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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

Wyze Biotech’s RJMty19 Injection Accepted for CDE Review for r/r B-Cell NHL

Fineline Cube Oct 30, 2023

Wyze Biotech Co., Ltd, a Guangdong-based developer of off-the-shelf universal DNT cell therapies, has announced...

Company

Shanghai Pharmaceuticals Posts 13.11% YOY Revenue Growth in Q3 2023 Financials

Fineline Cube Oct 30, 2023

China-based pharmaceutical distribution giant Shanghai Pharmaceuticals (SPH; HKG: 2607; SHA: 601607) has released its financial...

Company Deals

Shanghai Henlius Biotech and Intas Pharmaceuticals Ink New Licensing Deal for PD-1 mAb

Fineline Cube Oct 30, 2023

China’s Shanghai Henlius Biotech Inc., (HKG: 2696) has announced a new licensing agreement with India-based...

Company Drug

GSK’s ViiV Healthcare Secures NMPA Approval for Vocabria in HIV-1 Treatment

Fineline Cube Oct 27, 2023

UK pharmaceutical giant GlaxoSmithKline (GSK, NYSE: GSK) has announced that its HIV joint venture, ViiV...

Company Drug

AbbVie’s Rinvoq Gains Two New Indications in China: AxSpA and Ankylosing Spondylitis

Fineline Cube Oct 27, 2023

US-based pharmaceutical company AbbVie (NYSE: ABBV) has announced the receipt of two additional indication approvals...

Company

Takeda’s Global Revenues Grow: Strong Performance in Plasma Therapies and Gastroenterology

Fineline Cube Oct 27, 2023

Japan-based pharmaceutical giant Takeda (TYO: 4502) has released its financial results for the 6-month period...

Company

BMS Revenue Slips Due to Revlimid Erosion: Q3 2023 Insights

Fineline Cube Oct 27, 2023

Bristol Myers Squibb (BMS; NYSE: BMY) reported a 3% year-on-year (YOY) revenue decline, excluding foreign...

Company Drug

Eli Lilly’s Omvoh Receives FDA Approval for Ulcerative Colitis Treatment

Fineline Cube Oct 27, 2023

The US Food and Drug Administration (FDA) has granted regulatory approval to Eli Lilly (NYSE:...

Company

Merck Reports 9% Global Sales Growth in Q3 2023, Boosted by Keytruda and Gardasil

Fineline Cube Oct 27, 2023

US-based pharmaceutical giant Merck, Sharp & Dohme (MSD, NYSE: MRK) has reported a robust 9%...

Company Deals

Strategic Alliance Formed by uBriGene, Fraserna, and Virogin for Cell and Gene Therapy Services

Fineline Cube Oct 27, 2023

In a significant move to bolster the cell and gene therapy (CGT) sector, China-based biotechnology...

Company Drug

Fujian Cosunter Gains Ethical Approval for Phase IIa Study of GST-HG131 in Hepatitis B

Fineline Cube Oct 27, 2023

China-based Fujian Cosunter Pharmaceutical Co., Ltd (SHE: 300436) has announced the receipt of ethical approval...

Company Drug

Abbisko Therapeutics Gets NMPA Approval for Phase I Study of ABSK112 in NSCLC

Fineline Cube Oct 27, 2023

Shanghai-based biotechnology firm Abbisko Therapeutics Co., Ltd (HKG: 2256) has announced that it has received...

Policy / Regulatory

NMPA Unveils 73rd Batch of Reference Drugs for Generic Quality Consistency

Fineline Cube Oct 27, 2023

China’s National Medical Products Administration (NMPA) has released the 73rd batch of reference drugs as...

Company Drug

Biogen’s BIIB080 Shows Promise in Phase Ib Trial for Mild Alzheimer’s Disease

Fineline Cube Oct 26, 2023

Biogen (NASDAQ: BIIB) has released preliminary findings from a Phase Ib trial for BIIB080, a...

Company Deals

Sinotau Pharmaceutical Group Secures Rights to Blue Earth Diagnostics’ Flotufolastat in China

Fineline Cube Oct 26, 2023

Sinotau Pharmaceutical Group, a Beijing-based nuclear medicine enterprise, has entered into a licensing agreement with...

Company Deals

Shanghai Pharmaceuticals Partners with Asymchem for Advanced Drug Development and Production

Fineline Cube Oct 26, 2023

China-based pharmaceutical distribution giant Shanghai Pharmaceuticals (SPH; HKG: 2607; SHA: 601607) has entered into a...

Company Deals

Sonosemi Medical Secures Over USD 27.3 Million in Series B Funding for Vascular Intervention Devices

Fineline Cube Oct 26, 2023

Sonosemi Medical Co., Ltd., a Shenzhen-based innovator in vascular graft intervention devices, has reportedly secured...

Company Drug

Huadong Medicine’s Elahere Accepted for NMPA Review in China for Ovarian Cancer Treatment

Fineline Cube Oct 26, 2023

China-based Huadong Medicine Co., Ltd (SHE: 000963) has announced that the National Medical Products Administration...

Company Drug

MSD Halts Phase II Trials for Glutamate Modulator MK-1942 in Alzheimer’s and Depression

Fineline Cube Oct 26, 2023

Merck, Sharp & Dohme (MSD; NYSE: MRK) has announced the discontinuation of two Phase II...

Company Drug

Novartis’ Pluvicto Demonstrates Positive Phase III Results in mCRPC Treatment

Fineline Cube Oct 26, 2023

Swiss pharmaceutical giant Novartis (NYSE: NVS) has released encouraging data from a Phase III study...

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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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