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Licensing Partner of Shenzhen Chipscreen Biosciences - HUYABIO International, Receives Regulatory Approval for Chidamide Monotherapy of Peripheral T-Cell Lymphoma(PTCL) in Japan

/PRNewswire/ -- Shenzhen Chipscreen Biosciences licensing partner, HUYABIO International (HUYABIO™), today announced the regulatory approval for Chidamide...
Kensei Tobinai Chidamide Tucidinostat Chipscreen Bioscience Chipscreen Biosciences Lu Xianping Mireille Gillings

Licensing Partner of Shenzhen Chipscreen Biosciences - HUYABIO International, Receives Regulatory Approval for Chidamide Monotherapy of Peripheral T-Cell Lymphoma(PTCL) in Japan

/PRNewswire/ -- Shenzhen Chipscreen Biosciences licensing partner, HUYABIO International (HUYABIO™), today announced the regulatory approval for Chidamide...
Kensei Tobinai Chidamide Tucidinostat Chipscreen Bioscience Chipscreen Biosciences Lu Xianping Mireille Gillings

Merck & Co., Inc.: Merck and Eisai Receive Positive EU CHMP Opinions for KEYTRUDA (pembrolizumab) Plus LENVIMA (lenvatinib) in Two Different Types of Cancer

Positive Opinion Granted for Advanced Renal Cell Carcinoma Based on Significant Progression-Free Survival (PFS), Overall Survival (OS) and Objective Response Rate (ORR) Benefit Compared to Sunitinib
United States New Zealand Nikki Sullivan Peter Dannenbaum Melissa Moody Eisai Europe Ltd

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Merck and Eisai Receive Positive EU CHMP Opinions for KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenva

Positive Opinion Granted for Advanced Renal Cell Carcinoma Based on Significant Progression-Free Survival (PFS), Overall Survival (OS) and Objective Response Rate (ORR) Benefit Compared to Sunitinib in CLEAR/KEYNOTE-581 TrialPositive Opinion Granted for Advanced Endometrial Carcinoma Based on Significant OS and PFS...
United States Nikki Sullivan Peter Dannenbaum Melissa Moody European Union European Commission

Merck and Eisai Receive Positive EU CHMP Opinions for KEYTRUDA® Plus LENVIMA® in Two Different Types of Cancer

Positive Opinion Granted for Advanced Renal Cell Carcinoma Based on Significant Progression-Free Survival Overall Survival and Objective Response Rate Benefit Compared to Sunitinib in CLEARKEYNOTE-581 Trial Positive Opinion Granted for Advanced Endometrial Carcinoma Based on Significant OS and PFS Benefit Compared to Chemotherapy in KEYNOTE-775Study 309 Trial Merck known as MSD outside the United States and Canada, ...
United States New Zealand Gregory Lubiniecki Nikki Sullivan Peter Dannenbaum Melissa Moody

Ultimovacs ASA: Ultimovacs Presents the INITIUM Study Design as a Trial-in-Progress Poster at AACR Annual Meeting 2021

(0) Ultimovacs ASA ("Ultimovacs", ticker ULTI), announced that it is presenting a poster today on the trial design of its ongoing Phase II INITIUM clinical study evaluating nivolumab and ipilimumab in combination with the Companys proprietary universal cancer vaccine, UV1, as first line treatment in patients with metastatic malignant melanoma, at the 2021 AACR Annual Meeting, held virtually from April 9 to April 14, 2021. The poster, titled, "Nivolumab and ipilimumab +/- UV1 vaccine as 1st line...
Hans Vassg Progression Free Survival Overall Survival Objective Response Rate ப்ரோக்ரெஶந் இலவசம் பிழைப்பு ஓவரால் பிழைப்பு

Elevation Oncology Announces Clinical Cancer Research Publication Highlighting the Specific Inhibition of HER3 by Seribantumab in Preclinical NRG1 Fusion Models

Elevation Oncology Announces Clinical Cancer Research Publication Highlighting the Specific Inhibition of HER3 by Seribantumab in Preclinical NRG1 Fusion Models - Results show seribantumab efficiently inhibited HER3 and the entire ERBB family signaling pathway and established a biologically effective dose range for tumors driven by an NRG1 fusion - - Seribantumab is currently being evaluated in the tumor-agnostic Phase 2 CRESTONE trial for patients with any solid tumor harboring an NRG1 fusion ...
United States David Rosen Romel Somwar Shawn Leland Igor Odintsov American Association For Cancer Research

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