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Company Deals

Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal

Fineline Cube Jun 12, 2026
Company Deals

Kelun-Biotech Receives USD 89 Million Settlement Payment from Medilink Therapeutics Over ADC Pipeline Out-Licensing Dispute

Fineline Cube Jun 12, 2026
Company Deals

HJ Science Launches HK$1.11 Billion IPO on Hong Kong Exchange to Advance Clinical-Stage Pipeline in Autoimmune, Metabolic, and Oncology Therapies

Fineline Cube Jun 12, 2026
Company Deals

Cascade Pharmaceuticals Secures RMB 318 Million Series D Financing to Advance Bile Acid Metabolism Pipeline

Fineline Cube Jun 12, 2026
Company Deals

QuantumPharm (XtalPi) Secures $400 Million AI-Driven Partnership for Best-in-Class GPCR-Targeting Oral Small-Molecule Drug

Fineline Cube Jun 11, 2026
Policy / Regulatory

China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added

Fineline Cube Jun 12, 2026
Company Drug

Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC

Fineline Cube Jun 12, 2026
Company Drug

Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria

Fineline Cube Jun 12, 2026
Company Drug

AstraZeneca’s Imfinzi Gets Positive Opinion for Bladder Cancer Perioperative Treatment

Fineline Cube May 28, 2025

UK-based pharmaceutical giant AstraZeneca (AZ; NASDAQ: AZN) announced that the European Medicines Agency’s (EMA) Committee...

Company Drug

EyePoint’s Partner Betta Completes Enrollment for Duravyu’s Pivotal Phase III Study

Fineline Cube May 28, 2025

EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), the US partner of China-based Betta Pharmaceuticals (SHE: 300558), announced...

Company Drug

EMA Recommends Tevimbra for Nasopharyngeal Cancer First-line Treatment

Fineline Cube May 28, 2025

The European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended...

Company Drug

AbelZeta Pharma’s C-CAR168 Secures FDA RMAT Designation for Lupus Treatments

Fineline Cube May 28, 2025

Sino-US biotech AbelZeta Pharma, Inc., based in Rockville, Maryland, and with operations in Shanghai, announced...

Policy / Regulatory

FDA Rejects Data from Two Chinese Testing Labs Over Compliance Concerns

Fineline Cube May 28, 2025

The U.S. Food and Drug Administration (FDA) late last week issued General Correspondence Letters to...

Company Drug

CARsgen’s Satricabtagene Autoleucel Granted Priority Review by China’s CDE

Fineline Cube May 28, 2025

China-based CARsgen Therapeutics Holdings Ltd (HKG: 2171) has announced that the Center for Drug Evaluation...

Company Drug

Salubris Pharma’s Xinchaotuo Gains NMPA Approval for Primary Hypertension

Fineline Cube May 28, 2025

China-based Shenzhen Salubris Pharmaceuticals Co., Ltd (SHE: 002294) announced that it has received marketing approval...

Company Deals

Jiangsu Nhwa’s Investee Jiangsu Haoxinqing Plans Overseas Listing

Fineline Cube May 28, 2025

China-based Jiangsu Nhwa Pharmaceutical Co., Ltd (SHE: 002262) announced that its investee company Jiangsu Haoxinqing...

Company Deals

Shenyang Xingqi Pharmaceuticals Plans Private Placement to Fund R&D Center

Fineline Cube May 28, 2025

China-based Shenyang Xingqi Pharmaceutical Co., Ltd (SHE: 300573) announced plans for a private placement of...

Company Drug

Novartis’ Beovu Approved by NMPA for Diabetic Macular Edema Treatment

Fineline Cube May 28, 2025

Swiss giant Novartis’ (NYSE: NVS) Beovu (brolucizumab) received approval from China’s National Medical Products Administration...

Company Drug

Mabworks’ MIL62 Gains NMPA Review for NMOSD Treatment

Fineline Cube May 28, 2025

China-based Beijing Mabworks Biotech Co., Ltd announced that its New Drug Application (NDA) for MIL62,...

Company Deals

EpimAb Biotherapeutics and Juri Biosciences Ink Global Licensing Deal for KLK2-CD3 T-Cell Engager

Fineline Cube May 28, 2025

Shanghai-based biotech EpimAb Biotherapeutics announced a global licensing agreement with US-headquartered Juri Biosciences, Inc., a...

Company Deals Drug

Eli Lilly to Acquire SiteOne Therapeutics for Up to USD 1 Billion

Fineline Cube May 28, 2025

US-based pharmaceutical giant Eli Lilly & Co. (NYSE: LLY) announced plans to acquire compatriot biotech...

Company Drug

Junshi Biosciences’ Junshida Wins NMPA Approval for HeFH and Statin-Intolerant Patients

Fineline Cube May 28, 2025

China’s Shanghai Junshi Biosciences Co., Ltd (HKG: 1877, SHA: 688180) announced that it has received...

Company Drug

Sino Biopharmaceutical Presents TQB2102 Phase I Results at ASCO 2025

Fineline Cube May 28, 2025

China-based Sino Biopharmaceutical Ltd (HKG: 1177) presented preliminary results from a Phase I clinical study...

Company

BeiGene Rebrands to BeOne Medicines and Relocates to Switzerland

Fineline Cube May 28, 2025

BeiGene (NASDAQ: ONC, HKG: 6160, SHA: 688235), a global oncology company, has officially rebranded to...

Company Deals Drug

Betta Pharmaceuticals Partners with BioRay for Herceptin Biosimilar Anruize

Fineline Cube May 28, 2025

China-based Betta Pharmaceuticals (SHE: 300558) announced a strategic partnership with fellow domestic firm BioRay Biopharmaceutical....

Company Medical Device

China’s NMPA Approves Lifetech’s Aortic Fenestration Stent System

Fineline Cube May 28, 2025

China’s National Medical Products Administration (NMPA) recently approved an innovative aortic in-situ fenestration branch reconstruction...

Company Drug

Phanes Therapeutics Doses First Patient in CD73 Antibody Clinical Study

Fineline Cube May 28, 2025

Sino-US biotech Phanes Therapeutics Inc. announced the first patient dosing in a clinical study for...

Company Drug

StarryGene Initiates Phase II Study of XMVA09 for Wet AMD Treatment

Fineline Cube May 27, 2025

Hefei-based gene therapy biotech StarryGene announced the initiation of a Phase II clinical study for...

Posts pagination

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Recent updates

  • Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal
  • Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC
  • Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria
  • China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added
  • Takeda’s Zasocitinib Demonstrates Superior Efficacy Over Deucravacitinib in Phase III Psoriasis Trial with 35% PASI 100 Response Rate
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Company Deals

Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal

Company Drug

Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC

Company Drug

Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria

Policy / Regulatory

China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added

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