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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

Abbisko Therapeutics Initiates Phase II Study for Pimicotinib in Chronic Graft-Versus-Host Disease

Fineline Cube Jun 12, 2023

Shanghai-based biotech firm Abbisko Therapeutics Co., Ltd (HKG: 2256) has announced the first patient dosing...

Policy / Regulatory

NHSA Launches 2023 NRDL Update Process with New Work Plan and Public Feedback Period

Fineline Cube Jun 12, 2023

The National Healthcare Security Administration (NHSA) has commenced the process for the annual update of...

Company Drug

Genor Biopharma’s Geptanolimab NDA for PTCL Rejected by China’s NMPA

Fineline Cube Jun 12, 2023

China’s Genor Biopharma Co., Ltd (HKG: 6998) has announced that the National Medical Products Administration...

Company Drug

CSPC Pharmaceutical’s CPO301 Earns Fast-Track Status for EGFR Mutant NSCLC Treatment

Fineline Cube Jun 12, 2023

China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) has announced that its best-in-class antibody drug conjugate...

Company Drug

Salubris Pharmaceuticals’ Enarodustat Gains NMPA Approval for Renal Anemia Treatment

Fineline Cube Jun 12, 2023

China’s Shenzhen Salubris Pharmaceuticals Co., Ltd (SHE: 002294) has announced receiving market approval from the...

Company Deals

Baheal Pharmaceutical Partners with RabPharma for Commercialization of RAB001 in China

Fineline Cube Jun 12, 2023

China-based health services and distribution giant Baheal Pharmaceutical Group has announced a strategic partnership with...

Policy / Regulatory

CDE Releases 71st Batch of Generic Reference Preparations with Updates and New Injecables

Fineline Cube Jun 12, 2023

The Center for Drug Evaluation (CDE) has released the 71st batch of chemical generic reference...

Company Deals

Hainan Boao Lecheng Partners with Recordati on Rare Disease Drug Development

Fineline Cube Jun 12, 2023

The Hainan Boao Lecheng International Medical Tourism Pilot Zone has announced a strategic partnership with...

Company Medical Device

NMPA Approves Shanghai Magic Medicine’s Innovative Multimodal Tumor Treatment System

Fineline Cube Jun 12, 2023

The National Medical Products Administration (NMPA) has granted marketing approval to Shanghai Magic Medicine’s multimodal...

Company Drug

Keymed Biosciences’ CM313 Monoclonal Antibody Shows Promise in Phase I Study for Multiple Myeloma

Fineline Cube Jun 12, 2023

China-based Keymed Biosciences Inc., (HKG: 2162) has announced that the latest results from a Phase...

Company Deals

Eccogene Secures $25 Million in Series B Financing to Advance Metabolic Disease Therapies

Fineline Cube Jun 12, 2023

Sino-US firm Eccogene Inc. has announced the closure of a Series B financing round, raising...

Company Drug

HutchMed Presents Updated Data on Hematological Malignancy Therapies at EHA and ICML

Fineline Cube Jun 12, 2023

HutchMed (China) Ltd (NASDAQ: HCM, HKG: 0013) has announced that new and updated clinical data...

Company Drug

Reistone Biopharma’s Ivarmacitinib Accepted for Review by China’s CDE for Atopic Dermatitis

Fineline Cube Jun 9, 2023

Reistone Biopharma Co., Ltd, a company incubated by Hengrui Pharmaceuticals (SHA: 600276) with an investment...

Company Drug

CDE Indicates Priority Review for Overland ADCT’s Zynlonta and BeiGene’s Brukinsa

Fineline Cube Jun 9, 2023

The Center for Drug Evaluation (CDE) in China has indicated that Overland ADCT BioPharma (CY)...

Company Deals

Kexing Pharmaceutical Secures Commercial Rights for Convalife’s Neratinib Generic Outside China

Fineline Cube Jun 9, 2023

China-based Kexing Pharmaceutical (SHA: 688136) has announced a licensing agreement with compatriot firm Convalife, securing...

Company Deals

Lee’s Pharmaceutical Secures Rights to Eyedetec’s Dry Eye Device in Asia-Pacific

Fineline Cube Jun 9, 2023

China-based Lee’s Pharmaceutical Holdings Ltd (HKG: 0950) through its subsidiary Zhaoke Ophthalmology Ltd (HKG: 6622)...

Company Drug

NMPA Approves Betta Pharmaceuticals’ Vorolanib for Second-Line RCC Treatment in Combination with Everolimus

Fineline Cube Jun 9, 2023

The National Medical Products Administration (NMPA) has granted approval for Betta Pharmaceuticals Co., Ltd’s (SHE:...

Company Drug

Zelgen Biopharmaceuticals’ ZGGS15 Earns FDA Approval for Advanced Solid Tumor Clinical Trial

Fineline Cube Jun 9, 2023

Suzhou Zelgen Biopharmaceuticals Co., Ltd (SHA: 688266) has announced that it has received clinical trial...

Company Drug

CSPC Pharmaceutical’s CPO301 Receives Health Canada Approval for Phase I Study

Fineline Cube Jun 9, 2023

China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) has announced that it has received the green...

Company Deals R&D

Shanghai Fosun High Technology Partners with NICE for Joint Innovation Centers

Fineline Cube Jun 9, 2023

China-based conglomerate Shanghai Fosun High Technology (Group) Co., Ltd has entered into a partnership with...

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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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