Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 50/100

Failure Rate

5.4%

7 terminated/withdrawn out of 129 trials

Success Rate

80.0%

-6.5% vs industry average

Late-Stage Pipeline

19%

24 trials in Phase 3/4

Results Transparency

7%

2 of 28 completed trials have results

Key Signals

25 recruiting2 with results5 withdrawn

Enrollment Performance

Analytics

Phase 1
54(42.2%)
Phase 2
49(38.3%)
Phase 3
24(18.8%)
Early Phase 1
1(0.8%)
128Total
Phase 1(54)
Phase 2(49)
Phase 3(24)
Early Phase 1(1)

Activity Timeline

Global Presence

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Clinical Trials (129)

Showing 20 of 129 trials
NCT07416695Phase 1Recruiting

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of HLX3901 in Patients With Advanced SCLC or NEC

Role: lead

NCT07543471Phase 1Not Yet Recruiting

A Phase I Multicentre Randomized Double-Blind Parallel-Controlled Study of HLX05-N vs. ERBITUX® in Metastatic Colorectal Cancer

Role: lead

NCT06769152Phase 2Recruiting

A Phase II Clinical Study to Evaluate the Efficacy and Safety of HLX43 (Anti-PD-L1 ADC) in Patients With Advanced Gynecological Malignant Tumors

Role: lead

NCT07541534Phase 1Not Yet Recruiting

A Phase I Clinical Study of HLX316 in Participants With Advanced/Metastatic Solid Tumors

Role: lead

NCT07533708Phase 1Not Yet Recruiting

A Phase I Clinical Study of HLX3902 in Patients With mCRPC and Other Advanced Tumours

Role: lead

NCT07518043Phase 1Not Yet Recruiting

A Study of HLX18 vs. OPDIVO® in Multiple Resected Solid Tumors

Role: lead

NCT07495930Phase 1Not Yet Recruiting

Pharmacokinetic Characteristics, Safety, and Immunogenicity of HLX319 Compared With EU-Phesgo®

Role: lead

NCT07487519Phase 2Not Yet Recruiting

Phase II Study of HLX43 Monotherapy or Combined With Immune Checkpoint Inhibitors in Patients With Locally Advanced, Recurrent, or Metastatic Triple-negative Breast Cancer.

Role: lead

NCT07484893Phase 1Not Yet Recruiting

A Study to Evaluate the Safety, PK, and Immunogenicity of Recombinant Human Hyaluronidase in Healthy Subjects

Role: lead

NCT07294508Phase 2Recruiting

A Study to Evaluate HLX22 in Combination With HLX87 in Patients With HER2-Positive Recurrent or Metastatic Breast Cancer

Role: lead

NCT07480681Phase 1Not Yet Recruiting

Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of HLX97 (a KAT6A/B Inhibitor) in Patients With Advanced/Metastatic Solid Tumor

Role: lead

NCT07477587Phase 1Not Yet Recruiting

A Study to Compare the PK Characteristics, Safety, Tolerability, and Immunogenicity of HLX15-SC With DARZALEX FASPRO® in Combination With Lenalidomide and Dexamethasone (Rd) in Transplant-ineligible Patients With Newly Diagnosed Multiple Myeloma

Role: lead

NCT07473726Phase 1Not Yet Recruiting

A Phase I Clinical Study to Evaluate the Safety, Tolerability, and PK of HLX48 in Advanced/Metastatic Solid Tumors

Role: lead

NCT07176650Phase 1Recruiting

Phase I Clinical Study To Evaluate Pharmacokinetic Profile, Safety, Efficacy and Immunogenicity Of Ipilimumab Biosimilar HLX13 Vs. YERVOY® (US-Sourced YERVOY®) As A First-Line Treatment For Patients With Unresectable Hepatocellular Carcinoma

Role: lead

NCT07459751Phase 2Not Yet Recruiting

A Global Phase II/III Clinical Study to Evaluate the Efficacy and Safety of HLX43 Monotherapy or HLX43 in Combination With HLX07 Versus Docetaxel in Advanced or Metastatic Squamous Non-Small Cell Lung Cancer

Role: lead

NCT07459738Phase 2Not Yet Recruiting

A Phase II Study to Evaluate the Efficacy and Safety of HLX43 in Patients With Hormone Receptor Positive, HER2 Negative Locally Advanced or Metastatic Breast Cancer

Role: lead

NCT06857279Phase 2Recruiting

A Phase II Clinical Study to Evaluate HLX43 in Subjects With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Role: lead

NCT07274813Early Phase 1Recruiting

A Phase I Study to Evaluate the Safety, Tolerability, and PK of HLX37 in Advanced/Metastatic Solid Tumors

Role: lead

NCT06532006Phase 3Recruiting

A Phase Ⅲ Clinical Study of HLX22 in Combination With Trastuzumab and Chemotherapy for the Treatment of Gastroesophageal Junction and Gastric Cancer

Role: lead

NCT07160335Phase 1Recruiting

A Phase I Clinical Study to Evaluate the PK Profile, Efficacy, Safety and Immunogenicity of HLX17 vs. Keytruda® in Multiple Resected Solid Tumors

Role: lead