{"id":424577,"date":"2021-01-29T08:33:32","date_gmt":"2021-01-29T13:33:32","guid":{"rendered":"http:\/\/www.marketnewsdesk.com\/?p=424577"},"modified":"2021-01-29T08:33:32","modified_gmt":"2021-01-29T13:33:32","slug":"turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/","title":{"rendered":"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer"},"content":{"rendered":"<div class=\"mw_release\">\n<ul type=\"disc\">\n<li>\n          <strong><br \/>\n            <em>Phase 2 Confirmed Objective Response Rate is 93% (95% CI: 68-100); Pooled Phase 1\/2 Confirmed Objective Response Rate is 91% (95% CI: 71-99)<\/em><br \/>\n          <\/strong><\/p>\n<\/li>\n<li>\n          <strong><br \/>\n            <em>Approximately 40 Patients with ROS1-Positive TKI-Naive Non-Small Lung Cancer Now Enrolled in Phase 1\/2 TRIDENT-1 Study<\/em><br \/>\n          <\/strong><\/p>\n<\/li>\n<li>\n          <strong><br \/>\n            <em>Company Plans to Conduct Type B Meeting with Food and Drug Administration in 1H 2021 to Discuss Regulatory Path<\/em><br \/>\n          <\/strong><br \/>\n          \n        <\/li>\n<\/ul>\n<p>SAN DIEGO, Jan.  29, 2021  (GLOBE NEWSWIRE) &#8212; Turning Point Therapeutics, Inc. (NASDAQ: TPTX), a precision oncology company developing next-generation therapies that target genetic drivers of cancer, announced updated interim findings from the ongoing TRIDENT-1 registrational study of lead drug candidate repotrectinib in patients with ROS1-positive TKI-na\u00efve non-small cell lung cancer (NSCLC).<\/p>\n<p>In a total of 15 patients enrolled in the Phase 2 portion of the TRIDENT-1 study, the preliminary efficacy analysis showed the confirmed objective response rate (ORR) by physician assessment was 93% (95% CI: 68-100) and in 22 patients pooled from the Phase 1 (dosed at or above the Phase 2 dose) and Phase 2 portions, the confirmed ORR was 91% (95% CI: 71-99).<\/p>\n<p>The findings will be presented in a mini-oral presentation by Dr. Byoung Chul Cho, Division of Medical Oncology, Yonsei Cancer Center at Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea, at the International Association for the Study of Lung Cancer 2020 World Conference on Lung Cancer.<\/p>\n<p>\u201cThese interim data confirm our belief that repotrectinib has the potential to be the best-in-class treatment for patients with ROS1-positive TKI-na\u00efve advanced non-small cell lung cancer,\u201d said Mohammad Hirmand, M.D., chief medical officer. \u201cTo date, we have enrolled approximately 40 ROS1-positive TKI-na\u00efve patients in the Phase 1 and 2 portions of the TRIDENT-1 study dosed at or above the Phase 2 dose&#8211; an encouraging increase in enrollment following our data update from last August\u2014and we look forward to discussing next steps towards registration of repotrectinib in this patient population at a Type B meeting with the FDA anticipated in the first half of the year.\u201d<\/p>\n<p>\n        <strong>Interim Update <\/strong><br \/>\n        <br \/>Utilizing a Dec. 31, 2020 cutoff date, the TRIDENT-1 preliminary interim efficacy update includes 22 ROS1-positive TKI-na\u00efve NSCLC patients pooled from the Phase 1 portion of the study (dosed at or above the Phase 2 dose) with patients from the Phase 2 portion who had at least two post-baseline scans. Responses for patients in the Phase 2 portion of the study were determined by physician assessment. The interim safety update includes a total of 185 patients from the Phase 1 and Phase 2 portions of the study utilizing an Oct. 30, 2020 cutoff date.<\/p>\n<ul type=\"disc\">\n<li>14 of 15 patients treated in the Phase 2 portion achieved a confirmed ORR of 93% (95% CI: 68-100). At the time of the data cut-off, the one non-responder remained on treatment and in stable disease with a 13% tumor reduction. In addition, one of the 14 patients in a partial response at the time of the data cutoff date has since achieved a confirmed complete response.\n<\/li>\n<li>Duration of response ranged from 1.3+ to 7.4+ months, and the duration of treatment ranged from 3.7+ to 10.9+ months with 14 of the 15 patients remaining on treatment. As of the cutoff date, one additional patient (not included in the confirmed ORR calculation) had an unconfirmed partial response and was on treatment awaiting a confirmatory scan. The company\u2019s prior Phase 2 update with the data cutoff date of July 10, 2020 in 7 total patients, showed a confirmed ORR of 86% and a wider 95% confidence interval of 42 to 100.\n<\/li>\n<li>20 of 22 patients pooled from Phase 1 and Phase 2 achieved a confirmed ORR of 91% (95% CI: 71-99). In the 7 patients from the Phase 1 portion dosed at or above the Phase 2 dose, duration of treatment ranged from 10.9 to 37.3 months with a median of 30.9 months, with four patients receiving treatment for longer than 30 months.\n<\/li>\n<li>Repotrectinib was generally well tolerated in 185 patients treated in the\u00a0Phase 1 and Phase 2 portions of\u00a0the\u00a0study.\n<\/li>\n<li>Treatment-emergent adverse events (TEAE)\u00a0found in greater than\u00a015 percent of patients were dizziness (58%),\u00a0dysgeusia (43%),\u00a0constipation (32%), dyspnea (31%),\u00a0fatigue (27%),\u00a0paresthesia\u00a0(25%),\u00a0anemia (22%), nausea (20%),\u00a0and muscular weakness (16%).\n<\/li>\n<li>There were\u00a0four cases of Grade 3 dizziness\u00a0(2%) and no cases of dizziness have led\u00a0to treatment discontinuation. Dose modifications\u00a0due to\u00a0TEAEs\u00a0were infrequent, including 18% that led to dose reduction and 9% that led to drug discontinuation.\n<\/li>\n<li>The majority of treatment related AEs (TRAEs) were Grade 1 or 2 and there were no Grade 4 or Grade 5 TRAEs.<\/li>\n<\/ul>\n<p>\n        <strong>About Turning Point Therapeutics Inc.<\/strong><br \/>\n        <br \/>Turning Point Therapeutics\u00a0is a clinical-stage precision oncology company with a pipeline of internally discovered investigational drugs designed to address key limitations of existing cancer therapies. The company\u2019s lead drug candidate, repotrectinib, is a next-generation kinase inhibitor targeting the ROS1 and TRK oncogenic drivers of non-small cell lung cancer and advanced solid tumors. Repotrectinib, which is being studied in a registrational Phase 2 study in adults and a Phase 1\/2 study in pediatric patients, has shown antitumor activity and durable responses among kinase inhibitor treatment-na\u00efve and pre-treated patients. The company\u2019s pipeline of drug candidates also includes TPX-0022, targeting MET, CSF1R and SRC, which is being studied in a Phase 1 trial of patients with advanced or metastatic solid tumors harboring genetic alterations in <em>MET<\/em>; TPX-0046, targeting RET, which is being studied in a Phase 1\/2 trial of patients with advanced or metastatic solid tumors harboring genetic alterations in <em>RET<\/em>; and TPX-0131, a next-generation ALK inhibitor currently pending IND submission. Turning Point\u2019s next-generation kinase inhibitors are designed to bind to their targets with greater precision and affinity than existing therapies, with a novel, compact structure that has demonstrated an ability to potentially overcome treatment resistance common with other kinase inhibitors. The company is driven to develop therapies that mark a turning point for patients in their cancer treatment. For more information, visit <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=yKKrz19FOUbaQEitJQUsWSNg8CEi0h_RXACQ0p5k-HVfQtcx1q_TOuOhD_Qkt4f1a_JNoODreWkXlGwHQi2qrL3g6LLB6EOjIn-GCxOPx58=\" rel=\"nofollow noopener noreferrer\" target=\"_blank\">www.tptherapeutics.com<\/a>.<\/p>\n<p align=\"left\">\n        <strong>Forward Looking Statements<br \/><\/strong>Statements contained in this press release regarding matters that are not historical facts are \u201cforward-looking statements\u201d within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the efficacy, safety and therapeutic potential of repotrectinib, the results, conduct, progress and timing of the TRIDENT-1 clinical study, plans regarding future regulatory submissions, and the regulatory approval path for repotrectinib. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as \u201cplans\u201d, \u201cwill\u201d, \u201cbelieves,\u201d \u201canticipates,\u201d \u201cexpects,\u201d \u201cintends,\u201d \u201cgoal,\u201d \u201cpotential\u201d and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Turning Point Therapeutics\u2019 current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks and uncertainties associated with Turning Point Therapeutics\u2019 business in general, risks and uncertainties related to the impact of the COVID-19 pandemic to Turning Point\u2019s business and the other risks described in Turning Point Therapeutics\u2019 filings with the SEC. All forward-looking statements contained in this press release speak only as of the date on which they were made. Turning Point Therapeutics undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.<\/p>\n<p>Contact: <br \/>Jim Mazzola<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=0tLcMi7hqZr7x9wCEk-Ihy6tQBAIJxhfs2B488KsFz1SoSIxaq8G8BESkLQH4DTaEDenLQ6-3XJgigW1NK23G-izgBVSgD6S2EW3PqpNo0HirDAvPCPdNXFouJE_HDFP\" rel=\"nofollow noopener noreferrer\" target=\"_blank\">jim.mazzola@tptherapeutics.com<\/a><br \/>858-342-8272<\/p>\n<\/p>\n<p>      <img loading=\"lazy\" decoding=\"async\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODE0Mzg0NyMzOTUxMjA2IzIxNzcyMzE=\" width=\"1\" height=\"1\" \/><br \/>\n      <br \/>\n      <img loading=\"lazy\" decoding=\"async\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/ml.globenewswire.com\/release\/track\/ffaf6ee0-ba17-4d66-8526-8aa8b91e7cf1\" width=\"1\" height=\"1\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Phase 2 Confirmed Objective Response Rate is 93% (95% CI: 68-100); Pooled Phase 1\/2 Confirmed Objective Response Rate is 91% (95% CI: 71-99) Approximately 40 Patients with ROS1-Positive TKI-Naive Non-Small Lung Cancer Now Enrolled in Phase 1\/2 TRIDENT-1 Study Company Plans to Conduct Type B Meeting with Food and Drug Administration in 1H 2021 to Discuss Regulatory Path SAN DIEGO, Jan. 29, 2021 (GLOBE NEWSWIRE) &#8212; Turning Point Therapeutics, Inc. (NASDAQ: TPTX), a precision oncology company developing next-generation therapies that target genetic drivers of cancer, announced updated interim findings from the ongoing TRIDENT-1 registrational study of lead drug candidate repotrectinib in patients with ROS1-positive TKI-na\u00efve non-small cell lung cancer (NSCLC). In a total of 15 patients enrolled in the Phase &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-424577","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Phase 2 Confirmed Objective Response Rate is 93% (95% CI: 68-100); Pooled Phase 1\/2 Confirmed Objective Response Rate is 91% (95% CI: 71-99) Approximately 40 Patients with ROS1-Positive TKI-Naive Non-Small Lung Cancer Now Enrolled in Phase 1\/2 TRIDENT-1 Study Company Plans to Conduct Type B Meeting with Food and Drug Administration in 1H 2021 to Discuss Regulatory Path SAN DIEGO, Jan. 29, 2021 (GLOBE NEWSWIRE) &#8212; Turning Point Therapeutics, Inc. (NASDAQ: TPTX), a precision oncology company developing next-generation therapies that target genetic drivers of cancer, announced updated interim findings from the ongoing TRIDENT-1 registrational study of lead drug candidate repotrectinib in patients with ROS1-positive TKI-na\u00efve non-small cell lung cancer (NSCLC). In a total of 15 patients enrolled in the Phase &hellip; Continue reading &quot;Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2021-01-29T13:33:32+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODE0Mzg0NyMzOTUxMjA2IzIxNzcyMzE=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"6 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer\",\"datePublished\":\"2021-01-29T13:33:32+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\\\/\"},\"wordCount\":1190,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=ODE0Mzg0NyMzOTUxMjA2IzIxNzcyMzE=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\\\/\",\"name\":\"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer - 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Market Newsdesk","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/","og_locale":"en_US","og_type":"article","og_title":"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer - Market Newsdesk","og_description":"Phase 2 Confirmed Objective Response Rate is 93% (95% CI: 68-100); Pooled Phase 1\/2 Confirmed Objective Response Rate is 91% (95% CI: 71-99) Approximately 40 Patients with ROS1-Positive TKI-Naive Non-Small Lung Cancer Now Enrolled in Phase 1\/2 TRIDENT-1 Study Company Plans to Conduct Type B Meeting with Food and Drug Administration in 1H 2021 to Discuss Regulatory Path SAN DIEGO, Jan. 29, 2021 (GLOBE NEWSWIRE) &#8212; Turning Point Therapeutics, Inc. (NASDAQ: TPTX), a precision oncology company developing next-generation therapies that target genetic drivers of cancer, announced updated interim findings from the ongoing TRIDENT-1 registrational study of lead drug candidate repotrectinib in patients with ROS1-positive TKI-na\u00efve non-small cell lung cancer (NSCLC). In a total of 15 patients enrolled in the Phase &hellip; Continue reading \"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer\"","og_url":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/","og_site_name":"Market Newsdesk","article_published_time":"2021-01-29T13:33:32+00:00","og_image":[{"url":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODE0Mzg0NyMzOTUxMjA2IzIxNzcyMzE=","type":"","width":"","height":""}],"author":"Newsdesk","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Newsdesk","Est. reading time":"6 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/#article","isPartOf":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/"},"author":{"name":"Newsdesk","@id":"https:\/\/www.marketnewsdesk.com\/#\/schema\/person\/482f27a394d4fda80ecb5499e519d979"},"headline":"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer","datePublished":"2021-01-29T13:33:32+00:00","mainEntityOfPage":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/"},"wordCount":1190,"image":{"@id":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/#primaryimage"},"thumbnailUrl":"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODE0Mzg0NyMzOTUxMjA2IzIxNzcyMzE=","inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/","url":"https:\/\/www.marketnewsdesk.com\/index.php\/turning-point-therapeutics-reports-updated-interim-data-from-registrational-phase-2-trident-1-study-of-repotrectinib-in-patients-with-ros1-positive-tki-naive-non-small-cell-lung-cancer\/","name":"Turning Point Therapeutics Reports Updated Interim Data From Registrational Phase 2 Trident-1 Study of Repotrectinib in Patients With ROS1-Positive TKI-Na\u00efve Non-Small Cell Lung Cancer - 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