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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

We Doctor Holdings Limited Files for IPO on Hong Kong Stock Exchange

Fineline Cube Dec 31, 2024

China-based We Doctor Holdings Limited, a subsidiary of Chinese internet giant Tencent Corporate Venture Capital...

Company Deals

Shinva Medical Instrument to Acquire Stake in Wuhan Zhongzhi Biotechnologies for IVD Expansion

Fineline Cube Dec 31, 2024

China’s Shinva Medical Instrument Co., Ltd (SHA: 600587) has announced its intention to acquire a...

Company Drug

Hinova Pharmaceuticals’ HP568 Earns FDA Clinical Trial Approval for ER+/HER2- Breast Cancer

Fineline Cube Dec 31, 2024

Chengdu-based biotech Hinova Pharmaceuticals Inc., (SHA: 688302) has announced that it has received clinical trial...

Company Drug

CanSino Biologics’ Menhycia Receives Market Approval in Indonesia

Fineline Cube Dec 31, 2024

China-based CanSino Biologics (HKG: 6185) has received market approval from the Badan Pengawas Obat dan...

Company Drug

CSPC Pharmaceutical Group Receives NMPA Approval for SYH9016 Clinical Study in Solid Tumors

Fineline Cube Dec 31, 2024

China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) has announced that it has received approval from...

Company Drug

MicuRx Pharmaceuticals’ MRX-5 Receives FDA Orphan Drug Designation for NTM Infections

Fineline Cube Dec 30, 2024

Sino-US firm MicuRx Pharmaceuticals Inc. has announced that the US Food and Drug Administration (FDA)...

Company Deals

Hengrui Pharmaceuticals and IDEAYA Biosciences Ink Licensing Deal for SHR-4849

Fineline Cube Dec 30, 2024

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) has announced a significant licensing agreement with US-based...

Company Drug

CARsgen Therapeutics’ Satricabtagene Autoleucel Shows Positive Results in Phase II Study

Fineline Cube Dec 30, 2024

China-based CARsgen Therapeutics Holdings Ltd (HKG: 2171) has announced positive results from its pivotal Phase...

Company Drug

argenx’s Vygart Hytrulo Approved in Japan for Chronic Inflammatory Demyelinating Polyneuropathy

Fineline Cube Dec 30, 2024

Holland-based argenx SE (NASDAQ: ARGX) has announced receiving another indication approval from Japan’s Ministry of...

Company Drug

Daiichi Sankyo’s Datroway Approved in Japan for HR+, HER2- Breast Cancer

Fineline Cube Dec 30, 2024

Japan-based pharmaceutical company Daiichi Sankyo (TYO: 4568) has announced that it has received marketing approval...

Company Drug

MabPharm’s CMAB807 Biosimilar Receives Market Approval in Indonesia and Peru

Fineline Cube Dec 30, 2024

Taizhou-based MabPharm Ltd (HKG: 2181), a specialist in monoclonal antibody (mAb) biosimilars, has announced the...

Company Deals

Shanghai Ark Biopharmaceutical Partners with Partex to Advance AI-Driven Drug Development

Fineline Cube Dec 30, 2024

China’s Shanghai Ark Biopharmaceutical Co., Ltd. has formed a strategic alliance with Germany-based Partex, an...

Company Deals

Zhongheng Group and Fosun Pharmaceutical Form JV to Boost Overseas Business

Fineline Cube Dec 30, 2024

China-based Zhongheng Group (SHA: 600252) has announced plans to establish a joint venture (JV) with...

Company Drug

BeiGene’s Tevimbra Receives FDA Approval for HER2-Negative Gastric Cancer Treatment

Fineline Cube Dec 30, 2024

China-based biopharmaceutical company BeiGene Ltd (NASDAQ: BGNE, HKG: 6160, SHA: 688235) has announced that the...

Company Deals

Huadong Medicine Partners with SynerK PharmaTech for Hypertension siRNA Drug Development

Fineline Cube Dec 30, 2024

China-based Huadong Medicine Co., Ltd (SHE: 000963) has announced a strategic partnership agreement with SynerK...

Policy / Regulatory

NMPA Releases 87th Batch of Reference Drugs for Generic Quality Consistency

Fineline Cube Dec 30, 2024

The National Medical Products Administration (NMPA) has released the 87th batch of reference drugs for...

Company Drug

Bristol-Myers Squibb’s Opdivo Qvantig Receives FDA Approval for Expanded Indications

Fineline Cube Dec 30, 2024

Global biopharmaceutical company Bristol-Myers Squibb (BMS, NYSE: BMY) has announced that the US Food and...

Company Drug

HitGen Inc. Initiates Phase II Clinical Trial for HG146 in Adenoid Cystic Carcinoma

Fineline Cube Dec 30, 2024

China-based HitGen Inc. (SHA: 688222) has announced the commencement of the first patient enrollment in...

Company Deals

Reforgene Medicine Secures Hundreds of Millions in Financing for Gene Therapy Expansion

Fineline Cube Dec 30, 2024

Reforgene Medicine, a prominent gene editing therapy company headquartered in Guangzhou, has reportedly secured hundreds...

Company Deals

Xtalpi Inc. Partners with NCCS and Duke-NUS to Advance AI-Driven Drug Discovery

Fineline Cube Dec 30, 2024

Shenzhen-based QuantumPharm Inc., trading under the name Xtalpi Inc. (HKG: 2228), has announced a strategic...

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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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