Opdivo
Manufacturing · United States · <25 Employees
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Headquarters
United StatesWebsite
www.opdivo.comRevenue
<$5 MillionIndustry
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OPDIVO (Nivolumab) Drug Pipeline Research Report 2024: The First-in-human Immunoglobulin G4 (IgG4) PD-1 Immune Checkpoint Inhibitor Antibody - Market Size, Forecast, and Emerging Insights 2019-2032 - ResearchAndMarkets.com
DUBLIN--(BUSINESS WIRE)--The "OPDIVO Market Size, Forecast, and Emerging Insight - 2032" report has been added to ResearchAndMarkets.com's offering. This report provides comprehensive insights about OPDIVO for ovarian cancer in the six major markets. A detailed picture of the OPDIVO for ovarian cancer in the 6MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain), and the United Kingdom for the study period 2019 -2032 is provided in this report along with a detailed descriptionAgilent Companion Diagnostic Expands CE-IVD Mark for PD-L1 IHC 28-8 pharmDx to Include Esophageal Squamous Cell Carcinoma
SANTA CLARA, Calif.--(BUSINESS WIRE)--Agilent Technologies Inc. (NYSE: A) today announced it has expanded CE-IVD marking in the European Union for its PD-L1 IHC 28-8 pharmDx as an aid in identifying esophageal squamous cell carcinoma patients for treatment with Bristol Myers Squibb’s PD-1-targeted immunotherapeutic OPDIVO® (nivolumab), in combination with fluoropyrimidine and platinum-based chemotherapy or OPDIVO® in combination with YERVOY® (ipilimumab). These combined treatments provide new hBristol Myers Squibb Receives Positive CHMP Opinion for Opdivo (nivolumab) as Adjuvant Treatment for Esophageal or Gastroesophageal Junction Cancer Patients with Residual Pathologic Disease Following Chemoradiotherapy
PRINCETON, N.J.--(BUSINESS WIRE)---- $BMY #MEDIA--BMS Receives Positive CHMP Opinion for Opdivo as Adjuvant Treatment for Esophageal or Gastro Junction Cancer Patients w/ RPD Following ChemoUbiVac Announces Clinical Trial Collaboration with Bristol Myers Squibb on Combination Immunotherapy for Advanced Triple Negative Breast Cancer
PORTLAND, Ore.--(BUSINESS WIRE)--UbiVac, Inc. (www.ubivac.com) today announced it has entered into a clinical trial collaboration with Bristol Myers Squibb (NYSE:BMY) to evaluate the safety, tolerability, and preliminary efficacy of UbiVac’s investigational product, DPV-001™, a first-in-class cancer vaccine that exploits autophagy, in combination with Bristol Myers Squibb’s anti-OX40 (BMS-986178) combined with sequenced administration of the programmed death-1 (PD-1) immune checkpoint inhibitorBristol-Myers Squibb Reports Second Quarter Financial Results
NEW YORK--(BUSINESS WIRE)--Bristol-Myers Squibb Reports Second Quarter Financial Results
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Frequently Asked Questions Regarding Opdivo
Learn about OPDIVO® (nivolumab), a prescription medicine that treats certain types of cancers. Find the information you need to care for your OPDIVO® and OPDIVO + YERVOY® (ipilimumab) patients. Please see Indication and Important Safety Information.... Read More