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    <lastBuildDate>Fri, 16 Oct 2026 12:55:21 GMT</lastBuildDate>
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      <title>CHMP recommends approval of Johnson &amp; Johnson’s TALVEY®▼ (talquetamab) plus daratumumab in earlier line treatment of relapsed/refractory multiple myeloma</title>
      <link>https://www.jnj.com/media-center/press-releases/chmp-recommends-approval-of-johnson-johnsons-talvey-talquetamab-plus-daratumumab-in-earlier-line-treatment-of-relapsed-refractory-multiple-myeloma</link>
      <description>· If approved, TALVEY® plus daratumumab will be the only GPRC5D-targeting bispecific antibody combination therapy for relapsed or refractory multiple myeloma as early as second line · CHMP recommendation based on Phase 3 results where talquetamab and daratumumab, with or without pomalidomide, showed progression-free survival of up to 81% and overall survival of up to 89% at 24 months1</description>
      <pubDate>Fri, 16 Oct 2026 12:55:21 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/chmp-recommends-approval-of-johnson-johnsons-talvey-talquetamab-plus-daratumumab-in-earlier-line-treatment-of-relapsed-refractory-multiple-myeloma</guid>
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      <title>New TREMFYA® (guselkumab) study shows consistent perianal fistula remission across key Crohn’s disease patient subgroups</title>
      <link>https://www.jnj.com/media-center/press-releases/new-tremfya-guselkumab-study-shows-consistent-perianal-fistula-remission-across-key-crohns-disease-patient-subgroups</link>
      <description>· New prespecified analyses showed consistent findings across clinically important and difficult to treat subgroups, including patients with prior biologic exposure · Findings build on first positive results where TREMFYA achieved combined fistula remission rates of up to 28% across dosing groups · Results come from the first dedicated Phase 3 randomized, placebo-controlled trial in adults managing Crohn’s disease with perianal fistula in more than 20 years</description>
      <pubDate>Tue, 13 Oct 2026 20:10:51 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/new-tremfya-guselkumab-study-shows-consistent-perianal-fistula-remission-across-key-crohns-disease-patient-subgroups</guid>
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      <title>TREMFYA® (guselkumab) demonstrated sustained clinical and endoscopic remission through 3 years in moderately to severely active Crohn’s disease</title>
      <link>https://www.jnj.com/media-center/press-releases/tremfya-guselkumab-demonstrated-sustained-clinical-and-endoscopic-remission-through-3-years-in-moderately-to-severely-active-crohns-disease</link>
      <description>· New long-term data showed clinical remission rates of up to 94% and endoscopic remission rates of up to 61% in adults with moderately to severely active Crohn’s disease · 88% of patients achieved 90-day corticosteroid-free clinical remission</description>
      <pubDate>Tue, 13 Oct 2026 20:09:44 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/tremfya-guselkumab-demonstrated-sustained-clinical-and-endoscopic-remission-through-3-years-in-moderately-to-severely-active-crohns-disease</guid>
    </item>
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      <title>Johnson &amp; Johnson Q3 2026 earnings: CEO and CFO prepared remarks</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-q3-2026-earnings-ceo-and-cfo-prepared-remarks</link>
      <description>On the Q3 2026 earnings call, Johnson &amp; Johnson Chairman and CEO Joaquin Duato and Executive Vice President and CFO Joe Wolk discussed recent performance and long-term outlook.</description>
      <pubDate>Tue, 13 Oct 2026 13:07:42 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-q3-2026-earnings-ceo-and-cfo-prepared-remarks</guid>
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      <title>Johnson &amp; Johnson Announces Quarterly Dividend for Fourth Quarter 2026</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-announces-quarterly-dividend-for-fourth-quarter-2026</link>
      <description />
      <pubDate>Tue, 13 Oct 2026 10:25:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-announces-quarterly-dividend-for-fourth-quarter-2026</guid>
    </item>
    <item>
      <title>Johnson &amp; Johnson reports Q3 2026 results, raises 2026 guidance</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-reports-q3-2026-results-raises-2026-guidance</link>
      <description>2025 Second-Quarter reported sales growth of 5.8% to $23.7 Billion with operational growth of 4.6%* and adjusted operational growth of 3.0%* •</description>
      <pubDate>Tue, 13 Oct 2026 10:20:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-reports-q3-2026-results-raises-2026-guidance</guid>
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      <title>New Johnson &amp; Johnson ICOTYDE® (icotrokinra) long-term data demonstrate robust 2-year results in the treatment of adults and adolescents with plaque psoriasis</title>
      <link>https://www.jnj.com/media-center/press-releases/new-johnson-johnson-icotyde-icotrokinra-long-term-data-demonstrate-robust-2-year-results-in-the-treatment-of-adults-and-adolescents-with-plaque-psoriasis</link>
      <description>· Phase 3 data presented at Fall Clinical Dermatology show high, sustained response rates in adults and adolescents, with nearly three-quarters achieving clear or almost clear skin at two years and a continued favorable safety profile</description>
      <pubDate>Fri, 09 Oct 2026 11:01:23 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/new-johnson-johnson-icotyde-icotrokinra-long-term-data-demonstrate-robust-2-year-results-in-the-treatment-of-adults-and-adolescents-with-plaque-psoriasis</guid>
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      <title>Johnson &amp; Johnson announces new ICOTYDE® (icotrokinra) data in difficult-to-treat plaque psoriasis with proven durability through 2-years, affirming its use as a powerful first line systemic therapy</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-announces-new-icotyde-icotrokinra-data-in-difficult-to-treat-plaque-psoriasis-with-proven-durability-through-2-years-affirming-its-use-as-a-powerful-first-line-systemic-therapy</link>
      <description>• Revolutionary IL-23R targeted oral peptide delivers sustained skin clearance and a favorable safety profile in patients with psoriasis affecting sensitive, highly visible areas of the body • 60% of patients with scalp psoriasis and 89% with genital psoriasis achieved site-specific complete skin clearance at Week 112</description>
      <pubDate>Fri, 02 Oct 2026 10:12:35 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-announces-new-icotyde-icotrokinra-data-in-difficult-to-treat-plaque-psoriasis-with-proven-durability-through-2-years-affirming-its-use-as-a-powerful-first-line-systemic-therapy</guid>
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      <title>New Global Survey by Johnson &amp; Johnson Finds Most Women Don’t Connect Eye Health Changes with Menopause</title>
      <link>https://www.jnj.com/media-center/press-releases/new-global-survey-by-johnson-johnson-finds-most-women-dont-connect-eye-health-changes-with-menopause</link>
      <description>Johnson &amp; Johnson, Naomi Watts and the American Optometric Association encourage women to make eye health part of midlife care</description>
      <pubDate>Thu, 01 Oct 2026 11:45:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/new-global-survey-by-johnson-johnson-finds-most-women-dont-connect-eye-health-changes-with-menopause</guid>
    </item>
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      <title>Johnson &amp; Johnson presents new data reinforcing sustained disease control and improved daily function achieved with IMAAVY® (nipocalimab-aahu) in generalized myasthenia gravis (gMG)</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-presents-new-data-reinforcing-sustained-disease-control-and-improved-daily-function-achieved-with-imaavy-nipocalimab-aahu-in-generalized-myasthenia-gravis-gmg</link>
      <description>New two-year findings from the Phase 2/3 long-term extension demonstrate sustained disease control through two years, improvement in daily function and muscle strength, and reductions in corticosteroid use in anti-AChR+a adolescents Retrospective survey in adults identified fluctuating symptom control as a top driver for discontinuing prior advanced treatment, with most patient outcomes improving after transitioning to IMAAVY Data among 15 novel abstracts on IMAAVY to be presented at the MGFA Scientific Session during AANEM 2026</description>
      <pubDate>Tue, 29 Sep 2026 12:13:48 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-presents-new-data-reinforcing-sustained-disease-control-and-improved-daily-function-achieved-with-imaavy-nipocalimab-aahu-in-generalized-myasthenia-gravis-gmg</guid>
    </item>
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      <title>Johnson &amp; Johnson announces TREMFYA® (guselkumab) is the first and only IL-23 inhibitor to show significant improvement in spinal pain and stiffness in landmark axial psoriatic arthritis (PsA) study</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-announces-tremfya-guselkumab-is-the-first-and-only-il-23-inhibitor-to-show-significant-improvement-in-spinal-pain-and-stiffness-in-landmark-axial-psoriatic-arthritis-psa-study</link>
      <description>· Topline results show TREMFYA met the primary and major secondary endpoints of axial involvement in PsA - including spinal pain and stiffness - and demonstrated significant improvement in MRI-confirmed inflammation · First-ever study to use objective MRI assessments to confirm presence of axial involvement and demonstrate axial inflammation reduction in PsA</description>
      <pubDate>Fri, 25 Sep 2026 11:41:08 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-announces-tremfya-guselkumab-is-the-first-and-only-il-23-inhibitor-to-show-significant-improvement-in-spinal-pain-and-stiffness-in-landmark-axial-psoriatic-arthritis-psa-study</guid>
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      <title>Single infusion of CARVYKTI® (ciltacabtagene autoleucel) delivered five-year treatment-free remissions in 50% of patients in early line relapsed/refractory multiple myeloma</title>
      <link>https://www.jnj.com/media-center/press-releases/single-infusion-of-carvykti-ciltacabtagene-autoleucel-delivered-five-year-treatment-free-remissions-in-50-of-patients-in-early-line-relapsed-refractory-multiple-myeloma</link>
      <description>· New results suggest earlier treatment may increase the likelihood of long-term remission · Study adds to Johnson &amp; Johnson's overwhelming body of evidence supporting its innovative multiple myeloma therapies in second line, where earlier intervention may increase long-term remission and disease control</description>
      <pubDate>Fri, 25 Sep 2026 11:17:30 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/single-infusion-of-carvykti-ciltacabtagene-autoleucel-delivered-five-year-treatment-free-remissions-in-50-of-patients-in-early-line-relapsed-refractory-multiple-myeloma</guid>
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      <title>New model-based analysis further supports the potential of TECVAYLI® (teclistamab-cqyv) plus DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) to redefine long-term survival expectations in early line relapsed/refractory multiple myeloma</title>
      <link>https://www.jnj.com/media-center/press-releases/new-model-based-analysis-further-supports-the-potential-of-tecvayli-teclistamab-cqyv-plus-darzalex-faspro-daratumumab-and-hyaluronidase-fihj-to-redefine-long-term-survival-expectations-in-early-line-relapsed-refractory-multiple-myeloma</link>
      <description>· Analysis shows ~87% of patients treated with TECVAYLI® plus DARZALEX FASPRO® as early as second line were estimated to have comparable mortality risk to the general population · A separate analysis shows the survival benefit was driven by a 90% reduction in the risk of multiple myeloma progression versus standard of care, with no significant difference in rates of non-relapse mortality · Johnson &amp; Johnson is advancing a differentiated multiple myeloma portfolio designed to deliver deeper, more durable disease control and improve long-term outcomes for patients</description>
      <pubDate>Wed, 23 Sep 2026 14:12:59 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/new-model-based-analysis-further-supports-the-potential-of-tecvayli-teclistamab-cqyv-plus-darzalex-faspro-daratumumab-and-hyaluronidase-fihj-to-redefine-long-term-survival-expectations-in-early-line-relapsed-refractory-multiple-myeloma</guid>
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      <title>DePuy Synthes Showcases Next-Generation Trauma Innovations at OTA 2026</title>
      <link>https://www.jnj.com/media-center/press-releases/depuy-synthes-showcases-next-generation-trauma-innovations-at-ota-2026</link>
      <description>New innovations across fracture fixation, connected care, AI-assisted surgery and procedural solutions reinforce the company's leadership in trauma care.</description>
      <pubDate>Tue, 22 Sep 2026 12:07:33 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/depuy-synthes-showcases-next-generation-trauma-innovations-at-ota-2026</guid>
    </item>
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      <title>CAPLYTA® (lumateperone) shows significant and rapid improvement in bipolar mania in pivotal Phase 3 study</title>
      <link>https://www.jnj.com/media-center/press-releases/caplyta-lumateperone-shows-significant-and-rapid-improvement-in-bipolar-mania-in-pivotal-phase-3-study</link>
      <description>CAPLYTA® significantly reduced the signs and symptoms of acute manic episodes associated with bipolar I disorder as early as Day 3, with benefits sustained through Week 3 Results build on the established efficacy, safety and tolerability profile of CAPLYTA®, further supporting its potential to reach more patients across bipolar I and II disorders</description>
      <pubDate>Mon, 21 Sep 2026 13:45:12 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/caplyta-lumateperone-shows-significant-and-rapid-improvement-in-bipolar-mania-in-pivotal-phase-3-study</guid>
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      <title>RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) plus LAZCLUZE® (lazertinib) with prophylactic strategies shows low rates of treatment-related events at WCLC 2026</title>
      <link>https://www.jnj.com/media-center/press-releases/rybrevant-faspro-amivantamab-and-hyaluronidase-lpuj-plus-lazcluze-lazertinib-with-prophylactic-strategies-shows-low-rates-of-treatment-related-events-at-wclc-2026</link>
      <description>Low rates of rash, blood clots and administration-related reactions were observed with subcutaneous treatment and prophylaxis Fewer than 1% of patients discontinued treatment due to treatment-related events at one year New findings from Johnson &amp; Johnson build on the MARIPOSA survival benefit and strengthen evidence for RYBREVANT FASPRO plus LAZCLUZE as first-line treatment</description>
      <pubDate>Tue, 15 Sep 2026 12:30:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/rybrevant-faspro-amivantamab-and-hyaluronidase-lpuj-plus-lazcluze-lazertinib-with-prophylactic-strategies-shows-low-rates-of-treatment-related-events-at-wclc-2026</guid>
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      <title>Johnson &amp; Johnson’s 2026 Oncology Care Index Finds Community Oncologists Confident in AI’s Promise, but Practical Adoption Still Lags</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnsons-2026-oncology-care-index-finds-community-oncologists-confident-in-ais-promise-but-practical-adoption-still-lags</link>
      <description>• Reported AI adoption in oncology has increased from 19% of healthcare providers across all practice settings in 2025 to 49% of community oncologists specifically in 2026 • Meanwhile use of advanced tools like predictive models remains low, at just 19%, revealing a gap between adoption and deeper implementation</description>
      <pubDate>Mon, 14 Sep 2026 20:15:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnsons-2026-oncology-care-index-finds-community-oncologists-confident-in-ais-promise-but-practical-adoption-still-lags</guid>
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      <title>Johnson &amp; Johnson’s RYBREVANT® (amivantamab-vmjw) plus chemotherapy delivers longest reported median overall survival in EGFR exon 20 insertion mutation-positive lung cancer</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnsons-rybrevant-amivantamab-vmjw-plus-chemotherapy-delivers-longest-reported-median-overall-survival-in-egfr-exon-20-insertion-mutation-positive-lung-cancer</link>
      <description>RYBREVANT plus chemotherapy demonstrates durable benefit with a differentiated approach that dual-targets EGFR and MET Results mark significant progress for a patient population with poor outcomes and a historical five-year survival rate of just 8%</description>
      <pubDate>Mon, 14 Sep 2026 12:30:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnsons-rybrevant-amivantamab-vmjw-plus-chemotherapy-delivers-longest-reported-median-overall-survival-in-egfr-exon-20-insertion-mutation-positive-lung-cancer</guid>
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      <title>New overall survival data and treatment experience improvements reinforce the impact of RYBREVANT® (amivantamab-vmjw)-based regimens in EGFR-mutated lung cancer at WCLC 2026</title>
      <link>https://www.jnj.com/media-center/press-releases/new-overall-survival-data-and-treatment-experience-improvements-reinforce-the-impact-of-rybrevant-amivantamab-vmjw-based-regimens-in-egfr-mutated-lung-cancer-at-wclc-2026</link>
      <description>Presidential Symposium to feature final overall survival results for first-line RYBREVANT plus chemotherapy in EGFR exon 20 insertion-mutated NSCLC Additional findings show low rates of key treatment-related events with subcutaneous RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) and prophylactic strategies</description>
      <pubDate>Fri, 11 Sep 2026 21:00:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/new-overall-survival-data-and-treatment-experience-improvements-reinforce-the-impact-of-rybrevant-amivantamab-vmjw-based-regimens-in-egfr-mutated-lung-cancer-at-wclc-2026</guid>
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      <title>Johnson &amp; Johnson receives CE Marking for ACUVUE OASYS MAX Reusable Contact Lenses</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-receives-ce-marking-for-acuvue-oasys-max-reusable-contact-lenses</link>
      <description>New 2-week reusable contact lens brings advanced ACUVUE OASYS MAX technologies to deliver superior comfort and visual clarity to patients, even at day 14*†i Expands the ACUVUE OASYS MAX portfolio with an advanced option for reusable contact lens wearers Designed to meet the growing demand for lasting comfort and clear vision in today’s screen-intensive world *†1</description>
      <pubDate>Thu, 10 Sep 2026 11:45:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-receives-ce-marking-for-acuvue-oasys-max-reusable-contact-lenses</guid>
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      <title>Johnson &amp; Johnson presents new data at IMS 2026 highlighting its industry-leading multiple myeloma portfolio, with the goal of advancing the potential for cure</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-presents-new-data-at-ims-2026-highlighting-its-industry-leading-multiple-myeloma-portfolio-with-the-goal-of-advancing-the-potential-for-cure</link>
      <description>· 35+ abstracts demonstrate new findings across DARZALEX®, TECVAYLI® plus DARZALEX FASPRO®, CARVYKTI®, TALVEY®, and the investigational trispecific antibody ramantamig, highlighting the potential of early intervention with immune-based therapies to transform outcomes across the patient journey · With decades of leadership in multiple myeloma, Johnson &amp; Johnson continues to drive innovation throughout the patient journey, from market-leading backbone therapies to next-generation immune-based approaches</description>
      <pubDate>Wed, 09 Sep 2026 12:30:00 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-presents-new-data-at-ims-2026-highlighting-its-industry-leading-multiple-myeloma-portfolio-with-the-goal-of-advancing-the-potential-for-cure</guid>
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      <title>Johnson &amp; Johnson spotlights new neuropsychiatry data across bipolar mania, depression and schizophrenia at Psych Congress 2026</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-spotlights-new-neuropsychiatry-data-across-bipolar-mania-depression-and-schizophrenia-at-psych-congress-2026</link>
      <description>First presentation of pivotal Phase 3 CAPLYTA® data in adults with bipolar mania underscores the asset’s potential across mood disorders New SPRAVATO® analyses and schizophrenia research emphasize a focus on complex, high-burden neuropsychiatric conditions</description>
      <pubDate>Tue, 08 Sep 2026 12:00:07 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-spotlights-new-neuropsychiatry-data-across-bipolar-mania-depression-and-schizophrenia-at-psych-congress-2026</guid>
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      <title>Johnson &amp; Johnson to Participate in the Deutsche Bank 2026 Healthcare Summit</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-to-participate-in-the-deutsche-bank-2026-healthcare-summit</link>
      <description />
      <pubDate>Wed, 02 Sep 2026 20:07:36 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-to-participate-in-the-deutsche-bank-2026-healthcare-summit</guid>
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      <title>Johnson &amp; Johnson to Host Investor Conference Call on Third-Quarter Results</title>
      <link>https://www.jnj.com/media-center/press-releases/johnson-johnson-host-investor-conference-call-on-third-quarter-results</link>
      <description />
      <pubDate>Mon, 31 Aug 2026 21:02:23 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/johnson-johnson-host-investor-conference-call-on-third-quarter-results</guid>
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      <title>FDA approves IMAAVY® (nipocalimab-aahu) as first-ever treatment for warm autoimmune hemolytic anemia (wAIHA), representing a landmark advancement for patients</title>
      <link>https://www.jnj.com/media-center/press-releases/fda-approves-imaavy-nipocalimab-aahu-as-first-ever-treatment-for-warm-autoimmune-hemolytic-anemia-waiha-representing-a-landmark-advancement-for-patients</link>
      <description>· IMAAVY is an immunoselective FcRn blocker designed to target and reduce pathogenic immunoglobulin G (IgG) autoantibodies while also preserving B-cell function · Warm autoimmune hemolytic anemia is a rare, life-threatening disease in which autoantibodies cause the destruction of red blood cells, leading to severe anemia and debilitating fatigue · The approval is based on the pivotal Phase 2/3 study which demonstrated durable hemoglobin responsea · A mean increase in hemoglobin of 1 g/dL at Week 1b and improvement in FACIT-Fatiguec score at Week 24 were observed in IMAAVY-treated patientsd</description>
      <pubDate>Mon, 24 Aug 2026 22:26:56 GMT</pubDate>
      <guid>https://www.jnj.com/media-center/press-releases/fda-approves-imaavy-nipocalimab-aahu-as-first-ever-treatment-for-warm-autoimmune-hemolytic-anemia-waiha-representing-a-landmark-advancement-for-patients</guid>
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