Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

6.3%

5 terminated/withdrawn out of 80 trials

Success Rate

92.2%

+5.7% vs industry average

Late-Stage Pipeline

6%

5 trials in Phase 3/4

Results Transparency

0%

0 of 59 completed trials have results

Key Signals

10 recruiting

Enrollment Performance

Analytics

Phase 1
66(82.5%)
Phase 2
9(11.3%)
Phase 3
5(6.3%)
80Total
Phase 1(66)
Phase 2(9)
Phase 3(5)

Activity Timeline

Global Presence

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Clinical Trials (80)

Showing 20 of 80 trials
NCT05427682Phase 1Completed

A Clinical Trial to Evaluate the Pharmacokinetics and Safety of Pyroglutamate Rongliflozin Capsules in Subjects With Mild and Moderate Liver Damage

Role: lead

NCT04984512Phase 2Recruiting

The Efficacy And Safety Of Mitizodone Phosphate Tablets In The Treatment of Patient With Major Depressive Disorder

Role: lead

NCT03655873Phase 1Completed

The Study of a Selective 5-ht6 Receptor Antagonist, HEC30654AcOH,in Healthy Subjects

Role: lead

NCT04596007Phase 1Completed

The Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of HEC83518 Tablets in Chinses Healthy Subjects

Role: lead

NCT05802862Phase 3Completed

A Study of Insulin Degludec/Insulin Aspart Biosimilar (22011) Compared With Insulin Degludec/Insulin Aspart(Ryzodeg) in Participants With Type 2 Diabetes in China

Role: lead

NCT05127772Phase 1Completed

A Clinical Trial of HEC93077 in Chinese Healthy Subjects and HUA Patients With Single or Multiple Dosing

Role: lead

NCT04667429Phase 1Completed

the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of HEC83518 Tablets

Role: lead

NCT05374343Phase 1Completed

A Study of the Pharmacokinetics, Pharmacodynamics, and Safety of Rongliflozin in Type 2 Diabetic Subjects With Renal Impairment

Role: lead

NCT07376200Phase 1Recruiting

Single-ascending Dose Study of HEC-151 Injection

Role: lead

NCT05451602Phase 1Recruiting

HEC169096 in Participants With Advanced Solid Tumors

Role: lead

NCT05586074Phase 3Recruiting

HEC73543 Versus Salvage Chemotherapy in R/R FLT3-ITD AML

Role: lead

NCT07341672Phase 1Not Yet Recruiting

A Single-center, Randomized, Open-label, Parallel-design Clinical Study to Evaluate the Pharmacokinetic Effects of Itraconazole, Fluconazole or Efavirenz on a Single Dose of Clifutinib in Healthy Participants

Role: lead

NCT07099118Phase 1Recruiting

A Safety, Tolerability, Pharmacokinetics/Pharmacodynamics Study of HEC169584 Capsules in Healthy Subjects

Role: lead

NCT07102251Phase 1Recruiting

A Study to Evaluate the Safety, Tolerability, PK/PD of HEC-007 Injection in Healthy and Overweight/Obese Subjects

Role: lead

NCT05139719Phase 2Recruiting

A Study to Explore the Therapeutic Effect of HEC585 on Delaying Forced Vital Capacity (FVC) Decline and Tolerance in Progressive Fibrosing Interstitial Lung Disease (PF-ILD) Patients

Role: lead

NCT05060822Phase 2Active Not Recruiting

Phase ll Study of HEC585 in Patients With IPF

Role: lead

NCT07082842Phase 3Recruiting

Confirmatory Clinical Study of HEC585 Tablets in Patients With IPF

Role: lead

NCT07211165Phase 1Completed

Clinical Study on the Mass Balance of Clifutinib

Role: lead

NCT04415853Phase 3Recruiting

Study of Larotinib in Unresectable Advanced or Recurrent Esophageal Cancer

Role: lead

NCT05048368Phase 1Not Yet Recruiting

Pharmacokinetics Study of Larotinib in Subjects With Impaired Hepatic Function

Role: lead