Trials / Completed
CompletedNCT01444404
A Study of AMG 820 in Subjects With Advanced Solid Tumors
A Phase 1, First-In-Human Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Pharmacokinetics of AMG 820 in Adult Subjects With Advanced Solid Tumors
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 25 (actual)
- Sponsor
- AmMax Bio, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
First in human, open-label, sequential dose escalation and expansion study of AMG 820 in subjects with advanced solid tumors.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AMG 820 | AMG 820 is a fully human IgG2 c-fms antagonistic antibody and will be given every two weeks until progression or unacceptable toxicity develops. |
Timeline
- Start date
- 2008-03-31
- Primary completion
- 2014-02-06
- Completion
- 2014-02-06
- First posted
- 2011-09-30
- Last updated
- 2023-01-19
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01444404. Inclusion in this directory is not an endorsement.