Clinical trial · Interventional
Study of REGN1400 Alone and in Combination With Erlotinib or Cetuximab in Patients With Certain Types of Cancer
NCT01727869CI-TRIAL-00017392completedPhase 1ClinicalTrials.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)
This is an open-label, multicenter, ascending multiple dose study of REGN1400 alone and in combination with erlotinib or cetuximab administered to patients with certain types of 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 |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (3)
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Cohort 1
- description
- Dosing regimen 1: REGN1400 or REGN1400 and erlotinib or REGN1400 and cetuximab
- interventionNames
- Drug: REGN1400
- Drug: Erlotinib
- Drug: Cetuximab
- type
- EXPERIMENTAL
- label
- Cohort 2
- description
- Dosing regimen 2: REGN1400 or REGN1400 and erlotinib or REGN1400 and cetuximab
- interventionNames
- Drug: REGN1400
- Drug: Erlotinib
- Drug: Cetuximab
- type
- EXPERIMENTAL
- label
- Cohort 3
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria include, but are not limited to, the following: 1. Confirmed diagnosis of certain unresectable or metastatic cancers 2. Adequate Eastern Cooperative Oncology Group (ECOG) performance status 3. Adequate hepatic, renal and bone marrow function 4. Resolution of toxicity from prior therapy to grade less than/ = to 1 Exclusion Criteria include, but are not limited to, the following: 1. Active brain metastases 2. Thromboembolic events \< 6 months prior to study 3. Patients with a recent history (within 5 years) of another malignancy. 4. Investigational or any antitumor treatment with a maximum of 4 half-lives or administered 30 days prior to the initial administration of REGN1400 5. Patients who are pregnant or nursing 6. Prior treatment with ErbB3 inhibitors
References
Publications (0)
Data not yet available
No reference posted for this study.