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      <a target="_blank" rel="nofollow" href="https://www.etftrends.com/thematic-investing-content-hub/healthcare-etfs-broad-exposure-breakthroughs/">Healthcare ETFs: From Broad Exposure to Big Breakthroughs</a>
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        With AI and space dominating many of the market&#39;s most popular investment themes, it can be difficult to find differentiated opportunities. Healthcare is often viewed as one of the more defensive sectors, supported by relatively steady demand regardless of the economic environment.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/10/3309940/0/en/FDA-Issues-Complete-Response-Letter-for-AbbVie-s-Fast-Acting-Neurotoxin-TrenibotE-Spokane-dermatologist-Dr-Philip-Werschler-on-What-the-Letter-Means.html">FDA Issues Complete Response Letter for AbbVie&#39;s Fast-Acting Neurotoxin TrenibotE; Spokane dermatologist Dr. Philip Werschler on What the Letter Means</a>
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        The agency&#39;s letter cited manufacturing-related items and raised no safety or efficacy concerns. Werschler, a Spokane dermatologist who has served as a clinical trial investigator in dermatology and aesthetic medicine, explains how a Complete Response Letter functions and what a serotype E toxin could add to the category.
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/abbvie-presents-new-data-across-its-blood-cancer-portfolio-at-eha-2026-302793179.html">AbbVie Presents New Data Across Its Blood Cancer Portfolio at EHA 2026</a>
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        Data being presented, including six oral presentations, reinforce AbbVie&#39;s leadership and commitment to ongoing research to improve outcomes for people living with blood cancers NORTH CHICAGO, Ill., June 8, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced it will share new data at the European Hematology Association (EHA) 2026 Congress and will showcase clinical advancements from resear...
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/british-drug-cost-watchdog-recommends-use-abbvies-ovarian-cancer-therapy-2026-06-03/">British drug-cost watchdog recommends use of AbbVie&#39;s ovarian cancer therapy</a>
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        The UK cost-effectiveness watchdog on Thursday recommended AbbVie&#39;s &quot;guided missile&quot; cancer therapy, Elahere, for patients with a hard-to-treat form of ovarian cancer.
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/abbvie-to-present-at-the-goldman-sachs-47th-annual-global-healthcare-conference-302787501.html">AbbVie to Present at the Goldman Sachs 47th Annual Global Healthcare Conference</a>
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        NORTH CHICAGO, Ill., June 2, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV) will participate in the Goldman Sachs 47th Annual Global Healthcare Conference on Tuesday, June 9, 2026.
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/abbvie-announces-european-commission-authorization-of-expanded-label-for-venclyxto-venetoclax-to-include-additional-combinations-in-previously-untreated-chronic-lymphocytic-leukemia-302785137.html">AbbVie Announces European Commission Authorization of Expanded Label for VENCLYXTO® (venetoclax) to Include Additional Combinations in Previously Untreated Chronic Lymphocytic Leukemia</a>
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        Addition of VENCLYXTO plus acalabrutinib, with or without obinutuzumab, and VENCLYXTO plus ibrutinib supported by data from Phase 3 AMPLIFY trial, Phase 3 GLOW trial and Phase 2 CAPTIVATE trial Fixed-duration VENCLYXTO-based combination regimens provide patients with additional CLL treatment options that may offer the potential for treatment-free intervals NORTH CHICAGO, Ill., May 29, 2026 /PRN...
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/us-fda-approves-decnupaztm-pivekimab-sunirine-pvzy-for-treatment-of-adult-patients-with-blastic-plasmacytoid-dendritic-cell-neoplasm-an-ultra-rare-and-aggressive-blood-cancer-with-limited-treatment-options-302783714.html">U.S. FDA Approves DECNUPAZTM (pivekimab sunirine-pvzy) for Treatment of Adult Patients with Blastic Plasmacytoid Dendritic Cell Neoplasm, an Ultra-Rare and Aggressive Blood Cancer With Limited Treatment Options</a>
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        - DECNUPAZ is the first and only antibody-drug conjugate (ADC) approved for blastic plasmacytoid dendritic cell neoplasm (BPDCN) that is initiated in an outpatient setting - DECNUPAZ marks AbbVie&#39;s first ADC approved for blood cancer NORTH CHICAGO, Ill., May 27, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that the U.S. Food and Drug Administration (FDA) has approved DECNUPAZTM (piv...
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-approves-abbvies-rare-blood-cancer-drug-2026-05-27/">US FDA approves AbbVie&#39;s rare blood cancer drug</a>
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        The ​U.S. Food ‌and Drug ​Administration ​on Wednesday ⁠approved ​AbbVie&#39;s drug ​to treat blastic ​plasmacytoid ​dendritic cell ‌neoplasm, ⁠a very rare ​type ​of ⁠blood cancer.
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