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A Phase I Open Label Study Evaluating the Safety and Feasibility of Allogeneic Mesenchymal Stem Cells for Radiation-induced Hyposalivation and Xerostomia in Previous Oropharynx Cancer Patients
An investigator-initiated, non-randomized, open label study to investigate the safety, feasibility and tolerability of intraglandular injection of allogeneic mesenchymal stem/stromal cells (MSCs) into the submandibular and parotid glands of the patients with radiation-induced hyposalivation and xerostomia after radiation for a oropharyngeal squamous cell carcinoma
Patients with previous oropharyngeal cancer and radiation-induced hyposalivation and xerostomia (dry mouth syndrome) will receive intraglandular injections of allogeneic adipose-derived MSCs into the submandibular and parotid glands. The trial will be Good Clinical Practice (GCP) Monitored. From healthy donors, MSCs will be produced at a Good Manufacturing Practice (GMP) Facility. The patients will be followed for four months for safety, tolerability, and efficacy registration. Changes in quality of life, unstimulated, and stimulated whole saliva flow rate, salivary gland function will be assessed. Immune response towards receiving allogeneic MSCs will be evaluated in plasma and saliva. Changes in the composition and quality of the whole saliva will be investigated. Saliva from the participants will altså be compared to saliva from ten healthy controls.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
Yes
Department of Otolaryngology, Rigshospitalet, University Hospital of Copenhagen
Copenhagen, Denmark
Department of Otolaryngology, Rigshospitalet
Copenhagen, Denmark
Start Date
March 18, 2019
Primary Completion Date
June 22, 2020
Completion Date
December 1, 2025
Last Updated
January 29, 2021
10
ACTUAL participants
Allogeneic adipose derived stem/stromal cells
BIOLOGICAL
Lead Sponsor
Rigshospitalet, Denmark
NCT05926765
NCT04392622
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06414161