NCT07515079 Efficacy Evaluation Study of BAT5906 and Lucentis® in Patients With Diabetic Macular Edema Status RECRUITING Phase PHASE3
NCT07499700 A Clinical Study of BAT4406F Injection in Patients With Minimal Change Disease/Focal Segmental Glomerulosclerosis Status RECRUITING Phase PHASE2/PHASE3
NCT07180862 A Study Evaluating BAT3306 Compared With Keytruda® in NSCLC Cancer Participants Status RECRUITING Phase PHASE1
NCT06545617 A Clinical Study to Observe How Well That BAT8006 Works on Patients With Platinum Resistance Ovarian Cancer Status WITHDRAWN Phase PHASE1/PHASE2
NCT06376136 A Multicenter Open Clinical Study of Safety, Tolerability, Pharmacokinetic Profile, and Initial Clinical Efficacy of BAT 8010 for Injection Combined With BAT 1006 in the Treatment of Locally Advanced or Metastatic Tumors Status RECRUITING Phase PHASE1/PHASE2
NCT06341114 A Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy of the Combination of BAT8008 With BAT1308 in Patients With Advanced Solid Tumors Status ACTIVE_NOT_RECRUITING Phase PHASE1/PHASE2
NCT06321068 BAT1308 in Combination With Platinum-containing Chemotherapy is Used for the First-line Treatment of Advanced or Recurrent dMMR Endometrial Cancer Status TERMINATED Phase PHASE2/PHASE3
NCT06280196 A Study to Evaluate PK, Efficacy, and Safety of BAT3306 Plus Chemo and Compare With Keytruda®(EU/US) in Participants With IV nqNSCLC Status TERMINATED Phase PHASE3
NCT06139536 Assessment of Safety, Tolerability and Pharmacokinetics With BAT4706 and BAT1308 in Advanced Solid Tumors Patients Status RECRUITING Phase PHASE1
NCT06123884 BAT1308 Combined with Platinum-Based Chemotherapy± Bevacizumab for PDL1-Positive (CPS ≥1) Cervical Cancer Status RECRUITING Phase PHASE2/PHASE3
NCT06111196 Compare the Pharmacokinetics and Safety of BAT3306 Injection Versus KEYTRUDA® Administered in Healthy Male Subjects Status COMPLETED Phase PHASE1
NCT06094179 Evaluate the Safety, Tolerability of BAT6026 Status ACTIVE_NOT_RECRUITING Phase PHASE1/PHASE2
NCT06044350 A Clinical Trial of BAT4406F Injection in Patients With Neuromyelitis Optica Spectrum Disorders Status ACTIVE_NOT_RECRUITING Phase PHASE2
NCT05968508 A Randomized, Double-blind, Single-dose, Two-arm Parallel Study to Compare the Pharmacokinetics and Safety of BAT1806 Prefilled Subcutaneous Injection With RoActemra® in Healthy Chinese Male Subjects Status COMPLETED Phase PHASE1
NCT05879627 To Evaluate the Safety, Tolerance and Pharmacokinetics of BAT8007 for Injection in Patients With Advanced Solid Tumors Status TERMINATED Phase PHASE1
NCT05865574 A Comparative Pharmacokinetic Study to Evaluate Different Manufacturing Batches of BAT1706 Injection Status UNKNOWN Phase PHASE1
NCT05848466 Assessment of Safety, Tolerability and Pharmacokinetics With BAT8010 for Injection in Advanced Malignant Solid Tumors Patients Status COMPLETED Phase PHASE1
NCT05767060 BAT7104 Injection in Patients With Advanced Malignant Tumors. Status COMPLETED Phase PHASE1
NCT05620017 Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of BAT8008 for Injection Status RECRUITING Phase PHASE1