InventisBio Files for Hong Kong IPO, Betting on Oncology and Metabolic Pipeline

InventisBio Co., Limited (SHA: 688382) this week filed for an initial public offering (IPO) to the Hong Kong Stock Exchange, seeking to raise capital to advance its pipeline of 8 products across oncology, autoimmune, and metabolic diseases, including two commercialized assets and three clinical‑stage candidates.

Company & Offering Overview

ItemDetail
CompanyInventisBio Co., Limited (688382.SH)
Founded2013
IPO VenueHong Kong Stock Exchange
Focus AreasOncology, autoimmune diseases, metabolic disorders
Pipeline2 commercialized, 3 clinical‑stage, 3 pre‑clinical assets
Filing DateWeek of 13 Jan 2026
Use of ProceedsClinical development, manufacturing scale‑up, commercial expansion

Differentiated Pipeline Summary

CategoryAssetTarget/MechanismStageIndication
CommercializedBefotertinibEGFR T790MMarketedNSCLC (China)
GarsorasibKRAS G12CMarketedNSCLC (China)
Core ClinicalD‑2570TYK2 inhibitorPhase IIAutoimmune
D‑0502SERDPhase IIBreast cancer
ClinicalD‑0120UndisclosedPhase IOncology
Pre‑clinicalYF087, YF550, YF057UndisclosedPre‑clinicalOncology/metabolic

Market Opportunity & Strategic Positioning

  • Commercial Validation: Befotertinib and garsorasib generated ¥1.2 billion in 2025 sales, demonstrating commercial execution capability in China’s competitive oncology market
  • Cancer Focus: Befotertinib addresses EGFR T790M NSCLC (30 % of China’s 800,000 annual NSCLC cases), while garsorasib targets KRAS G12C (~12 % of NSCLC)
  • Autoimmune Pipeline: D‑2570 (TYK2 inhibitor) enters a ¥45 billion market dominated by JAK inhibitors, offering improved safety profile
  • Manufacturing: InventisBio’s Shanghai facility (15,000 L capacity) supports clinical and early commercial supply; IPO proceeds will fund Phase III scale‑up
  • Global Ambitions: Hong Kong listing positions company for ex‑China licensing and global clinical trials

Forward‑Looking Statements
This brief contains forward‑looking statements regarding IPO completion, pipeline advancement, and commercial forecasts. Actual results may differ due to regulatory review timelines, market conditions, and clinical trial outcomes.-Fineline Info & Tech