An Open-Label Study Following Oral Dosing of Seladelpar to Participants With Primary Biliary Cholangitis (PBC) and Hepatic Impairment (HI)
1期
已完成
NCT04950764
| 适应症 | Primary Biliary Cholangitis, Compensated Cirrhosis, Hepatic Impairment |
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| 分期 | 1期 |
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| 申办方 | Gilead Sciences |
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| 状态 | 已完成 |
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| 受试者人数 | 24 人 |
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| 干预（药物） | Seladelpar |
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| 开始日期 | 2021年11月16日 |
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| 完成日期 | 2025年2月24日 |
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| 结果公布日 | 2026年5月4日 |
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摘要
The Effect of Hepatic Impairment on The Pharmacokinetics of Seladelpar: An Open-Label Study Following Oral Dosing of Seladelpar to Participants with Primary Biliary Cholangitis (PBC) and Hepatic Impairment (HI)
Part A: Pharmacokinetic (PK) Parameter: Cmax of Seladelpar and Its Metabolites (M1, M2, and M3)
Day 1: Predose; 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 48 and 72 hours postdose · nanograms per milliliter (ng/mL)
| Part A: Cohort 1 - CP-A Without PHT (Seladelpar 10 mg) | 182.0 ± 60.68 nanograms per milliliter (ng/mL) |
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| Part A: Cohort 2 - CP-A With PHT (Seladelpar 10 mg) | 367.7 ± 238.28 nanograms per milliliter (ng/mL) |
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| Part A: Cohort 3 - CP-B (Seladelpar 10 mg) | 359.2 ± 158.61 nanograms per milliliter (ng/mL) |
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| Part A: Cohort 4 - CP-C (Seladelpar 10 mg) | 388.5 ± 153.45 nanograms per milliliter (ng/mL) |
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| Part A: Cohort 1 - CP-A Without PHT (Seladelpar 10 mg) | 20.08 ± 9.012 nanograms per milliliter (ng/mL) |
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| Part A: Cohort 2 - CP-A With PHT (Seladelpar 10 mg) | 33.17 ± 9.913 nanograms per milliliter (ng/mL) |
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| Geometric Least-squares Mean Ratio | 183 (95% CI 114–295) |
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Part A: PK Parameter: Tmax of Seladelpar and Its Metabolites (M1, M2, and M3)
Day 1: Predose; 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 48 and 72 hours postdose · hours (h)
| Part A: Cohort 1 - CP-A Without PHT (Seladelpar 10 mg) | 1.208 hours (h) |
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| Part A: Cohort 2 - CP-A With PHT (Seladelpar 10 mg) | 0.758 hours (h) |
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| Part A: Cohort 3 - CP-B (Seladelpar 10 mg) | 1.250 hours (h) |
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| Part A: Cohort 4 - CP-C (Seladelpar 10 mg) | 1.250 hours (h) |
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| Part A: Cohort 1 - CP-A Without PHT (Seladelpar 10 mg) | 4.000 hours (h) |
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| Part A: Cohort 2 - CP-A With PHT (Seladelpar 10 mg) | 4.500 hours (h) |
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Part A: PK Parameter: AUC0-t of Seladelpar and Its Metabolites (M1, M2, and M3)
Day 1: Predose; 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 48 and 72 hours postdose · h*ng/mL
| Part A: Cohort 1 - CP-A Without PHT (Seladelpar 10 mg) | 800 ± 214 h*ng/mL |
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| Part A: Cohort 2 - CP-A With PHT (Seladelpar 10 mg) | 1390 ± 504 h*ng/mL |
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| Part A: Cohort 3 - CP-B (Seladelpar 10 mg) | 1390 ± 812 h*ng/mL |
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| Part A: Cohort 4 - CP-C (Seladelpar 10 mg) | 1970 ± 416 h*ng/mL |
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| Part A: Cohort 1 - CP-A Without PHT (Seladelpar 10 mg) | 239 ± 41.3 h*ng/mL |
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| Part A: Cohort 2 - CP-A With PHT (Seladelpar 10 mg) | 324 ± 117 h*ng/mL |
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| Geometric Least-squares Mean Ratio | 171 (95% CI 124–235) |
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本页整理自 ClinicalTrials.gov 的公开数据，不构成医疗建议，也不构成投资建议。请务必咨询专业医师。