Clinical trial · Interventional
E7080 in Combination With Carboplatin and Paclitaxel in Patients With Non-small Cell Lung Cancer (NSCLC)
NCT00832819CI-TRIAL-00017741completedPhase 1Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to determined the maximum tolerated dose (MTD), safety and tolerability, pharmacokinetics, pharmacodynamics, and anti-tumor effect of E7080 administered continually twice daily in combination with carboplatin and paclitaxel to patients with advanced or metastatic non-small cell lung cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small-cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Carboplatin | Drug | Carboplatin | ALIAS |
| E7080 | Drug | Lenvatinib | ALIAS |
| Paclitaxel | Drug | Paclitaxel | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- E7080 (Dose Escalation Cohort)
- description
- This will be a dose-escalation evaluation of 12-18 participants to determine the maximum tolerated dose of E7080 in combination with paclitaxel and carboplatin.
- interventionNames
- Drug: E7080
- Drug: Paclitaxel
- Drug: Carboplatin
- type
- EXPERIMENTAL
- label
- E7080 (Expansion Cohort)
- description
- Dosage of E7080 for Expansion Cohort will be determined based on the maximum tolerated dose in the Dose-Escalation Cohort.
- interventionNames
- Drug: E7080
- Drug: Paclitaxel
- Drug: Carboplatin
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 74 Years
Show eligibility criteria text
Inclusion criteria: 1. Subjects with a histologically or cytologically confirmed diagnosis of non-small cell lung cancer (NSCLC). 2. Locally advanced and/or metastatic non-small cell lung cancer (NSCLC) (Stage IIIB/IV). 3. Subjects with at least one measurable tumor lesion by Response Evaluation Criteria In Solid Tumors (RECIST). 4. Subjects with Performance Status (PS) 0-1. 5. Subjects with adequate organ function. Exclusion criteria: 1. Subjects who have ever received the following therapy for non-small cell lung cancer (NSCLC): 1. Chemotherapy 2. Biological or immunotherapies 3. Surgery for primary focus 4. The radiation therapy for primary focus 2. Subjects with the severe complications or disease history. 3. Subjects with brain metastasis accompanying clinical symptoms or requiring treatment. 4. Subjects with simultaneous or metachronous cancers. 5. Subjects who cannot take oral medication. 6. Subjects who are using drugs that strongly inhibit or induce cytochrome P450 (CYP) 3A4.
References
Publications (1)
- DERIVEDNishio M, Horai T, Horiike A, Nokihara H, Yamamoto N, Takahashi T, Murakami H, Yamamoto N, Koizumi F, Nishio K, Yusa W, Koyama N, Tamura T. Phase 1 study of lenvatinib combined with carboplatin and paclitaxel in patients with non-small-cell lung cancer. Br J Cancer. 2013 Aug 6;109(3):538-44. doi: 10.1038/bjc.2013.374. Epub 2013 Jul 16. PMID 23860537