Trials / Approved For Marketing
Approved For MarketingNCT02307812
Ramucirumab Use in Combination With Paclitaxel in Gastric or Gastroesophageal Junction Adenocarcinoma; Temporary Authorization for Use (ATU) in France
- Status
- Approved For Marketing
- Phase
- —
- Study type
- Expanded Access
- Enrollment
- —
- Sponsor
- Eli Lilly and Company · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- —
Summary
The treating physician/investigator contacts Lilly when, based on their medical opinion, a patient meets the criteria for inclusion in the ATU.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ramucirumab | Administered intravenously (IV) |
| DRUG | Paclitaxel | Administered IV |
Timeline
- First posted
- 2014-12-04
- Last updated
- 2025-01-09
Source: ClinicalTrials.gov record NCT02307812. Inclusion in this directory is not an endorsement.