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To Evaluate Pharmacokinetics (PK) and Safety of Tavapadon in Participants With Severe Renal Impairment Compared to Participants With Normal Renal Function

A Phase 1 Open-label Trial to Evaluate the Pharmacokinetics and Safety Following Single Dose of Tavapadon in Participants With Severe Renal Impairment Compared to Participants With Normal Renal Function

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05404542
Enrollment
14
Registered
2022-06-03
Start date
2022-05-10
Completion date
2023-08-14
Last updated
2024-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal Impairment

Keywords

Healthy Volunteer, Severe Renal Impairment

Brief summary

The primary purpose is to assess the effect of renal impairment on the PK of tavapadon following administration of a single oral dose in participants with severe renal impairment relative to age, body weight, and sex-matched participants with normal renal function.

Interventions

Oral tablets

Sponsors

Cerevel Therapeutics, LLC
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

Key Inclusion Criteria: 1. Body mass index of ≥18.0 to 40.0 kilograms per meter square (kg/m\^2), inclusive, and a total body weight \>50 kilograms (kg) \[(110 pounds (lbs)\]. 2. Age that is within ±10 years of the median age for the severe renal impairment cohort. Bodyweight that is within ±15 kg of the median bodyweight for the severe renal impairment cohort. 3. Severe renal function: estimated glomerular filtration rate (eGFR) \<30 mL/min (not requiring dialysis) determined using Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. 4. Stable disease, defined as no clinically significant changes in disease status as documented by the most recent eGFR assessment (within at least 3 months before Screening). 5. Stable concomitant medications for the management of individual participants medical history. Key

Exclusion criteria

1. Serious risk of suicide in the opinion of the investigator. 2. History of substance or alcohol use disorder (excluding nicotine or caffeine) within 12 months prior to signing the informed consent form (ICF). 3. Receipt of severe acute respiratory syndrome coronavirus 2(SARS-CoV2) vaccine or booster within 7 days of planned dosing. 4. Have recently been diagnosed with symptomatic Coronavirus Disease 2019 (COVID-19) or test positive for COVID-19 within 30 days prior to signing the ICF. 5. Positive drug screen including tetrahydrocannabinol (THC). 6. Positive result for human immunodeficiency virus (HIV) antibody, hepatitis B surface antigen, hepatitis B core antibody, or hepatitis C antibody with detectable viral ribonucleic acid (RNA) levels at Screening. 7. Positive drug screen including THC (except with a vail prescription other than medical marijuana). 8. Participants who have received an organ transplant or are currently waiting for an organ transplant and are listed on the national transplant list. 9. Participants who require dialysis. 10. Participant with nephrotic syndrome. 11. Abnormal hemoglobin. 12. Abnormal blood pressure measurement or heart rate at Screening or Check-in. Note: Other protocol defined Inclusion/

Design outcomes

Primary

MeasureTime frame
Maximum Observed Plasma Concentration (Cmax) of Tavapadonpre-dose and at multiple timepoints post-dose up to Day 7
Area Under the Plasma Concentration-time Curve from Time Zero to Time t (AUC0-t) of Tavapadonpre-dose and at multiple timepoints post-dose up to Day 7
Area Under the Plasma Concentration-time Curve from Time Zero to Infinity (AUCinf) of Tavapadonpre-dose and at multiple timepoints post-dose up to Day 7

Secondary

MeasureTime frame
Number of Participants with Clinically Significant Abnormalities in Laboratory ValuesDay 1 up to Follow-up (Day 15)
Number of Participants with Adverse Events (AEs) and AEs by SeverityDay 1 up to Follow-up (Day 15)
Number of Participants with Change in Columbia Suicide Severity Rating Scale (C-SSRS) ScoreDay 1 up to Follow-up (Day 15)
Number of Participants with Clinically Significant Abnormalities in Physical and Neurological Examination ResultsDay 1 up to Follow-up (Day 15)
Number of Participants with Clinically Significant Abnormalities in Electrocardiogram (ECG) ValuesDay 1 up to Follow-up (Day 15)
Number of Participants with Clinically Significant Abnormalities in Vital Sign ValuesDay 1 up to Follow-up (Day 15)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026