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CStone presents updated results of anti-PD-1 antibody nofazinlimab in combination with lenvatinib as first-line treatment in patients with unresectable hepatocellular carcinoma (HCC) at ASCO 2022 | Antibodies

CStone presents updated results of anti-PD-1 antibody nofazinlimab in combination with lenvatinib as first-line treatment in patients with unresectable hepatocellular carcinoma (HCC) at ASCO 2022

United statesJason yangJia fanCstone pharmaceuticalsInternational agency for research on cancerFudan universityAmerican society of clinical oncologyI cstone pharmaceuticalsWorld health organizationChinese academy of sciencesOrphan drug designationChinai juneClinical oncologyChief medical officerGlobal cancer incidenceInternational agency

Innovent Presents Clinical Data of IBI110 (Anti-LAG-3 Monoclonal Antibody) at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting | Antibodies

Innovent Presents Clinical Data of IBI110 (Anti-LAG-3 Monoclonal Antibody) at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting

Rhui zhouUnited statesHong kongInnovent biologicsAdimab incyteCaicun zhouEli lillySchool of medicineAmerican society of clinical oncologyMd anderson cancer centerZhejiang universityI innovent biologics incInnovent presents clinical dataClinical oncologyAnnual meetingChinai june

U S Food and Drug Administration Approves Two Opdivo® (nivolumab)-Based Regimens as First-Line Treatments for Unresectable Advanced or Metastatic Esophageal Squamous Cell Carcinoma | Antibodies

U.S. Food and Drug Administration Approves Two Opdivo® (nivolumab)-Based Regimens as First-Line Treatments for Unresectable Advanced or Metastatic Esophageal Squamous Cell Carcinoma

United statesSouth koreaJapan generalI bristol myers squibbBristol myers squibbJaffera ajaniAdam lenkowskyDrug administration approves two opdivoNational cancer instituteAmerican society of clinical oncologyBristol myers squibb companyTime oncology review pilot programVirtual congressAmerican cancer societyUniversity of texas md anderson cancer centerDrug administration

Alvotech Clinical Study Results Demonstrate Therapeutic Equivalence between Biosimilar Candidate AVT04 and Reference Product Stelara® | Antibodies

Alvotech Clinical Study Results Demonstrate Therapeutic Equivalence between Biosimilar Candidate AVT04 and Reference Product Stelara®

United statesUnited kingdomLichtenstein hukyndraLos angelesMark levickRobert wessmanAlvotech lux holdingsExchange commissiona registration statement on formAlvotech holdingsOaktree acquisition corpTeva pharmaceuticalsTeva pharmaceutical industries ltdI alvotech holdings saBiosimilar candidateReference product stelaraIcelandi may

Evusheld significantly protected against symptomatic COVID-19 for at least six months in PROVENT Phase III trial in high-risk populations | Antibodies

Evusheld significantly protected against symptomatic COVID-19 for at least six months in PROVENT Phase III trial in high-risk populations

United kingdomUnited statesCity ofGreat britainAstrazeneca evusheldMyronj levinVanderbilt university medical centerDepartment of defenseCompany on twitter astrazenecaDepartment of healthUniversity of colorado school medicineEuropean unionNuclear defenseCenters for diseaseEuropean congressBiomedical advanced research

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