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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

Organon Reports Q4 2023 Revenue Growth Driven by Women’s Health and Biosimilars

Fineline Cube Feb 18, 2024

Organon (NYSE: OGN), the U.S.-based pharmaceutical company, has reported its fourth-quarter 2023 financial results, revealing...

Company Drug

Roche’s Xolair Gains FDA Approval to Combat IgE-Mediated Food Allergies in Patients Aged 1 and Up

Fineline Cube Feb 18, 2024

Roche (SWX: ROG) has announced that the U.S. Food and Drug Administration (FDA) has granted...

Company Drug

Ipsen Secures FDA Approval for Onivyde Regimen as First-Line Treatment for Metastatic Pancreatic Adenocarcinoma

Fineline Cube Feb 18, 2024

Ipsen (EPA: IPN, OTCMKTS: IPSEY), the France-based biopharmaceutical company, has announced that the U.S. Food...

Company Drug

FDA Approves Takeda’s Eohilia as First Oral Therapy for Eosinophilic Esophagitis in Patients Aged 11 and Up

Fineline Cube Feb 18, 2024

The U.S. Food and Drug Administration (FDA) has granted approval to Takeda Pharmaceutical Company (TYO:...

Company Drug

Roche’s Piasky (Crovalimab) Secures NMPA Approval for Untreated Paroxysmal Nocturnal Hemoglobinuria

Fineline Cube Feb 9, 2024

The National Medical Products Administration (NMPA) has granted marketing approval to Swiss pharmaceutical giant Roche...

Company Drug

Roche Secures NMPA Approval for Rozlytrek to Treat Pediatric NTRK Fusion-Positive Tumors

Fineline Cube Feb 9, 2024

Swiss pharmaceutical giant Roche (SWX: ROG) has received a new indication approval from the National...

Company Deals

Akeso Biopharma to Acquire 35% Stake in AD Pharmaceuticals for RMB 267 Million

Fineline Cube Feb 9, 2024

Akeso Biopharma (HKG: 9926) is poised to acquire a 35% stake in AD Pharmaceuticals Co.,...

Company

AstraZeneca Reports 6% Revenue Growth in 2023, Driven by Oncology and Diabetes Drug Sales

Fineline Cube Feb 9, 2024

AstraZeneca (AZ; NASDAQ: AZN), the UK-based multinational, reported its financial results for 2023 this week,...

Company Deals

I-Mab to Become U.S.-Based Biotech, Divesting All China Assets for Up to $80 Million

Fineline Cube Feb 8, 2024

I-Mab (NASDAQ: IMAB), a biotech company transitioning to a U.S.-based entity, has announced plans to...

Company Deals

AbbVie Expands Licensing Agreement for Innovative sCAR-T Platform with Scripps Research

Fineline Cube Feb 8, 2024

AbbVie (NYSE: ABBV) has expanded its collaboration with Scripps Research’s Calibr-Skaggs Institute, securing licensing rights...

Company

AstraZeneca Announces $300 Million Investment in Next-Gen Cell Therapies Manufacturing in the U.S.

Fineline Cube Feb 8, 2024

AstraZeneca (AZ; NASDAQ: AZN), headquartered in the UK, has announced a significant investment of $300...

Company Drug

FDA Grants Priority Review for GSK’s Arexvy to Expand RSV Vaccine Age Range to 50-59

Fineline Cube Feb 8, 2024

The U.S. Food and Drug Administration (FDA) has initiated a priority review of GlaxoSmithKline’s (GSK;...

Company Drug

CMS Secures NMPA Approval for Clinical Trials of TYK2 Inhibitor CMS-D001 and GnRH Antagonist CMS-D002

Fineline Cube Feb 8, 2024

China Medical System Holdings Ltd (CMS, HKG: 0867) has announced that it has received clinical...

Company Drug

Evopoint Biosciences Enrolls First Patient in Phase III Trial for Gout Drug XNW3009

Fineline Cube Feb 8, 2024

Suzhou-based Evopoint Biosciences Co., Ltd. has announced the enrollment of its first patient in a...

Company Drug

ChinaGene Secures CDE Approval for ZVS101e Gene Therapy Targeting Retinitis Pigmentosa

Fineline Cube Feb 8, 2024

Beijing-based ChinaGene Technology Co., Ltd. has announced that it has received tacit clinical approval from...

Company Deals

Yantai Dongcheng Acquires Full Rights to Alfatide II, Targeting Diagnostic and Therapeutic Applications

Fineline Cube Feb 8, 2024

Yantai Dongcheng Pharmaceutical Group Co., Ltd. (SHE: 002675) has announced its acquisition of all rights...

Company Drug

Nanjing Zenshine’s ZX-7101A NDA Accepted by NMPA for Uncomplicated Influenza Treatment

Fineline Cube Feb 8, 2024

Nanjing Zenshine Pharmaceuticals Co., Ltd., a China-based small molecule drug developer, has announced that the...

Company

Gilead’s 2023 Flat Sales Reflect Stagnation and COVID-19 Demand Decline

Fineline Cube Feb 7, 2024

Gilead Sciences Inc. (NASDAQ: GILD) has reported a stagnant performance for the year 2023, with...

Company

Astellas Pharma Inc. Reports 2.1% YOY Growth in Q1-Q3 Fiscal 2023 Revenues

Fineline Cube Feb 7, 2024

Tokyo-based pharmaceutical company Astellas Pharma Inc., (TYO: 4503) has announced financial results for the first...

Company

Gilead’s 2023 Stagnation Foresees Flat 2024 Sales as Veklury Revenues Dwindle

Fineline Cube Feb 7, 2024

Gilead Sciences (NASDAQ: GILD) has reported a stagnant performance for 2023, with product sales remaining...

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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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