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Company Deals

MiniMed Diabetes Files for IPO, Seeking Nasdaq Listing as MMED

Fineline Cube Dec 22, 2025
Company Deals

Simcere Zaiming Licenses ADC SIM0613 to Ipsen in $1.06 Billion Deal

Fineline Cube Dec 22, 2025
Company Deals

Fosun Pharma Partners with Clavis Bio in $362.5M Strategic Collaboration

Fineline Cube Dec 21, 2025
Company Deals

Leadingtac Raises RMB 200M Series B to Advance Protein Degradation Pipeline

Fineline Cube Dec 20, 2025
Company Deals

Baiyunshan to Acquire Zhejiang Pharma‑Industry for $500.5M, Expanding Distribution Network

Fineline Cube Dec 19, 2025
Policy / Regulatory

CDE Reference Standards 101st Batch Seeks Public Feedback

Fineline Cube Dec 23, 2025
Company Drug

Alphamab JSKN003 ADC FDA Breakthrough Therapy Targets Ovarian Cancer

Fineline Cube Dec 23, 2025
Company Drug

Jemincare JMX-2005 PAD Injection Secures NMPA Clinical Trial Approval

Fineline Cube Dec 23, 2025
Company Drug

CARsgen’s BCMA-Targeted CAR-T Therapy CT053 Gains Priority Review in China

Fineline Cube Oct 14, 2022

The Center for Drug Evaluation (CDE) website indicates that China-based chimeric antigen receptor (CAR)-T cell...

Company Drug

LianBio Cancels Phase III Trial for Truseltiq in China Amid Global Halt

Fineline Cube Oct 14, 2022

China-based LianBio (OTCMKTS: LIANY) revealed in an SEC filing that it is canceling work on...

Company Drug

Accutar Biotechnology Initiates Phase I Trial for ERα Targeting Degradation Molecule AC0682

Fineline Cube Oct 14, 2022

New Jersey-based Accutar Biotechnology Inc., which is heavily backed by Chinese funds, has announced the...

Policy / Regulatory R&D

CDE Releases Draft Guidelines for Extrapolating Adult Drug Data to Pediatric Use

Fineline Cube Oct 14, 2022

The Center for Drug Evaluation (CDE) has released the “Guidelines on Quantitative Methodology for Extrapolating...

Company Drug

RemeGen’s Telitacicept Receives FDA Orphan Drug Designation for Myasthenia Gravis

Fineline Cube Oct 13, 2022

China-based pharma firm RemeGen (HKG: 9995, SHA: 688331) has announced receiving Orphan Drug Designation (ODD)...

Company Deals

Jacobio Partners with Merck KGaA for KRAS G12C Inhibitor Clinical Study

Fineline Cube Oct 13, 2022

China-based Jacobio Pharmaceuticals Group Co., Ltd (HKG: 1167) has announced a clinical study collaboration partnership...

Company Medical Device

Hotgen Biotech Gains Regulatory Approvals in Saudi Arabia and India

Fineline Cube Oct 13, 2022

China-based Hotgen Biotech Co., Ltd (SHA: 688068) has announced receiving one certificate from the Saudi...

Company Drug

BeiGene’s Brukinsa Outperforms Imbruvica in Phase III ALPINE Study

Fineline Cube Oct 13, 2022

China-based biotech BeiGene Inc. (HKG: 6160, SHA: 688235, NASDAQ: BGNE) has announced that its Bruton’s...

Company

Hengrui Medicine’s Deputy GM Tao Weikang Resigns, Joins Qilu Pharma

Fineline Cube Oct 13, 2022

China-based Jiangsu Hengrui Medicine Co., Ltd (SHA: 600276) has announced that its deputy general manager...

Company Deals

Proxinse Medtech Raises Series A Funding for Endoscope Camera System

Fineline Cube Oct 13, 2022

Shenzhen Proxinse Medical Technology Co., Ltd, a provider of minimally invasive surgery endoscope camera systems...

Company Deals

AlphaLife Sciences Raises Series A+ Funding for Clinical Research SaaS

Fineline Cube Oct 13, 2022

China-based clinical research SaaS service provider AlphaLife Sciences has reportedly raised “tens of millions” of...

Company Drug

Aosaikang’s Neratinib Maleate API Market Filing Accepted by NMPA

Fineline Cube Oct 13, 2022

Beijing Aosaikang Pharmaceutical Co., Ltd (SHE: 002755) has announced that the market filing for its...

Drug Policy / Regulatory

Azvudine Included in China’s COVID-19 Treatment Protocol

Fineline Cube Oct 12, 2022

The National Healthcare Commission and the National Administration of Traditional Chinese Medicine have released a...

Company Drug

NMPA Approves IND Filing for Henan Genuine Biotech’s Long-Acting HIV Drug CL-197

Fineline Cube Oct 12, 2022

China-based Henan Genuine Biotech Co., Ltd’s investigational new drug (IND) filing for its oral long-acting...

Company Deals

WuXi Biologics Partners with Toregem BioPharma on Anti-USAG-1 Monoclonal Antibody

Fineline Cube Oct 12, 2022

China-based Contract Research, Development, and Manufacturing Organization (CRDMO) WuXi Biologics (HKG: 2269) has entered into...

Company Deals

BeiGene Partners with Amoy Diagnostics for Companion Diagnostics Development

Fineline Cube Oct 12, 2022

China-based biotech BeiGene Inc. (HKG: 6160, SHA: 688235, NASDAQ: BGNE) has entered into a partnership...

Company Medical Device

NMPA Approves Beijing Union Strong’s Intracranial Aneurysm Surgical Planning Software

Fineline Cube Oct 12, 2022

The National Medical Products Administration (NMPA) has approved the marketing of Beijing Union Strong Technology...

Company Deals

Aier Eye Hospital Group Plans IPO on ChiNext Board

Fineline Cube Oct 12, 2022

China-based ophthalmic medical services provider Aier Eye Hospital Group Co., Ltd (SHE: 300015) is set...

Company Deals

BeiGene Partners with Immune-Onc for Clinical Development of Myeloid Checkpoint Inhibitors

Fineline Cube Oct 12, 2022

China-based biotech BeiGene (HKG: 6160, SHA: 688235, NASDAQ: BGNE) has entered into a clinical study...

Company Deals

Cyagen Biosciences Partners with Neurophth for Ophthalmology AAV Capsid Development

Fineline Cube Oct 12, 2022

Cyagen Biosciences, a provider of custom-engineered mouse and rat models with operations in the US...

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Recent updates

  • Alphamab JSKN003 ADC FDA Breakthrough Therapy Targets Ovarian Cancer
  • CDE Reference Standards 101st Batch Seeks Public Feedback
  • Jemincare JMX-2005 PAD Injection Secures NMPA Clinical Trial Approval
  • J&J TREMFYA Pediatric Psoriasis EC Approval Targets First IL-23 Indication
  • Takeda Zasocitinib TYK2 Phase III Shows Positive Psoriasis Results
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

Alphamab JSKN003 ADC FDA Breakthrough Therapy Targets Ovarian Cancer

Policy / Regulatory

CDE Reference Standards 101st Batch Seeks Public Feedback

Company Drug

Jemincare JMX-2005 PAD Injection Secures NMPA Clinical Trial Approval

Company Drug

J&J TREMFYA Pediatric Psoriasis EC Approval Targets First IL-23 Indication

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