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Company Deals

Junshi Biosciences Forms Strategic JV with Zhiyu Biomedicine, Contributing Oncology Antibody IP and ADC Platform for Multispecific Development

Fineline Cube Jun 8, 2026
Company Deals

Everest Medicines Licenses LNZ100 Presbyopia Treatment from Corxel for Greater China – Aceclidine-Based Eye Drop Offers Novel Miotic Mechanism

Fineline Cube Jun 8, 2026
Company Deals

SSY Group Secures Global Rights to Pediatric Antispasmodic and COPD Drugs from Xinzheng Heying – Full IP Transfer in Category 2.2 and 2.3 Assets

Fineline Cube Jun 5, 2026
Company Deals

Lonza and Stipple Bio Forge Strategic ADC Partnership – Combining Epitope Discovery with Glyco Connect Platform for Next-Generation Oncology Therapies

Fineline Cube Jun 5, 2026
Company Deals

Gilead and Lakefront Complete $1.675B Acquisition of Ouro Medicines – Securing BCMAxCD3 T Cell Engager for Autoimmune Diseases

Fineline Cube Jun 5, 2026
Policy / Regulatory

China’s NHC Releases Sixth Pediatric Drug Priority List – 27 Varieties Including Emicizumab, Pembrolizumab, and Omalizumab Targeted for Development

Fineline Cube Jun 5, 2026
Company Drug

Bayer’s Kerendia (Finerenone) Demonstrates Significant Kidney Protection in Non-Diabetic CKD Phase III Trial – First Mineralocorticoid Receptor Antagonist to Show Efficacy Beyond Diabetes Population

Fineline Cube Jun 8, 2026
Company Drug

Novo Nordisk’s Zenagamtide (Amycretin) Delivers 1.71% A1C Reduction and 14.6% Weight Loss in Phase 2 Type 2 Diabetes Trial – Dual GLP-1/Amylin Agonist Advances to Phase 3

Fineline Cube Jun 8, 2026
Company Medical Device

Acotec Scientific’s Micro-Guidewire Receives Beijing Medical Products Administration Approval

Fineline Cube Aug 19, 2025

China-based Acotec Scientific Holdings Limited (HKG: 6669) announced that its micro-guidewire has received registration approval...

Company Deals

Skyhawk Therapeutics Collaborates with Merck on RNA-Targeting Small Molecules for Neurological Diseases

Fineline Cube Aug 19, 2025

Skyhawk Therapeutics, Inc. announced on August 18, 2025, a strategic research collaboration with Merck KGaA...

Company Drug

Sichuan Biokin’s Iza-Bren Granted FDA Breakthrough Therapy Designation for NSCLC

Fineline Cube Aug 19, 2025

Sichuan Biokin Pharmaceutical Co., Ltd (SHA: 688506) announced that its bispecific antibody-drug conjugate (ADC), izalontamab...

Company Drug

Ascentage Pharma’s Lisaftoclax Gains FDA and EMA Clearance for Global Phase III Trial

Fineline Cube Aug 18, 2025

Ascentage Pharma Group International (HKG: 6855) announced that it has received clearance from the U.S....

Company Drug

Novo Nordisk’s Wegovy Granted FDA Approval for Metabolic-Associated Steatohepatitis

Fineline Cube Aug 18, 2025

Danish biopharmaceutical giant Novo Nordisk A/S (NYSE: NVO) announced on August 15, 2025, that its...

Company Drug

Livzon Announces NMPA Acceptance of JP-1366 Tablets Application for Reflux Esophagitis

Fineline Cube Aug 18, 2025

Livzon Pharmaceutical Group Inc. (HKG: 1513) announced that the drug registration application for its JP-1366...

Company Drug

iRegene Therapeutics’ NouvNeu001 Receives FDA Fast Track Designation for Parkinson’s Therapy

Fineline Cube Aug 18, 2025

China-based iRegene Therapeutics announced on August 15, 2025, that its self-developed injectable product, NouvNeu001, has...

Company Drug

Ab&B Bio-Tech’s RSV Vaccine Gains IND Approval in China and the U.S.

Fineline Cube Aug 18, 2025

China-based Ab&B Bio-Tech CO., LTD. JS (HKG: 2627) announced that its self-developed investigational new drug...

Company Drug

Haisco’s HSK39297 Gains NMPA Approval for AMD and gMG Trials

Fineline Cube Aug 18, 2025

Haisco Pharmaceutical Group Co., Ltd. (SHE: 002653) announced that the National Medical Products Administration (NMPA)...

Company Drug

FDA Accelerates Approval of Dordaviprone for H3 K27M-Mutant Diffuse Midline Glioma

Fineline Cube Aug 18, 2025

The U.S. Food and Drug Administration (FDA) granted accelerated approval on August 6, 2025, to...

Company Deals

Ajinomoto and Amphastar Ink Licensing Pact for Oncology and wAMD Drug Candidates

Fineline Cube Aug 18, 2025

Nanjing Ajinomoto Bio-Pharma Services and Amphastar Pharmaceuticals (NASDAQ: AMPH) announced on August 12, 2025, the...

Company Drug

Hengrui Pharmaceuticals Gains NMPA Approval for SHR-7782 Clinical Trials in Advanced Solid Tumors

Fineline Cube Aug 15, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) announced that its independently developed therapeutic...

Company Deals

FosunInsightec and Shanghai International Medical Center Establish National Focused Ultrasound Demonstration Center

Fineline Cube Aug 15, 2025

FosunInsightec partnered with the Shanghai International Medical Center (SIMC) on August 11, 2025, to establish...

Company Deals

Minghui Pharmaceutical Secures $131M Pre-IPO Funding Led by OrbiMed and Qiming Ventures

Fineline Cube Aug 15, 2025

China-based Minghui Pharmaceutical Inc. announced the successful completion of a $131 million Pre-IPO financing round....

Company Drug

FDA Approves Precigen’s Papzimeos for Recurrent Respiratory Papillomatosis”

Fineline Cube Aug 15, 2025

The U.S. Food and Drug Administration (FDA) has approved Papzimeos (zopapogene imadenovec-drba), developed by Precigen,...

Company Deals

Shanghai Pharmaceuticals and Baxter China Forge Strategic Partnership for Anesthesia Products

Fineline Cube Aug 15, 2025

Shanghai Pharmaceuticals Holding Co., Ltd. (SPH, HKG: 2607, SHA: 601607) announced the signing of a...

Company

CARsgen Therapeutics Reports 2025 Interim Results and Regulatory Progress

Fineline Cube Aug 15, 2025

CARsgen Therapeutics Holdings Limited (HKG: 2171) has announced its 2025 Interim Results, highlighting significant progress...

Company Deals

Superluminal Collaborates With Eli Lilly on Small Molecule Therapeutics for Cardiometabolic Diseases

Fineline Cube Aug 15, 2025

Superluminal Medicines announced on August 14, 2025, a collaboration with Eli Lilly (NYSE: LLY) to...

Company Drug

Sanofi’s Rilzabrutinib Granted Orphan Drug Designation for IgG4-Related Disease by EMA

Fineline Cube Aug 15, 2025

French pharmaceutical major Sanofi (NASDAQ: SNY) announced that it has received another orphan drug designation...

Policy / Regulatory

China’s NHSA Releases Interim Measures for Medical Case-Based Payment Management

Fineline Cube Aug 15, 2025

The National Healthcare Security Administration (NHSA) issued the “Interim Measures for Medical Security Case-Based Payment...

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Recent updates

  • Bayer’s Kerendia (Finerenone) Demonstrates Significant Kidney Protection in Non-Diabetic CKD Phase III Trial – First Mineralocorticoid Receptor Antagonist to Show Efficacy Beyond Diabetes Population
  • Novo Nordisk’s Zenagamtide (Amycretin) Delivers 1.71% A1C Reduction and 14.6% Weight Loss in Phase 2 Type 2 Diabetes Trial – Dual GLP-1/Amylin Agonist Advances to Phase 3
  • Oricell Therapeutics Receives NMPA Clearance for World’s First GPC3-Targeted CAR-T Therapy in Advanced Liver Cancer – Ori-C101 Enters Confirmatory Phase II
  • Boehringer Ingelheim’s Survodutide Dual Agonist Achieves 34% Visceral Fat Reduction and 60% MASLD Resolution in Phase III ADA 2026 Data
  • Eli Lilly’s Retatrutide Delivers Unprecedented 28.3% Weight Loss and Resolves Multiple Obesity Comorbidities in Phase III TRIUMPH-1 and TRANSCEND-T2D-1 Trials
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

Bayer’s Kerendia (Finerenone) Demonstrates Significant Kidney Protection in Non-Diabetic CKD Phase III Trial – First Mineralocorticoid Receptor Antagonist to Show Efficacy Beyond Diabetes Population

Company Drug

Novo Nordisk’s Zenagamtide (Amycretin) Delivers 1.71% A1C Reduction and 14.6% Weight Loss in Phase 2 Type 2 Diabetes Trial – Dual GLP-1/Amylin Agonist Advances to Phase 3

Company Drug

Oricell Therapeutics Receives NMPA Clearance for World’s First GPC3-Targeted CAR-T Therapy in Advanced Liver Cancer – Ori-C101 Enters Confirmatory Phase II

Company Drug

Boehringer Ingelheim’s Survodutide Dual Agonist Achieves 34% Visceral Fat Reduction and 60% MASLD Resolution in Phase III ADA 2026 Data

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