Inhibrx To Host Webcast Presentation of Topline Results from its Registrational Trial of Ozekibart (INBRX-109) in Chondrosarcoma and to Provide Updates on Colorectal Cancer and Ewing Sarcoma Expansion Cohorts
Inhibrx (Nasdaq: INBX) will webcast topline results from the registrational ChonDRAgon study of ozekibart (INBRX-109) versus placebo in advanced/metastatic unresectable chondrosarcoma on Thursday, October 23, 2025 at 1:30 p.m. PT.
The company will also provide updates on two expansion cohorts: ozekibart plus FOLFIRI in late-line colorectal cancer and ozekibart with irinotecan and temozolomide in refractory Ewing sarcoma. Investors can join via webcast or listen by dial-in; the webcast will be available for 60 days after the event and the corporate presentation will be updated in the Investors section of the company website.
Inhibrx (Nasdaq: INBX) trasmetterà in webcast i risultati principali dello studio registrazionale ChonDRAgon di ozekibart (INBRX-109) rispetto al placebo in sarcoma cartilagineo avanzato/metastatico non resecabile giovedì 23 ottobre 2025 alle 13:30 PT.
L’azienda fornirà anche aggiornamenti su due coorti di espansione: ozekibart più FOLFIRI in cancro colorettale in stadio avanzato/ultime linee di trattamento e ozekibart con irinotecano e temozolomide nello sarcoma di Ewing refrattario. Gli investitori possono partecipare via webcast o ascoltare tramite dial-in; il webcast sarà disponibile per 60 giorni dopo l’evento e la presentazione aziendale sarà aggiornata nella sezione Investitori del sito web dell’azienda.
Inhibrx (Nasdaq: INBX) transmitirá por webcast los resultados clave del estudio registracional ChonDRAgon de ozekibart (INBRX-109) frente a placebo en sarcoma condroblástico avanzado/metastásico no resecable el jueves 23 de octubre de 2025 a la 1:30 p.m. PT.
La compañía también ofrecerá actualizaciones sobre dos cohortes de expansión: ozekibart más FOLFIRI en cáncer colorrectal en etapas tardías/últimas líneas de tratamiento y ozekibart con irinotecán y temozolomida en sarcoma de Ewing refractario. Los inversores pueden unirse por webcast o escuchar mediante dial-in; el webcast estará disponible durante 60 días tras el evento y la presentación corporativa se actualizará en la sección de Inversores del sitio web de la empresa.
Inhibrx (나스닥: INBX)는 고도/전이성 재발 불가성 연골육종에서 오제키바트(INBRX-109)의 위약 대비 registrational 연구 ChonDRAgon의 주요 topline 결과를 2025년 10월 23일 목요일 오후 1:30 PT에 webcast로 중계합니다.
또한 두 개의 확장 코호트에 대한 업데이트도 제공합니다: ozekibart + FOLFIRI를 말기 colorectal cancer에서, irinotecan 및 temozolomide를 포함한 ozekibart를 난치성 Ewing sarcoma에서. 투자자들은 webcast에 참여하거나 다이얼 인으로 청취할 수 있습니다; webcast는 행사 후 60일간 이용 가능하며 기업 프레젠테이션은 회사 웹사이트의 투자자 섹션에서 업데이트될 예정입니다.
Inhibrx (Nasdaq: INBX) diffusera en webcast les résultats préliminaires de l’étude registrational ChonDRAgon sur l’ozekibart (INBRX-109) versus placebo chez les patients atteints de cartilaginous sarcoma avancé/metastatique non résécable, le jeudi 23 octobre 2025 à 13h30 PT.
L’entreprise fournira également des mises à jour sur deux cohortes d’expansion : ozekibart plus FOLFIRI dans un cancer colorectal en phase tardive/dernières lignes et ozekibart avec irinotécan et temozolomide dans le sarcome d’Ewing réfractaire. Les investisseurs peuvent se joindre par webcast ou écouter par dial-in; le webcast sera disponible pendant 60 jours après l’événement et la présentation d’entreprise sera mise à jour dans la section Investisseurs du site de l’entreprise.
Inhibrx (Nasdaq: INBX) wird die Topline-Ergebnisse der registrationalen Studie ChonDRAgon zu Ozekibart (INBRX-109) vs. Placebo bei fortgeschrittenem/metastatischem, unresectablem Chondrosarkom am Donnerstag, 23. Oktober 2025 um 13:30 PT webcasten.
Das Unternehmen wird außerdem Updates zu zwei Expansionskohorten geben: ozekibart plus FOLFIRI beim späten/Letzte-Zeile-Colorektalkrebs und ozekibart mit Irinotecan und Temozolomid beim refraktären Ewing-Sarkom. Investoren können per Webcast teilnehmen oder über Dial-in zuhören; der Webcast steht 60 Tage nach der Veranstaltung zur Verfügung und die Firmenpräsentation wird im Bereich Investorenseite der Unternehmenswebsite aktualisiert.
Inhibrx (ناسداك: INBX) سيبث نتائج الخطوط العريضة من دراسة ChonDRAgon التسجيلية لدواذيبارت (INBRX-109) مقابل الدواء الوهمي في ورم غضروفي عظمي متقدم/منتشر غير قابل للإزالة يوم الخميس 23 أكتوبر 2025 في الساعة 1:30 مساءً بتوقيت المحيط الهادئ عبر webcast.
ستقدم الشركة أيضاً تحديثات حول مجموعتين توسيعيتين: ozekibart إضافة FOLFIRI في سرطان القولون والمستقيم في مراحل متأخرة/آخر خطوط العلاج و< b>ozekibart مع irinotecan و temozolomide في ساركومة أينغ refractor. يمكن للمستثمرين الانضمام عبر webcast أو الاستماع عبر dial-in؛ وسيكون webcast متاحاً لمدة 60 يوماً بعد الحدث وسيتم تحديث العرض المؤسسي في قسم المستثمرين من موقع الشركة الإلكتروني.
Inhibrx(纳斯达克:INBX) 将通过网络广播披露有关 ChonDRAgon 注册性研究中 ozekibart(INBRX-109)对比安慰剂在晚期/转移性不可切除性软骨肉瘤的初步 topline 结果,时间为 2025 年 10 月 23 日星期四,太平洋夏令时下午 1:30。
公司还将提供关于两个扩展队列的更新:晚期结直肠癌中的 ozekibart 加 FOLFIRI,以及对难治性 Ewing 肉瘤的 ozekibart 与 irinotecan 和 temozolomide。投资者可通过 webcast 参加或通过拨号收听; webcast 将在事件后 60 天 内可用,公司的投资者页面将更新企业演示文稿。
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– Event to be webcast live on Thursday, October 23, 2025 at 1:30 p.m. PT –
Investors may join via the web: https://app.webinar.net/RdZmlEPaEyw or may listen to the call by dialing (1-888-880-3330). Please refer to Inhibrx Biosciences, Inc. or the conference ID 9577647 when calling in. Following the webcast, the presentation may be accessed through a link on the investors section of Inhibrx's website at https://inhibrx.com/inhibrx-biosciences-inc-investors/events-and-presentations. The webcast will be available for 60 days following the event. Following the presentation, Inhibrx will update its corporate presentation within the "Investors" section of its website at www.inhibrx.com.
About ozekibart (INBRX-109)
Ozekibart is a precision-engineered, tetravalent death receptor 5 (DR5) agonist antibody designed to exploit the tumor-biased cell death induced by DR5 activation. In January 2021, the FDA granted Fast Track designation to ozekibart for the treatment of patients with metastatic or unresectable conventional chondrosarcoma, and, in November 2021, the FDA granted orphan drug designation to ozekibart for chondrosarcoma.
In June 2021, Inhibrx initiated a randomized, blinded, placebo-controlled, registration-enabling Phase 2 trial of ozekibart in metastatic, unresectable conventional chondrosarcoma.
Additionally, in Phase 1/2 trials, Inhibrx is investigating ozekibart in colorectal cancer in combination with FOLFIRI and Ewing sarcoma in combination with irinotecan/temozolomide, as well as other tumor types.
About Inhibrx Biosciences, Inc.
Inhibrx Biosciences is a clinical-stage biopharmaceutical company focused on developing a broad pipeline of novel biologic therapeutic candidates. Inhibrx Biosciences utilizes diverse methods of protein engineering to address the specific requirements of complex target and disease biology, including its proprietary protein engineering platforms. Inhibrx Biosciences was incorporated in January 2024 as a direct, wholly-owned subsidiary of Inhibrx, Inc. Prior to the sale of Inhibrx, Inc. and the INBRX-101 program to Sanofi S.A., Inhibrx Biosciences acquired certain corporate infrastructure and other assets and liabilities through a series of internal restructuring transactions effected by Inhibrx, Inc. Inhibrx, Inc. also completed a distribution to holders of its shares of common stock of
Forward-Looking Statements
Inhibrx cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. These statements are based on Inhibrx's current beliefs and expectations. These forward-looking statements include, but are not limited to, statements regarding the clinical development of ozekibart. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in Inhibrx's business, including, without limitation, risks and uncertainties regarding: the initiation, timing, progress and results of its preclinical studies and clinical trials, and its research and development programs; its ability to advance therapeutic candidates into, and successfully complete, clinical trials; its interpretation of initial, interim or preliminary data from its clinical trials, including interpretations regarding disease control and disease response; results from preclinical studies or early clinical trials not necessarily being predictive of future results; unexpected adverse side effects or inadequate efficacy of its therapeutic candidates that may limit their development, regulatory approval and/or commercialization; the potential for its programs and prospects to be negatively impacted by developments relating to its competitors, including the results of studies or regulatory determinations relating to its competitors; the timing or likelihood of regulatory filings and approvals and regulatory developments in the
Investor and Media Contact:
Kelly Deck, CFO
ir@inhibrx.com
858-795-4260
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