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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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04043104
Recruitment Status : Completed
First Posted : August 2, 2019
Last Update Posted : April 24, 2023
Sponsor:
Information provided by (Responsible Party):
MeiraGTx UK II Ltd

Study Description
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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 evaluate the safety and identify either a maximum tolerated dose or a maximum feasible dose of a single dose of AAV2hAQP1 infused into one or both parotid glands:

To evaluate subject improvement of xerostomia symptoms, to evaluate the increase in parotid gland salivary output after treatment with AAV2hAQP1, to evaluate additional efficacy outcomes.


Condition or disease Intervention/treatment Phase
Radiation-Induced Parotid Gland Hypofunction Xerostomia Due to Radiotherapy Head and Neck Cancer Drug: AAV2hAQP1: 1 x 10^11 vg/gland (single gland) Drug: AAV2hAQP1: 3 x 10^10 vg/gland (both glands) Drug: AAV2hAQP1: 3 x 10^11 vg/gland (single gland) Drug: AAV2hAQP1: 1 x 10^11 vg/gland (both glands) Drug: AAV2hAQP1: 1 x 10^12 vg/gland (single gland) Drug: AAV2hAQP1: 3 x 10^11 vg/gland (both glands) Drug: AAV2hAQP1: 3 x 10^12 vg/gland (single gland) Drug: AAV2hAQP1: 1 x 10^12 vg/gland (both glands) Phase 1

Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 24 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: 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
Actual Study Start Date : June 30, 2019
Actual Primary Completion Date : March 28, 2023
Actual Study Completion Date : March 28, 2023

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dry Mouth Safety

Arms and Interventions
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Arm Intervention/treatment
Experimental: 1 x 10^11 vg/gland (single gland) Drug: AAV2hAQP1: 1 x 10^11 vg/gland (single gland)
Intra-parotid administration of AAV2hAQP1 via Stensen's duct to a single parotid gland at a dose level of 1 x 10^11 vg/gland
Experimental: 3 x 10^10 vg/gland (both glands) Drug: AAV2hAQP1: 3 x 10^10 vg/gland (both glands)
Intra-parotid administration of AAV2hAQP1 via Stensen's duct to both parotid glands at a dose level of 3 x 10^10 vg/gland
Experimental: 3 x 10^11 vg/gland (single gland) Drug: AAV2hAQP1: 3 x 10^11 vg/gland (single gland)
Intra-parotid administration of AAV2hAQP1 of via Stensen's duct to a single parotid gland at a dose level of 3 x 10^11 vg/gland
Experimental: 1 x 10^11 vg/gland (both glands) Drug: AAV2hAQP1: 1 x 10^11 vg/gland (both glands)
intra-parotid administration of AAV2hAQP1 via Stensen's duct to both parotid glands at a dose level of 1 x 10^11 vg/gland
Experimental: 1 x 10^12 vg/gland (single gland) Drug: AAV2hAQP1: 1 x 10^12 vg/gland (single gland)
Intra-parotid administration of AAV2hAQP1 via Stensen's duct to a single parotid gland at a dose level of 1 x 10^12 vg/gland
Experimental: 3 x 10^11 vg/gland (both glands) Drug: AAV2hAQP1: 3 x 10^11 vg/gland (both glands)
Intra-parotid administration of AAV2hAQP1 via Stensen's duct to both parotid glands at a dose level of 3 x 10^11 vg/gland
Experimental: 3 x 10^12 vg/gland (single gland) Drug: AAV2hAQP1: 3 x 10^12 vg/gland (single gland)
Intra-parotid administration of AAV2hAQP1 via Stensen's duct to a single parotid gland at a dose level of 3 x 10^12 vg/gland
Experimental: 1 x 10^12 vg/gland (both glands) Drug: AAV2hAQP1: 1 x 10^12 vg/gland (both glands)
Intra-parotid administration of AAV2hAQP1 via Stensen's duct to both parotid glands at a dose level of 1 x 10^12 vg/gland


Outcome Measures
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Primary Outcome Measures :
  1. The primary outcome is safety of AAV2hAQP1 administered to the parotid gland of adult subjects with radiation-induced xerostomia [ Time Frame: one day to one year ]
    Safety will be assessed by number of adverse events occurring with treatment


Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Male or female subjects ≥18 years of age.
  2. History of radiation therapy for head and neck cancer.
  3. 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.
  4. 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.

  5. 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 Criteria:

  1. Pregnant or lactating women or women planning to become pregnant.
  2. Any experimental therapy within 3 months before Day 1.
  3. Active infection that requires the use of intravenous antibiotics and does not resolve at least 1 week before Day 1.
  4. Uncontrolled ischemic heart disease (i.e., unstable angina, evidence of active ischemic heart disease on electrocardiogram [ECG]).
  5. History of systemic autoimmune diseases affecting the salivary glands.

  6. Use of systemic immunosuppressive medications (i.e., corticosteroids).

    o Note: Topical, inhaled, or intranasal corticosteroids are allowed.

  7. 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.
  8. Active infections including, Epstein-Barr virus (EBV), cytomegalovirus (CMV), hepatitis B (HBV), hepatitis C (HCV), or human immunodeficiency virus (HIV) infection.
  9. 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.
  10. 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.
  11. Estimated glomerular filtration rate <60 mL/min/1.73 m2 using the Modification of Diet in Renal Disease equation.
  12. Active use of tobacco products as determined by self-reporting.
  13. Allergy to iodine or shellfish, and thus unable to have sialographic evaluations.
  14. Allergy or hypersensitivity to glycopyrrolate.
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04043104


Locations
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United States, California
Leland Stanford Junior University
Stanford, California, United States, 94305
United States, Kentucky
University of Louisville
Louisville, Kentucky, United States, 40202
United States, Massachusetts
Brigham and Women's Hospital
Boston, Massachusetts, United States, 02184
United States, New York
Memorial Sloan Kettering Cancer Center
New York, New York, United States, 10065
United States, North Carolina
Atrium Health
Charlotte, North Carolina, United States, 28209
Canada, Ontario
Health Sciences North - Northeast Cancer Center
Sudbury, Ontario, Canada
Sponsors and Collaborators
MeiraGTx UK II Ltd
More Information
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Responsible Party: MeiraGTx UK II Ltd
ClinicalTrials.gov Identifier: NCT04043104    
Other Study ID Numbers: MGT016
First Posted: August 2, 2019    Key Record Dates
Last Update Posted: April 24, 2023
Last Verified: April 2023

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Xerostomia
Salivary Gland Diseases
Mouth Diseases
Stomatognathic Diseases