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| Sponsor: | Hollis-Eden Pharmaceuticals |
|---|---|
| Information provided by: | Hollis-Eden Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT00716794 |
Purpose
This is a phase I/II, open-label, dose escalation study of HE3235 administered orally to patients with advanced prostate cancer who have failed hormone therapy and at least one taxane based chemotherapy regimen.
| Condition | Intervention | Phase |
|---|---|---|
|
Prostate Cancer |
Drug: HE3235 |
Phase I Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Open Label, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | A Phase I/II, Open-Label, Dose Ranging Study of the Safety, Tolerance, Pharmacokinetics and Potential Activity of HE3235 When Administered Orally to Patients With Prostate Cancer |
| Estimated Enrollment: | 44 |
| Study Start Date: | July 2008 |
| Estimated Study Completion Date: | December 2009 |
| Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Main Inclusion Criteria:
Patient has progression of disease despite adequate hormone therapy, demonstrated by one of the following:
Exclusion Criteria:
Contacts and Locations| Contact: HollisEden Clinical Trials | 858-320-2591 | clinicaltrials@holliseden.com |
| United States, California | |
| Recruiting | |
| San Francisco, California, United States, 94115 | |
| Recruiting | |
| Roseville, California, United States, 95661 | |
| Recruiting | |
| Encinitas, California, United States, 92024 | |
| United States, New York | |
| Recruiting | |
| New York, New York, United States, 10065 | |
| United States, Texas | |
| Recruiting | |
| San Antonio, Texas, United States, 78229 | |
| United States, Washington | |
| Recruiting | |
| Seattle, Washington, United States, 98109 | |
| Study Director: | Dwight Stickney, MD | Hollis-Eden Pharmaceuticals |
More Information
| Responsible Party: | Hollis-Eden Pharmaceuticals ( Nanette Onizuka-Handa/Sr. Vice President, Regulatory Affairs and Quality ) |
| Study ID Numbers: | HE3235-0201 |
| Study First Received: | July 14, 2008 |
| Last Updated: | June 15, 2009 |
| ClinicalTrials.gov Identifier: | NCT00716794 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Prostate cancer HE3235 Apoptone |
|
Neoplasms Prostatic Diseases Neoplasms by Site Genital Neoplasms, Male |
Prostatic Neoplasms Urogenital Neoplasms Genital Diseases, Male |