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Company Deals Digital PIC

Takeda and Ant Group Form Digital Healthcare Partnership to Advance AI‑Driven Patient Care in China

Fineline Cube Aug 26, 2026
Company Deals

Haisco Signs Exclusive Licensing Deal with Sentivera for Preclinical Autoimmune Asset – Up to USD 1.46 Billion in Milestones

Fineline Cube Aug 26, 2026
Company Deals PIC

Mirxes Signs Strategic MOU With GAIA Health to Expand Early Cancer Screening in the Philippines

Fineline Cube Aug 25, 2026
Company Deals

Hanmi Pharm Strikes Up to $2.3 Billion Licensing Deal With Genentech for Muscle‑Sparing Obesity Candidate HM17321

Fineline Cube Aug 25, 2026
Company Deals Digital

METiS and WestVac Biopharma Forge AI Partnership to Develop Personalized mRNA Cancer Vaccines

Fineline Cube Aug 21, 2026
Hospital Policy / Regulatory

China’s NHC Issues Notice Deepening “Six Expansions” to Strengthen Family Doctor Contracted Services With AI Integration

Fineline Cube Aug 25, 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

Regor Therapeutics Strikes Deal with Genentech for CDK Inhibitors, Fetching USD 850 Million Upfront

Fineline Cube Oct 8, 2024

Regor Therapeutics Group, a US-based biotech with significant ties to China, has entered into a...

Company Drug

China’s CDE Announces “Care Plan” to Include Pfizer’s Marstaximab for Rare Disease Drug Development

Fineline Cube Oct 8, 2024

The National Health Commission (NHC) of China, through its Center for Drug Evaluation (CDE), has...

Company Deals

Genor Biopharma to Acquire EOC Pharma Group in a Merger Deal, Eyeing Commercialization Synergies

Fineline Cube Oct 8, 2024

Genor Biopharma Holdings Limited (HKG: 6998) has announced a definitive merger agreement with EOC Pharma...

Company

WuXi AppTec and WuXi Biologics Weigh Asset Sales in US and Europe Over Biosecure Act Concerns

Fineline Cube Oct 8, 2024

Reports emerged last week in the Financial Times suggesting that WuXi AppTec (HKG: 2359) and...

Company Deals

Tigermed Announces Acquisition of Majority Stake in Shanghai Guanhe Pharmaceutical for CNY 140 Million

Fineline Cube Oct 8, 2024

Tigermed (SHE: 300347, HKG: 3347) has announced its intention to acquire a 40.5650% stake in...

Policy / Regulatory

China’s National Healthcare Security Administration Issues Draft Guidelines for Long-Term Care Insurance

Fineline Cube Oct 8, 2024

The National Healthcare Security Administration (NHSA) has released the “Draft Technical Guidelines for the Preparation...

Company Deals

Insilico Medicine and Seto Biopartner to Leverage AI in Synthetic Biology and Drug Discovery

Fineline Cube Oct 8, 2024

Insilico Medicine has announced a strategic partnership with Seto Bio (SHE: 300583) to harness cutting-edge...

Policy / Regulatory

China’s CDE Releases Draft Guidelines for Biosimilar Drug Labeling

Fineline Cube Oct 8, 2024

On September 29, 2024, the Center for Drug Evaluation (CDE) of China’s National Medical Products...

Company R&D

Legend Biotech Corporation to Establish Advanced R&D Center in Philadelphia for Next-Generation Cell Therapies

Fineline Cube Oct 8, 2024

Legend Biotech Corporation (NASDAQ: LEGN), a leading chimeric antigen receptor (CAR) T cell therapy specialist...

Company Drug

BeiGene Prices TEVIMBRA 10% Below Competitors Following FDA Approval for Esophageal Cancer Treatment

Fineline Cube Oct 7, 2024

BeiGene (NASDAQ: BGNE; HKG: 6160; SHA: 688235) has announced the commercial availability of TEVIMBRA (Tislelizumab)...

Company Drug

Unixell Advances in Cell Therapy with CDE IND Acceptance

Fineline Cube Oct 6, 2024

Shanghai-based Unixell Biotechnology Co., Ltd. has announced that its Investigational New Drug (IND) application for...

Company Drug

Duality Biotherapeutics’ BDCA2 ADC DB-2304 Phase I Trial Registered on ClinicalTrials.gov

Fineline Cube Oct 5, 2024

Duality Biologics, Inc., a biopharmaceutical company specializing in the development of innovative therapies, has registered...

Company Drug

BeiGene’s FGFR2b ADC BG-C137 Enters Phase I Clinical Trial for Advanced Solid Tumors

Fineline Cube Oct 5, 2024

On October 3, 2024, BeiGene (NASDAQ: BGNE; HKG: 6160; SHA: 688235) registered a Phase I...

Company Drug

BMS Expands Opdivo Indication with FDA Approval for NSCLC Combo Therapy

Fineline Cube Oct 4, 2024

The U.S. Food and Drug Administration (FDA) has granted approval for Bristol Myers Squibb’s (BMS,...

Company Drug

InnoCare Pharma’s Orelabrutinib Achieves Milestone in SLE Clinical Trial Enrollment

Fineline Cube Oct 4, 2024

InnoCare Pharma announced on October 4, 2024, that it has completed patient enrollment in a...

Company Drug

Akeso Biopharma’s PD-1/VEGF Bispecific Antibody Study Completes Enrollment

Fineline Cube Oct 4, 2024

On October 4, 2024, Summit Therapeutics (referred to as “Summit”), a partner of Akeso Biopharma...

Company Deals Drug

FRα ADC Rina-S by Genmab Enters Late-Stage Clinical Trial Following ProfoundBio Acquisition

Fineline Cube Oct 3, 2024

Genmab A/S (NASDAQ: GMAB) has initiated a Phase III clinical trial for its FRα ADC...

Company Drug

Dizal Pharmaceutical’s Surufatinib Earns CDE Consideration for Breakthrough Therapy in EGFR exon20ins NSCLC

Fineline Cube Oct 3, 2024

Dizal Pharmaceutical, a biopharmaceutical company based in China, has announced that the Center for Drug...

Company Drug

Hengrui Pharmaceuticals’ HR19042 Capsules Designated as Breakthrough Therapy for Autoimmune Hepatitis by China NMPA

Fineline Cube Oct 2, 2024

The Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA) has recently...

Company Drug

NMPA Clears AbbVie’s ABBV-706 for Clinical Trials Targeting SCLC and Neuroendocrine Tumors

Fineline Cube Oct 2, 2024

The China National Medical Products Administration (NMPA) has granted clinical trial approval to ABBV-706, a...

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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