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Company Deals

Allogene Therapeutics Terminates Asian CAR-T Joint Venture with Overland Pharmaceuticals – Strategic Retreat from Allogeneic Cell Therapy Market in Asia

Fineline Cube May 18, 2026
Company Deals

Eli Lilly Commits $50M to UNICEF USA Alliance Targeting Non-Communicable Disease Prevention in Children Across 21 LMICs

Fineline Cube May 15, 2026
Company Deals

TenNor Therapeutics Raises $71M in Hong Kong IPO – Antimicrobial Pipeline Targets H. pylori and Implant-Associated Infections

Fineline Cube May 14, 2026
Company Deals Drug

Fosun Pharma Secures Global Rights to AriBio’s Alzheimer’s Drug AR1001 in $240M Deal – PDE-5 Inhibitor Shows Promise in Phase III

Fineline Cube May 14, 2026
Company Deals

Merck & Co. Forges Four Strategic Partnerships with Chinese Biotechs to Advance Autoimmune and Oncology Pipeline Through MCICC Platform

Fineline Cube May 14, 2026
Policy / Regulatory

China Issues National Guidelines for Home Hospital Bed Services to Address Healthcare Access for Vulnerable Populations

Fineline Cube May 15, 2026
Company Drug

Harbour BioMed Unveils Preclinical Data for LET003 – AI-Discovered ACVR2A/2B Antibody Shows Best-in-Class Potential in Obesity Combination Therapy with GLP-1 Drugs

Fineline Cube May 18, 2026
Company Drug

AstraZeneca and Daiichi Sankyo’s ENHERTU Secures Dual FDA Approval for HER2-Positive Early Breast Cancer – Neoadjuvant and Adjuvant Indications Supported by Landmark Phase 3 Data

Fineline Cube May 18, 2026
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...

Company Drug

Zelgen’s ZG006 Wins BTD for Neuroendocrine Carcinoma as First DLL3 Trispecific

Fineline Cube Nov 25, 2025

Suzhou Zelgen Biopharmaceuticals Co., Ltd. (SHA: 688266) announced that ZG006, the world’s first trispecific antibody...

Company Drug

Hengrui’s Ivarmacitinib NDA Accepted for Non‑Radiographic Axial Spondyloarthritis

Fineline Cube Nov 25, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276, HKG: 1276) announced that the China National Medical...

Company Drug

AstraZeneca’s Durvalumab Wins China Approval for Stage III NSCLC After Sequential Chemoradiotherapy

Fineline Cube Nov 25, 2025

AstraZeneca (AZ, NASDAQ: AZN) announced that Imfinzi (durvalumab) received National Medical Products Administration (NMPA) approval...

Company Drug

Qihan-Biotech’s QT-019B Universal CAR-T Wins Implied NMPA Approval

Fineline Cube Nov 25, 2025

Hangzhou Qihan Biotech Co., Ltd. announced that its New Drug Clinical Trial (IND) application for...

Company Drug

Junshi’s JS001sc Subcutaneous PD-1 Meets Phase 3 Endpoint in NSCLC

Fineline Cube Nov 25, 2025

Shanghai Junshi Biosciences Co., Ltd. (HKG: 1877, SHA: 688180) announced that its Phase 3 trial JS001sc-002-III-NSCLC...

Company Deals Digital

Rimag Partners with Qingyang Government on AI Medical Imaging Infrastructure

Fineline Cube Nov 25, 2025

Jiangxi Rimag Group Co., Ltd. (HKG: 2522) announced a Strategic Framework Cooperation Agreement with the...

Company Deals

Biogen Dayra Partnership Targets Immunology with Macrocyclic Peptides

Fineline Cube Nov 25, 2025

Biogen Inc. (NASDAQ: BIIB) and Dayra Therapeutics announced a research collaboration to discover and develop...

Company Drug

CStone’s Sugemalimab Wins EU Approval for Stage III NSCLC, Expanding European Indication

Fineline Cube Nov 25, 2025

CStone Pharmaceuticals (HKG: 2616) announced that the European Commission (EC) has approved a new indication...

Company Drug

Salubris’ SAL0139 Wins NMPA Nod for Hyperlipidemia Clinical Trial

Fineline Cube Nov 24, 2025

Shenzhen Salubris Pharmaceuticals Co., Ltd. (SHE: 002294) announced that its independently developed innovative small molecule...

Company Drug

Zhongsheng’s Onradivir Granules Enroll First Phase 3 Pediatric Influenza Patient

Fineline Cube Nov 24, 2025

Guangdong Zhongsheng Pharmaceutical Co., Ltd. (SHE: 002317) announced the enrollment and dosing of the first...

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Recent updates

  • Harbour BioMed Unveils Preclinical Data for LET003 – AI-Discovered ACVR2A/2B Antibody Shows Best-in-Class Potential in Obesity Combination Therapy with GLP-1 Drugs
  • Allogene Therapeutics Terminates Asian CAR-T Joint Venture with Overland Pharmaceuticals – Strategic Retreat from Allogeneic Cell Therapy Market in Asia
  • AstraZeneca and Daiichi Sankyo’s ENHERTU Secures Dual FDA Approval for HER2-Positive Early Breast Cancer – Neoadjuvant and Adjuvant Indications Supported by Landmark Phase 3 Data
  • Roche’s Tecentriq Secures FDA Approval for ctDNA-Guided Adjuvant Treatment in Muscle-Invasive Bladder Cancer – First MRD-Directed Immunotherapy with 41% Mortality Reduction
  • Biogen’s Zorevunersen Receives China Breakthrough Therapy Designation for Dravet Syndrome – First ASO Targeting SCN1A Gene in Rare Epileptic Encephalopathy
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

Harbour BioMed Unveils Preclinical Data for LET003 – AI-Discovered ACVR2A/2B Antibody Shows Best-in-Class Potential in Obesity Combination Therapy with GLP-1 Drugs

Company Deals

Allogene Therapeutics Terminates Asian CAR-T Joint Venture with Overland Pharmaceuticals – Strategic Retreat from Allogeneic Cell Therapy Market in Asia

Company Drug

AstraZeneca and Daiichi Sankyo’s ENHERTU Secures Dual FDA Approval for HER2-Positive Early Breast Cancer – Neoadjuvant and Adjuvant Indications Supported by Landmark Phase 3 Data

Company Drug

Roche’s Tecentriq Secures FDA Approval for ctDNA-Guided Adjuvant Treatment in Muscle-Invasive Bladder Cancer – First MRD-Directed Immunotherapy with 41% Mortality Reduction

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