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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 Medical Device

MicroTech’s LinX CGM Wins India Approval, Expanding Asia Diabetes Monitoring

Fineline Cube Nov 27, 2025

MicroTech Medical (Hangzhou) Co., Ltd. (HKG: 2235) announced that its LinX Continuous Glucose Monitoring (CGM)...

Medical Device

Bio-heart’s IberiRDN Wins New Zealand Nod as Only Dual-Approach Renal Denervation System

Fineline Cube Nov 27, 2025

Shanghai Bio-heart Biological Technology Co., Ltd. (HKG: 2185) announced that its Iberis Multi-Electrode Renal Denervation...

Company Drug

IASO-Bio’s Fucaso Wins Hong-Kong Approval as First China CAR-T

Fineline Cube Nov 27, 2025

IASO Biotherapeutics announced that Fucaso (equecabtagene autoleucel injection), its proprietary fully human BCMA‑targeted CAR‑T cell...

Company Drug

BeOne’s Sotoclax Wins FDA Priority Review for Mantle Cell Lymphoma

Fineline Cube Nov 27, 2025

BeOne Medicines Ltd. (NASDAQ: ONC, HKG: 6160, SHA: 688235) announced that the U.S. FDA has accepted its...

Company Deals

Patronus Biotech Gates Foundation Grant Accelerates Malaria Vaccine Development

Fineline Cube Nov 27, 2025

Patronus Biotech Pte. Ltd. announced it has received a grant from the Gates Foundation to...

Company Deals

Innova Therapeutics Acquires Enci Therapeutics’ IVT-8086 Cancer Program

Fineline Cube Nov 27, 2025

Innova Therapeutics announced the acquisition of Enci Therapeutics, gaining its primary cancer therapeutic program IVT‑8086,...

Company Drug

Gene Key’s iNKT Cell Therapy Wins NMPA Nod for ARDS, First Allogeneic Ready-to-Use

Fineline Cube Nov 27, 2025

Beijing Gene Key Life Technology Co., Ltd. announced that its GKL‑006RTU Injection, China’s first novel...

Company Drug

SciClone’s Meropenem-Vaborbactam Wins GBA Approval as First Antibiotic Under Medical Connect

Fineline Cube Nov 27, 2025

SciClone Pharmaceuticals Inc. announced that Meropenem/Vaborbactam for Injection has been approved under the “Hong Kong-Macau...

Company Drug

Novartis’ Remibrutinib Wins NMPA Approval for Chronic Spontaneous Urticaria

Fineline Cube Nov 26, 2025

Novartis AG (NYSE: NVS) announced that remibrutinib tablets received National Medical Products Administration (NMPA) approval...

Policy / Regulatory

CMS IRA Drug-Pricing Round 2 Delivers 62% Average Cut, Ozempic Falls 71%

Fineline Cube Nov 26, 2025

The U.S. Centers for Medicare & Medicaid Services (CMS) announced results of the second round...

Company Drug

Hengrui’s Three Oncology Assets Win NMPA Clinical Trial Approval

Fineline Cube Nov 26, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276, HKG: 1276) announced that three of its investigational...

Company Drug

Humanwell’s Lisdexamfetamine NDA Accepted by NMPA for ADHD, First Generic Potential

Fineline Cube Nov 26, 2025

Humanwell Healthcare (Group) Co., Ltd. (SHA: 600079) announced that the National Medical Products Administration (NMPA)...

Company Drug

Innovent’s mazdutide 9mg Obesity Application Accepted by NMPA

Fineline Cube Nov 26, 2025

Innovent Biologics, Inc. (HKG: 1801) announced that China’s National Medical Products Administration (NMPA) has accepted...

Company Drug

Fosun’s Luvometinib Gets NMPA Priority Review for Pediatric LCH

Fineline Cube Nov 26, 2025

Fosun Pharma (SHA: 600196, HKG: 2196) announced that the National Medical Products Administration (NMPA) has...

Company Deals

Kelonia JNJ Partnership Targets In Vivo CAR-T for Multiple Myeloma

Fineline Cube Nov 26, 2025

Kelonia Therapeutics announced a strategic collaboration with Johnson & Johnson (J&J, NYSE: JNJ) to develop...

Company Drug

Otsuka’s VOYXACT Wins FDA Accelerated Approval for IgAN, First APRIL Blocker

Fineline Cube Nov 26, 2025

Otsuka Pharmaceutical (OTCMKTS: OTSKY) announced that VOYXACT (sibeprenlimab‑szsi) received U.S. FDA Accelerated Approval for reducing...

Company

Wuzhong Pharma Faces Mandatory Delisting After CSRC Violations

Fineline Cube Nov 26, 2025

Jiangsu Wuzhong Pharmaceutical Group Corp. (SHA: 600200) received an Administrative Penalty Decision ( No. 145) from...

Company Drug

Novartis’s Itvisma Wins FDA Approval as First Gene Therapy for SMA

Fineline Cube Nov 26, 2025

Novartis AG (NYSE: NVS) announced that Itvisma (onasemnogene abeparvovec‑brve) received U.S. FDA approval for children...

Company Drug

Novo’s Kyinsu Wins EU Approval for Type 2 Diabetes, a Once-Weekly Combo First

Fineline Cube Nov 26, 2025

Novo Nordisk A/S (NYSE: NVO) announced that the European Commission (EC) has granted marketing authorization...

Company Drug

Novo Nordisk’s Semaglutite Alzheimer’s Failure Sends Stock to 4-Year Low

Fineline Cube Nov 25, 2025

Novo Nordisk A/S (NYSE: NVO) announced that semaglutide failed to slow disease progression in two...

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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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