Johnson & Johnson Strengthens Neuroscience Leadership with Acquisition of Intra-Cellular Therapies, Inc. |
2025-01-13 06:30 | UU:JNJ | | News Release200 | Johnson & Johnson Strengthens Neuroscience Leadership with Acquisition of Intra-Cellular Therapies, Inc. |
2025-01-09 08:04 | UU:JNJ | | News Release200 | Nipocalimab granted U.S. FDA Priority Review for the treatment of generalized myasthenia gravis |
2025-01-08 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson's Posdinemab and Tau Active Immunotherapy Receive U.S. FDA Fast Track Designations for the Treatment of Alzheimer's Disease |
2025-01-07 08:00 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus LAZCLUZE(TM) (lazertinib) show statistically significant and clinically meaningful improvement in overall survival versus osimertinib |
2025-01-02 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson Announces Quarterly Dividend for First Quarter 2025 |
2024-12-12 16:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the 43rd Annual J.P. Morgan Healthcare Conference |
2024-12-10 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson to Host Investor Conference Call on Fourth-Quarter Results |
2024-12-09 19:30 | UU:JNJ | | News Release200 | CARVYKTI(TM) (ciltacabtagene autoleucel) demonstrated significantly higher rates of minimal residual disease (MRD) negativity compared to standard therapies in the CARTITUDE-4 study |
2024-12-09 08:00 | UU:JNJ | | News Release200 | Warm autoimmune hemolytic anemia (wAIHA) research presented by Johnson & Johnson highlights profound disease burden and unmet need for targeted treatment options |
2024-12-08 19:30 | UU:JNJ | | News Release200 | DARZALEX FASPRO(TM) (daratumumab and hyaluronidase-fihj)-based regimens demonstrate improved rates of minimal residual disease (MRD) negativity and progression-free survival in patients with newly diagnosed multiple myeloma |
2024-12-08 12:33 | UU:JNJ | | News Release200 | TECVAYLI(TM) (teclistamab-cqyv) demonstrates potential as frontline combination therapy for patients with newly diagnosed multiple myeloma |
2024-12-08 11:21 | UU:JNJ | | News Release200 | DARZALEX FASPRO(TM) (daratumumab and hyaluronidase-fihj) shows 51 percent reduction in risk of progression to active multiple myeloma for patients with high-risk smoldering multiple myeloma |
2024-12-02 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson seeks U.S. FDA approval for first pediatric indications for TREMFYA(TM) (guselkumab) |
2024-11-22 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson seeks U.S. FDA approval for subcutaneous induction regimen of TREMFYA(TM) (guselkumab) in ulcerative colitis, a first for an IL-23 inhibitor |
2024-11-19 09:02 | UU:JNJ | | News Release200 | Johnson & Johnson to showcase strength of its broad hematology portfolio and pipeline at the 2024 American Society of Hematology Annual Meeting |
2024-11-18 16:30 | UU:JNJ | | News Release200 | Icotrokinra delivered an industry-leading combination of significant skin clearance with demonstrated tolerability in a once daily pill in Phase 3 topline results |
2024-11-14 10:00 | UU:JNJ | | News Release200 | Nipocalimab demonstrates significant clinical improvement in disease activity and IgG reduction in Phase 2 Sjogren's disease study |
2024-11-11 16:05 | UU:JNJ | | News Release200 | Nipocalimab is the first and only investigational therapy granted U.S. FDA Breakthrough Therapy Designation for the treatment of adults living with moderate-to-severe Sjogren's disease |
2024-11-08 07:00 | UU:JNJ | | News Release200 | Johnson & Johnson submits applications in the U.S. and EU seeking approval of DARZALEX FASPRO(TM) / DARZALEX(TM) as subcutaneous monotherapy for high-risk smoldering multiple myeloma |
2024-11-07 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson advances leadership in rheumatic disease innovation with 43 abstracts at ACR 2024 |
2024-11-04 15:11 | UU:JNJ | | News Release200 | Empower 2024 Delivers Groundbreaking Insights and Innovation to Achieve Data-Driven Healthcare |
2024-10-28 15:40 | UU:JNJ | | SEDAR Interim Financial Statements812 | SEDAR Interim MD & A |
2024-10-28 07:30 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) is the first and only IL-23 inhibitor to demonstrate robust results with a fully subcutaneous regimen in both induction and maintenance in Crohn's disease |
2024-10-25 08:05 | UU:JNJ | | News Release200 | New SPECTREM study findings reveal TREMFYA(TM) (guselkumab) effectively clears overlooked and undertreated plaque psoriasis |
2024-10-24 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson highlights innovative neuropsychiatry portfolio and pipeline at Psych Congress |
2024-10-15 08:00 | UU:JNJ | | News Release200 | Nipocalimab demonstrates sustained disease control in adolescents living with generalized myasthenia gravis in Phase 2/3 study |
2024-10-15 06:25 | UU:JNJ | | News Release200 | Johnson & Johnson Announces Quarterly Dividend for Fourth Quarter 2024 |
2024-10-15 06:20 | UU:JNJ | | News Release200 | Johnson & Johnson Reports Q3 2024 Results |
2024-10-10 16:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the Stifel 2024 Healthcare Conference |
2024-10-10 08:00 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) demonstrates impressive results across biologic-naive and biologic-refractory patients in Crohn's disease and ulcerative colitis |
2024-10-09 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson Completes Acquisition of V-Wave |
2024-10-04 16:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the Guggenheim Global Healthcare Conference |
2024-10-02 09:00 | UU:JNJ | | News Release200 | ERLEADA(TM) (apalutamide) demonstrates statistically significant and clinically meaningful improvement in overall survival compared to enzalutamide in patients with metastatic castration-sensitive prostate cancer |
2024-09-30 16:05 | UU:JNJ | | News Release200 | Johnson & Johnson files for U.S. FDA approval of DARZALEX FASPRO(TM)-based quadruplet regimen for newly diagnosed multiple myeloma patients for whom transplant is not planned |
2024-09-30 08:05 | UU:JNJ | | News Release200 | Johnson & Johnson Rolls Out New TECNIS Odyssey Next-Generation Intraocular Lens Offering Cataract Patients Precise Vision at Every Distance in Any Lighting |
2024-09-27 16:30 | UU:JNJ | | News Release200 | CARVYKTI(TM) is the first and only cell therapy to significantly extend overall survival versus standard therapies for patients with multiple myeloma as early as second line |
2024-09-27 13:05 | UU:JNJ | | News Release200 | DARZALEX(TM) (daratumumab)-based maintenance regimens show clinically meaningful deep and durable responses in transplant-eligible patients with newly diagnosed multiple myeloma |
2024-09-27 13:00 | UU:JNJ | | News Release200 | DARZALEX FASPRO(TM)-based quadruplet regimen significantly improves minimal residual disease negativity for newly diagnosed multiple myeloma patients for whom transplant is not planned |
2024-09-27 08:05 | UU:JNJ | | News Release200 | Novel combination of TALVEY(TM) (talquetamab-tgvs) and TECVAYLI(TM) (teclistamab-cqyv) suggests high response rates and durable responses in triple-class refractory patients with relapsed or refractory multiple myeloma, including those with extramedullary |
2024-09-27 08:00 | UU:JNJ | | News Release200 | TALVEY(TM) (talquetamab-tgvs) and DARZALEX FASPRO(TM) (daratumumab and hyaluronidase-fihj) based combination shows deep and durable responses in patients with relapsed or refractory multiple myeloma |
2024-09-20 15:43 | UU:JNJ | | News Release200 | Johnson & Johnson Announces that its Subsidiary, Red River Talc LLC, has Filed a Voluntary Prepackaged Chapter 11 Case to Resolve All Current and Future Ovarian Cancer Talc Claims |
2024-09-19 18:54 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus standard of care approved in the U.S. as first and only targeted regimen to cut risk of disease progression by more than half in second-line EGFR-mutated advanced lung cancer |
2024-09-16 02:50 | UU:JNJ | | News Release200 | Neoadjuvant TAR-200 plus cetrelimab nearly doubles the pathological complete response rate compared to cetrelimab alone in patients with muscle-invasive bladder cancer |
2024-09-15 02:30 | UU:JNJ | | News Release200 | New data from TAR-200 Phase 2b SunRISe-1 study show 84 percent complete response rate in patients with high-risk non-muscle-invasive bladder cancer |
2024-09-14 09:45 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus chemotherapy show 49 percent overall response rate in metastatic colorectal cancer |
2024-09-14 03:10 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus chemotherapy shows positive overall survival trend versus chemotherapy in patients with previously treated EGFR-mutated lung cancer |
2024-09-11 18:22 | UU:JNJ | | News Release200 | TREMFYA(TM) (guselkumab) receives U.S. FDA approval for adults with moderately to severely active ulcerative colitis, strengthening Johnson & Johnson's leadership in inflammatory bowel disease |
2024-09-10 17:15 | UU:JNJ | | News Release200 | Dexamethasone reduces infusion-related reactions in patients with EGFR-mutated non-small cell lung cancer treated with intravenous RYBREVANT(TM) (amivantamab-vmjw) |
2024-09-08 13:47 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus LAZCLUZE(TM) (lazertinib) show strong favorable overall survival trend versus osimertinib in EGFR-mutated advanced lung cancer |
2024-09-05 16:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Host Investor Conference Call on Third-Quarter Results |
2024-08-29 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson seeks first approval of nipocalimab to treat broadest population living with antibody positive generalized myasthenia gravis |
2024-08-27 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson is transforming solid tumor cancer outcomes with new data at the 2024 World Conference on Lung Cancer and European Society for Medical Oncology Congress |
2024-08-26 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson's Executive Vice President, Chief Human Resources Officer Peter Fasolo to Retire; Kristen Mulholland Named Chief Human Resources Officer, Effective October 1, 2024 |
2024-08-20 07:30 | UU:JNJ | | News Release200 | Johnson & Johnson to Acquire V-Wave |
2024-08-20 07:00 | UU:JNJ | | News Release200 | RYBREVANT(TM) (amivantamab-vmjw) plus LAZCLUZE(TM) (lazertinib) approved in the U.S. as a first-line chemotherapy-free treatment for patients with EGFR-mutated advanced lung cancer |
2024-08-07 17:00 | UU:JNJ | | News Release200 | Groundbreaking nipocalimab study of pregnant individuals at high risk for early onset severe hemolytic disease of the fetus and newborn published in The New England Journal of Medicine |
2024-08-06 09:00 | UU:JNJ | | News Release200 | Alzheimer's Disease Diagnostics & Therapeutics Market Driven by Use of Biomarkers and Advancing R&D Activities |
2024-07-30 18:45 | UU:JNJ | | SEDAR Interim Financial Statements812 | SEDAR Interim MD & A |
2024-07-30 18:42 | UU:JNJ | | News Release200 | DARZALEX FASPRO(TM) (daratumumab and hyaluronidase-fihj)-based quadruplet regimen approved in the U.S. for patients with newly diagnosed multiple myeloma who are transplant-eligible |
2024-07-29 16:00 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the 2024 Wells Fargo Healthcare Conference |
2024-07-23 16:00 | UU:JNJ | | News Release200 | Johnson & Johnson to Participate in the Morgan Stanley 22nd Annual Global Healthcare Conference |
2024-07-22 08:00 | UU:JNJ | | News Release200 | Johnson & Johnson seeks U.S. FDA approval of SPRAVATO(TM) (esketamine) as the first and only monotherapy for adults with treatment-resistant depression |
2024-07-17 06:25 | UU:JNJ | | News Release200 | Johnson & Johnson Announces Quarterly Dividend for Third Quarter 2024 |
2024-07-17 06:20 | UU:JNJ | | News Release200 | Johnson & Johnson reports Q2 2024 results |
2024-07-15 08:05 | UU:JNJ | | News Release200 | NKGen Biotech Appoints Dr. Marco Gottardis to its Board of Directors |
2024-07-11 07:30 | UU:JNJ | | News Release200 | Johnson & Johnson Strengthens Pipeline to Lead in Atopic Dermatitis With the Completion of the Acquisition of Yellow Jersey Therapeutics, Gaining Ownership of NM26 |