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Company Deals

Sihuan Pharmaceutical and dProtein Biotechnology Form AI-Powered Medical Aesthetics Joint Venture

Fineline Cube May 29, 2026
Company Deals Drug

Salvectors Receives NMPA Clinical Approval for YB1-X7, World’s First Oncolytic Salmonella Therapy for Advanced Solid Tumors

Fineline Cube May 29, 2026
Company Deals

Kexing Pharmaceutical and Sinotherapeutics Partner to Commercialize Tofacitinib Extended-Release Tablets in Kuwait and Mexico

Fineline Cube May 29, 2026
Company Deals

Genrix Bio Licenses BCMA×CD3 Bispecific Velinotamig to Fosun’s Yaopharma for Greater China in $268M Deal

Fineline Cube May 29, 2026
Company Deals

Innovent Biologics and Pfizer Forge $10.5B Global Oncology Partnership Spanning 12 First-in-Class Programs

Fineline Cube May 29, 2026
Policy / Regulatory

China’s NHSA Proposes First National Basic Medical Insurance Medical Service Items List to Standardize Reimbursement Framework

Fineline Cube May 29, 2026
Company Drug

Sanofi’s Venglustat Receives FDA Priority Review and Breakthrough Therapy Designation for Type 3 Gaucher Disease

Fineline Cube May 29, 2026
Company Drug

BeOne Medicines and Amgen’s Tarlatamab Receives NMPA Conditional Approval for Second-Line ES-SCLC in China

Fineline Cube May 29, 2026
Company Drug

Brii Biosciences’ HBV Drug Candidates Receive NMPA’s Breakthrough Therapy Designations

Fineline Cube May 14, 2024

Brii Biosciences Ltd (HKG: 2137) has announced that two of its hepatitis B virus (HBV)...

Company Drug

HutchMed’s HMPL-306 Advances to Phase III Trial in R/R AML Patients

Fineline Cube May 14, 2024

HutchMed (China) Ltd (NASDAQ: HCM; HKG: 0013) has announced the commencement of the RAPHAEL study,...

Company Drug

Zai Lab’s ROS1 Inhibitor Augtyro Earns NMPA Nod for Advanced NSCLC Treatment

Fineline Cube May 13, 2024

Zai Lab Ltd (NASDAQ: ZLAB; HKG: 9688), a biopharmaceutical company based in China, has announced...

Company Drug Medical Device

NMPA Accepts Jiangsu Yahong Meditech’s Application for Cervical HSIL Treatment Cevira

Fineline Cube May 13, 2024

Jiangsu Yahong Meditech Co., Ltd (Asieris, SHA: 688176), a specialist in urogenital cancer treatments in...

Company Drug

Mabwell’s 9MW2821 ADC for Triple Negative Breast Cancer Accepted for Review by NMPA

Fineline Cube May 13, 2024

Mabwell (Shanghai) Bioscience Co., Ltd (SHA: 688062), a biopharmaceutical company based in China, has announced...

Company Drug

Huadong Medicine’s EGFR Inhibitor Mefatinib for NSCLC Accepted by NMPA for Review

Fineline Cube May 13, 2024

Huadong Medicine Co., Ltd (SHE: 000963), a leading pharmaceutical company based in China, has announced...

Company Deals Medical Device

Subtle Medical Inc Closes USD 10 Million Series B+ Round to Accelerate Global Expansion

Fineline Cube May 13, 2024

Subtle Medical Inc, a medical imaging specialist and Stanford University spin-off, has reportedly raised close...

Company Drug

Shenzhen Hepalink’s Enoxaparin Sodium Gets Green Light in Singapore

Fineline Cube May 13, 2024

Shenzhen Hepalink Pharmaceutical Group Co., Ltd (SHE: 002399), a leading pharmaceutical company based in China,...

Policy / Regulatory

NMPA Updates In Vitro Diagnostic Reagents Classification List for Enhanced Regulatory Oversigh

Fineline Cube May 13, 2024

The National Medical Products Administration (NMPA) has coordinated the revision and release of the In...

Company Deals

Novartis Inks Deal to Acquire Mariana Oncology, Bolstering Radioligand Therapy Portfolio

Fineline Cube May 13, 2024

Swiss pharmaceutical giant Novartis (NYSE: NVS) is poised to expand its oncology portfolio by acquiring...

Policy / Regulatory

China’s NMPA Revamps Medical Device Classification Rules to Improve Regulatory Efficiency

Fineline Cube May 13, 2024

The National Medical Products Administration (NMPA) has revised the “Notice on Standardizing the Classification of...

Company Drug

BMS’s Opdivo/Yervoy Combo Misses PFS Endpoint in Unresectable Stage III NSCLC Trial

Fineline Cube May 13, 2024

Bristol-Myers Squibb (BMS; NYSE: BMY) has announced that a late-stage trial for its checkpoint inhibitors...

Company Drug

FDA Reviews BMS’ Opdivo Subcutaneous Formulation for Broad Indications

Fineline Cube May 13, 2024

The US Food and Drug Administration (FDA) has agreed to review a submission from Bristol-Myers...

Company Policy / Regulatory

BIO Survey Highlights Extensive Dependence on Chinese CDMOs in Life Sciences

Fineline Cube May 11, 2024

The Biotechnology Innovation Organization (BIO), a US industry trade group, has completed a survey among...

Company Drug

Yunnan Baiyao’s Radiopharmaceutical INR101 Advances to Clinical Trial Stage with NMPA Approval

Fineline Cube May 11, 2024

Yunnan Baiyao Group Co., Ltd (SHE: 000538), a traditional Chinese medicine (TCM) company based in...

Company Drug

Eisai’s Fycompa Gains New Indication for Generalized Tonic-Clonic Seizures in China

Fineline Cube May 11, 2024

Eisai Co Ltd (TYO: 4523), a Japanese pharmaceutical company, has announced that its antiepilepsy drug...

Company Deals

Ribobay Pharma and General Biol to Commence GMP-Grade Oligonucleotide Manufacturing Services

Fineline Cube May 11, 2024

Shanghai-based contract research, development, and manufacturing organization (CRDMO) Ribobay Pharma has announced plans to commence...

Company Policy / Regulatory

BioSecure Act Advances in US, Aiming to Curb Ties with Chinese Bioscience Firms

Fineline Cube May 11, 2024

US legislators are working expeditiously to finalize the BioSecure Act, legislation that, if enacted, would...

Company Drug

Jacobio Pharma’s KRAS G12C Inhibitor Gains NMPA Approval for Phase III CRC Study

Fineline Cube May 11, 2024

Jacobio Pharma (HKG: 1167), a biopharmaceutical company based in China, has announced that it has...

Company Deals

Tianjin Lisheng Pharmaceutical Co., Ltd. to Sell Stake in Mitsubishi Tanabe’s China Subsidiary

Fineline Cube May 11, 2024

Tianjin Lisheng Pharmaceutical Co., Ltd. (SHE: 002393), a Chinese pharmaceutical company, has announced plans to...

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Recent updates

  • Sanofi’s Venglustat Receives FDA Priority Review and Breakthrough Therapy Designation for Type 3 Gaucher Disease
  • BeOne Medicines and Amgen’s Tarlatamab Receives NMPA Conditional Approval for Second-Line ES-SCLC in China
  • Northland Biotech’s Engensis Gene Therapy Receives NMPA Approval for Severe Lower Limb Ischemia Ulcers
  • AstraZeneca’s Fasenra Becomes First Biologic Approved in China for Hypereosinophilic Syndrome
  • Shionogi’s Symproic (Naldemedine) Receives NMPA Approval for Opioid-Induced Constipation in China
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 Drug

Sanofi’s Venglustat Receives FDA Priority Review and Breakthrough Therapy Designation for Type 3 Gaucher Disease

Company Drug

BeOne Medicines and Amgen’s Tarlatamab Receives NMPA Conditional Approval for Second-Line ES-SCLC in China

Company Drug

Northland Biotech’s Engensis Gene Therapy Receives NMPA Approval for Severe Lower Limb Ischemia Ulcers

Company Drug

AstraZeneca’s Fasenra Becomes First Biologic Approved in China for Hypereosinophilic Syndrome

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