Drugs / TQH2722
Regulatory milestones approvals, filings & regulatory actions · 1 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Filed | China (NMPA) | — | atopic eczema | 2026-09-16 | “注射用TQB2102及TQH2722注射液的上市申请同日被受理,分别用于既往在复发或转移性疾病阶段未接受过化疗的不可切除或转移性HER2低表达(IHC 1+或IHC 2+/ISH-)成人乳腺癌患者,及治疗外用药控制不佳或不适合外用药治疗的成人中重度特应性皮炎(AD)。” cttq.com ↗ |
Trials 7
Evidence & citations 5 cited values
Every value below carries the sentence it was read from. 8 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | TQH2722 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT07398859 ↗ |
| Known as | TQH2722 injection | “TQH2722 injection is a fully human monoclonal antibody that interfering with the signal cascade.” NCT06439381 ↗ |
| Modality | Monoclonal antibody | “TQH2722 is a fully human monoclonal antibody” NCT05409326 ↗ |
| Route | Subcutaneous | “TQH2722 was subcutaneously injected” PMID 40221092 ↗ Apr 2025 |
| Target | IL4R | “TQH2722 is a fully human monoclonal antibody directed against the interleukin (IL)-4 receptor α subunit (IL-4Rα)” NCT05409326 ↗ |