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Company Deals

Gilead Exercises Option on Kymera’s KT-200 for $45M – Advances CDK2 Molecular Glue Degrader to IND-Enabling Studies

Fineline Cube Apr 12, 2026
Company Deals

Sinocelltech to Raise RMB 900M via Private Placement – Funds Working Capital for Biologics Pipeline

Fineline Cube Apr 12, 2026
Company Deals

NorrDia Medical Raises RMB 100M+ to Complete Bellco Acquisition – Builds Global Blood Purification Platform

Fineline Cube Apr 12, 2026
Company Deals

Vivatides Therapeutics Closes $54M Series A to Advance Extrahepatic Oligonucleotide Delivery Platform – Led by Qiming Venture Partners

Fineline Cube Apr 12, 2026
Company Deals

C4 Therapeutics and Roche Forge $1B+ DAC Collaboration to Pioneer Degrader-Antibody Conjugates in Oncology

Fineline Cube Apr 10, 2026
Policy / Regulatory

Beijing Unveils 32-Point Framework to Accelerate Healthcare Innovation, AI Integration, and Medical Device Development

Fineline Cube Apr 8, 2026
Company Drug

Henlius Biotech Secures Two New NMPA Approvals for Hanlikang – Expands Rituximab Biosimilar into DLBCL Combination Therapies

Fineline Cube Apr 12, 2026
Company Drug

Konruns Pharma Wins NMPA Approval for KC1036 Phase III in Esophageal Cancer – Multi‑Target TKI Advances in 2L+ ESCC

Fineline Cube Apr 12, 2026
Company Medical Device

Yantai Dongcheng Pharmaceutical’s Radiopharmaceutical 18F-LNC1007 Cleared for Australian Phase I Trial

Fineline Cube May 7, 2024

Yantai Dongcheng Pharmaceutical Group Co., Ltd (SHE: 002675), a Chinese pharmaceutical company, has announced that...

Company Drug

Sichuan Biokin’s EGFR/HER3 ADC Expands Phase II Clinical Program with NMPA Approval

Fineline Cube May 7, 2024

Sichuan Biokin Pharmaceutical Co., Ltd (SHA: 688506), a Chinese biopharmaceutical company, has received approval from...

Company

Bio-Bank Corp. Aims for HKEX IPO with Focus on PDGF Drug Development

Fineline Cube May 7, 2024

B&K Corporation Limited, known as Bio-Bank Corp., has recently filed an initial public offering (IPO)...

Policy / Regulatory

China Upgrades Midazolam to Category I Psychotropic Drug List in Regulatory Rescheduling

Fineline Cube May 7, 2024

In a joint notification, the National Medical Products Administration (NMPA), Ministry of Public Security, and...

Company Drug

Merus’s Zenocutuzumab Receives Priority Review Status from FDA for Lung and Pancreatic Cancer Indications

Fineline Cube May 7, 2024

Dutch biotechnology company Merus (NASDAQ: MRUS) has announced that the US Food and Drug Administration...

Policy / Regulatory

Lei Haichao Takes Over as Party Secretary of China’s National Health Commission

Fineline Cube May 7, 2024

The National Health Commission (NHC) of China has undergone a leadership change, with Lei Haichao...

Company Drug

Betta Pharmaceuticals Files for Market Approval of CDK4/6 Inhibitor BPI-16350 in China

Fineline Cube May 7, 2024

Betta Pharmaceuticals Co., Ltd (SHE: 300558), a Chinese pharmaceutical company, has announced that it has...

Company Drug

Tonghua Dongbao Pharmaceuticals Commences Phase IIa Trial for Dual-Targeted Gout Drug Candidate

Fineline Cube May 7, 2024

Tonghua Dongbao Pharmaceuticals (SHA: 600867), a China-based pharmaceutical company, has announced that the first patient...

Company Policy / Regulatory

BIO Surveys Members on China-CDMO Dependence Amid BioSecurity Bill Deliberations

Fineline Cube May 7, 2024

The Biotechnology Innovation Organization (BIO), a prominent US industry trade group, is conducting a survey...

Company Drug

Henlius’ HER2 Dual-Targeted Therapy Gets Green Light for Global Phase III Trial by FDA

Fineline Cube May 7, 2024

Shanghai Henlius Biotech Co., Ltd (HKG: 2696) has announced that it has received approval from...

Company Drug

Jacobio Pharma Applies for Approval of KRAS G12C Inhibitor Gecirasib in China

Fineline Cube May 7, 2024

Jacobio Pharma (HKG: 1167), a China-based biopharmaceutical company, has announced the submission of a New...

Company Drug

China’s CDE Gives Tacit Approval to Keymed Biosciences’ Alzheimer’s Drug CM383 for Clinical Trials

Fineline Cube May 7, 2024

The Center for Drug Evaluation (CDE) has indicated on its website that China-based Keymed Biosciences...

Company Deals

Biocytogen and BioCopy AG Collaborate on TCR-Mimic Antibody Development for Cancer Therapies

Fineline Cube May 7, 2024

Biocytogen Pharmaceuticals (Beijing) Co., Ltd (HKG: 2315), a China-based biopharmaceutical company, has announced an evaluation...

Policy / Regulatory

CDE Seeks Public Comment on Latest Generic Chemical Reference Preparations

Fineline Cube May 7, 2024

The Center for Drug Evaluation (CDE), China’s regulatory body, is currently seeking public feedback on...

Company

GSK’s Q1 2024 Results Beat Forecasts with 10% YOY Revenue Increase; Upgrades Full-Year Outlook

Fineline Cube May 7, 2024

GSK plc (NYSE: GSK), the UK pharmaceutical giant, announced its financial results for the first...

Company

Eli Lilly & Co. Raises Full-Year Guidance on Strength of Q1 2024 Results and Production Expansion

Fineline Cube May 7, 2024

Eli Lilly & Co. (NYSE: LLY) has reported financial results for the first quarter of...

Company

Pfizer Appoints Citigroup’s Andrew Baum as Executive Vice-President for Strategy and Innovation

Fineline Cube May 7, 2024

Pfizer Inc. (NYSE: PFE) has announced the appointment of Andrew Baum, M.D., to serve as...

Company Drug

EyePoint Pharmaceuticals’ Durvayu Fails to Meet Primary Endpoint in NPDR Trial

Fineline Cube May 7, 2024

EyePoint Pharmaceuticals Inc., (NASDAQ: EYPT) has announced that its drug candidate Durvayu (vorolanib intravitreal insert;...

Company

Pfizer’s Q1 2024 Results Highlight Robust Portfolio Growth and Profitability

Fineline Cube May 6, 2024

Pfizer Inc. (NYSE: PFE) saw its share price surge over 5% following the release of...

Company Policy / Regulatory

US Legislature Reviews BioSecurity Bill to Sever Biotech Industry Ties with Chinese Companies

Fineline Cube May 6, 2024

On May 15, 2024, the US House Oversight Committee is set to review a “BioSecurity”...

Posts pagination

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Recent updates

  • Peijia Medical Doses First Patient in US Early Feasibility Study for GeminiOne TEER System – Expands Global Mitral Regurgitation Pipeline
  • Henlius Biotech Secures Two New NMPA Approvals for Hanlikang – Expands Rituximab Biosimilar into DLBCL Combination Therapies
  • Gilead Exercises Option on Kymera’s KT-200 for $45M – Advances CDK2 Molecular Glue Degrader to IND-Enabling Studies
  • Konruns Pharma Wins NMPA Approval for KC1036 Phase III in Esophageal Cancer – Multi‑Target TKI Advances in 2L+ ESCC
  • Sinocelltech to Raise RMB 900M via Private Placement – Funds Working Capital for Biologics Pipeline
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 Medical Device

Peijia Medical Doses First Patient in US Early Feasibility Study for GeminiOne TEER System – Expands Global Mitral Regurgitation Pipeline

Company Drug

Henlius Biotech Secures Two New NMPA Approvals for Hanlikang – Expands Rituximab Biosimilar into DLBCL Combination Therapies

Company Deals

Gilead Exercises Option on Kymera’s KT-200 for $45M – Advances CDK2 Molecular Glue Degrader to IND-Enabling Studies

Company Drug

Konruns Pharma Wins NMPA Approval for KC1036 Phase III in Esophageal Cancer – Multi‑Target TKI Advances in 2L+ ESCC

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