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BRUKINSA® Receives Positive Recommendation from NICE in U K for Adult Patients with Chronic Lymphocytic Leukemia

BRUKINSA® Receives Positive Recommendation from NICE in U K for Adult Patients with Chronic Lymphocytic Leukemia
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United kingdomSouth koreaUnited statesGreat britainMaryline ivaRobert mulrooneyLiza heapesTalha munirCancer research united kingdomBeigene ltdScottish medicines consortiumNational cancer instituteNational institute for healthAmerican cancer societyExchange commissionNational institute

BeiGene, Ltd : BRUKINSA Receives Positive Recommendation from NICE in U K for Adult Patients with Chronic Lymphocytic Leukemia

BeiGene, Ltd : BRUKINSA Receives Positive Recommendation from NICE in U K for Adult Patients with Chronic Lymphocytic Leukemia
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South koreaUnited kingdomUnited statesGreat britainMaryline ivaIhre chancenRobert mulrooneyIndiens wirtschaftTalha munirLiza heapesNational institute for healthCancer research united kingdomNational cancer instituteBeigene ltdScottish medicines consortiumExchange commission

BeiGene, Ltd : BeiGene Announces the Phase 3 RATIONALE 315 Trial Met Primary Endpoints of Major Pathological Response Rate and Event-Free Survival for Tislelizumab Plus Chemotherapy in Patients with Resectable Non-Small Cell Lung Cancer (NSCLC)

BeiGene, Ltd : BeiGene Announces the Phase 3 RATIONALE 315 Trial Met Primary Endpoints of Major Pathological Response Rate and Event-Free Survival for Tislelizumab Plus Chemotherapy in Patients with Resectable Non-Small Cell Lung Cancer (NSCLC)
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New zealandUnited kingdomIhre chancenLiza heapesKyle blankenshipIndiens wirtschaftMaryline ivaDrug administrationBeigene ltdExchange commissionEuropean commissionEuropean society for medical oncologyEuropean medicines agencyBlinded independent pathology reviewBlinded independent central reviewEuropean society

BeiGene, Ltd : BeiGene Announces Late-Breaking Data at ESMO Showing Tislelizumab plus Chemotherapy Significantly Improved Overall Survival at Final Analysis in First-Line Advanced Gastric or Gastroesophageal Junction Adenocarcinoma

BeiGene, Ltd : BeiGene Announces Late-Breaking Data at ESMO Showing Tislelizumab plus Chemotherapy Significantly Improved Overall Survival at Final Analysis in First-Line Advanced Gastric or Gastroesophageal Junction Adenocarcinoma
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United kingdomNew zealandRui hua xuIhre chancenLiza heapesMaryline ivaMark lanasaKyle blankenshipIndiens wirtschaftEuropean society for medical oncologyEuropean commissionCancer control centerSun yat sen universityEuropean medicines agencyExchange commissionDrug administration

BeiGene Receives Positive CHMP Opinion for BRUKINSA® (zanubrutinib) in Relapsed or Refractory Follicular Lymphoma

BASEL, Switzerland & BEIJING & CAMBRIDGE, Mass., October 13, 2023 BeiGene (Nasdaq: BGNE; HKEX: 06160; SSE: 688235), a global biotechnology company, today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive opinion recommending approval of BRUKINSA® (zanubrutinib), a Bruton’s tyrosine kinase inhibitor (BTKi), in combination with obinutuzumab for the treatment of adult patients with relapsed or refractory (R/R) follicul

South koreaUnited statesUnited kingdomGreat britainMehrdad mobasherLiza heapesMaryline ivaKyle blankenshipEuropean commissionEuropean unionAccess consortium new active substance initiativeAmerican cancer societyWorld health organizationLeukemia lymphoma societyEuropean medicines agencyCommittee for medicinal products human use