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Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Company Deals PIC

WestGene and CREATE Sign License Deal to Co‑Develop In Vivo CAR‑T Therapies

Fineline Cube Aug 31, 2026
Company Deals PIC

Simnova Closes nearly RMB 400 Million Series B to Advance CAR‑NK Candidate SNC103

Fineline Cube Aug 31, 2026
Company Deals PIC

Leaderna Therapeutics Closes Series A+ Led by Grand View Capital to Advance Oligonucleotide Pipeline

Fineline Cube Aug 31, 2026
Company Drug PIC

Eli Lilly Wins FDA Approval for Mounjaro Cardiovascular Risk Reduction in Type 2 Diabetes

Fineline Cube Aug 31, 2026
Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Fineline Cube Sep 1, 2026
Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Fineline Cube Sep 1, 2026
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),...

Company Drug

Jiangsu Hengrui Receives NMPA Approval to Begin Clinical Trials for New Anticancer Biologic

Fineline Cube Jun 5, 2024

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

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Recent updates

  • NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment
  • Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment
  • Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States
  • Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market
  • Laekna Doses First Patient in Phase I Study of LAE118 PI3Kα Inhibitor for Advanced Solid Tumors, Licensed to Vasque Bio for Up to USD 527 Million
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Company Drug

Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States

Policy / Regulatory

Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market

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