Trials / Completed
CompletedNCT00306618
Safety and Efficacy Study of Panzem NCD to Treat Glioblastoma
A Single-Center, Open-Label, Phase II, Safety, Pharmacokinetic and Efficacy of Panzem Nanocrystal Colloidal Dispersion Administered Orally to Patients With Recurrent Glioblastoma Multiforme
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- CASI Pharmaceuticals, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This single-center, open-label, phase 2 study will evaluate the anti-tumor activity, as well as the safety and pharmacokinetics, of Panzem (2-methoxyestradiol, 2ME2) Nanocrystal Colloidal Dispersion (NCD) administered in patients with recurrent glioblastoma multiforme (GBM)
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Panzem Nanocrystal Colloidal Dispersion | Panzem NCD suspension, 100 mg/mL, four times daily continuous dosing |
Timeline
- Start date
- 2006-01-01
- Primary completion
- 2007-11-01
- Completion
- 2008-12-01
- First posted
- 2006-03-24
- Last updated
- 2008-12-10
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00306618. Inclusion in this directory is not an endorsement.