Overview
An Investigational Immuno-therapy Study to Investigate the Safety and Effectiveness of Nivolumab, and Nivolumab Combination Therapy in Virus-associated Tumors
Status:
Active, not recruiting
Active, not recruiting
Trial end date:
2022-08-04
2022-08-04
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study to investigate the safety and effectiveness of nivolumab, and nivolumab combination therapy, to treat patients who have virus-associated tumors. Certain viruses have been known to play a role in tumor formation and growth. This study will investigate the effects of the study drugs, in patients who have the following types of tumors: - Anal canal cancer-No longer enrolling this tumor type - Cervical cancer - Epstein Barr Virus (EBV) positive gastric cancer-No longer enrolling this tumor type - Merkel Cell Cancer - Penile cancer-No longer enrolling this tumor type - Vaginal and vulvar cancer-No longer enrolling this tumor type - Nasopharyngeal Cancer - No longer enrolling this tumor type - Head and Neck Cancer - No longer enrolling this tumor typePhase:
Phase 1/Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Bristol-Myers SquibbCollaborator:
Ono Pharmaceutical Co. LtdTreatments:
Antibodies, Monoclonal
Daratumumab
Ipilimumab
Nivolumab
Criteria
For more information regarding BMS clinical trial participation, please visitwww.BMSStudyConnect.com
Inclusion Criteria:
- Histopathologic confirmation of the following tumor types (please refer to protocol
for full details pertaining to eligible tumor types):
1. Merkel Cell Carcinoma
2. Gastric or Gastro-Esophageal junction carcinoma (No longer enrolling this tumor
type)
3. Nasopharyngeal Carcinoma
4. Squamous cell carcinoma (SCC) of the cervix, vagina, or vulva
5. Squamous cell carcinoma of the Head and Neck
6. Squamous cell carcinoma of the anal canal and penis
7. Recurrent/metastatic SCC of the cervix not amenable to curative treatment with
surgery and/or radiation therapy who are unsuitable for platinum-based therapy
may enroll in the cervical cancer Combination B expansion cohort
- Measurable disease by CT or MRI
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Patient willing to comply to provide tumor tissue (archival or fresh biopsy specimen)
- Men and women of age 18 or older
Exclusion Criteria:
- Active brain metastases or leptomeningeal metastases
- Patients with active, known or suspected autoimmune disease
- Patients with a condition requiring systemic treatment with either corticosteroids or
other immunosuppressive medications
- Patients with hepatitis
- Patients with HIV
- Pregnant or breastfeeding women