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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

Pfizer Adjusts 2023 Revenue Projections Amidst Decreased COVID-19 Solution Demand

Fineline Cube Oct 16, 2023

Pharmaceutical giant Pfizer Inc. (NYSE: PFE) has revised its projected 2023 revenues downward, reflecting a...

Policy / Regulatory

Fujian’s Fourth Round VBP Seeks Public Feedback on Drug Procurement List

Fineline Cube Oct 16, 2023

The Fujian drug and device joint procurement center has published the “Fujian Fourth Round Drug...

Company Drug

FDA Approves Pfizer’s Braftovi + Mektovi Combo for BRAF V600E Metastatic NSCLC

Fineline Cube Oct 13, 2023

The US Food and Drug Administration (FDA) has granted Pfizer (NYSE: PFE) regulatory approval for...

Policy / Regulatory

China Introduces Trial Measures for Science and Technology Ethics Review

Fineline Cube Oct 13, 2023

The National Health Commission, Ministry of Science and Technology, Ministry of Education, and eight other...

Company Drug

Roche’s Ocrevus Demonstrates Long-Term Efficacy in Multiple Sclerosis Treatment

Fineline Cube Oct 13, 2023

Swiss pharmaceutical giant Roche (SWX: ROG) has presented compelling long-term efficacy data for its selective...

Policy / Regulatory

China Releases First Supplement to 2020 Pharmacopoeia with 47 New Drug Varieties

Fineline Cube Oct 13, 2023

The National Medical Products Administration (NMPA) and the National Health Commission have announced the release...

Company Drug

Sichuan Huiyu Pharmaceutical’s HYP2090PTSA Gains NMPA Approval for KRAS G12C Solid Tumors

Fineline Cube Oct 13, 2023

Sichuan Huiyu Pharmaceutical Co., Ltd (SHA: 688553), a China-based pharmaceutical company, has announced that it...

Company Deals

Livzon Pharmaceutical Secures Licensing Agreement for LanssonPharm’s PDE4 Inhibitor in China

Fineline Cube Oct 13, 2023

China-based Livzon Pharmaceutical Group Inc., (HKG: 1513, SHE: 000513) has announced a significant licensing agreement...

Company Drug

AbbVie’s Rinvoq Demonstrates Sustained Efficacy in Late-Stage Atopic Dermatitis Study

Fineline Cube Oct 13, 2023

AbbVie (NYSE: ABBV) has announced late-stage results for its JAK inhibitor Rinvoq (upadacitinib) in the...

Policy / Regulatory

China’s Healthcare Landscape: Key Insights from the 2022 Statistical Communique

Fineline Cube Oct 13, 2023

The National Health Commission (NHC) has released “China’s Healthcare Statistical Communique 2022,” providing a comprehensive...

Company Drug

Lee’s Pharmaceutical’s Subsidiary Announces Positive Results for Myopia Treatment NVK002

Fineline Cube Oct 13, 2023

China-based Lee’s Pharmaceutical Holdings Ltd (HKG: 0950), through its subsidiary Zhaoke Ophthalmology Ltd (HKG: 6622),...

Company Drug

J&J’s Cetrelimab and TAR-200 Gain Tacit Approvals for Bladder Cancer Trials

Fineline Cube Oct 13, 2023

The Center for Drug Evaluation (CDE) website has indicated that Johnson & Johnson (J&J; NYSE:...

Company Medical Device

Nanjing Geneseeq’s NSCLC TMB Detection Kit Approved by NMPA

Fineline Cube Oct 13, 2023

China-based Nanjing Geneseeq Medical Device and Diagnostic Inc. has announced that its tissue tumor mutation...

Company Drug

RemeGen Secures NMPA Approval for Phase II Study of Disitamab Vedotin in Breast Cancer

Fineline Cube Oct 13, 2023

China-based biopharma RemeGen Ltd (HKG: 9995) has announced that it has received approval from the...

Company Deals

Genetron Holdings Enters Privatization Agreement with Consortium

Fineline Cube Oct 13, 2023

Beijing-based Genetron Holdings Ltd (NASDAQ: GTH) has officially entered into a privatization and merger agreement...

Company Drug

Ascentage Pharma Initiates Phase III Study for APG-2575 and Calquence in CLL/SLL

Fineline Cube Oct 13, 2023

Suzhou-based Ascentage Pharma (HKG: 6855) has announced the approval to commence a global multi-center, randomized,...

Company Drug

Betta Pharmaceuticals Secures NMPA Approval for Befotertinib in NSCLC Treatment

Fineline Cube Oct 13, 2023

China-based Betta Pharmaceuticals Co., Ltd. (SHE: 300558) has officially announced its receipt of market approval...

Company Drug

KPC Pharmaceuticals Secures WHO Prequalification for Dihydroartemisinin/Piperaquine

Fineline Cube Oct 13, 2023

Yunnan-based KPC Pharmaceuticals Inc. (SHA: 600422) has announced that its dihydroartemisinin/piperaquine 40mg/320mg formulation has received...

Company

Novartis Halts Phase II Clinical Study for MIJ821 in Major Depressive Disorder

Fineline Cube Oct 12, 2023

Novartis (NYSE: NVS), the Swiss pharmaceutical giant, has decided to hold the Phase II clinical...

Company Drug

MSD’s Keytruda Achieves Primary Endpoint in Late-Stage NSCLC Trial

Fineline Cube Oct 12, 2023

Merck, Sharp & Dohme (MSD; NYSE: MRK) has announced that a late-stage trial for its...

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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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