Nivolumab Plus Pemetrexed for Head and Neck Squamous Cell Carcinoma
- Sponsor
- AHS Cancer Control Alberta
- Study ID
- NCT04107103
- Phase
- PHASE2
- Status
- Completed
Conditions
- SCCHN
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Combination Product: Nivolumab with Pemetrexed — DRUGNivolumab 3 mg/kg IV q.2 weekly in combination with pemetrexed 500mg/m2 q.6weekly. Treatment with nivolumab will continue every 14-days, and pemetrexed treatment will continue every 42-days. Treatment continues until disease progression or toxicity resulting in treatment discontinuation or until 2 years of treatment.
Study Details
The purpose of this study is to find out what effects the combination of Nivolumab and Pemetrexed has on you and your cancer. The safety of this combination and the effectiveness of this treatment will be studied.
Key Dates
- Start date
- Mar 19, 2020
- Status verified
- Jun 2024
- Primary completion
- Apr 14, 2023
- Completion
- Apr 28, 2023
Study Design
- Enrollment
- 6 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Single ArmA single-arm combining nivolumab with pemetrexed
Primary Outcome Measure
Feasibility [ Time Frame: 1 year after enrollment of last participant ]
Related Studies
- Intratumoral Delivery of Viral Replicon (saRNA) Particles Expressing IL-12 in Head and Neck CancerPHASE1 · Recruiting · VLP Therapeutics · Stanford, California