A Study of AAV2-hAQP1 Gene Therapy in Participants With Radiation-Induced Late Xerostomia

Inclusion Criteria:

• Completed beam radiation therapy for head and neck cancer at least 3 years prior tothe first screening visit

• No history of parotid gland cancer, recurrent cancer, or a second primary cancer

• An unstimulated whole saliva flow rate (mL/min) >0 (i.e., at least one drop ofsaliva in the collection tube)

• A stimulated whole saliva flow rate (mL/min) within a specified range aftermechanical stimulation by chewing

• Average screening XQ Total Score at or above a specified threshold

• No evidence of head and neck cancer, defined as a negative otolaryngology exam and anegative computed tomography (CT) scan of the head, neck, and chest with contrast.If a participant has had a magnetic resonance imaging (MRI) study, CT scan, positronemission tomography (PET), or fluorodeoxyglucose-positron emission tomography (FDG-PET) scan of the head, neck, and chest within 6 months of study entry (and atleast 3 years after the completion of radiotherapy), then that image may be used foreligibility determination and a CT scan at screening will not be required.

• Either received treatment with one or more prescription sialagogues and elected todiscontinue therapy or, in consultation with their physician, elected to notinitiate such treatment

• Participants taking a prescription sialagogue (specifically, pilocarpine orcevimeline) must stop that medication at least 2 weeks prior to Screening and bewilling to refrain from taking such medications for the duration of the study

• Participants who require medication for an underlying medical condition that isknown to affect salivary output must be on stable doses of such medications for atleast one month prior to the first screening visit

Exclusion Criteria:

• Any malignancy within the preceding 3 years, except for treated basal cell orsquamous cell carcinoma of the skin or in situ cervical carcinoma

• History of systemic autoimmune disease affecting the salivary glands (e.g.,Sjogren's disease)

• Currently using systemic immunosuppressive medication(s) (e.g., corticosteroids orbiologics) or treated with one within 4 weeks of the first screening visit. Note:Topical, inhaled, or intranasal corticosteroids are permitted.

• Active viral infection with Epstein-Barr virus (EBV), defined as a positive anti-VCAIgM. In the event a potential participant has a positive anti-VCA IgM, they may berescreened 2-4 months later at which time a positive Epstein-Barr Virus NuclearAntigen (EBNA) will be considered as evidence of resolved EBV infection.

• Evidence of active Hepatitis C virus (HCV) infection

• Evidence of human immunodeficiency virus (HIV) infection

• Diagnosis of myasthenia gravis

• Personal or family history of acute or chronic angle-closure glaucoma (ACG), or atincreased risk of developing ACG, or had prophylactic treatment to reduce the riskof developing ACG

• Known allergy or hypersensitivity to glycopyrrolate

• Current smokers or history of smoking within the preceding 3 years (includes vapingwith tobacco additives)

• Current alcohol misuse or a history of the same within the preceding 3 years (defined for men as an average intake of more than 14 drinks per week and for womenas more than 7 drinks per week)

• Poorly controlled diabetes (hemoglobin A1c >7%)