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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 Hospital

HKSH Medical Partners with United Imaging to Advance CT Technology

Fineline Cube May 28, 2025

Hong Kong-based private healthcare provider HKSH Medical Group announced the signing of a Memorandum of...

Company Drug

AstraZeneca’s Imfinzi Gets Positive Opinion for Bladder Cancer Perioperative Treatment

Fineline Cube May 28, 2025

UK-based pharmaceutical giant AstraZeneca (AZ; NASDAQ: AZN) announced that the European Medicines Agency’s (EMA) Committee...

Company Drug

EyePoint’s Partner Betta Completes Enrollment for Duravyu’s Pivotal Phase III Study

Fineline Cube May 28, 2025

EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), the US partner of China-based Betta Pharmaceuticals (SHE: 300558), announced...

Company Drug

EMA Recommends Tevimbra for Nasopharyngeal Cancer First-line Treatment

Fineline Cube May 28, 2025

The European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended...

Company Drug

AbelZeta Pharma’s C-CAR168 Secures FDA RMAT Designation for Lupus Treatments

Fineline Cube May 28, 2025

Sino-US biotech AbelZeta Pharma, Inc., based in Rockville, Maryland, and with operations in Shanghai, announced...

Policy / Regulatory

FDA Rejects Data from Two Chinese Testing Labs Over Compliance Concerns

Fineline Cube May 28, 2025

The U.S. Food and Drug Administration (FDA) late last week issued General Correspondence Letters to...

Company Drug

CARsgen’s Satricabtagene Autoleucel Granted Priority Review by China’s CDE

Fineline Cube May 28, 2025

China-based CARsgen Therapeutics Holdings Ltd (HKG: 2171) has announced that the Center for Drug Evaluation...

Company Drug

Salubris Pharma’s Xinchaotuo Gains NMPA Approval for Primary Hypertension

Fineline Cube May 28, 2025

China-based Shenzhen Salubris Pharmaceuticals Co., Ltd (SHE: 002294) announced that it has received marketing approval...

Company Deals

Jiangsu Nhwa’s Investee Jiangsu Haoxinqing Plans Overseas Listing

Fineline Cube May 28, 2025

China-based Jiangsu Nhwa Pharmaceutical Co., Ltd (SHE: 002262) announced that its investee company Jiangsu Haoxinqing...

Company Deals

Shenyang Xingqi Pharmaceuticals Plans Private Placement to Fund R&D Center

Fineline Cube May 28, 2025

China-based Shenyang Xingqi Pharmaceutical Co., Ltd (SHE: 300573) announced plans for a private placement of...

Company Drug

Novartis’ Beovu Approved by NMPA for Diabetic Macular Edema Treatment

Fineline Cube May 28, 2025

Swiss giant Novartis’ (NYSE: NVS) Beovu (brolucizumab) received approval from China’s National Medical Products Administration...

Company Drug

Mabworks’ MIL62 Gains NMPA Review for NMOSD Treatment

Fineline Cube May 28, 2025

China-based Beijing Mabworks Biotech Co., Ltd announced that its New Drug Application (NDA) for MIL62,...

Company Deals

EpimAb Biotherapeutics and Juri Biosciences Ink Global Licensing Deal for KLK2-CD3 T-Cell Engager

Fineline Cube May 28, 2025

Shanghai-based biotech EpimAb Biotherapeutics announced a global licensing agreement with US-headquartered Juri Biosciences, Inc., a...

Company Deals Drug

Eli Lilly to Acquire SiteOne Therapeutics for Up to USD 1 Billion

Fineline Cube May 28, 2025

US-based pharmaceutical giant Eli Lilly & Co. (NYSE: LLY) announced plans to acquire compatriot biotech...

Company Drug

Junshi Biosciences’ Junshida Wins NMPA Approval for HeFH and Statin-Intolerant Patients

Fineline Cube May 28, 2025

China’s Shanghai Junshi Biosciences Co., Ltd (HKG: 1877, SHA: 688180) announced that it has received...

Company Drug

Sino Biopharmaceutical Presents TQB2102 Phase I Results at ASCO 2025

Fineline Cube May 28, 2025

China-based Sino Biopharmaceutical Ltd (HKG: 1177) presented preliminary results from a Phase I clinical study...

Company

BeiGene Rebrands to BeOne Medicines and Relocates to Switzerland

Fineline Cube May 28, 2025

BeiGene (NASDAQ: ONC, HKG: 6160, SHA: 688235), a global oncology company, has officially rebranded to...

Company Deals Drug

Betta Pharmaceuticals Partners with BioRay for Herceptin Biosimilar Anruize

Fineline Cube May 28, 2025

China-based Betta Pharmaceuticals (SHE: 300558) announced a strategic partnership with fellow domestic firm BioRay Biopharmaceutical....

Company Medical Device

China’s NMPA Approves Lifetech’s Aortic Fenestration Stent System

Fineline Cube May 28, 2025

China’s National Medical Products Administration (NMPA) recently approved an innovative aortic in-situ fenestration branch reconstruction...

Company Drug

Phanes Therapeutics Doses First Patient in CD73 Antibody Clinical Study

Fineline Cube May 28, 2025

Sino-US biotech Phanes Therapeutics Inc. announced the first patient dosing in a clinical study for...

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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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