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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

Hengrui’s Ivarmacitinib NDA Accepted for Non‑Radiographic Axial Spondyloarthritis

Fineline Cube Nov 25, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276, HKG: 1276) announced that the China National Medical...

Company Drug

AstraZeneca’s Durvalumab Wins China Approval for Stage III NSCLC After Sequential Chemoradiotherapy

Fineline Cube Nov 25, 2025

AstraZeneca (AZ, NASDAQ: AZN) announced that Imfinzi (durvalumab) received National Medical Products Administration (NMPA) approval...

Company Drug

Qihan-Biotech’s QT-019B Universal CAR-T Wins Implied NMPA Approval

Fineline Cube Nov 25, 2025

Hangzhou Qihan Biotech Co., Ltd. announced that its New Drug Clinical Trial (IND) application for...

Company Drug

Junshi’s JS001sc Subcutaneous PD-1 Meets Phase 3 Endpoint in NSCLC

Fineline Cube Nov 25, 2025

Shanghai Junshi Biosciences Co., Ltd. (HKG: 1877, SHA: 688180) announced that its Phase 3 trial JS001sc-002-III-NSCLC...

Company Deals Digital

Rimag Partners with Qingyang Government on AI Medical Imaging Infrastructure

Fineline Cube Nov 25, 2025

Jiangxi Rimag Group Co., Ltd. (HKG: 2522) announced a Strategic Framework Cooperation Agreement with the...

Company Deals

Biogen Dayra Partnership Targets Immunology with Macrocyclic Peptides

Fineline Cube Nov 25, 2025

Biogen Inc. (NASDAQ: BIIB) and Dayra Therapeutics announced a research collaboration to discover and develop...

Company Drug

CStone’s Sugemalimab Wins EU Approval for Stage III NSCLC, Expanding European Indication

Fineline Cube Nov 25, 2025

CStone Pharmaceuticals (HKG: 2616) announced that the European Commission (EC) has approved a new indication...

Company Drug

Salubris’ SAL0139 Wins NMPA Nod for Hyperlipidemia Clinical Trial

Fineline Cube Nov 24, 2025

Shenzhen Salubris Pharmaceuticals Co., Ltd. (SHE: 002294) announced that its independently developed innovative small molecule...

Company Drug

Zhongsheng’s Onradivir Granules Enroll First Phase 3 Pediatric Influenza Patient

Fineline Cube Nov 24, 2025

Guangdong Zhongsheng Pharmaceutical Co., Ltd. (SHE: 002317) announced the enrollment and dosing of the first...

Company Deals

HBM and AstraZeneca Deepen ADC/TCE Collaboration as AstraZeneca Exercises License Options

Fineline Cube Nov 24, 2025

HBM Holdings Limited (HKG: 2142) announced the renewal and deepening of its global strategic collaboration...

Company Drug

Kelun-Biotech’s Sac-TMT Achieves First ADC-IO NSCLC Success

Fineline Cube Nov 24, 2025

Kelun-Biotech Biopharmaceutical Co., Ltd. (HKG: 6990) announced that sacituzumab tirumotecan (sac-TMT), its proprietary TROP2 ADC,...

Company Drug

Luye’s LY03017 Wins FDA Nod for Psychosis Trials in Alzheimer’s and Parkinson’s

Fineline Cube Nov 24, 2025

Luye Pharma Group Limited (HKG: 2186) announced that its independently developed LY03017 received U.S. FDA...

Others

CSPC’s SYH2056 Wins NMPA Nod for Depression Trials as Fast‑Acting 5‑HT2A Agonist

Fineline Cube Nov 24, 2025

CSPC Pharmaceutical Group Limited (HKG: 1093) announced that SYH2056, a selective 5‑HT2A receptor agonist, received...

Company Drug

Biokin’s iza-bren NDA Accepted for Nasopharyngeal Carcinoma, Advancing Bispecific ADC

Fineline Cube Nov 24, 2025

Sichuan Biokin Pharmaceutical Co., Ltd. (SHA: 688506) announced that its New Drug Application (NDA) for...

Company Deals

Phrontline Raises $60M Series Pre‑A+ to Advance Bispecific ADC Pipeline

Fineline Cube Nov 24, 2025

Phrontline Biopharma, a next‑generation antibody‑drug conjugate (ADC) company, announced the close of an oversubscribed USD...

Company Deals

Valo Health Partners with Merck on $3B Parkinson’s Disease Discovery Deal

Fineline Cube Nov 24, 2025

Valo Health, Inc. announced a strategic collaboration with Merck KGaA (ETR: MRK) to advance therapeutic...

Policy / Regulatory

NMPA Issues Export Drug Certification Rules, Expanding Scope and Validity

Fineline Cube Nov 24, 2025

China’s National Medical Products Administration (NMPA) released the “Regulations on Inspection and Export Certification Management...

Company Drug

Bayer’s HYRNUO Wins FDA Approval for HER2-Mutated Lung Cancer

Fineline Cube Nov 24, 2025

Bayer AG (ETR: BAYN) announced that sevabertinib (trade name HYRNUO) received U.S. FDA approval for...

Company

Johnson & Johnson China PINS Head Alex He to Depart, Driving Leadership Transition Amid Key NRDL Product Success

Fineline Cube Nov 24, 2025

Johnson & Johnson (J&J, NYSE: JNJ) China confirmed a significant leadership change today, announcing that...

Company Deals

3SBio’s Mandi Spin-Off Targets HKEX IPO as Hair Health Leader

Fineline Cube Nov 23, 2025

3SBio Inc. (HKG: 1530) announced plans to spin off its consumer healthcare subsidiary Mandi International...

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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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