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Company Deals

Gilead Sciences to Acquire Arcellx for $7.8B – Bolsters CAR‑T Pipeline with BCMA‑Targeted Anito‑cel

Fineline Cube Feb 24, 2026
Company Deals

Findcure Bio Raises $14.5 Million Series B to Advance Radiopharmaceutical Platform

Fineline Cube Feb 14, 2026
Company Deals

Siemens Healthineers Deepens Mayo Clinic Partnership on AI Neurology and Precision Oncology

Fineline Cube Feb 14, 2026
Company Deals

VivaVision Biotech Files Hong Kong IPO to Advance Ophthalmology Pipeline

Fineline Cube Feb 14, 2026
Company Deals

Genhouse Bio Partners with Gilead on $1.5 Billion Synthetic Lethal Cancer Project GH31

Fineline Cube Feb 14, 2026
Policy / Regulatory

FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies

Fineline Cube Feb 24, 2026
Company Drug

CSPC Pharmaceutical Wins NMPA Approval for Phase II Study of SYS6023 HER3 ADC in Metastatic Breast Cancer

Fineline Cube Feb 24, 2026
Company Drug

Sichuan Biokin’s Iza‑Bren Hits PFS and OS Endpoints in Phase III TNBC Study – First Bispecific ADC to Show Dual Survival Benefit

Fineline Cube Feb 24, 2026
Company Medical Device

Sansure Biotech’s HBV RNA Detection Kit Receives NMPA Marketing Approval

Fineline Cube Jun 7, 2024

Sansure Biotech Inc., (SHA: 688289), a leading molecular diagnostics company based in China, has announced...

Company Medical Device

MicroPort Endovascular MedTech Secures NMPA Approval for Vena Cava Filter

Fineline Cube Jun 7, 2024

Shanghai MicroPort Endovascular MedTech Co., Ltd (SHA: 688016), a prominent medical device company based in...

Company Drug

Qilu Pharmaceutical’s Generic Pomalidomide Wins NMPA Nod for Multiple Myeloma Treatment

Fineline Cube Jun 7, 2024

Qilu Pharmaceutical, a leading pharmaceutical company based in China, has received approval from the National...

Company Drug

Fosun Pharma’s FCN-159 Receives Priority Review Status from NMPA for Pediatric Neurofibromatosis

Fineline Cube Jun 7, 2024

Shanghai Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196) has announced that the National...

Company Drug

Luye Pharma Submits Market Approval Application for Rivastigmine Patch in Japan

Fineline Cube Jun 7, 2024

Luye Pharma Group (HKG: 2186), a leading pharmaceutical company based in China, has announced a...

Company Drug

HutchMed Initiates Phase I Clinical Trial for HMPL-506 in Hematologic Malignancies

Fineline Cube Jun 7, 2024

HutchMed (HKG: 0013, NASDAQ: HCM) has announced the commencement of a Phase I clinical study...

Company Deals

Alphamab Oncology Partners with ArriVent BioPharma for Global ADC Development and Commercialization

Fineline Cube Jun 6, 2024

Alphamab Oncology (HKG: 9966), a biopharmaceutical company based in China, has entered into a research...

Company Drug

Sino Biopharmaceutical Presents FS222 Phase I Results at ASCO Annual Meeting

Fineline Cube Jun 6, 2024

Sino Biopharmaceutical Ltd (HKG: 1177), a prominent biopharmaceutical company in China, has presented updates from...

Company Drug

Jiangsu Hengrui’s HER2 Targeted ADC SHR-A1811 Poised to Earn Breakthrough Designation in China

Fineline Cube Jun 6, 2024

Jiangsu Hengrui Pharmaceuticals Co., Ltd (SHA: 600276), a leading pharmaceutical company in China, has announced...

Company Deals

3SBio Secures Exclusive Licensing Agreement for Seven Drug Candidates from Subsidiary

Fineline Cube Jun 6, 2024

Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd, a subsidiary of 3SBio Inc. (HKG: 1530), has disclosed...

Company Medical Device

Rightongene Bio Receives NMPA Approval for BCR-ABL P210 Fusion Gene Detection Kit

Fineline Cube Jun 6, 2024

Shanghai Rightongene Biotechnology Co., Ltd (SHA: 688217), a biopharmaceutical company based in China, has announced...

Company

WuXi Biologics Expands Manufacturing Capacity with New Bioreactors at Hangzhou Facility

Fineline Cube Jun 6, 2024

WuXi Biologics (HKG: 2269), a leading Contract Research, Development, and Manufacturing Organization (CRDMO) based in...

Company Drug

J&J’s Tecvayli Shows Promising Response Rates in Multiple Myeloma Trial

Fineline Cube Jun 6, 2024

Johnson & Johnson (J&J; NYSE: JNJ) has reported updates from a Phase I/II clinical trial...

Company Policy / Regulatory

Jiangsu Hengrui Pharmaceuticals Receives FDA Form 483 Following Inspection Discrepancies

Fineline Cube Jun 6, 2024

The U.S. Food and Drug Administration (FDA) has issued a Form 483 to Jiangsu Hengrui...

Company Deals

Cloudbreak Pharma Files for Hong Kong IPO with Focus on Ophthalmic Innovations

Fineline Cube Jun 6, 2024

Cloudbreak Pharma Inc., a Cayman Islands-registered pharmaceutical company, has filed for an initial public offering...

Company Deals

Xtalpi Inc. Makes a Splash with HKD 1.13 Billion IPO on Hong Kong Stock Exchange

Fineline Cube Jun 6, 2024

XtalPi (QuantumPharm, HKG: 2228) has successfully conducted an initial public offering (IPO) on the Hong...

Policy / Regulatory

China’s NHC Launches Health Literacy Plan to Shift Focus to Preventative Healthcare

Fineline Cube Jun 6, 2024

China’s National Health Commission (NHC), in collaboration with two other bureaus, has unveiled the “All-Citizen...

Company Drug

Bristol Myers Squibb’s Breyanzi Shows Promising Results in Three Lymphoma Trials

Fineline Cube Jun 6, 2024

Bristol Myers Squibb (BMS; NYSE: BMY) has announced results from three distinct clinical trials assessing...

Company Drug

AbelZeta and AstraZeneca’s C-CAR031 Shows Promising Results in HCC Treatment

Fineline Cube Jun 5, 2024

AbelZeta, a Sino-US biotech company with operations in Rockville, Maryland, and Shanghai, has presented data...

Company Drug

InnoCare’s Tafasitamab-Lenalidomide Combo on Track for Priority Review in China for DLBCL Treatment

Fineline Cube Jun 5, 2024

The Center for Drug Evaluation (CDE) website has indicated that InnoCare (HKG: 9969; SHA: 688428),...

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Recent updates

  • CSPC Pharmaceutical Wins NMPA Approval for Phase II Study of SYS6023 HER3 ADC in Metastatic Breast Cancer
  • Trinomab’s Retavibart NDA Accepted by NMPA – First Long‑Acting RSV mAb for Infant Protection in China
  • Sichuan Biokin’s Iza‑Bren Hits PFS and OS Endpoints in Phase III TNBC Study – First Bispecific ADC to Show Dual Survival Benefit
  • FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies
  • Gilead Sciences to Acquire Arcellx for $7.8B – Bolsters CAR‑T Pipeline with BCMA‑Targeted Anito‑cel
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

CSPC Pharmaceutical Wins NMPA Approval for Phase II Study of SYS6023 HER3 ADC in Metastatic Breast Cancer

Others

Trinomab’s Retavibart NDA Accepted by NMPA – First Long‑Acting RSV mAb for Infant Protection in China

Company Drug

Sichuan Biokin’s Iza‑Bren Hits PFS and OS Endpoints in Phase III TNBC Study – First Bispecific ADC to Show Dual Survival Benefit

Policy / Regulatory

FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies

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