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Company Drug PIC

NMPA Approves Novartis’ Pluvicto Plus ARPI for PSMA‑Positive mHSPC in China, Advancing Radioligand Therapy to Earlier Prostate Cancer

Fineline Cube Aug 26, 2026
Company Drug PIC

FDA Approves J&J’s IMAAVY for Warm Autoimmune Hemolytic Anemia, Marking Second Indication for Nipocalimab

Fineline Cube Aug 26, 2026
Company Drug PIC

FDA Approves BeOne’s Tevimbra Plus Zanidatamab and Chemotherapy for First‑Line HER2‑Positive Gastroesophageal Adenocarcinoma

Fineline Cube Aug 26, 2026
Company Drug PIC

MHLW Approves Takeda’s First‑in‑Class ORZEYFUL (Oveporexton) for Narcolepsy Type 1 in Japan

Fineline Cube Aug 26, 2026
Company PIC

WuXi Biologics 2026H1 Revenue Climbs 18.4% to RMB 11.8 Billion as Project Pipeline Hits 1,064 Integrated Programs

Fineline Cube Aug 26, 2026
Company Drug PIC

NMPA Approves Novartis’ Pluvicto Plus ARPI for PSMA‑Positive mHSPC in China, Advancing Radioligand Therapy to Earlier Prostate Cancer

Fineline Cube Aug 26, 2026
Company Drug PIC

NMPA Approves Novartis’ Pluvicto Plus ARPI for PSMA‑Positive mHSPC in China, Advancing Radioligand Therapy to Earlier Prostate Cancer

Fineline Cube Aug 26, 2026
Company Drug PIC

FDA Approves J&J’s IMAAVY for Warm Autoimmune Hemolytic Anemia, Marking Second Indication for Nipocalimab

Fineline Cube Aug 26, 2026
Company Deals

Eurofarma Invests in Abcuro as Part of $100 Million Disruptive Startups and Biotech Initiative

Fineline Cube Sep 11, 2023

Brazil-based multinational company (MNC) Eurofarma has announced an investment in US immunotherapy developer Abcuro as...

Company Drug

EMA Reviews Janssen’s Balversa for Advanced Urothelial Carcinoma with FGFR3 Alterations

Fineline Cube Sep 11, 2023

The European Medicines Agency (EMA) has accepted for review a filing made by the Janssen...

Company Drug

United Laboratories Receives Tacit Approval for JAK1 Inhibitor TUL01101 Clinical Trial

Fineline Cube Sep 11, 2023

Hong Kong-listed United Laboratories International Holdings Ltd (HKG: 3933) has announced tacit clinical trial approval...

Company Drug

Jiangsu Hengrui Pharmaceuticals Gets NMPA Approval for Phase Ib/III Study of Dalpiciclib in mHSPC

Fineline Cube Sep 11, 2023

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd (SHA: 600276) has announced that it has received approval...

Company Deals

Otsuka and Shape Therapeutics Partner on Ophthalmology Gene Therapies Development

Fineline Cube Sep 11, 2023

Japan drug maker Otsuka (OTCMKTS: OTSKY) and US firm Shape Therapeutics have announced a strategic...

Company Drug

Roche and Alnylam’s Zilebesiran Achieves Primary Endpoint in Hypertension Phase II Trial

Fineline Cube Sep 8, 2023

Roche (SWX: ROG) and Alnylam (NASDAQ: ALNY) have announced that a Phase II trial for...

Policy / Regulatory

CDE Annual Report: Clinical Trials for Innovative Drugs in China Reach Record High

Fineline Cube Sep 8, 2023

The Center for Drug Evaluation (CDE) has released its annual report on clinical trials in...

Company Drug

Pfizer and Valneva’s Lyme Disease Vaccine VLA15 Shows Promise as Booster in Pediatric Trials

Fineline Cube Sep 8, 2023

Partners Pfizer (NYSE: PFE) and Valneva SE (NASDAQ: VALN) have revealed that their Lyme disease...

Company Drug

European Commission Approves Pediatric Indication for MSD’s Ervebo Ebola Vaccine

Fineline Cube Sep 8, 2023

The European Commission (EC) has granted Merck, Sharp & Dohme (MSD; NYSE: MRK) approval for...

Company Drug

Cutia Therapeutics’ CU-40102 Meets Primary Endpoint in Phase III Study for Androgenic Alopecia

Fineline Cube Sep 8, 2023

Dermatology therapy developer Cutia Therapeutics (HKG: 2487) has announced that its Phase III clinical study...

Company Drug

AstraZeneca’s Ultomiris Faces FDA Rejection for NMOSD Indication Extension

Fineline Cube Sep 8, 2023

UK pharmaceutical company AstraZeneca (AZ; NASDAQ: AZN) has received a rejection from the US Food...

Company Drug

Chengdu Kanghua Receives FDA Approval for Clinical Trial of Norovirus Vaccine

Fineline Cube Sep 8, 2023

China-based Chengdu Kanghua Biological Products Co., Ltd (SHE: 300841) has announced that it has received...

Company Drug

Merck’s Keytruda Approved in China for MSI-H/dMMR Advanced Solid Tumors: A Biomarker-Driven Milestone

Fineline Cube Sep 8, 2023

US pharmaceutical major Merck, Sharp & Dohme (MSD; NYSE: MRK) has announced that its programmed...

Company Deals

Biocytogen Pharmaceuticals Enters Agreement with Myricx Bio for ADC Development

Fineline Cube Sep 8, 2023

China-based Biocytogen Pharmaceuticals (Beijing) Co., Ltd (HKG: 2315) has announced an antibody evaluation, option, and...

Company Deals

Danaher Partners with Beijing’s Changping District to Accelerate Science and Technology Innovation Center

Fineline Cube Sep 8, 2023

US-headquartered Danaher (NYSE: DHR), a Fortune 500 science and technology innovator, has entered into a...

Policy / Regulatory

Chongqing Unveils Three-Year Public Health Action Plan Draft for Public Feedback

Fineline Cube Sep 8, 2023

The health commission of Chongqing province has released the “Chongqing Public Health Capacity Improvement Three-year...

Company Drug

Immunofoco’s IMC008 Earns Orphan Drug Designation for Pancreatic Cancer from FDA

Fineline Cube Sep 8, 2023

Suzhou-based cell therapy developer Immunofoco has announced that it has received orphan drug designation (ODD)...

Company Drug

Shanghai Haihe Pharmaceutical’s Glumetinib Filed for Marketing in Japan for NSCLC Treatment

Fineline Cube Sep 8, 2023

Shanghai Haihe Pharmaceutical Co., Ltd has announced the filing for marketing approval in Japan for...

Company

Eminence Biotechnology Launches Fully Operational Cell Culture Media Facility in Suzhou

Fineline Cube Sep 8, 2023

China-based Eminence Biotechnology (Suzhou) Co., Ltd. has announced the full operation of its state-of-the-art cell...

Company Medical Device

LIQUIK Study Interim Results to Showcase Lucence’s Liquid Biopsy Advancements at WCLC 2023

Fineline Cube Sep 8, 2023

Precision medicine specialist Lucence, with a presence in Suzhou, Hong Kong, and Palo Alto, California,...

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Recent updates

  • NMPA Approves Novartis’ Pluvicto Plus ARPI for PSMA‑Positive mHSPC in China, Advancing Radioligand Therapy to Earlier Prostate Cancer
  • FDA Approves J&J’s IMAAVY for Warm Autoimmune Hemolytic Anemia, Marking Second Indication for Nipocalimab
  • FDA Approves BeOne’s Tevimbra Plus Zanidatamab and Chemotherapy for First‑Line HER2‑Positive Gastroesophageal Adenocarcinoma
  • MHLW Approves Takeda’s First‑in‑Class ORZEYFUL (Oveporexton) for Narcolepsy Type 1 in Japan
  • WuXi Biologics 2026H1 Revenue Climbs 18.4% to RMB 11.8 Billion as Project Pipeline Hits 1,064 Integrated Programs
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 PIC

NMPA Approves Novartis’ Pluvicto Plus ARPI for PSMA‑Positive mHSPC in China, Advancing Radioligand Therapy to Earlier Prostate Cancer

Company Drug PIC

FDA Approves J&J’s IMAAVY for Warm Autoimmune Hemolytic Anemia, Marking Second Indication for Nipocalimab

Company Drug PIC

FDA Approves BeOne’s Tevimbra Plus Zanidatamab and Chemotherapy for First‑Line HER2‑Positive Gastroesophageal Adenocarcinoma

Company Drug PIC

MHLW Approves Takeda’s First‑in‑Class ORZEYFUL (Oveporexton) for Narcolepsy Type 1 in Japan

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