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Company Deals

Junshi Biosciences Licenses Anti-IL-17A Antibody Roconkibart to Fosun Wanbang for Greater China – $1.34B Deal Secures Commercialization of Phase III-Ready Psoriasis Therapy

Fineline Cube Jul 2, 2026
Company Deals Digital

Insilico Medicine and Takeda Launch $600M Strategic AI Drug Discovery Collaboration – Pharma.AI Platform to Drive Candidate Identification for High-Potential Therapeutic Targets

Fineline Cube Jul 2, 2026
Company Deals

Nona Biosciences and Lonza Forge Strategic Alliance to Develop Best-in-Class Blood-Brain Barrier Penetration Technology for CNS Therapeutics

Fineline Cube Jul 2, 2026
Company Deals

Ipsen to Acquire Memo Therapeutics for €200M Plus Milestones, Gaining Phase II BK Virus Antibody Potravitug for Transplant Nephropathy

Fineline Cube Jul 2, 2026
Company Deals

Ribo Life Science Achieves First Milestone in siRNA Collaboration with Madrigal for MASH Therapeutics

Fineline Cube Jul 2, 2026
Policy / Regulatory

China’s CDE Unveils 108th Batch of Reference Preparations for Generic Drug Evaluation, Adds 28 New Drugs

Fineline Cube Jun 29, 2026
Company Drug

Hangzhou Adamerck’s Aom0498 Receives NMPA Approval as China’s First Homegrown Neuromuscular Blockade Reversal Agent – Completing Decade-Long National Innovation Program

Fineline Cube Jul 2, 2026
Company Drug

Jingxin Pharmaceutical Secures NMPA Approval for China’s First Generic Cariprazine in Schizophrenia – Capturing Market Opportunity as Reference Product Remains Unlaunched

Fineline Cube Jul 2, 2026
Company Medical Device

Blue Sail Medical Receives NMPA Approval for Disposable Coronary Intravascular Impact Waveguide

Fineline Cube May 28, 2024

China’s Blue Sail Medical Co., Ltd (SHE: 002382) has announced that it has received marketing...

Company Drug

RareStone Group’s Pitolisant Secures NMPA Approval to Treat Narcolepsy in Children and Adolescents

Fineline Cube May 28, 2024

RareStone Group, a China-based company specializing in rare diseases (formerly known as Citrine Medicine), has...

Company Drug

Sanofi’s Sarclisa Receives FDA Priority Review for Newly Diagnosed Multiple Myeloma Treatment

Fineline Cube May 28, 2024

Sanofi plc (NYSE: SNY), a leading pharmaceutical company based in France, has announced that the...

Company Policy / Regulatory

Beijing Unveils Action Plan to Boost Pharmaceutical and Health Industry by 2026

Fineline Cube May 27, 2024

The Beijing People’s Government has issued an “Action Plan” outlining measures and targets to “Accelerate...

Company Drug

Yantai Dongcheng Pharmaceutical Receives NMPA Approval for SSTR2 Targeted Radioactive Drug

Fineline Cube May 27, 2024

Yantai Dongcheng Pharmaceutical Group Co., Ltd (SHE: 002675), a pharmaceutical company based in China, has...

Company Deals

Medilink Therapeutics Partners with BioNTech to Develop ADC Products Using TMALIN Technology

Fineline Cube May 27, 2024

Medilink Therapeutics, based in Suzhou, has entered into another partnership agreement with German biotechnology company...

Company Drug

Jiangsu Hengrui’s SHR-A1921 Anticipated to Gain NMPA Breakthrough Designation for Ovarian Cancer

Fineline Cube May 27, 2024

Jiangsu Hengrui Pharmaceuticals Co., Ltd (SHA: 600276) has announced that its drug candidate SHR-A1921 is...

Company Drug

Chinese Biopharma Companies Set to Showcase Oncology Pipelines at ASCO 2024

Fineline Cube May 27, 2024

A cohort of Chinese biopharmaceutical companies, including Wuhan YZY Biopharma Co., Ltd (HKG: 2496), Suzhou...

Company Drug

Novartis’ Fabhalta Shows Promise in Late-Stage C3 Glomerulopathy Trial

Fineline Cube May 27, 2024

Novartis AG (NYSE: NVS), a leading Swiss pharmaceutical company, last week announced positive preliminary data...

Company Drug

Kexing Pharmaceutical Secures NMPA Approval for Childhood Growth Hormone Deficiency Study

Fineline Cube May 27, 2024

Kexing Pharmaceutical (SHA: 688136), based in China, has received approval from the National Medical Products...

Company Drug

Henlius Biotech’s Denosumab Biosimilar Secures EMA Review for European Market Entry

Fineline Cube May 27, 2024

Shanghai Henlius Biotech Inc. (HKG: 2696), a biopharmaceutical company based in China, has announced that...

Company Deals

Sihuan Pharma Halts Xuanzhu Biopharm’s IPO on Shanghai Sci-Tech Innovation Board

Fineline Cube May 27, 2024

Sihuan Pharmaceutical Holdings Group Ltd (HKG: 0460), a Chinese pharmaceutical company, has announced the cancellation...

Company Deals

Bayer’s Consumer Health Division to Invest $83 Million in New Supply Center in China

Fineline Cube May 27, 2024

Bayer (ETR: BAYN)’s Consumer Health Division has entered into an agreement with Qidong city in...

Company Drug

Bio-Thera Solutions Receives NMPA Approval for BAT6005 and BAT1308 Combination Therapy Trial

Fineline Cube May 27, 2024

Bio-Thera Solutions Ltd (SHA: 688177), a biopharmaceutical company based in China, has announced that it...

Company Medical Device

Boston Scientific Gets NMPA Approval for Agent DCB, First of Its Kind for Coronary ISR Treatment

Fineline Cube May 27, 2024

Boston Scientific Corporation (NYSE: BSX), a leading medical device manufacturer in the U.S., has announced...

Company

Eli Lilly Invests $5.3 Billion to Expand Manufacturing Capacity for Incretin Receptor Agonists

Fineline Cube May 27, 2024

Eli Lilly and Company (NYSE: LLY) has announced a significant investment of USD 5.3 billion...

Company Drug

Novartis’ Atrasentan Shows Significant Reduction in Proteinuria in IgA Nephropathy Trial

Fineline Cube May 27, 2024

Novartis AG (NYSE: NVS), a Swiss pharmaceutical company, last week presented interim results for the...

Company Drug

AccurEdit Therapeutics Publishes Positive Data for Gene-Edited Drug ART001 in Amyloidosis Treatment

Fineline Cube May 27, 2024

AccurEdit Therapeutics (Suzhou) Co., Ltd., a leading gene editing therapy specialist based in China, has...

Company Drug

Shanghai Fosun Pharma’s FCN-159 File for Dendritic and Histiocytic Tumors Accepted by China’s NMPA

Fineline Cube May 27, 2024

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

Policy / Regulatory

China’s CDE Issues Draft Guidelines for Patient-Centric Rare Disease Drug R&D

Fineline Cube May 27, 2024

The Center for Drug Evaluation (CDE) has issued a notification regarding the patient-centric rare disease...

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Recent updates

  • Hangzhou Adamerck’s Aom0498 Receives NMPA Approval as China’s First Homegrown Neuromuscular Blockade Reversal Agent – Completing Decade-Long National Innovation Program
  • Junshi Biosciences Licenses Anti-IL-17A Antibody Roconkibart to Fosun Wanbang for Greater China – $1.34B Deal Secures Commercialization of Phase III-Ready Psoriasis Therapy
  • Jingxin Pharmaceutical Secures NMPA Approval for China’s First Generic Cariprazine in Schizophrenia – Capturing Market Opportunity as Reference Product Remains Unlaunched
  • TransThera Completes Patient Enrollment in Global Phase III Trial of Tinengotinib for Advanced Cholangiocarcinoma – Multi-Kinase Inhibitor Backed by Multiple Regulatory Designations
  • TransThera Advances Phase II Trial of Selective BTK Inhibitor TT-01488 with Anti-CD20 Antibodies for Mantle Cell Lymphoma – Novel Non-Covalent Approach Shows Enhanced Safety Profile
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

Hangzhou Adamerck’s Aom0498 Receives NMPA Approval as China’s First Homegrown Neuromuscular Blockade Reversal Agent – Completing Decade-Long National Innovation Program

Company Deals

Junshi Biosciences Licenses Anti-IL-17A Antibody Roconkibart to Fosun Wanbang for Greater China – $1.34B Deal Secures Commercialization of Phase III-Ready Psoriasis Therapy

Company Drug

Jingxin Pharmaceutical Secures NMPA Approval for China’s First Generic Cariprazine in Schizophrenia – Capturing Market Opportunity as Reference Product Remains Unlaunched

Company Drug

TransThera Completes Patient Enrollment in Global Phase III Trial of Tinengotinib for Advanced Cholangiocarcinoma – Multi-Kinase Inhibitor Backed by Multiple Regulatory Designations

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