Junshi Biosciences Q3 2025 Revenue Climbs 31%, Toripalimab Drives Growth, NMPA Approves sNDA

Junshi Biosciences Q3 2025 Revenue Climbs 31%, Toripalimab Drives Growth, NMPA Approves sNDA

Shanghai Junshi Biosciences Co., Ltd. (HKG: 1877,  SHA: 688180) today released its third‑quarter 2025 financial results. Operating revenue rose RMB 637 million, a 31.4 % year‑on‑year increase. For the first nine months of 2025, total revenue reached RMB 1.806 billion, up 42.06 % YoY.

Highlights

MetricQ3 2025YoY Change
Operating RevenueRMB 637 million+31.4 %
9‑Month RevenueRMB 1.806 billion+42.06 %
Cash & Cash‑Equivalents (End‑of‑Period)RMB 3.270 billion

Revenue Drivers

  • Toripalimab (LOQTORZI, JS001) sold ≈ RMB 1.495 billion in the domestic Chinese market, up ~40 % YoY.
  • Net loss narrowed significantly versus the same period in 2024.

Regulatory Milestones

  • NMPA accepted a supplemental New Drug Application (sNDA) for toripalimab as first‑line therapy in HER2‑expressing urothelial carcinoma.
  • 12 indications approved in mainland China; 10 listed on China’s National Reimbursement Drug List (NRDL).
  • Toripalimab approved in > 40 countries/regions (incl. U.S., EU, India, U.K., Australia, Canada, UAE, etc.) and is under review in multiple other markets.

Pipeline & Clinical Development

AssetDevelopment StageTarget IndicationRegulatory Status
JS207 (PD‑1/VEGF bispecific)Phase II/IIINeoadjuvant NSCLCFDA IND approved
JS005 (Anti‑IL‑17A mAb)Phase IIIModerate‑to‑severe plaque psoriasisPrimary endpoint met
JT118 (Monkeypox vaccine)Phase I/IIMonkeypoxNMPA CTA approved

Forward‑Looking Statements
This release contains forward‑looking statements that involve risks and uncertainties. Actual results may differ materially.-Fineline Info & Tech