COMPANY
Geron
Geron is a hematology biopharmaceutical company. From company website Source · Oct 13, 2026
Timeline
- Raise Private placement: $375M (up to, as announced), announced Nov 7, 2024. Source: SEC filing. source ↗
- Trial start Phase 1: A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis source ↗
- Trial start Phase 3: 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 source ↗
- Trial start Phase 2/Phase 3: Study to Evaluate Imetelstat (GRN163L) in Participants With International Prognostic Scoring System (IPSS) Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS) source ↗
- Trial start Phase 2: 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 source ↗
- Trial start Phase 2: Imetelstat Sodium in Treating Participants With Primary or Secondary Myelofibrosis source ↗
- Trial start Phase 2: Open Label Study to Evaluate the Activity of Imetelstat in Patients With Essential Thrombocythemia or Polycythemia Vera source ↗
- Trial start Phase 2: Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple Myeloma source ↗
- Trial start Phase 2: Imetelstat in Combination With Paclitaxel (With or Without Bevacizumab) in Patients With Locally Recurrent or Metastatic Breast Cancer source ↗
- Trial start Phase 2: Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC) source ↗
- Trial start Phase 1: A Study of GRN163L With Paclitaxel and Bevacizumab to Treat Patients With Locally Recurrent Or Metastatic Breast Cancer source ↗
- Trial start Phase 1: Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma source ↗
- Trial start Phase 1: Safety and Dose Study of GRN163L Administered to Treat Patients With Refractory or Relapsed Multiple Myeloma source ↗
- Trial start Phase 1: Study of GRN163L With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non Small Cell Lung Cancer source ↗
- Trial start Phase 1: Safety and Dose Study of GRN163L Administered to Patients With Refractory or Relapsed Solid Tumor Malignancies source ↗
- Trial start Phase 1: Safety and Dose Study of GRN163L to Treat Patients With Chronic Lymphoproliferative Disease(CLD) source ↗
Upcoming milestones
- 2027-02 (ESTIMATED) · Phase 1 · A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis · NCT05371964
- Jun 30, 2028 (ESTIMATED) · Phase 3 · 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 · NCT04576156
Funding
- Private placement: $375M (up to, as announced), announced Nov 7, 2024. Source: SEC filing. source ↗
Clinical trials (lead sponsor) 16
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT05371964 | A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With Myelofibrosis | Phase 1 | Active, not recruiting | May 4, 2022 | 2027-02 (estimated) |
| NCT02598661 | Study to Evaluate Imetelstat (GRN163L) in Participants With International Prognostic Scoring System (IPSS) Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS) | Phase 2/Phase 3 | Active, not recruiting | Jan 12, 2016 | Oct 13, 2023 (actual) |
| NCT04576156 | 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 | Phase 3 | Active, not recruiting | Apr 12, 2021 | Jun 30, 2028 (estimated) |
| NCT01242930 | Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple Myeloma | Phase 2 | Completed | 2010-11 | 2014-11 (actual) |
| NCT05937568 | Expanded Access for Treatment With Imetelstat | Not listed | Approved for marketing | Not listed | Not listed |
| NCT01731951 | Imetelstat Sodium in Treating Participants With Primary or Secondary Myelofibrosis | Phase 2 | Completed | Oct 29, 2012 | May 24, 2018 (actual) |
| NCT02426086 | 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 | Phase 2 | Completed | Aug 28, 2015 | Apr 26, 2018 (actual) |
| NCT01243073 | Open Label Study to Evaluate the Activity of Imetelstat in Patients With Essential Thrombocythemia or Polycythemia Vera | Phase 2 | Completed | 2010-12 | 2013-10 (actual) |
| NCT01137968 | Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC) | Phase 2 | Completed | 2010-05 | 2013-09 (actual) |
| NCT01256762 | Imetelstat in Combination With Paclitaxel (With or Without Bevacizumab) in Patients With Locally Recurrent or Metastatic Breast Cancer | Phase 2 | Completed | 2010-11 | 2012-10 (actual) |
| NCT00510445 | Study of GRN163L With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non Small Cell Lung Cancer | Phase 1 | Completed | 2007-07 | 2011-04 (actual) |
| NCT00594126 | Safety and Dose Study of GRN163L Administered to Treat Patients With Refractory or Relapsed Multiple Myeloma | Phase 1 | Completed | 2007-11 | 2011-07 (actual) |
| NCT00124189 | Safety and Dose Study of GRN163L to Treat Patients With Chronic Lymphoproliferative Disease(CLD) | Phase 1 | Completed | 2005-07 | 2013-03 (actual) |
| NCT00732056 | A Study of GRN163L With Paclitaxel and Bevacizumab to Treat Patients With Locally Recurrent Or Metastatic Breast Cancer | Phase 1 | Completed | 2008-07 | 2011-09 (actual) |
| NCT00718601 | Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma | Phase 1 | Completed | 2008-07 | 2011-10 (actual) |
| NCT00310895 | Safety and Dose Study of GRN163L Administered to Patients With Refractory or Relapsed Solid Tumor Malignancies | Phase 1 | Completed | 2006-03 | 2013-03 (actual) |