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Company Deals

Tonghua Dongbao Partners with Huisheng Biopharma – Secures China Rights to First Domestic Insulin Degludec Biosimilars

Fineline Cube Feb 27, 2026
Company Deals Drug

Jumpcan Pharma Secures China Rights to Thederma’s TAP-1503 – First AhR Modulator for Atopic Dermatitis

Fineline Cube Feb 27, 2026
Company Deals

WuXi XDC Licenses WuXiTecan-2 Technology to Earendil Labs – $885M Deal Powers AI‑Driven ADC Development

Fineline Cube Feb 27, 2026
Company Deals

SteinCares Partners with Shilpa Biologicals on Latin America Biosimilar Deal – Regional Commercialization Agreement

Fineline Cube Feb 26, 2026
Company Deals

Danaher to Acquire Masimo for $9.9B – Expands Diagnostics Platform with Pulse Oximetry Leader

Fineline Cube Feb 26, 2026
Policy / Regulatory

NMPA Approves 76 Innovative Medical Devices in 2025 – 17% YoY Growth Driven by AI and Priority Review Surge

Fineline Cube Feb 26, 2026
Company Drug

Dupixent Wins Two NMPA Approvals in China – First Biologic for Bullous Pemphigoid and Pediatric Asthma Expansion

Fineline Cube Feb 28, 2026
Company Drug

Olumiant Wins CHMP Positive Opinion for Pediatric Alopecia – JAK Inhibitor Nears EU Approval for Teens with Severe AA

Fineline Cube Feb 28, 2026
Company Drug

Biosion’s SIRPα-Targeting Monoclonal Antibody BSI-082 Clears US FDA Clinical Trial Hurdle

Fineline Cube Jan 25, 2024

Biosion, a global clinical-stage biotechnology company dedicated to developing antibody-based therapies for immune and oncologic...

Company Drug

IASO Biotherapeutics Secures NMPA Approval for Fucaso in Refractory Myasthenia Gravis

Fineline Cube Jan 25, 2024

China-based IASO Biotherapeutics has received clinical trial approval from the National Medical Products Administration (NMPA)...

Company Drug

MSD’s Keytruda Combines with PharmAbcine’s PMC-309 in Phase Ia/b Solid Tumor Trial

Fineline Cube Jan 25, 2024

Merck, Sharp & Dohme (MSD; NYSE: MRK) has announced that its blockbuster anti-PD-1 drug Keytruda...

Policy / Regulatory

NMPA Proposes Streamlined Market Approval Process for Domestically Produced Overseas Drugs

Fineline Cube Jan 25, 2024

The National Medical Products Administration (NMPA) has released a draft proposal titled “Optimizing the Market...

Company Deals

GSK In-Licenses Elegen’s Cell-Free DNA Tech to Advance Next-Gen Gene Therapies and Vaccines

Fineline Cube Jan 25, 2024

GlaxoSmithKline (GSK; NYSE: GSK), a UK-based pharmaceutical giant, has this week in-licensed US partner Elegen’s...

Policy / Regulatory

NMPA Expands Generic Drug Catalog with 74th and 75th Batches for Quality Consistency Evaluation

Fineline Cube Jan 25, 2024

The National Medical Products Administration (NMPA) has released the 74th and 75th batches of reference...

Company Drug

China Grand Pharmaceutical Gets NMPA Green Light for mRNA Cancer Vaccine ARC01 Phase I Study

Fineline Cube Jan 25, 2024

China Grand Pharmaceutical and Healthcare Holdings Ltd (HKG: 0512; CGP) has announced that it has...

Company Deals Hospital

China Anti-Cancer Association Forms Consortium for Standardizing Cancer Research Ethics Reviews

Fineline Cube Jan 25, 2024

The medical ethics professional committee of the China Anti-Cancer Association (CACA) has announced the formation...

Company Drug

Boan Biotech Secures FDA Orphan Drug Designations for Two Claudin18.2 Targeting Candidates

Fineline Cube Jan 25, 2024

Boan Biotech (HKG: 6955), a Chinese biotechnology company, has announced that it has received orphan...

Company Deals

Alphamab and 3D Medicines License Envafolimab Rights to Glenmark for Multiple Regions

Fineline Cube Jan 25, 2024

Alphamab Oncology (HKG: 9966) and 3D Medicines (HKG: 1244), two Chinese pharmaceutical companies, have announced...

Company Drug

Lingyi Biotechnology’s Gene Therapy Candidate LY-M001 Gets FDA Green Light for Gaucher’s Disease

Fineline Cube Jan 25, 2024

Lingyi Biotechnology Co., Ltd, a China-based gene therapy developer, has secured clinical trial approval from...

Company R&D

WuXi Biologics Launches WuXiaADCC PLUS Platform for Non-Fucosylated Antibody Development

Fineline Cube Jan 25, 2024

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

Company Drug

Phanes Therapeutics’ First-in-Class BsAb PT217 Accepted for Review by China’s CDE

Fineline Cube Jan 25, 2024

Sino-US biotechnology company Phanes Therapeutics Inc. has announced that the Investigational New Drug (IND) filing...

Company Drug

Zhaoke Ophthalmology Secures NMPA Approval for Presbyopia Treatments Brimochol PF and CarbacholPF

Fineline Cube Jan 25, 2024

Lee’s Pharmaceutical Holdings Ltd (HKG: 0950), a China-based pharmaceutical company, through its subsidiary Zhaoke Ophthalmology...

Company

Harbour BioMed Gets FDA Green Light for Phase I Study of BsAb Targeting PD-L1 and CD40

Fineline Cube Jan 25, 2024

Harbour BioMed (HKG: 2142), a biotechnology company with operations in Suzhou, China, Cambridge in the...

Company

Abbott Reports Mixed 2023 Results with Q4 Growth Offsetting Full-Year Decline

Fineline Cube Jan 25, 2024

US healthcare company Abbott (NYSE: ABT) has released its financial results for the fourth quarter...

Company Deals

Sanofi Acquires Rare Disease Candidate INBRX-101 in $1.7 Billion Deal

Fineline Cube Jan 24, 2024

French pharmaceutical giant Sanofi (NASDAQ: SNY) has announced the acquisition of INBRX-101, a promising candidate...

Company Drug Legal / IP

Eli Lilly’s Olumiant Patent Invalidated in China, Generic Version Approved

Fineline Cube Jan 24, 2024

The China National Intellectual Property Administration (CNIPA) has declared the compound patent CN200980116857.7 for Eli...

Company Drug

BMS’s Opdivo-Yervoy Combo Cuts Cancer Progression Risk by 79% in Phase III Study

Fineline Cube Jan 24, 2024

Bristol Myers Squibb (BMS; NYSE: BMY) has published late-stage and long-term data for its anti-PD-1...

Company Drug

Tcelltech’s B7-H3 Targeting CAR-T Therapy TX103 Gets Tacit Clinical Approval for Glioblastoma

Fineline Cube Jan 24, 2024

The Center for Drug Evaluation (CDE) website in China has indicated that Tcelltech’s TX103, a...

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Recent updates

  • Dupixent Wins Two NMPA Approvals in China – First Biologic for Bullous Pemphigoid and Pediatric Asthma Expansion
  • Olumiant Wins CHMP Positive Opinion for Pediatric Alopecia – JAK Inhibitor Nears EU Approval for Teens with Severe AA
  • Henlius’ HLX11 Wins CHMP Positive Opinion – Perjeta Biosimilar Nears EU Approval for HER2+ Breast Cancer
  • Shionogi Files CORECTIM Lotion for Japan Approval – Expands Topical JAK Inhibitor Franchise in Atopic Dermatitis
  • Dupixent Wins CHMP Positive Opinion for Pediatric CSU – EU Approval Nears for Children Aged 2–11 Years
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

Dupixent Wins Two NMPA Approvals in China – First Biologic for Bullous Pemphigoid and Pediatric Asthma Expansion

Company Drug

Olumiant Wins CHMP Positive Opinion for Pediatric Alopecia – JAK Inhibitor Nears EU Approval for Teens with Severe AA

Company Drug

Henlius’ HLX11 Wins CHMP Positive Opinion – Perjeta Biosimilar Nears EU Approval for HER2+ Breast Cancer

Company Drug

Shionogi Files CORECTIM Lotion for Japan Approval – Expands Topical JAK Inhibitor Franchise in Atopic Dermatitis

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