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Company Deals

Simcere Secures Greater China Rights to Reyoung Bio’s Long‑Acting RSV Antibody RB0026 Under Priority Review

Fineline Cube Aug 20, 2026
Company Deals

VectorBuilder and Lir Therapeutics Forge AI Collaboration to Optimize AAV Capsids for Clinical Translation

Fineline Cube Aug 20, 2026
Company Deals

LEO Pharma to Acquire Global Rights to Dersimelagon From Tanabe – Late‑Stage Oral Therapy for Rare Protoporphyrias Nears FDA Decision

Fineline Cube Aug 20, 2026
Company Deals

Bio-Thera Solutions Expands Partnership with Avalon Pharma: Exclusive MENA Licensing Deal for Dupixent Biosimilar BAT2406 – Second Collaboration After BAT3306

Fineline Cube Aug 19, 2026
Company Deals

OmniAb Signs Global Collaboration and License Agreement with Eli Lilly for Ion Channel Program – Up to $370 Million in Milestones Plus Royalties

Fineline Cube Aug 18, 2026
Company Policy / Regulatory

China’s CDE Opens Public Comment on “Pioneer Program” for Cell and Gene Therapy Products, Capping Intake at 15 Drugs Per Year

Fineline Cube Aug 20, 2026
Company Drug

Abbisko Wins NMPA IND Clearance for Pan‑KRAS Inhibitor ABSK211 in Advanced Solid Tumors, Following FDA Green Light

Fineline Cube Aug 20, 2026
Company Drug

Haisco Pharmaceutical Wins NMPA Clinical Approval for Nav1.8 Inhibitor HSK51155 – Pain Drug Licensed to AbbVie in USD 700 Million Deal Advances in China

Fineline Cube Aug 19, 2026
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...

Company Deals

HBM and AstraZeneca Deepen ADC/TCE Collaboration as AstraZeneca Exercises License Options

Fineline Cube Nov 24, 2025

HBM Holdings Limited (HKG: 2142) announced the renewal and deepening of its global strategic collaboration...

Company Drug

Kelun-Biotech’s Sac-TMT Achieves First ADC-IO NSCLC Success

Fineline Cube Nov 24, 2025

Kelun-Biotech Biopharmaceutical Co., Ltd. (HKG: 6990) announced that sacituzumab tirumotecan (sac-TMT), its proprietary TROP2 ADC,...

Company Drug

Luye’s LY03017 Wins FDA Nod for Psychosis Trials in Alzheimer’s and Parkinson’s

Fineline Cube Nov 24, 2025

Luye Pharma Group Limited (HKG: 2186) announced that its independently developed LY03017 received U.S. FDA...

Others

CSPC’s SYH2056 Wins NMPA Nod for Depression Trials as Fast‑Acting 5‑HT2A Agonist

Fineline Cube Nov 24, 2025

CSPC Pharmaceutical Group Limited (HKG: 1093) announced that SYH2056, a selective 5‑HT2A receptor agonist, received...

Company Drug

Biokin’s iza-bren NDA Accepted for Nasopharyngeal Carcinoma, Advancing Bispecific ADC

Fineline Cube Nov 24, 2025

Sichuan Biokin Pharmaceutical Co., Ltd. (SHA: 688506) announced that its New Drug Application (NDA) for...

Company Deals

Phrontline Raises $60M Series Pre‑A+ to Advance Bispecific ADC Pipeline

Fineline Cube Nov 24, 2025

Phrontline Biopharma, a next‑generation antibody‑drug conjugate (ADC) company, announced the close of an oversubscribed USD...

Company Deals

Valo Health Partners with Merck on $3B Parkinson’s Disease Discovery Deal

Fineline Cube Nov 24, 2025

Valo Health, Inc. announced a strategic collaboration with Merck KGaA (ETR: MRK) to advance therapeutic...

Policy / Regulatory

NMPA Issues Export Drug Certification Rules, Expanding Scope and Validity

Fineline Cube Nov 24, 2025

China’s National Medical Products Administration (NMPA) released the “Regulations on Inspection and Export Certification Management...

Company Drug

Bayer’s HYRNUO Wins FDA Approval for HER2-Mutated Lung Cancer

Fineline Cube Nov 24, 2025

Bayer AG (ETR: BAYN) announced that sevabertinib (trade name HYRNUO) received U.S. FDA approval for...

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Recent updates

  • Simcere Secures Greater China Rights to Reyoung Bio’s Long‑Acting RSV Antibody RB0026 Under Priority Review
  • China’s CDE Opens Public Comment on “Pioneer Program” for Cell and Gene Therapy Products, Capping Intake at 15 Drugs Per Year
  • CARsgen 1H 2026: Satricabtagene Autoleucel Wins NMPA Approval as World’s First CAR‑T for Solid Tumors; Cash Runway Seen Into 2030
  • Abbisko Wins NMPA IND Clearance for Pan‑KRAS Inhibitor ABSK211 in Advanced Solid Tumors, Following FDA Green Light
  • VectorBuilder and Lir Therapeutics Forge AI Collaboration to Optimize AAV Capsids for Clinical Translation
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 Deals

Simcere Secures Greater China Rights to Reyoung Bio’s Long‑Acting RSV Antibody RB0026 Under Priority Review

Company Policy / Regulatory

China’s CDE Opens Public Comment on “Pioneer Program” for Cell and Gene Therapy Products, Capping Intake at 15 Drugs Per Year

Company

CARsgen 1H 2026: Satricabtagene Autoleucel Wins NMPA Approval as World’s First CAR‑T for Solid Tumors; Cash Runway Seen Into 2030

Company Drug

Abbisko Wins NMPA IND Clearance for Pan‑KRAS Inhibitor ABSK211 in Advanced Solid Tumors, Following FDA Green Light

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