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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

Novartis Invests USD 86.4 Million in New Radiotherapy Facility in China

Fineline Cube Dec 4, 2023

Swiss pharmaceutical giant Novartis (NYSE: NVS) has invested over 600 million Chinese yuan (approximately USD...

Company Deals

AbbVie to Acquire ImmunoGen for USD 10.1 Billion, Expanding Oncology Portfolio

Fineline Cube Dec 4, 2023

AbbVie (NYSE: ABBV) has reached an agreement to acquire fellow U.S. biotech ImmunoGen (NASDAQ: IMGN)...

Company Drug

Akeso Biopharma Files New Indication for Penpulimab in First-Line NPC Treatment

Fineline Cube Dec 4, 2023

Akeso Biopharma (HKG: 9926) has announced a new indication filing for its programmed death-1 (PD-1)...

Company Deals

SanegeneBio Secures Over USD 80 Million in Series A+ Funding to Advance RNAi Therapeutics

Fineline Cube Dec 4, 2023

SanegeneBio, a Suzhou-based developer of RNA interference (RNAi) therapeutics, has successfully raised over USD 80...

Company Drug

Shanghai Junshi’s Loqtorzi Enters Australian Market Approval Process for Nasopharyngeal Carcinoma

Fineline Cube Dec 4, 2023

Shanghai Junshi Biosciences Co., Ltd (HKG: 1877; SHA: 688180) has announced that the Therapeutic Goods...

Company Drug

CARsgen Therapeutics Secures U.S. FDA Approval for CT071 Clinical Trials in Multiple Myeloma

Fineline Cube Dec 4, 2023

CARsgen Therapeutics Holdings Ltd (HKG: 2171), based in China, has announced that it has received...

Company Drug

Lepu Biotechnology’s MRG003 Gains Fast-Track Status from U.S. FDA for Nasopharyngeal Carcinoma

Fineline Cube Dec 4, 2023

Lepu Biotechnology Co., Ltd (HKG: 2157), based in China, has announced that its flagship product...

Company Deals

Nona Biosciences Partners with Lycia Therapeutics to Advance LYTAC Platform for Novel Therapies

Fineline Cube Dec 4, 2023

Nona Biosciences, a wholly-owned subsidiary of HBM Holdings Ltd (HKG: 2142), has announced a collaboration...

Company Deals

Concentra Biosciences Targets China-Based Biotech LianBio in Unsolicited Takeover Bid

Fineline Cube Dec 4, 2023

LianBio (OTCMKTS: LIANY), a China-based biotech firm, has become the target of an unsolicited takeover...

Medical Device Policy / Regulatory

FDA Investigates Safety of China-Made Plastic Syringes Due to Quality Concerns

Fineline Cube Dec 4, 2023

The US Food and Drug Administration (FDA) has issued a warning that it is investigating...

Policy / Regulatory

China’s State Council Unveils Comprehensive Plan to Boost Beijing’s Healthcare Sector

Fineline Cube Dec 1, 2023

The State Council has unveiled a comprehensive “Work Plan” aimed at enhancing Beijing’s service industry...

Company Deals

Bayer Partners with CrossBay Medical to Enhance Hormonal IUS Delivery System

Fineline Cube Dec 1, 2023

Germany’s Bayer (ETR: BAYN) has announced a strategic partnership with women’s health innovator CrossBay Medical...

Company Deals

Johnson & Johnson Acquires Laminar for $400 Million to Enhance Heart Rhythm Solutions

Fineline Cube Dec 1, 2023

Johnson & Johnson (J&J; NYSE: JNJ) has finalized the acquisition of medical device manufacturer Laminar...

Company Drug

Yingli Pharma Enrolls First Patient in Phase I Study for KRAS Inhibitor YL-17231 at MD Anderson

Fineline Cube Dec 1, 2023

Yingli Pharma, a US-based biopharmaceutical company focused on developing therapies for both the Chinese and...

Company Deals

MSD to Migrate IT Systems to AWS, Aiming for Faster Drug Discovery and Clinical Trials

Fineline Cube Dec 1, 2023

Merck, Sharp & Dohme (MSD; NYSE: MRK) has announced plans to transition a significant portion...

Company Drug

Akeso’s AK111 Achieves Key Efficacy Milestones in Phase III Trial for Plaque Psoriasis

Fineline Cube Dec 1, 2023

Akeso Biopharma (HKG: 9926), based in China, has announced that its pivotal Phase III clinical...

Company Drug

Sichuan Kelun-Biotech to Present Promising Phase II Results for SKB264 in mTNBC at SABCS 2023

Fineline Cube Dec 1, 2023

Sichuan Kelun Pharmaceutical Co., Ltd’s (SHE: 002422) innovative drug development subsidiary, Sichuan Kelun-Biotech Biopharmaceutical Co.,...

Company Drug

TG ImmunoPharma Secures U.S. FDA IND Approval for Promising mAb TGI-5 Targeting Multiple Cancers

Fineline Cube Dec 1, 2023

TG ImmunoPharma Co., Ltd, based in China, has announced that it has received Investigational New...

Company Drug

Insilico Medicine Launches Clinical Study for First-in-Class PHD Inhibitor ISM5411 in IBD

Fineline Cube Dec 1, 2023

Insilico Medicine, a China-based biotech leveraging generative artificial intelligence (AI), has announced the initiation of...

Company Drug

Simcere Secures NMPA Approval for Edaravone Sublingual Tablets Targeting Post-Stroke Cognitive Impairment

Fineline Cube Dec 1, 2023

Jiangsu Simcere Pharmaceutical Co., Ltd (HKG: 2096) has received clinical trial approval from the National...

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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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