drugset / Trial / NCT06118333
A Study Comparing BL-B01D1 With Physician's Choice of Chemotherapy in Patients With Recurrent or Metastatic Nasopharyngeal Carcinoma(PANKU-NPC01)
Phase 3
Active not recruiting
386 enrolled
Sichuan Baili Pharmaceutical Co., Ltd.
Baili-Bio (Chengdu) Pharmaceutical Co., Ltd. · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
A phase III, randomized, open-label, multicenter study to evaluate the efficacy and safety of BL-B01D1 in patients with recurrent or metastatic nasopharyngeal carcinoma who had failed at least two lines of platinum-based chemotherapy after receiving PD-1/PD-L1 monoclonal antibody as the last line of therapy.
Timeline
- Start
- 2023-12-04
- Primary completion
- 2026-11
- Completion
- 2026-11
Outcome
Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)
paper Overall survival data were not mature at data cutoff. PMID 41125110 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BL-B01D1 | Unknown | 2.5 mg/kg | Intravenous |
| Subject | Capecitabine | Small molecule | — | Oral |
| Subject | Docetaxel | Small molecule | — | Intravenous |
| Subject | Gemcitabine | Small molecule | — | Intravenous |