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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

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...

Company Deals Drug

Sanofi to Acquire Vicebio Ltd for Up to USD 1.6 Billion, Advancing Next-Gen Vaccine Development

Fineline Cube Jul 22, 2025

Vicebio Ltd has entered into an exclusive, definitive agreement to be acquired by France-based major...

Company

AstraZeneca to Invest $50 Billion in US Manufacturing and R&D Expansion by 2030

Fineline Cube Jul 22, 2025

UK-based AstraZeneca (AZ, NASDAQ: AZN) announced plans to invest $50 billion in the United States by...

Company Drug

Genentech’s Astegolimab Shows Promising Results in Phase IIb COPD Trial

Fineline Cube Jul 22, 2025

Genentech, a member of the Roche Group (SWX: ROG, OTCMKTS: RHHBY), announced the results of...

Company Drug

AstraZeneca’s FLAURA2 Study Confirms Osimertinib Combo’s Survival Benefit in NSCLC

Fineline Cube Jul 22, 2025

UK-based AstraZeneca (AZ, NASDAQ: AZN) announced the final overall survival (OS) results from the Phase III...

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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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