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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 Drug

Sanofi’s Dupixent Approved in Japan for Chronic Obstructive Pulmonary Disease

Fineline Cube Mar 31, 2025

Sanofi (EPA: SAN, NASDAQ: SNY) announced that it has received approval from Japan’s Ministry of...

Company Deals

Pacific Shuanglin Bio-pharmacy Partners with XtalPi for Blood Product Innovation

Fineline Cube Mar 31, 2025

China-based Pacific Shuanglin Bio-pharmacy Co., Ltd (SHE: 000403) has formed a strategic partnership with Shenzhen-based...

Company Drug

Novartis’ Pluvicto Gains Expanded FDA Approval for Prostate Cancer Treatment

Fineline Cube Mar 31, 2025

Swiss pharmaceutical giant Novartis (NYSE: NVS) announced that it has received expanded indication approval from...

Company Drug

EMA’s CHMP Issues Negative Opinion on Lilly’s Kisunla for Alzheimer’s

Fineline Cube Mar 31, 2025

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA)...

Policy / Regulatory

China’s IAC Drafts Commercial Health Insurance Drug List A-Series to Bridge NRDL Coverage Gaps

Fineline Cube Mar 31, 2025

The Insurance Association of China (IAC) has unveiled its inaugural draft for the Commercial Health...

Policy / Regulatory

China Scraps Outpatient Prepayment in Public Hospitals by 2025: Healthcare Reform Shifts Financial Burden

Fineline Cube Mar 31, 2025

The National Health Commission (NHC) will eliminate outpatient prepayment requirements across public medical institutions by...

Company

uBriGene Appoints Dr. Joy Zhou to Lead Cell Therapy Development

Fineline Cube Mar 31, 2025

China-based advanced therapy medicinal product (ATMP) contract development and manufacturing organization (CDMO) uBriGene Biosciences announced...

Company Drug

BMS’s Opdivo/Yervoy Combo Approved by NMPA for First-Line HCC Treatment

Fineline Cube Mar 31, 2025

Bristol-Myers Squibb (BMS, NYSE: BMY) announced that it has received approval from China’s National Medical...

Company Drug

Roche’s Ocrevus Approved by China’s NMPA for Multiple Sclerosis Treatment

Fineline Cube Mar 31, 2025

Swiss pharmaceutical giant Roche (SWX: ROG, OTCMKTS: RHHBY) announced that it has received marketing approval...

Company Medical Device

Shanghai Bio-heart Launches SAKURA-SCB Study for Drug-Coated Balloon in Japan

Fineline Cube Mar 31, 2025

China-based Shanghai Bio-heart Biological Technology Co., Ltd (HKG: 2185) announced the first patient enrollment for...

Company Drug

AstraZeneca’s Imfinzi Approved by FDA for Bladder Cancer Treatment

Fineline Cube Mar 31, 2025

The US Food and Drug Administration (FDA) has approved AstraZeneca’s (NASDAQ: AZN) PD-L1 inhibitor Imfinzi...

Company

MicroPort Endovascular Reports 1.61% Revenue Growth in 2024 with Strong Profit Increase

Fineline Cube Mar 31, 2025

Shanghai MicroPort Endovascular MedTech Co., Ltd (SHA: 688016) released its 2024 financial report, showing a...

Company

Luye Pharma Group Reports 2024 Revenue Dip Despite Growth in Product Sales

Fineline Cube Mar 31, 2025

China-based Luye Pharma Group (HKG: 2186) announced its 2024 financial performance, recording RMB 6.061 billion...

Company

Hengrui Pharmaceuticals Reports 22.63% Revenue Growth in 2024 with Strong Innovative Drug Sales

Fineline Cube Mar 31, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) released its 2024 financial report, recording RMB...

Company Drug Medical Device

Sanofi’s Qfitlia Approved by FDA for Hemophilia A and B Prophylaxis

Fineline Cube Mar 31, 2025

France-based Sanofi (EPA: SAN, NASDAQ: SNY) has announced receiving marketing approval from the US Food...

Company Drug

Brii Biosciences Presents Elebsiran Phase II Data at APASL 2025 Meeting

Fineline Cube Mar 31, 2025

China-based Brii Biosciences Ltd (HKG: 2137) has published the latest data from its ongoing Phase...

Company

Akeso Biopharma Reports 53% Revenue Decline in 2024 Despite Growth in Product Sales

Fineline Cube Mar 31, 2025

China-based Akeso Biopharma (HKG: 9926) released its 2024 financial report, recording RMB 2.124 billion (USD...

Company Drug

IASO Biotherapeutics’ Fucaso Approved in Macao for Relapsed Multiple Myeloma

Fineline Cube Mar 31, 2025

China-based IASO Biotherapeutics announced that the New Drug Application (NDA) for its BCMA-targeted chimeric antigen...

Company Drug

Eli Lilly Launches Kisunla in China for Early Alzheimer’s Treatment

Fineline Cube Mar 31, 2025

US pharmaceutical giant Eli Lilly and Company (NYSE: LLY) has officially launched Kisunla (donanemab) in...

Company Drug

Laekna Submits Revised Protocol for LAE102 Obesity Trial with Eli Lilly

Fineline Cube Mar 31, 2025

Sino-US biotech Laekna Therapeutics (HKG: 2105) announced the submission of a revised clinical protocol to...

Posts pagination

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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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