The purpose of this study is to determine whether an investigationalcombination immuno-therapy of nivolumab and daratumumab is safe andeffective in the treatment of advanced or metastatic solid tumors.
- Conditions
- Advanced or metastatic solid tumorsMedDRA version: 21.1Level: PTClassification code 10061873Term: Non-small cell lung cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)MedDRA version: 21.1Level: LLTClassification code 10051971Term: Pancreatic adenocarcinomaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)MedDRA version: 20.0Level: PTClassification code 10075566Term: Triple negative breast cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)Therapeutic area: Diseases [C] - Cancer [C04]
- Registration Number
- EUCTR2017-000367-33-IT
- Lead Sponsor
- BRISTOL-MYERS SQUIBB INTERNATIONAL CORPORATIO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 105
- Patients must have metastatic or advanced solid tumors.
- Women with histologically or cytologically confirmed triple negative breast carcinoma.
- Participants with histologically confirmed pancreatic adenocarcinoma.
- Participants must have histologic or cytologic confirmation of Non
Small Cell Lung Cancer (NSCLC).
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 66
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 94
-Active brain metastases or leptomeningeal metastases.
- Any serious or uncontrolled medical disorder.
- Prior malignancy active within the previous 3 years.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method