Project Details
Description
A Phase I, Multicenter, Open label does escalation Safety Pharmacokinetic and Pharmacodynamic Study of Minnelide given daily for 21 days followed by 7 days off schedule in patients with Advanced GI Tumors
| Status | Finished |
|---|---|
| Effective start/end date | 8/8/13 → 8/30/18 |
Funding
- MINNEAMRITA THERAPEUTICS, LLC
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