Clinical trial
Safety and Dose Study of GRN163L to Treat Patients With Chronic…
NCT00124189 · Geron Corporation, Industry · Completed
Key facts
| NCT number | NCT00124189 |
|---|---|
| Title | Safety and Dose Study of GRN163L to Treat Patients With Chronic Lymphoproliferative Disease(CLD) |
| Official title | A Phase I, Sequential Cohort, Dose Escalation Trial to Determine the Safety, Tolerability, and Maximum Tolerated Dose of GRN163L in Patients With Chronic Lymphoproliferative Disease |
| Lead sponsor | Geron Corporation, Industry |
| Status | Completed |
| Phase | Phase 1 |
| Study type | Interventional |
| Conditions | Chronic Lymphoproliferative Diseases |
| Intervention type | Drug |
| Interventions | GRN163L |
| Enrollment | 48 |
| Start date | Jul 1, 2005 |
| Primary completion | Mar 1, 2013 |
| Completion | Mar 1, 2013 |
| First posted | Jul 27, 2005 |
| Last update posted | Dec 24, 2015 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: