Jazz Pharmaceuticals to Present Data Across Growing Oncology Pipeline and Portfolio at ASCO 2024

PR Newswire04-25

Overall survival and additional long-term follow-up data from the Phase 2b HERIZON-BTC-01 trial in previously treated HER2-positive metastatic biliary tract cancer (BTC) to be presented at ASCO 2024 ...

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DUBLIN, April 24, 2024 /PRNewswire/ --Jazz Pharmaceuticals plc today announced that the company, along with its partners, will presentor publish eight abstracts at the American Society of Clinical Oncology  Annual Meeting from May 31-June 4, 2024 in Chicago. Presentations include data from trials of zanidatamab, Zepzelca , and Rylaze . A poster featuring the study design for the JZP898 Phase 1 trial in progress will also be presented.Updated data with longer follow-up, including overall survival findings, will be presented from the Phase 2b HERIZON-BTC-01 trial of zanidatamab, a HER2-targeted bispecific, biparatopic antibody, in previously treated HER2-positive biliary tract cancer . Data from the HERIZON-BTC-01 trial were the backbone of the recently completed Biologics License Application  su","collect":0,"end_time":0,"defaultTopTitle":"yahoo.com","property":[],"viewcount":null,"language":"en","relate_stocks":{"BK4017":"黄金","BK4585":"ETF&股票定投概念","LU0889565916.HKD":"FRANKLIN BIOTECHNOLOGY DISCOVERY \"A\" (HKD) ACC","CDE":"科尔黛伦矿业","LU0985320562.USD":"NORDEA 1 GLOBAL STARS EQUITY \"BP\" (USD) ACC","BK4588":"碎股","BK4533":"AQR资本管理(全球第二大对冲基金)","LU0320765992.SGD":"FTIF - Franklin Biotechnology Discovery A Acc SGD","BTC":"ClearShares Piton Intermediate Fixed Income ETF","BK4007":"制药","LU0109394709.USD":"富兰克林生物科技新领域基金A (acc)","LU2355687059.USD":"NORDEA 1 GLOBAL IMPACT  \"BP\" (USD) ACC","BK4107":"财产与意外伤害保险","BK4532":"文艺复兴科技持仓","JAZZ":"爵士制药","ALL":"好事达"},"translate_title":"Jazz Pharmaceuticals将在ASCO 2024上展示不断增长的肿瘤管道和产品组合的数据","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"ALL":1,"BTC":1,"CDE":1,"JAZZ":0.9},"content_text":"Overall survival and additional long-term follow-up data from the Phase 2b HERIZON-BTC-01 trial in previously treated HER2-positive metastatic biliary tract cancer (BTC) to be presented at ASCO 2024\nDUBLIN, April 24, 2024 /PRNewswire/ -- Jazz Pharmaceuticals plc (Nasdaq: JAZZ) today announced that the company, along with its partners, will present or publish eight abstracts at the American Society of Clinical Oncology (ASCO) Annual Meeting from May 31-June 4, 2024 in Chicago. Presentations include data from trials of zanidatamab, Zepzelca® (lurbinectedin), and Rylaze® (asparaginase erwinia chrysanthemi (recombinant)-rywn). A poster featuring the study design for the JZP898 Phase 1 trial in progress will also be presented.\nUpdated data with longer follow-up, including overall survival findings, will be presented from the Phase 2b HERIZON-BTC-01 trial of zanidatamab, a HER2-targeted bispecific, biparatopic antibody, in previously treated HER2-positive biliary tract cancer (BTC). Data from the HERIZON-BTC-01 trial were the backbone of the recently completed Biologics License Application (BLA) submission for previously treated HER2-positive metastatic BTC.\n\"We are excited to present data across our oncology pipeline and portfolio at ASCO, particularly the opportunity to provide updated data from the pivotal Phase 2b HERIZON-BTC-01 trial of zanidatamab in HER2-positive BTC presented at last year's meeting. BTC is often associated with a poor prognosis, and we believe zanidatamab has the potential to be transformative to the current standard of care in BTC and multiple HER2-expressing cancers, including in cases resistant to prior HER2-targeted therapies,\" said Rob Iannone, M.D., M.S.C.E., executive vice president, global head of research and development of Jazz Pharmaceuticals. \"The abstracts accepted for presentation by Jazz and our partners at this year's meeting demonstrate our commitment to advancing our portfolio of innovative oncology products and investigational therapies at all stages of development as we seek to deliver on our goal to help people with cancer live longer, fuller lives.\"\nThe full ASCO abstracts will be available on May 23, 2024, after 5 p.m. ET. The abstract titles are available at: https://www.asco.org/abstracts. \nA full list of Jazz or partner-supported presentations at the 2024 ASCO Annual Meeting follows:\nZanidatamab\n\n\n\n\nPresentation Title \nAuthor \nPresentation Details \n\n\nZanidatamab in previously-treated HER2+ BTC: OS and longer follow-up from the phase 2b HERIZON-BTC-01 study \nShubham Pant, Jia Fan, Do-Youn Oh, Hye Jin Choi, Jin Won Kim, Heung-Moon Chang, Lequn Bao, Hui-Chuan Sun, Teresa Macarulla, Feng Xie, Jean-Philippe Metges, Jie-Er Ying, John A Bridgewater, Mohamedtaki A Tejani, Emerson Y Chen, Harpreet Wasan, Michel Ducreux, Yi Zhao, Phillip M Garfin, James J Harding \n\n\nType: Poster\nSession: Gastrointestinal Cancer – Gastroesophageal, Pancreatic, and Hepatobiliary\nDate/Time: Saturday, June 1, 2024, 1:30-4:30 PM CDT\nNumber: 4091\n \n\n\n\n\nZepzelca\n\n\n\n\nPresentation Title \nAuthor \nPresentation Details \n\n\nReal-world safety and Healthcare Resource Utilization (HCRU) of lurbinectedin in patients with SCLC: Jazz EMERGE 402 updated analysis \nFiras Badin, Philip Lammers, Mehul Patel, Leonid Shunyakov, Dennis Slater, Catherine Labbé, Navit Naveh, Anne Boccuti, Raj Hanvesakul, Wenyan Li, Badri Rengarajan, Balazs Halmos \nType: ePublication Number: e23266 \n\n\nEfficacy and safety of lurbinectedin with irinotecan in a phase 2 expansion cohort of patients with synovial sarcoma (PharmaMar-supported presentation) \nGregory M Cote, Javier Martin Broto, Sant P Chawla, Bruno Bockorny, Alejandro Falcon, Antonio Lopez Pousa, Luis Paz-Ares, Benjamin Verret, Sara Martinez, Sonia Extremera, Martin Cullell-Young, Salvador Fudio, Carmen Kahatt, Ali Zeaiter, Axel Le Cesne \nType: Poster Session: Sarcoma Date/Time: Saturday, June 1, 2024, 1:30-4:30 PM CDT Number: 11560 \n\n\nRandomized Controlled, Open-label, Phase IIb/III Study of Lurbinectedin in Combination with Doxorubicin versus Doxorubicin Alone as First-line Treatment in Patients with Metastatic Leiomyosarcoma – Trial in progress (PharmaMar-supported presentation) \nGregory M Cote, Sant P Chawla, George Demetri, Bernd Kasper, Robin Jones, Javier Martin Broto, Joseph Wooley, Mia Weiss, Salvatore Tafuto, Giuseppe Badalamenti, Irene Carrasco, Paloma Peinado, Jean-Yves Blay, Gaston Boggio, Cristian Fernandez, Antonio Nieto, Carmen Kahatt, Ali Zeaiter, Axel Le Cesne \nType: Poster Session: Sarcoma Date/Time: Saturday, June 1, 2024, 1:30-4:30 PM CDT Number: TPS11590 \n\n\nA phase II study of lurbinectedin ± avelumab in small cell carcinoma of the bladder (LASER) – Trial in Progress [IST] \nNicholas Simon, Elias Chandran, Scot Niglio, Andre R Kydd, Saad Atiq, Lisa Ley, Lisa Cordes, Tzu-fang Wang, Salah Boudjadi, Elizabeth Smith, Dilara Akbulut, Seth Steinberg, Andrea B Apolo \nType: Poster Session: Genitourinary Cancer – Kidney and Bladder Date/Time: Sunday, June 2, 2024, 9:00 AM - 12:00 PM CDT Number: TPS4629 \n\n\nEfficacy and safety of lurbinectedin in combination with irinotecan in patients with relapsed SCLC: results from a phase 2 expansion cohort(PharmaMar-supported presentation) \nLuis Paz-Ares, Alejandro Falcon, Alejandro Navarro, Amparo Sanchez, Gregory M Cote, Javier Molina-Cerrillo, Vicente Alonso, Javier Baena, Ana Gil, Santiago Ponce-Aix, Helena Bote de Cabo, Sara Martinez, Julia Martinez, Jose Antonio López-Vilariño, Carmen Kahatt, Ali Zeaiter, Javier Gomez, Jon Zugazagoitia \nType: Poster Session: Lung Cancer – Non-Small Cell Local-Regional/Small Cell/Other Thoracic Cancers Date/Time: Monday, June 3, 2024, 1:30-4:30 PM CDT Number: 8094 \n\n\n\n\nJZP898\n\n\n\n\nPresentation Title \nAuthor \nPresentation Details \n\n\nA phase 1/1b first-in-human (FIH) study of JZP898 as monotherapy and in combination with pembrolizumab in adult patients with advanced or metastatic solid tumors – Trial in Progress \nMeredith McKean, Thomas Hutson, Sarina A Piha-Paul, Ida Micaily, Mingxiang Liao, Robin Humphreys, Graham Brock, Natasha Sahr, Vian Amber, Alexander Spira \nType: Poster Session: Developmental Therapeutics—Molecularly Targeted Agents and Tumor Biology Date/Time: Saturday, June 1, 2024. 9:00 AM–12:00 PM CDT  Number: TPS3190 \n\n\n\n\nRylaze\n\n\n\n\nPresentation Title \nAuthor \nPresentation Details \n\n\nRecombinant Erwinia asparaginase (JZP458) in acute lymphoblastic leukemia/lymphoblastic lymphoma (ALL/LBL): post hoc analysis of adverse events of interest from AALL1931 \nEtsuko Aoki, Luke Maese, Mignon L Loh, Shirali Agarwal, Vijayalakshmi Chandrasekaran, Yali Liang, Nalina Dronamraju, Robert Iannone, Lewis B Silverman, Elizabeth A Raetz, Rachel E Rau \nType: Poster Session: Hematologic Malignancies – Leukemia, Myelodysplastic Syndromes, and Allotransplant Date/Time: Monday, June 3, 2024, 9:00 AM–12:00 PM CDT  Number: 6521 \n\n\n\n\nAbout Zanidatamab Zanidatamab is an investigational bispecific antibody that can simultaneously bind two non-overlapping epitopes of HER2, known as biparatopic binding. This unique design and increased binding results in multiple mechanisms of action, including dual HER2 signal blockade, removal of HER2 protein from the cell surface, and immune-mediated cytotoxicity leading to encouraging antitumor activity in patients. Zanidatamab is being developed in multiple clinical trials as a targeted treatment option for patients with solid tumors that express HER2. Zanidatamab is being developed by Jazz and BeiGene, Ltd. (BeiGene) under license agreements from Zymeworks, which first developed the molecule. \nThe U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy designation for zanidatamab development in patients with previously treated HER2 gene-amplified biliary tract cancers (BTC), and two Fast Track designations for zanidatamab: one as a single agent for refractory BTC and one in combination with standard of care chemotherapy for 1L gastroesophageal adenocarcinoma (GEA). Additionally, zanidatamab has received Orphan Drug designations from FDA for the treatment of BTC and GEA, as well as Orphan Drug designation from the European Medicines Agency for the treatment of BTC and gastric cancer. Zanidatamab was also granted Breakthrough Therapy designation from the Center for Drug Evaluation (CDE) in China.\nAbout Zepzelca® (lurbinectedin)Zepzelca is an alkylating drug that binds guanine residues within DNA. This triggers a cascade of events that can affect the activity of DNA binding proteins, including some transcription factors, and DNA repair pathways, resulting in disruption of the cell cycle and eventual cell death.1\nThe FDA approved Zepzelca under accelerated approval in June 2020 for the treatment of adult patients with metastatic SCLC with disease progression on or after platinum-based chemotherapy. The approval is based on overall response rate (ORR) and duration of response demonstrated in an open-label, monotherapy clinical study. In December 2021, Jazz and PharmaMar announced the initiation of LAGOON, a confirmatory Phase 3 clinical trial of Zepzelca for the treatment of patients with relapsed small cell lung cancer. If positive, LAGOON could confirm the benefit of Zepzelca in the treatment of small cell lung cancer (SCLC) when patients progress following 1L treatment with a platinum-based regimen and support full approval in the U.S.\nZepzelca is a prescription medicine used to treat adults with SCLC that has spread to other parts of the body (metastatic) and who have received treatment with chemotherapy that contains platinum, and it did not work or is no longer working. Zepzelca is approved based on response rate and how long the response lasted. Additional studies will further evaluate the benefit of Zepzelca for this use. \nImportant Safety Information for ZEPZELCA\nBefore receiving ZEPZELCA, tell your healthcare provider about all of your medical conditions, including if you:\n\nhave liver or kidney problems.\nare pregnant or plan to become pregnant. ZEPZELCA can harm your unborn baby.\n\nFemales who are able to become pregnant:\n\nYour healthcare provider should do a pregnancy test before you start treatment with ZEPZELCA.\nYou should use effective birth control (contraception) during treatment with and for 6 months after your last dose of ZEPZELCA.\nTell your healthcare provider right away if you become pregnant or think that you are pregnant during treatment with ZEPZELCA.\n\nMales with female partners who are able to become pregnant should use effective birth control during treatment with and for 4 months after your last dose of ZEPZELCA.\nFemales who are breastfeeding or plan to breastfeed. It is not known if ZEPZELCA passes into your breastmilk. Do not breastfeed during treatment with ZEPZELCA and for 2 weeks after your last dose of ZEPZELCA. Talk to your healthcare provider about the best way to feed your baby during treatment with ZEPZELCA.\nTell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Certain other medicines may affect how ZEPZELCA works.\nWhat should I avoid while using ZEPZELCA?Avoid eating or drinking grapefruit, Seville oranges, or products that contain grapefruit juice and Seville oranges during treatment with ZEPZELCA.\nZEPZELCA can cause serious side effects, including:\n\nLow blood cell counts. Low blood counts including low neutrophil counts (neutropenia) and low platelet counts (thrombocytopenia) are common with ZEPZELCA and can also be severe. Some people with low white blood cell counts may get fever, or an infection throughout the body (sepsis), that can cause death. Your healthcare provider should do blood tests before you receive each treatment with ZEPZELCA to check your blood cell counts.\n\nTell your healthcare provider right away if you develop:\n\nfever or any other signs of infection\nunusual bruising or bleeding\ntiredness\npale colored skin\nLiver problems. Increased liver function tests are common with ZEPZELCA and can also be severe. Your healthcare provider should do blood tests to check your liver function before you start and during treatment with ZEPZELCA.\n\nTell your healthcare provider right away if you develop symptoms of liver problems including:\n\nloss of appetite\nnausea or vomiting\npain on the right side of your stomach area (abdomen)\nYour healthcare provider may temporarily stop treatment, lower your dose, or permanently stop ZEPZELCA if you develop low blood cell counts or liver problems during treatment with ZEPZELCA.\n\nThe most common side effects of ZEPZELCA include:\n\ntiredness\nlow white and red blood cell counts\nincreased kidney function blood test (creatinine)\nincreased liver function blood tests\nincreased blood sugar (glucose)\nnausea\ndecreased appetite\nmuscle and joint (musculoskeletal) pain\nlow level of albumin in the blood\nconstipation\ntrouble breathing\nlow levels of sodium and magnesium in the blood\nvomiting\ncough\ndiarrhea\n\nThese are not all of the possible side effects of ZEPZELCA.\nCall your doctor for medical advice about side effects. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. You may also report side effects to Jazz Pharmaceuticals at 1-800-520-5568.\nMore information about Zepzelca, including Full Prescribing Information and Patient Information, is available here.\nZEPZELCA is a trademark of Pharma Mar, S.A. used by Jazz Pharmaceuticals under license.\nAbout JZP898JZP898 (also known as WTX-613) is an investigational differentiated, conditionally-activated interferon alpha (IFNα) INDUKINE™ molecule. JZP898 is an engineered IFN⍺2b cytokine pro-drug that is activated specifically within the tumor microenvironment where it can stimulate IFNα receptors on cancer-fighting immune effector cells. JZP898 was created leveraging Werewolf Therapeutics' proprietary PREDATOR™ protein engineering technology, which integrates specialized protein design elements to enhance activity, stability and tumor selectivity within a single molecule, called INDUKINE molecules.\nAbout RYLAZE® (asparaginase erwinia chrysanthemi (recombinant)-rywn)RYLAZE, also known as JZP458, is approved in the U.S. for use as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LBL) in adult and pediatric patients one month or older who have developed hypersensitivity to E. coli-derived asparaginase. RYLAZE has orphan drug designation for the treatment of ALL/LBL in the United States. RYLAZE is a recombinant erwinia asparaginase that uses a novel Pseudomonas fluorescens expression platform. JZP458 was granted Fast Track designation by the U.S. Food and Drug Administration (FDA) in October 2019 for the treatment of this patient population. RYLAZE was approved as part of the Real-Time Oncology Review program, an initiative of the FDA's Oncology Center of Excellence designed for efficient delivery of safe and effective cancer treatments to patients.4 \nThe full U.S. Prescribing Information for RYLAZE is available at: https://pp.jazzpharma.com/pi/rylaze.en.USPI.pdf \nImportant Safety Information for RYLAZE\nRYLAZE should not be given to people who have had:\n\nSerious allergic reactions to RYLAZE\nSerious swelling of the pancreas (stomach pain), serious blood clots, or serious bleeding during previous asparaginase treatment\n\nRYLAZE may cause serious side effects, including:\n\nAllergic reactions (a feeling of tightness in your throat, unusual swelling/redness in your throat and/or tongue, rash, or trouble breathing), some of which may be life-threatening\nSwelling of the pancreas (stomach pain), which, if left untreated, may be fatal\nBlood clots (may be experienced as headache, arm or leg swelling, shortness of breath, or chest pain), which may be life-threatening\nBleeding, which may be life-threatening\nLiver problems\n\nContact your doctor immediately if any of these side effects occur.\nSome of the most common side effects with RYLAZE include: liver problems, nausea and vomiting, bone and muscle pain, infection, tiredness, headache, fever with low white blood cell count, fever, bleeding, mouth swelling (sometimes with sores), pain in the abdomen, decreased appetite, allergic reactions, high blood sugar levels, diarrhea, swelling of the pancreas, and low levels of potassium in your blood.\nRYLAZE can harm your unborn baby. Inform your doctor if you are pregnant, planning to become pregnant, or nursing. Females of reproductive potential should use effective contraception (other than hormonal contraceptives) during treatment and for 3 months following the final dose. Do not breastfeed while receiving RYLAZE and for 1 week after the final dose.\nTell your healthcare provider if there are any side effects that are bothersome or that do not go away.\nThese are not all the possible side effects of RYLAZE. For more information, ask your healthcare provider.\nCall your doctor for medical advice about any side effects.\nYou are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088 (1-800-332-1088).\nAbout Jazz PharmaceuticalsJazz Pharmaceuticals plc (Nasdaq: JAZZ) is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases—often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.\nJazz Pharmaceuticals plc Caution Concerning Forward-Looking StatementsThis press release contains forward-looking statements, including, but not limited to, statements related to growing our portfolio of innovative oncology products and investigational therapies at all stages of development as we seek to deliver on our goal to help people with cancer live longer, fuller lives, and other statements that are not historical facts. These forward-looking statements are based on Jazz Pharmaceuticals' current plans, objectives, estimates, expectations and intentions and inherently involve significant risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, risks and uncertainties associated with pharmaceutical product development, and other risks and uncertainties affecting Jazz Pharmaceuticals and its development programs, including those described from time to time under the caption \"Risk Factors\" and elsewhere in Jazz Pharmaceuticals plc's Securities and Exchange Commission filings and reports (Commission File No. 001-33500), including Jazz Pharmaceuticals' Annual Report on Form 10-K for the year ended December 31, 2023, and future filings and reports by Jazz Pharmaceuticals. Other risks and uncertainties of which Jazz Pharmaceuticals is not currently aware may also affect Jazz Pharmaceuticals' forward-looking statements and may cause actual results and the timing of events to differ materially from those anticipated. The forward-looking statements herein are made only as of the date hereof or as of the dates indicated in the forward-looking statements, even if they are subsequently made available by Jazz Pharmaceuticals on its website or otherwise. Jazz Pharmaceuticals undertakes no obligation to update or supplement any forward-looking statements to reflect actual results, new information, future events, changes in its expectations or other circumstances that exist after the date as of which the forward-looking statements were made.\nContacts:\nJazz Media Contact:Kristin BhavnaniHead of Global Strategic Brand EngagementJazz Pharmaceuticals plcCorporateAffairsMediaInfo@jazzpharma.comIreland +353 1 637 2141U.S. +1 215 867 4948\nJazz Investor Contact:Andrea N. Flynn, Ph.D.Vice President, Head, Investor RelationsJazz Pharmaceuticals plcinvestorinfo@jazzpharma.com Ireland +353 1 634 3211U.S. +1 650 496 2717\n\n\n\n\n\n View original content to download multimedia:https://www.prnewswire.com/news-releases/jazz-pharmaceuticals-to-present-data-across-growing-oncology-pipeline-and-portfolio-at-asco-2024-302126649.html\nSOURCE Jazz Pharmaceuticals plc","kind":null,"is_publish_news":null,"is_publish_highlight":null,"is_publish_live":null,"is_publish_wemedia":null,"editions":null,"symbols":[],"gpt_button":1},"commentList":[],"isCommentEnd":true,"newsSizeData":{"likeSize":0,"commentSize":0,"repostSize":0,"favoriteSize":0,"likeStatus":false,"favoriteStatus":false},"APP":{"userAgent":"Mozilla/5.0 AppleWebKit/537.36 (KHTML, like Gecko; compatible; ClaudeBot/1.0; +claudebot@anthropic.com)","isDev":false,"isTTM":true,"deviceId":"web-server-community-laohu8-v3","version":"4.22.4","shortVersion":"4.22.4","platform":"web","vendor":"web","appName":"ttm","isIOS":false,"isAndroid":false,"isTiger":false,"isTHS":false,"isWeiXin":false,"isWeiXinMini":false,"isWeiBo":false,"isQQ":false,"isBaiduSwan":false,"isBaiduBox":false,"isDingTalk":false,"isToutiao":false,"isOnePlus":false,"isHuaWei":false,"isXiaomi":false,"isXiaomiWebView":false,"isOppo":false,"isVivo":false,"isSamsung":false,"isMobile":false},"href":"/m/news/2430496385"}