Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of GT-02287 in Parkinson's Disease

Prior treatment

• Concomitant medications metabolized primarily by cytochrome P450 3A4 (CYP3A4) that have a narrow therapeutic window, concomitant medications that are substrates of breast cancer resistance protein and/or P-glycoprotein and that have a narrow therapeutic window, concomitant medications that are potent inhibitors or inducers of CYP3A4
• Use of dopamine antagonists (antipsychotics) or anticholinergic medications
• Concomitant disease including, but not limited to cardiovascular conditions, diabetes, autoimmune disease, cancer, active infectious disease, psychotic disorders and symptoms, depressive symptoms, drug and/or alcohol misuse as defined in the protocol
• participation in any interventional clinical study within 3 months or 5 half-lives, whichever is longer, prior to Screening

Other illness

• Other neurological disorders, including but not limited to Alzheimer's disease, amyotrophic lateral sclerosis, frontotemporal dementia, progressive supranuclear palsy, corticobasal syndrome, Huntington's disease, multiple system atrophy, dementia with Lewy bodies, secondary (e.g. drug-induced) parkinsonism, multiple sclerosis, or epilepsy
• A history of Gaucher disease or homozygous for a GBA1 pathogenic variant known to be associated with GD or compound heterozygous for 2 alleles that are known to be associated with GD.
• Dementia or a moderate cognitive impairment (score ≥17 on the Montreal Cognitive Assessment)
• Hypersensitivity to GT-02287 or any of its excipients
• Malabsorption or relevant disorder which may impact the absorption of GT-02287

Lab values

• Clinically significant abnormalities in laboratory test

Other

• Known PD-associated LRRK2 pathogenic variant or other PD-associated genetic mutations other than GBA1
• Contraindications to lumbar puncture (LP)
• Blood donation \>500 mL within 3 months
• Unable to comply with restrictions on food products, smoking, and /or alcohol use as defined in protocol

• Able and willing to provide written informed consent and be willing to comply with the requirements and restrictions of the study
• Any sex, ≥30 and ≤85 years of age
• Diagnosis of PD based on MDS criteria
• Within 7 years of PD diagnosis
• Body mass index of ≥18 and ≤40 kg/m2, and a body weight ≥45 kg and ≤120 kg
• Willing to provide a blood sample for PD-related genetic testing
• Hoehn \& Yahr 1-3, inclusive
• No severe motor fluctuations or disabling dyskinesias based on the investigator's clinical assessment
• Naïve to pharmacological treatment for PD or on stable PD medication for ≥3 months prior to Screening, including ≥4 weeks at the same dose(s) immediately before Screening
• Not pregnant or breastfeeding
• If participant is either of childbearing potential or produces potentially viable sperm, participant must agree to use 2 forms of contraception (barrier method and a second highly effective form of birth control/contraception, as defined in the protocol) if engaging in potentially reproductive intercourse (with a partner who produces potentially viable sperm or is of childbearing potential, respectively)
• Agreeing to not participate in another investigational study while taking part in this study
• For participants with known GBA1 mutations, presence of a GBA1 mutation that has been associated with an increased risk of PD