Trials / Unknown
UnknownNCT00706862
Safety and Efficacy of Talactoferrin in Addition to Standard Chemotherapy in Patients With Non-small Cell Lung Cancer
FORTIS-C: A Phase 3, Randomized, Placebo-controlled Study of Oral Talactoferrin in Combination With Carboplatin and Paclitaxel as First-line Therapy in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 1,100 (estimated)
- Sponsor
- Agennix · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to determine whether the combination of talactoferrin, carboplatin and paclitaxel improves progression free survival and overall survival in patients with non-small cell lung cancer compared to the combination of paclitaxel and carboplatin alone
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Talactoferrin | Oral, 1.5 grams twice per day |
| DRUG | Placebo | Oral, twice per day |
Timeline
- Start date
- 2009-02-01
- Primary completion
- 2015-06-01
- Completion
- 2016-03-01
- First posted
- 2008-06-30
- Last updated
- 2012-03-15
Locations
6 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00706862. Inclusion in this directory is not an endorsement.