Merck's Zilovertamab Vedotin Shows Promising Results in Phase 2 Trial for Relapsed/Refractory DLBCL at 2025 ASCO Meeting

Reuters

05-30

Merck's Zilovertamab Vedotin Shows Promising Results in Phase 2 Trial for Relapsed/Refractory DLBCL at 2025 ASCO Meeting

Merck & Co. Inc. unveiled promising results from the Phase 2 portion of the waveLINE-003 trial involving their investigational drug zilovertamab vedotin. Administered at a dose of 1.75 mg/kg in combination with rituximab, gemcitabine, and oxaliplatin, the treatment demonstrated significant antitumor activity and a complete response rate in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). Dr. Gregory Lubiniecki from Merck Research Laboratories highlighted the manageable safety profile and potential of this ROR1-directed antibody-drug conjugate to treat multiple hematologic malignancies. Dr. Philippe Armand of the Dana-Farber Cancer Institute noted the encouraging outcomes for patients, emphasizing the need for additional treatment options for those with relapsed/refractory DLBCL. The trial's success supports further research, with the Phase 3 portion already underway.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck & Co. Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20250530306112) on May 30, 2025, and is solely responsible for the information contained therein.

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Inc. unveiled promising results from the Phase 2 portion of the waveLINE-003 trial involving their investigational drug zilovertamab vedotin. Administered at a dose of 1.75 mg/kg in combination with rituximab, gemcitabine, and oxaliplatin, the treatment demonstrated significant antitumor activity and a complete response rate in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). Dr. Gregory Lubiniecki from Merck Research Laboratories highlighted the manageable safety profile and potential of this ROR1-directed antibody-drug conjugate to treat multiple hematologic malignancies. Dr. Philippe Armand of the Dana-Farber Cancer Institute noted the encouraging outcomes for patients, emphasizing the need for additional treatment options for those with relapsed/refractory DLBCL. 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While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck & Co. Inc. published the original content used to generate this news brief via Business Wire  on May 30, 2025, and is solely responsible for the information contained therein.","collect":0,"end_time":0,"defaultTopTitle":"","property":[],"viewcount":null,"language":"en","relate_stocks":{},"translate_title":"默克的Zilovertamab Vedotin在2025年ASCO会议上针对复发/难治性DLBCL的2期试验中显示出有希望的结果","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"MRK":0.9},"content_text":"Merck's Zilovertamab Vedotin Shows Promising Results in Phase 2 Trial for Relapsed/Refractory DLBCL at 2025 ASCO Meeting\n    \n\n        Merck & Co. Inc. unveiled promising results from the Phase 2 portion of the waveLINE-003 trial involving their investigational drug zilovertamab vedotin. 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