A Study of Nivolumab by Itself or Nivolumab Combined With Ipilimumab in Patients With Advanced or Metastatic Solid Tumors
Part of paid clinical trials in Muscle Shoals, Alabama.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT01928394
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Advanced or Metastatic Solid Tumors
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab — BIOLOGICAL
- Ipilimumab — BIOLOGICAL
- Cobimetinib — DRUG
Study Details
To investigate the safety and efficacy of nivolumab as a single agent or in combination with ipilimumab in 6 tumor types - triple-negative breast cancer (TNBC), gastric cancer (GC), pancreatic adenocarcinoma (PC), small cell lung cancer (SCLC), bladder cancer (BC), and ovarian cancer (OC). A combination of nivolumab with ipilimumab and cobimetinib is also investigated in PC.
Key Dates
- Start date
- Oct 24, 2013
- Status verified
- Dec 2024
- Primary completion
- Feb 5, 2019
- Completion
- Nov 18, 2024
Study Design
- Enrollment
- 1,163 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm N - NivolumabNivolumab 3 mg/kg solution intravenously every 2 weeks until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends
- Experimental: Arm N-I, Level 1: Nivolumab+IpilimumabNivolumab 1 mg/kg solution intravenously plus Ipilimumab 1 mg/kg solution every 3 weeks for 4 doses followed by Nivolumab 3 mg/kg every 2 weeks until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends
- Experimental: Arm N-I, Level 2: Nivolumab+IpilimumabNivolumab 1 mg/kg solution intravenously plus Ipilimumab 3 mg/kg every 3 weeks for 4 doses followed by nivolumab 3 mg/kg every 2 weeks until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends
- Experimental: Arm N-I, Level 2b: Nivolumab+IpilimumabNivolumab 3 mg/kg solution intravenously plus Ipilimumab 1 mg/kg every 3 weeks for 4 doses followed by nivolumab 3 mg/kg every 2 weeks until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends
- Experimental: Arm N-I, Level 2c: Nivolumab+IpilimumabNivolumab 3 mg/kg solution intravenously every 3 weeks combined with ipilimumab 1 mg/kg every 6 weeks until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends
- Experimental: Arm N-I, Level 2d: Nivolumab+Ipilimumab+CobimetinibNivolumab 3 mg/kg solution intravenously every 3 weeks combined with ipilimumab 1 mg/kg every 6 weeks and cobimetinib 60mg once daily 21days on/7 days off until documented disease progression, discontinuation due to toxicity, withdrawal of consent or the study ends
Primary Outcome Measure
Objective Response Rate ( ORR ) [ Time Frame: 60 months ]
Locations (19)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution - 0047 | Muscle Shoals | Alabama | 35661 | - |
| Local Institution - 0044 | Aurora | Colorado | 80045 | - |
| Local Institution - 0015 | New Haven | Connecticut | 06520 | - |
| Local Institution - 0046 | Gainesville | Florida | 32610 | - |
| Local Institution - 0021 | Tampa | Florida | 33612 | - |
| Local Institution - 0001 | Atlanta | Georgia | 30322 | - |
| Local Institution - 0004 | Baltimore | Maryland | 21287 | - |
| Local Institution - 0005 | Boston | Massachusetts | 02215 | - |
| Local Institution - 0043 | Boston | Massachusetts | 02215 | - |
| Local Institution - 0049 | Omaha | Nebraska | 68130 | - |
| Local Institution - 0045 | Mineola | New York | 11501 | - |
| Local Institution - 0006 | New York | New York | 10065 | - |
| Local Institution - 0003 | Charlotte | North Carolina | 28204 | - |
| Local Institution - 0008 | Durham | North Carolina | 27710 | - |
| Local Institution - 0007 | Portland | Oregon | 97239 | - |
| Local Institution - 0011 | Franklin | Tennessee | 37067 | - |
| Local Institution - 0002 | Nashville | Tennessee | 37232 | - |
| Local Institution - 0009 | Houston | Texas | 77030 | - |
| Local Institution - 0042 | Seattle | Washington | 98104 | - |
Find similar trials in Muscle Shoals, AL
Related Studies
- A Study to Learn About the Study Medicine Called PF-07799544 as Monotherapy or in Combination in People With Advanced Solid TumorsPHASE1 · Recruiting · Pfizer · Birmingham, Alabama
- A First-in-human Study of PRTH-101 Monotherapy +/- Pembrolizumab in Subjects With Advanced MalignanciesPHASE1 · Recruiting · Incendia Therapeutics · Scottsdale, Arizona
- DCSZ11 as a Monotherapy and in Combination in Patients With Advanced or Metastatic Solid TumorsPHASE1 · Recruiting · DynamiCure Biotechnology · Birmingham, Alabama
- Dose Escalation and Expansion Study of BH3120 Alone or With Pembrolizuamb in Advanced or Metastatic Solid TumorsPHASE1 · Recruiting · Hanmi Pharmaceutical Company Limited · Tampa, Florida