Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

4.5%

1 terminated/withdrawn out of 22 trials

Success Rate

92.9%

+6.4% vs industry average

Late-Stage Pipeline

5%

1 trials in Phase 3/4

Results Transparency

23%

3 of 13 completed trials have results

Key Signals

3 recruiting3 with results

Enrollment Performance

Analytics

Phase 1
11(52.4%)
Phase 2
9(42.9%)
Phase 3
1(4.8%)
21Total
Phase 1(11)
Phase 2(9)
Phase 3(1)

Activity Timeline

Global Presence

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Clinical Trials (22)

Showing 20 of 22 trials
NCT07549451Phase 2Not Yet Recruiting

Phase 2 Study Of Imetelstat for Patient With Myelodysplastic/Myeloproliferative Neoplasms

Role: collaborator

NCT07320235Phase 1Recruiting

Imetelstat Combinations in Relapsed AML

Role: collaborator

NCT06247787Phase 1Recruiting

A Study to Find the Highest Dose of Imetelstat in Combination With Fludarabine and Cytarabine for Patients With AML, MDS or JMML That Has Come Back or Does Not Respond to Therapy

Role: collaborator

NCT05371964Phase 1Recruiting

A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis

Role: lead

NCT02598661Phase 2Active Not Recruiting

Study to Evaluate Imetelstat (GRN163L) in Participants With International Prognostic Scoring System (IPSS) Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)

Role: lead

NCT04576156Phase 3Active Not Recruiting

A Study Comparing Imetelstat Versus Best Available Therapy for the Treatment of Intermediate-2 or High-risk Myelofibrosis (MF) Who Have Not Responded to Janus Kinase (JAK)-Inhibitor Treatment

Role: lead

NCT05583552Phase 2Active Not Recruiting

Study to Evaluate Imetelstat in Patients With High-Risk MDS or AML Failing HMA-based Therapy

Role: collaborator

NCT05937568Unknown

Expanded Access for Treatment With Imetelstat

Role: lead

NCT01731951Phase 2Completed

Imetelstat Sodium in Treating Participants With Primary or Secondary Myelofibrosis

Role: lead

NCT02426086Phase 2Completed

Study to Evaluate Activity of 2 Dose Levels of Imetelstat in Participants With Intermediate-2 or High-Risk Myelofibrosis (MF) Previously Treated With Janus Kinase (JAK) Inhibitor

Role: lead

NCT01916187Phase 1Withdrawn

Imetelstat Given Intravenously Alone and With Standard 13-Cis-Retinoic Acid in Children With Neuroblastoma

Role: collaborator

NCT01242930Phase 2Completed

Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple Myeloma

Role: lead

NCT01137968Phase 2Completed

Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC)

Role: lead

NCT01243073Phase 2Completed

Open Label Study to Evaluate the Activity of Imetelstat in Patients With Essential Thrombocythemia or Polycythemia Vera

Role: lead

NCT01256762Phase 2Completed

Imetelstat in Combination With Paclitaxel (With or Without Bevacizumab) in Patients With Locally Recurrent or Metastatic Breast Cancer

Role: lead

NCT00718601Phase 1Completed

Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma

Role: lead

NCT00310895Phase 1Completed

Safety and Dose Study of GRN163L Administered to Patients With Refractory or Relapsed Solid Tumor Malignancies

Role: lead

NCT00124189Phase 1Completed

Safety and Dose Study of GRN163L to Treat Patients With Chronic Lymphoproliferative Disease(CLD)

Role: lead

NCT00510445Phase 1Completed

Study of GRN163L With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non Small Cell Lung Cancer

Role: lead

NCT00594126Phase 1Completed

Safety and Dose Study of GRN163L Administered to Treat Patients With Refractory or Relapsed Multiple Myeloma

Role: lead