Safety and Tolerability Study of Nivolumab and Cabiralizumab for Resectable Biliary Tract Cancer
| Status: | Not yet recruiting |
|---|---|
| Healthy: | No |
| Age Range: | 18 - 100 |
| Updated: | 4/6/2019 |
| Start Date: | May 2019 |
| End Date: | January 2023 |
| Contact: | Susan Sartorius-Mergenthaler, RN |
| Email: | Sartosu@jhmi.edu |
| Phone: | 410-614-3644 |
Safety and Tolerability Study of Combination Nivolumab and Cabiralizumab as Neoadjuvant and Adjuvant Therapy for Resectable Biliary Tract Cancer
The purposed of this research is to study the safety and clinical activity of the combination
of nivolumab and cabiralizumab in people with resectable biliary tract cancers (BTC).
of nivolumab and cabiralizumab in people with resectable biliary tract cancers (BTC).
Inclusion Criteria:
- Has confirmed biliary tract cancer
- Ability to understand and willingness to sign a written informed consent document.
- Age ≥18 years
- Have biopsiable disease
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
- Patient must have adequate organ function defined by the study-specified laboratory
tests.
- Must use acceptable form of birth control while on study.
Exclusion Criteria:
- Has active autoimmune disease that requires systemic treatment.
- Has a known additional malignancy that is progressing or has required active treatment
within the past 2 years or that is expected to require active treatment within two
years.
- Prior treatment with immunotherapy agents (including, anti-PD-1, anti-PD-L1,
anti-PD-L2, anti-CTLA4, etc.).
- Has known central nervous system (CNS) metastases and/or carcinomatous meningitis.
- Has evidence of interstitial lung disease or active, non-infectious pneumonitis.
- Has evidence of an uncontrolled, active infection requiring parenteral anti-bacterial,
anti-viral or anti-fungal therapy ≤ 7 days prior to administration of study
medication.
- Has received a blood transfusion within 72 hours prior to first dose of study drug
administration
- Unwilling or unable to follow the study schedule for any reason.
- Major surgery within 4 weeks prior to initiation of study treatment.
- Patient with uncontrolled intercurrent illness including, but not limited to,
uncontrolled infection, symptomatic congestive heart failure, unstable angina
pectoris, cardiac arrhythmia, significant muscle disorders or psychiatric
illness/social situations that would limit compliance with study requirements.
- Pregnant or breastfeeding women.
- Have known history of infection with HIV, hepatitis B, or hepatitis C.
- Received any prophylactic vaccine within 30 days of first dose of study drug
treatment.
- Has a history of allergy to study treatments or any of its components of the study.
We found this trial at
1
site
Click here to add this to my saved trials
