Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

3.7%

3 terminated/withdrawn out of 82 trials

Success Rate

89.3%

+2.8% vs industry average

Late-Stage Pipeline

24%

20 trials in Phase 3/4

Results Transparency

4%

1 of 25 completed trials have results

Key Signals

14 recruiting1 with results

Enrollment Performance

Analytics

Phase 1
41(50.0%)
Phase 2
21(25.6%)
Phase 3
12(14.6%)
Phase 4
8(9.8%)
82Total
Phase 1(41)
Phase 2(21)
Phase 3(12)
Phase 4(8)

Activity Timeline

Global Presence

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Clinical Trials (82)

Showing 20 of 82 trials
NCT06375044Phase 1Recruiting

Study of SIM0500 Alone in Participants With Relapsed or Refractory Multiple Myeloma

Role: lead

NCT06331559Phase 1Terminated

Study of SIM0501 Alone and in Combination in Patients With Advanced Solid Tumors

Role: lead

NCT06370416Phase 2Enrolling By Invitation

the Prevention of Bone Marrow Suppression Caused by Chemotherapy in Advanced NSCLC With Trilaciclib

Role: collaborator

NCT07348211Phase 1Recruiting

First in Human Study of SIM0610 in Solid Tumors

Role: lead

NCT07361003Phase 3Recruiting

A Phase Ib/III Study of Suvemcitug Plus FTD/TPI in Participants With Refractory Metastatic Colorectal Cancer

Role: lead

NCT07357610Phase 1Recruiting

An Open-Label Drug Interaction Clinical Study to Evaluate Itraconazole, Rifampin, Midazolam and SIM0270 in Chinese Healthy Adult Participants

Role: lead

NCT07345364Phase 1Not Yet Recruiting

A Phase I, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses of SIM0811 Injection in Healthy Chinese Adult Subjects

Role: lead

NCT04914598Phase 3Active Not Recruiting

A Phase Ⅲ Clinical Study of Combined Cisplatin Versus Placebo Combined With Intracavitary Cisplatin Injection in the Treatment of Malignant Pleural Effusions

Role: lead

NCT07266493Phase 2Recruiting

Efficacy and Safety of Neoadjuvant Envafolimab Combined With Albumin-bound Paclitaxel and Carboplatin for Resectable Locally Advanced Esophageal Squamous Cell Carcinoma

Role: collaborator

NCT07265921Phase 1Recruiting

A Phase I Study of SIM0609 in Adult Participants With Locally Advanced/Metastatic Solid Tumors

Role: lead

NCT07175233Phase 2Not Yet Recruiting

A Phase 2 Study to Evaluate the Efficacy, Safety of SIM0278 in Subjects With Moderate to Severe Atopic Dermatitis

Role: lead

NCT06680921Phase 3Recruiting

A Study of SIM0270 Combined With Everolimus vs. Treatment of Physician's Choice in Patients With ER+/HER2- Advanced Breast Cancer (SIMRISE)

Role: lead

NCT06022354Phase 1Completed

To Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SIM0278 in Chinese Healthy Subjects

Role: lead

NCT04908787Phase 3Completed

A Phase III Study of BD0801 Combined With Chemotherapy in Recurrent, Platinum-resistant Epithelial Ovarian Cancer

Role: lead

NCT05718219Phase 1Active Not Recruiting

Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of SIM0348 in Advanced Solid Tumors

Role: lead

NCT07050459Phase 1Recruiting

A Phase I Study of SIM0686 in Participants With Locally Advanced/Metastatic Solid Tumors

Role: lead

NCT07007988Phase 1Recruiting

A Phase I Study of SIM0388 in Participants With Malignant Ascites.

Role: lead

NCT06186414Phase 1Recruiting

A Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SIM0237 Alone or in Combination with BCG in NMIBC

Role: lead

NCT06686745Phase 1Recruiting

Study of SIM0508 Alone and in Combination in Patients With Advanced Solid Tumors

Role: lead

NCT05781360Phase 1Terminated

A Study to Investigate the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of SIM0237 in Adult Participants with Advanced Solid Tumors

Role: lead