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Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Company Deals PIC

WestGene and CREATE Sign License Deal to Co‑Develop In Vivo CAR‑T Therapies

Fineline Cube Aug 31, 2026
Company Deals PIC

Simnova Closes nearly RMB 400 Million Series B to Advance CAR‑NK Candidate SNC103

Fineline Cube Aug 31, 2026
Company Deals PIC

Leaderna Therapeutics Closes Series A+ Led by Grand View Capital to Advance Oligonucleotide Pipeline

Fineline Cube Aug 31, 2026
Company Drug PIC

Eli Lilly Wins FDA Approval for Mounjaro Cardiovascular Risk Reduction in Type 2 Diabetes

Fineline Cube Aug 31, 2026
Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Fineline Cube Sep 1, 2026
Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Fineline Cube Sep 1, 2026
Company Drug

Ipsen’s Cabometyx Approved by European Commission for Neuroendocrine Tumors

Fineline Cube Jul 25, 2025

France-based pharmaceutical company Ipsen S.A. (EPA: IPN, OTCMKTS: IPSEY) announced that its anticancer drug Cabometyx...

Policy / Regulatory

NHSA Announces Reforms to Centralized Drug Procurement Policies Beyond Lowest Price

Fineline Cube Jul 24, 2025

The National Healthcare Security Administration (NHSA) held a press conference today on the “High-Quality Completion...

Company

Boehringer Ingelheim Reports 6.3% Sales Growth in First Half of 2025

Fineline Cube Jul 24, 2025

Boehringer Ingelheim announced today its financial results for the first half of 2025, reporting group...

Company Drug

Kelun-Biotech’s SKB378/WIN378 Enters Global Phase II Trial for Asthma Treatment

Fineline Cube Jul 24, 2025

Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. (HKG: 6990) announced on July 23, 2025, that its partner...

Company Drug

Sirius Therapeutics’ SRSD107 Receives EMA Approval for Phase II Clinical Trials in Thromboembolic Diseases

Fineline Cube Jul 24, 2025

China-based Sirius Therapeutics announced on July 23, 2025, that its next-generation siRNA therapy, SRSD107, has...

Company Drug

Akeso Enrolls First Patient in Phase III Trial of Ivonescimab for Pancreatic Cancer

Fineline Cube Jul 24, 2025

China-based Akeso Biopharma (HKG: 9926) announced on July 24, 2025, that the first patient has...

Company Drug

Youcare Pharma’s YKYY029 Receives FDA IND Approval for Hypertension Treatment

Fineline Cube Jul 24, 2025

China-based Youcare Pharmaceutical Group (SHA: 688658) announced on July 24, 2025, that its subsidiary, Beijing...

Policy / Regulatory

National Health Commission Launches Integrated Medical and Elder Care Demonstration Projects

Fineline Cube Jul 24, 2025

On July 22, 2025, China’s National Health Commission (NHC) issued the “Work Plan for Integrated...

Company Drug

Kintor’s KX-826 Topical Solution Meets Primary Endpoint in AGA Phase II Trial

Fineline Cube Jul 24, 2025

China-based Kintor Pharmaceutical (HKG: 9939) announced on July 24, 2025, that its self-developed 1.0% KX-826...

Company Deals

Ascentage Pharma Collaborates with Major Chinese Firms to Commercialize Lisaftoclax

Fineline Cube Jul 23, 2025

China-based Ascentage Pharma (NASDAQ: AAPG, HKG: 6855) announced today that it has entered into cooperation...

Company Medical Device

Shanghai Kehua Bioengineering Subsidiary Receives Two IVD Certificates from NMPA

Fineline Cube Jul 23, 2025

China-based Shanghai Kehua Bioengineering Co., Ltd. (KHB) (SHE: 002022) announced on July 23, 2025, that...

Company Drug

Shenzhen Beimei’s TWYNEO Receives NMPA Clinical Trial Approval for Acne Treatment

Fineline Cube Jul 23, 2025

Shenzhen Beimei Pharmaceutical Co., Ltd. announced on July 22, 2025, that its drug TWYNEO (tretinoin...

Company Deals

Chison Medical and Gates Foundation Collaborate on Innovative Ultrasound Equipment

Fineline Cube Jul 23, 2025

China-based Chison Medical Technologies (SHA: 688358) announced on July 23, 2025, a partnership with the...

Company Medical Device

Shanghai MicroPort EP MedTech’s IceMagic Catheter Receives EU MDR Certification

Fineline Cube Jul 23, 2025

Shanghai-based Shanghai MicroPort EP MedTech Co., Ltd. (SHA: 688351) announced on July 23, 2025, that...

Company Drug

CTTQ Doses First Patient in China for TQB6411 Phase I Clinical Trial

Fineline Cube Jul 23, 2025

Subsidiary of China based Sino Biopharmaceutical Ltd (HKG: 1177) Jiangsu Chia Tai Tianqing Pharmaceutical Co.,...

Company Drug

FDA-Approved Smile System Launches in Lecheng for ADHD Treatment

Fineline Cube Jul 23, 2025

On July 22, 2025, the innovative non-pharmacological ADHD treatment medical device “Smile” (ADHD Transcutaneous Nerve...

Company Drug

Grand Pharma’s TLX591 Granted NMPA Approval for Phase III Prostate Cancer Trial

Fineline Cube Jul 23, 2025

China-based Grand Pharmaceutical Group Limited (HKG: 0512) announced that its innovative radiolabeled drug conjugate (RDC)...

Company Drug

Abbisko Therapeutics Completes First Patient Dosing for PRMT5×MTA Inhibitor ABSK131

Fineline Cube Jul 23, 2025

Shanghai-based biotech Abbisko Therapeutics Co., Ltd (HKG: 2256) announced the completion of the first patient...

Company Deals

Novatim and ERIGEN Ink Licensing Pact for Dual-Target CAR-T Therapy KQ-2003

Fineline Cube Jul 22, 2025

Novatim Immune Therapeutics (Zhejiang) Co., Ltd. announced a strategic cooperation with US-based biopharmaceutical company ERIGEN...

Company Drug

AusperBio Gains NMPA Approval for Phase III Trials of AHB-137 in Chronic Hepatitis B

Fineline Cube Jul 22, 2025

Sino-US liver therapy developer AusperBio announced that the National Medical Products Administration (NMPA) has approved...

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Recent updates

  • NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment
  • Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment
  • Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States
  • Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market
  • Laekna Doses First Patient in Phase I Study of LAE118 PI3Kα Inhibitor for Advanced Solid Tumors, Licensed to Vasque Bio for Up to USD 527 Million
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Company Drug

Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States

Policy / Regulatory

Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market

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