Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 70/100

Failure Rate

4.8%

1 terminated/withdrawn out of 21 trials

Success Rate

0.0%

-86.5% vs industry average

Late-Stage Pipeline

14%

3 trials in Phase 3/4

Results Transparency

0%

0 of 0 completed trials have results

Key Signals

4 recruiting

Enrollment Performance

Analytics

Phase 1
16(76.2%)
Phase 3
3(14.3%)
Phase 2
1(4.8%)
Early Phase 1
1(4.8%)
21Total
Phase 1(16)
Phase 3(3)
Phase 2(1)
Early Phase 1(1)

Activity Timeline

Global Presence

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Clinical Trials (21)

Showing 20 of 21 trials
NCT06788431Early Phase 1Recruiting

A Clinical Study of IMC-001 for Injection in Improving Atherosclerotic Plaque Stability in Patients With Acute Coronary Syndrome.

Role: lead

NCT07355283Phase 3Not Yet Recruiting

IMM0306 in Combination With Lenalidomide vs Placebo in Combination With Lenalidomide in Patients With Relapsed/Refractory Follicular Lymphoma

Role: lead

NCT07118085Phase 1Recruiting

A Randomized, Double-blind, Placebo-controlled, Single and Multiple Dose Escalation Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of IMC-003 for Injection in Healthy Postmenopausal Women

Role: lead

NCT06647862Phase 3Recruiting

IMM01+Azacitidine VS Placebo +Azacitidine in Patients With Newly Diagnosed Chronic Myelomonocytic Leukemia (CMML1-2)

Role: lead

NCT07170787Phase 1Not Yet Recruiting

A Study of IMM2510 + IMM01 Combination Therapy in Patients With Advanced Solid Tumors

Role: lead

NCT06764836Phase 1Recruiting

A Study of IMM2510 + IMM27M Combination Therapy in Patients With Advanced Solid Tumors

Role: lead

NCT06746870Phase 2Not Yet Recruiting

A Phase II Clinical Study to Evaluate the Safety, Pharmacokinetic Profile, and Preliminary Efficacy of IMM2510 in Combination with Chemotherapy As First-line Treatment in Subjects with Non-small Cell Lung Cancer or Triple-negative Breast Cancer

Role: lead

NCT05076591Phase 1Suspended

IMM2902, a HER2/SIRPα Bispecific MAb-Trap Antibody-receptor Fusion Protein, in Patients with HER2-expressing Advanced Solid Tumors

Role: lead

NCT06465446Phase 3Not Yet Recruiting

A Study of IMM01 Plus Tiselizumab Versus Physician's Choice Chemotherapy in PD(L)1-refractory Classical Hodgkin Lymphoma

Role: lead

NCT05985083Phase 1Unknown

A Study Of IMM47 In Subjects With Advanced Solid Tumors

Role: lead

NCT05972460Phase 1Unknown

IMM2510, a PD-L1 and VEGF Bispecific Fusion Protein, in Patients With Advanced Solid Tumors

Role: lead

NCT05780307Phase 1Unknown

IMM2520, a PD-L1 and CD47 Bispecific Antibody in Patients With Advanced Solid Tumors

Role: lead

NCT05140811Phase 1Unknown

A Study of IMM01 Combined With Azacitidine in Patients With Acute Myeloid Leukemia and Myelodysplastic Syndrome

Role: lead

NCT05235438Phase 1Unknown

Safety and Toxicity Study of IMM27M in Patients With Advanced Solid Tumor

Role: lead

NCT05771883Phase 1Unknown

A Clinical Study of Injectable IMM0306 in Combination With Lenalidomide

Role: lead

NCT05860075Phase 1Terminated

Exploratory Study of IMM01 for Injection in the Treatment of Refractory or Recurrent Hematologic Malignancy

Role: lead

NCT05833984Phase 1Unknown

Safety and Efficacy of IMM01 Plus Tislelizumab in Patients With Advanced Solid Tumors and Lymphomas

Role: lead

NCT05805956Phase 1Unknown

IMM2902 in Patients With Advanced Solid Tumors Expressing HER2

Role: lead

NCT05805943Phase 1Unknown

Study of IMM0306 in Patients With Relapsed or Refractory CD20-positive B-cell Non-Hodgkin's Lymphoma

Role: lead

NCT04746131Phase 1Suspended

Safety and Pharmacokinetic Study of IMM0306 in Patients With Refractory or Relapsed CD20-positive B-cell Non-Hodgkin's Lymphoma (B-NHL)

Role: lead