Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 65/100

Failure Rate

16.1%

9 terminated/withdrawn out of 56 trials

Success Rate

78.0%

-8.5% vs industry average

Late-Stage Pipeline

18%

10 trials in Phase 3/4

Results Transparency

3%

1 of 32 completed trials have results

Key Signals

6 recruiting1 with results7 terminated

Enrollment Performance

Analytics

Phase 1
40(72.7%)
Phase 3
9(16.4%)
Phase 2
5(9.1%)
Phase 4
1(1.8%)
55Total
Phase 1(40)
Phase 3(9)
Phase 2(5)
Phase 4(1)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (56)

Showing 20 of 56 trials
NCT05879627Phase 1Terminated

To Evaluate the Safety, Tolerance and Pharmacokinetics of BAT8007 for Injection in Patients With Advanced Solid Tumors

Role: lead

NCT05148325Phase 1Completed

Assessment of Safety ,Tolerance and Pharmacokinetics Clinical Efficacy With BAT4706 in Advanced Solid Tumors

Role: lead

NCT05848466Phase 1Completed

Assessment of Safety, Tolerability and Pharmacokinetics With BAT8010 for Injection in Advanced Malignant Solid Tumors Patients

Role: lead

NCT07499700Phase 2Recruiting

A Clinical Study of BAT4406F Injection in Patients With Minimal Change Disease/Focal Segmental Glomerulosclerosis

Role: lead

NCT05803187Completed

Clinical Study of Stage IV Psoriasis in Children With Geleli

Role: lead

NCT06094179Phase 1Active Not Recruiting

Evaluate the Safety, Tolerability of BAT6026

Role: lead

NCT05620017Phase 1Recruiting

Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of BAT8008 for Injection

Role: lead

NCT06545617Phase 1Withdrawn

A Clinical Study to Observe How Well That BAT8006 Works on Patients With Platinum Resistance Ovarian Cancer

Role: lead

NCT05378737Phase 1Completed

Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of BAT8006 for Injection

Role: lead

NCT07180862Phase 1Recruiting

A Study Evaluating BAT3306 Compared With Keytruda® in NSCLC Cancer Participants

Role: lead

NCT06341114Phase 1Active Not Recruiting

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

Role: lead

NCT05155722Phase 1Completed

Assessment of Safety ,Tolerance and Pharmacokinetics Clinical Efficacy With BAT1308 in Advanced Solid Tumors

Role: lead

NCT06044350Phase 2Active Not Recruiting

A Clinical Trial of BAT4406F Injection in Patients With Neuromyelitis Optica Spectrum Disorders

Role: lead

NCT05439629Phase 3Completed

Efficacy Evaluation Study of BAT5906 and Lucentis® in Patients With Macular Degeneration

Role: lead

NCT05105971Phase 1Completed

Assessment of Safety and Preliminary Efficacy With BAT6026 in Solid Tumor Patients in China

Role: lead

NCT05767060Phase 1Completed

BAT7104 Injection in Patients With Advanced Malignant Tumors.

Role: lead

NCT06280196Phase 3Terminated

A Study to Evaluate PK, Efficacy, and Safety of BAT3306 Plus Chemo and Compare With Keytruda®(EU/US) in Participants With IV nqNSCLC

Role: lead

NCT06321068Phase 2Terminated

BAT1308 in Combination With Platinum-containing Chemotherapy is Used for the First-line Treatment of Advanced or Recurrent dMMR Endometrial Cancer

Role: lead

NCT06376136Phase 1Recruiting

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

Role: lead

NCT05109650Phase 1Terminated

Assessment of Safety and Preliminary Efficacy With BAT6026 in Solid Tumour Patients

Role: lead