Status:
COMPLETED
A Phase 1 Open-Label, Dose Escalation Study to Determine the Optimal Dose, Safety, and Activity of AAV2hAQP1 in Subjects With Radiation-Induced Parotid Gland Hypofunction and Xerostomia
Lead Sponsor:
MeiraGTx UK II Ltd
Conditions:
Radiation-Induced Parotid Gland Hypofunction
Xerostomia Due to Radiotherapy
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
Open-label, non-randomized, dose escalation trial of AAV2hAQP1 administered via Stensen's duct to a single or both parotid glands in subjects with radiation-induced xerostomia The objectives are to ev...
Eligibility Criteria
Inclusion
- Male or female subjects ≥18 years of age.
- History of radiation therapy for head and neck cancer.
- Abnormal parotid gland function as judged by both absence of unstimulated parotid salivary flow and a stimulated parotid salivary flow in the targeted parotid gland \>0 and \<0.3 mL/min/gland after 2% citrate stimulation.
- No evidence of recurrence of the primary malignancy by an otolaryngology (ears, nose, and throat \[ENT\]) assessment. Additionally, all subjects must be disease-free of head and neck cancer for at least 5 years following the end of treatment at screening, with the exception of subjects with a history of HPV+ OPC (base of tongue, oropharynx, pharynx, soft palate, tonsil) who must be disease free for at least 2 years following the end of treatment. Disease status will be determined by negative clinical examinations and computed tomography (CT) scans of the neck and chest. If subjects have had a magnetic resonance imaging (MRI) of the neck or a positron emission tomography (PET) scan within 6 months of screening, then a CT scan is not required, except for HPV+ OPC subjects who must have scans at 2 years post treatment.
- Female subjects of childbearing potential (i.e., ovulating, pre-menopausal, and not surgically sterile) and all male subjects must use a medically accepted contraceptive regimen during their participation in the study and until all samples collected at 2 consecutive visits following AAV2hAQP1 administration are negative. Acceptable methods of contraception for male subjects include the following:
- Condoms with spermicide. Acceptable methods of contraception for female subjects include the following:
- Intrauterine device for at least 12 weeks prior to Screening.
- Hormonal contraception (oral, implant, injection, ring, or patch) for at least 12 weeks prior to Screening.
- Diaphragm used in combination with spermicide.
Exclusion
- Pregnant or lactating women or women planning to become pregnant.
- Any experimental therapy within 3 months before Day 1.
- Active infection that requires the use of intravenous antibiotics and does not resolve at least 1 week before Day 1.
- Uncontrolled ischemic heart disease (i.e., unstable angina, evidence of active ischemic heart disease on electrocardiogram \[ECG\]).
- History of systemic autoimmune diseases affecting the salivary glands.
- Use of systemic immunosuppressive medications (i.e., corticosteroids).
- o Note: Topical, inhaled, or intranasal corticosteroids are allowed.
- Malignancy, other than head and neck cancer, within the past 3 years, with the exception of adequately treated basal cell or squamous cell carcinoma of the skin or in situ cervical carcinoma.
- Active infections including, Epstein-Barr virus (EBV), cytomegalovirus (CMV), hepatitis B (HBV), hepatitis C (HCV), or human immunodeficiency virus (HIV) infection.
- White blood cell count \<3000/μL, absolute neutrophil count \<1500/μL, hemoglobin \<10.0 g/dL, platelet count \<100,000/μL, or absolute lymphocyte count ≤500/μL.
- Alanine aminotransferase and/or aspartate aminotransferase \>1.5 × the upper limit of normal (ULN), alkaline phosphatase \>1.5 × ULN, or total bilirubin \>1.5 × ULN with any elevation of liver enzymes.
- Estimated glomerular filtration rate \<60 mL/min/1.73 m2 using the Modification of Diet in Renal Disease equation.
- Active use of tobacco products as determined by self-reporting.
- Allergy to iodine or shellfish, and thus unable to have sialographic evaluations.
- Allergy or hypersensitivity to glycopyrrolate.
Key Trial Info
Start Date :
June 30 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 28 2023
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT04043104
Start Date
June 30 2019
End Date
March 28 2023
Last Update
April 24 2023
Active Locations (6)
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1
Leland Stanford Junior University
Stanford, California, United States, 94305
2
University of Louisville
Louisville, Kentucky, United States, 40202
3
Brigham and Women's Hospital
Boston, Massachusetts, United States, 02184
4
Memorial Sloan Kettering Cancer Center
New York, New York, United States, 10065