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Geron

HQ: Parsippany, NJ source · geron.com ↗ · West Coast

Clinical Phase 3

Geron is a hematology biopharmaceutical company. From company website Source · Oct 13, 2026

Keywords: hematology biopharmaceutical Myelofibrosis Multiple Myeloma Myelodysplastic Syndromes Primary Myelofibrosis Secondary Myelofibrosis Myeloid Malignancies Essential Thrombocythemia Polycythemia Vera Non-small Cell Lung Cancer Locally Recurrent or Metastatic Breast Cancer Lung Cancer Chronic Lymphoproliferative Diseases Breast Cancer Solid Tumor Malignancies Imetelstat Imetelstat Sodium (GRN163L) GRN163L

Location: Parsippany, NJ · source · Oct 15, 2026

Profile checked Oct 10, 2026

$375.0MRaised (2 yrs)16Trials (company is sponsor)

Timeline

  1. Raise Private placement: $375M (up to, as announced), announced Nov 7, 2024. Source: SEC filing. source ↗
  2. 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 ↗
  3. 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 ↗
  4. 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 ↗
  5. 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 ↗
  6. Trial start Phase 2: Imetelstat Sodium in Treating Participants With Primary or Secondary Myelofibrosis source ↗
  7. Trial start Phase 2: Open Label Study to Evaluate the Activity of Imetelstat in Patients With Essential Thrombocythemia or Polycythemia Vera source ↗
  8. Trial start Phase 2: Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple Myeloma source ↗
  9. Trial start Phase 2: Imetelstat in Combination With Paclitaxel (With or Without Bevacizumab) in Patients With Locally Recurrent or Metastatic Breast Cancer source ↗
  10. Trial start Phase 2: Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC) source ↗
  11. Trial start Phase 1: A Study of GRN163L With Paclitaxel and Bevacizumab to Treat Patients With Locally Recurrent Or Metastatic Breast Cancer source ↗
  12. Trial start Phase 1: Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma source ↗
  13. Trial start Phase 1: Safety and Dose Study of GRN163L Administered to Treat Patients With Refractory or Relapsed Multiple Myeloma source ↗
  14. Trial start Phase 1: Study of GRN163L With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non Small Cell Lung Cancer source ↗
  15. Trial start Phase 1: Safety and Dose Study of GRN163L Administered to Patients With Refractory or Relapsed Solid Tumor Malignancies source ↗
  16. Trial start Phase 1: Safety and Dose Study of GRN163L to Treat Patients With Chronic Lymphoproliferative Disease(CLD) source ↗

Upcoming milestones

Estimated primary completion per ClinicalTrials.gov. Dates move.

Funding

Raised: $375.0M. Last 2 years.

Clinical trials (lead sponsor) 16

RecordTitlePhaseStatusStartPrimary completion
NCT05371964A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of Imetelstat in Combination With Ruxolitinib in Participants With MyelofibrosisPhase 1Active, not recruitingMay 4, 20222027-02 (estimated)
NCT02598661Study to Evaluate Imetelstat (GRN163L) in Participants With International Prognostic Scoring System (IPSS) Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)Phase 2/Phase 3Active, not recruitingJan 12, 2016Oct 13, 2023 (actual)
NCT04576156A 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 TreatmentPhase 3Active, not recruitingApr 12, 2021Jun 30, 2028 (estimated)
NCT01242930Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple MyelomaPhase 2Completed2010-112014-11 (actual)
NCT05937568Expanded Access for Treatment With ImetelstatNot listedApproved for marketingNot listedNot listed
NCT01731951Imetelstat Sodium in Treating Participants With Primary or Secondary MyelofibrosisPhase 2CompletedOct 29, 2012May 24, 2018 (actual)
NCT02426086Study 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) InhibitorPhase 2CompletedAug 28, 2015Apr 26, 2018 (actual)
NCT01243073Open Label Study to Evaluate the Activity of Imetelstat in Patients With Essential Thrombocythemia or Polycythemia VeraPhase 2Completed2010-122013-10 (actual)
NCT01137968Imetelstat as Maintenance Therapy After Initial Induction Chemotherapy in Non-small Cell Lung Cancer (NSCLC)Phase 2Completed2010-052013-09 (actual)
NCT01256762Imetelstat in Combination With Paclitaxel (With or Without Bevacizumab) in Patients With Locally Recurrent or Metastatic Breast CancerPhase 2Completed2010-112012-10 (actual)
NCT00510445Study of GRN163L With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non Small Cell Lung CancerPhase 1Completed2007-072011-04 (actual)
NCT00594126Safety and Dose Study of GRN163L Administered to Treat Patients With Refractory or Relapsed Multiple MyelomaPhase 1Completed2007-112011-07 (actual)
NCT00124189Safety and Dose Study of GRN163L to Treat Patients With Chronic Lymphoproliferative Disease(CLD)Phase 1Completed2005-072013-03 (actual)
NCT00732056A Study of GRN163L With Paclitaxel and Bevacizumab to Treat Patients With Locally Recurrent Or Metastatic Breast CancerPhase 1Completed2008-072011-09 (actual)
NCT00718601Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed MyelomaPhase 1Completed2008-072011-10 (actual)
NCT00310895Safety and Dose Study of GRN163L Administered to Patients With Refractory or Relapsed Solid Tumor MalignanciesPhase 1Completed2006-032013-03 (actual)
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