Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 60/100

Failure Rate

3.2%

1 terminated/withdrawn out of 31 trials

Success Rate

80.0%

-6.5% vs industry average

Late-Stage Pipeline

3%

1 trials in Phase 3/4

Results Transparency

0%

0 of 4 completed trials have results

Key Signals

9 recruiting

Enrollment Performance

Analytics

Phase 1
4(44.4%)
N/A
3(33.3%)
Phase 3
1(11.1%)
Phase 2
1(11.1%)
9Total
Phase 1(4)
N/A(3)
Phase 3(1)
Phase 2(1)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (31)

Showing 20 of 31 trials
NCT06924710Not ApplicableRecruiting

Adaptive Therapy for Resected Stage ⅠA2-Ⅱ NSCLC Patients With Undetectable MRD

Role: collaborator

NCT04405557Active Not Recruiting

The PREDICT Study: Prospective Early Detection In a Population at High-risk for Common Malignant Tumor

Role: lead

NCT05415670Completed

Benign/Malignant Pulmonary Nodule Classification Based on High-throughput Whole-genome Methylation Sequencing(GM-seq)

Role: lead

NCT06098560Recruiting

Circulating Tumor DNA (ctDNA) as a Predictive Biomarker for Immunotherapy in Advanced or Locally Advanced dMMR/MSI-H Colorectal Patients

Role: lead

NCT05965557Recruiting

Exploration of Predictive Markers of Neoadjuvant Immunotherapy in Non-Small Cell Lung Cancer

Role: lead

NCT05713994Recruiting

Combined HAIC, TKI/Anti-VEGF and ICIs as Conversion Therapy for Unresectable Hepatocellular Carcinoma

Role: collaborator

NCT06876610Recruiting

Application of CfDNA Methylation Detection in Auxiliary Diagnosis of Breast Cancer

Role: lead

NCT04566432Recruiting

Therapeutic ResistAnce and Clonal Evolution Assessed With Liquid Biopsy in ICIs Treated NSCLC Patients

Role: lead

NCT06283875Not Yet Recruiting

The Exploration of Personalized ctDNA Based MRD in the Clinical Significance of Cervical Cancer

Role: lead

NCT04353557Recruiting

ctDNA Monitoring in Early Breast Cancer

Role: lead

NCT03614689Active Not Recruiting

Assessment of the Minimal Residual Disease in Ovarian Cancer From Circulating Tumor DNA and Immune Repertoire

Role: lead

NCT05717738Recruiting

Combined TACE, TKI/Anti-VEGF and ICIs as Conversion Therapy for Advanced Hepatocellular Carcinoma

Role: collaborator

NCT06341855Not ApplicableRecruiting

Exploring the Potential of ctDNA-MRD for Recurrence Surveillance and Prognostic Evaluation in High-risk Endometrial Cancer

Role: collaborator

NCT05292443Withdrawn

Therapeutic ResistAnce and Clonal Evolution Assessed With Liquid Biopsy in ICIs Treated Primary Liver Cancer

Role: lead

NCT06074029Phase 1Active Not Recruiting

Exploratory Study on the Therapeutic Effect Prediction Model of Advanced BTC Immunotherapy

Role: collaborator

NCT03360630Phase 1Completed

Anti-PD-1 Alone or Combined With Autologous Cell Therapy in Advanced NSCLC

Role: collaborator

NCT06192784Phase 2Unknown

Combined DEB-TACE, Lenvatinib and Pucotenlimab as Conversion Therapy for Unresectable Intrahepatic Cholangiocarcinoma

Role: collaborator

NCT06194695Unknown

DEB-TACE, Lenvatinib and Anti-PD(L)1 Antibody as Conversion Therapy for Intrahepatic Cholangiocarcinoma

Role: collaborator

NCT05533892Phase 1Unknown

Nocardia Rubra Cell Wall Skeleton (N-CWS) Plus HAIC, Lenvatinib and Tislelizumab in Treating Patients With Advanced HCC

Role: collaborator

NCT05520801Unknown

Primary Hepatobiliary Cancer Cohort of Central China

Role: collaborator