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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 Deals

Neowise Biotechnology Secures RMB 200 Million in Series A+ Financing Round

Fineline Cube Mar 15, 2023

Neowise Biotechnology Co., Ltd, a T cell receptor (TCR)-therapy developer based in Suzhou, reportedly raised...

Company Deals

Singde Yiyang Secures Series A Financing to Expand Wellness Services in China

Fineline Cube Mar 15, 2023

Singde Yiyang, a leading wellness service provider based in Qingdao, reportedly raised “hundreds of millions”...

Drug Policy / Regulatory

NMPA Releases 65th Batch of Reference Drugs for Generic Quality Consistency Evaluation

Fineline Cube Mar 15, 2023

The National Medical Products Administration (NMPA) has released the 65th batch of reference drugs for...

Hospital Policy / Regulatory

NHSA Launches Crackdown on Medical Insurance Fund Management with New Inspection Measures

Fineline Cube Mar 15, 2023

The National Healthcare Security Administration (NHSA) is intensifying efforts to manage medical insurance funds at...

Company Deals

Meinian Onehealth and Astra Biotechnology Partner on Hypersensitive Blood Biomarker Detection

Fineline Cube Mar 15, 2023

China-based Meinian Onehealth Healthcare (Group) Co., Ltd (SHE: 002044) has entered into a partnership with...

Company Drug

Immorna Enrolls First Patient in Phase I Study of JCXH-211 for Malignant Tumors

Fineline Cube Mar 15, 2023

Immorna (Hangzhou) Biotechnology, an mRNA-based vaccine developer based in Hangzhou, has announced the enrollment of...

Policy / Regulatory R&D

CDE Issues Guidelines on Single-Arm Clinical Trials for Antitumor Drugs

Fineline Cube Mar 15, 2023

The Center for Drug Evaluation (CDE) has released the “Technical Guidelines for the Applicability of...

Company Deals R&D

XtalPi and DP Technology Partner to Accelerate Pre-Clinical Drug Development with AI

Fineline Cube Mar 15, 2023

Sino-US artificial intelligence (AI) firm XtalPi Inc. has entered into a partnership with Beijing-based DP...

Company Deals

Laekna Therapeutics Files for IPO on Hong Kong Stock Exchange, Aims to Expand Cancer and Hepatic Fibrosis Therapies

Fineline Cube Mar 15, 2023

China’s Laekna Therapeutics Shanghai Co., Ltd has filed for an initial public offering (IPO) with...

Company Drug

LanssonPharm’s Anti-Depression Drug LS21031 Receives CDE Approval for Clinical Trials

Fineline Cube Mar 14, 2023

China-based central nervous system (CNS) drug developer LanssonPharm has announced that it has received clinical...

Company Drug

GSK’s Nucala Gains NMPA Approval for Severe Eosinophilic Asthma in China

Fineline Cube Mar 14, 2023

UK-based GSK plc (NYSE: GSK) has announced that a market approval filing for Nucala (mepolizumab)...

Company Drug

Juventas Cell Therapy’s CNCT19 Receives FDA IND Approval for r/r B-ALL Treatment

Fineline Cube Mar 14, 2023

China-based Juventas Cell Therapy Ltd’s chimeric antigen receptor (CAR) T-cell therapy, CNCT19 (Inaticabtagene Autoleucel), has...

Company Drug

Bio-Thera Solutions Initiates First Patient Dosing in Phase I Study of BAT8007

Fineline Cube Mar 14, 2023

China-based Bio-Thera Solutions, Ltd. (SHA: 688177) has announced the first patient dosing in a multi-center,...

Company Drug

Antengene to Begin Phase I Clinical Study of ATG-022 for Advanced Solid Tumors

Fineline Cube Mar 14, 2023

China-based Antengene Corporation Ltd (HKG: 6996) is poised to commence a Phase I clinical study...

Company Drug

Guangdong Zhongsheng’s RAY1225 Receives NMPA Approval for Clinical Study

Fineline Cube Mar 14, 2023

China-based Guangdong Zhongsheng Pharmaceutical Co., Ltd (SHE: 002317) has announced that it has received approval...

Company Deals

AnnJi Pharma Signs USD 250 Million Licensing Deal with Avenue Therapeutics for Kennedy’s Disease Drug

Fineline Cube Mar 14, 2023

Taiwan-based AnnJi Pharmaceutical Co., Ltd has announced the signing of a licensing agreement with US...

Company Drug

Vcanbio’s VUM02 Gains CDE Review for Liver Failure and ARDS Clinical Trials

Fineline Cube Mar 14, 2023

Vcanbio Cell & Gene Engineering Corp., Ltd (SHA: 600645) has announced that two additional clinical...

Company Drug

Luye Pharma’s Biosimilar BA9101 Completes Phase III Study Enrollment with Ocumension

Fineline Cube Mar 14, 2023

China-based Luye Pharma Group’s (HKG: 2186) controlling subsidiary, Shandong Boan Biotechnology Co., Ltd, has completed...

Company Deals

Immunophage Biotech Raises RMB 200 Million in Series B1 Financing for Clinical Trials

Fineline Cube Mar 14, 2023

Nanjing-based Immunophage Biotech Co., Ltd reportedly raised close to RMB 200 million (USD 29.1 million)...

Company Drug

Akeso Biopharma Enrolls First Subject in Phase III Study of Cadonilimab for Gastric Cancer

Fineline Cube Mar 14, 2023

China-based Akeso Biopharma (HKG: 9926) has announced the enrollment of the first subject in a...

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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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