Clinical trial
A Double Blind, Placebo Controlled Dose Range Finding Study to Assess the Safety, Pharmacokinetics, and Efficacy of Tempol for the Reduction of Severe Mucositis in Head and Neck Cancer Patients Undergoing Combined Radio- and Chemotherapy
NCT03480971 is registered in ClinicalTrials.gov with Matrix Biomed, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Double Blind, Placebo Controlled Dose Range Finding Study to Assess the Safety, Pharmacokinetics, and Efficacy of Tempol for the Reduction of Severe Mucositis in Head and Neck Cancer Patients Undergoing Combined Radio- and Chemotherapy
- Lead sponsor
- Matrix Biomed, Inc.
- Phase
- Phase 2
- Overall status
- Recruiting
- Start date
- May 13, 2019
- Completion date
- December 31, 2025
- Enrollment
- 120 (estimated)
- Sites
- 9
Conditions
As the registry lists them; a condition with its own page is linked.
mucositis, nephrotoxicity, ototoxicity