- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT03961932
Safety and Pharmacokinetics of Linzagolix in Female Subjects With Normal and Impaired Renal Function
Evaluation of the Safety and Pharmacokinetics of a Single Dose of Linzagolix in Female Subjects With Normal and Impaired Renal Function
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
This is a Phase 1, non-randomized, open label, single-dose study to evaluate the effect of varying degrees of impaired renal function (i.e., mild, moderate, severe Renal Impairment (RI), and End-Stage Renal Disease (ESRD) on hemodialysis) on the PK, safety, and tolerability of linzagolix and its major metabolite, KP017.
Up to 40 adult female participants will be enrolled.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
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Florida
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Orlando, Florida, Stati Uniti, 32809
- Clinical Site
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Minnesota
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Saint Paul, Minnesota, Stati Uniti, 55114
- Clinical Site
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Key Inclusion Criteria:
Renal Impaired Subjects
- Adult female, ≥ 18 years of age at screening
- Has a BMI ≥ 18.0 and ≤ 42.0 kg/m^2 and weight ≥ 40 kg, at screening
Aside from RI, be sufficiently healthy for study participation based upon medical history, physical examination, vital signs, electrocardiograms (ECGs), and screening clinical laboratory profiles, as deemed by the Principal Investigator (PI) or designee
Subjects with mild, moderate, or severe RI:
Has estimated glomerular filtration rate (eGFR) based on Modification of Diet in Renal Disease (MDRD) equation at screening as follows:
- Severe RI only: ≤ 29 mL/min/1.73m^2 not on hemodialysis
- Moderate RI only: 30 - 59 mL/min/1.73m^2
- Mild RI only: 60 - 89 mL/min/1.73m^2
Has a stable renal function with no clinically significant change in renal status at least 1 month prior to study drug administration and is not currently or has not been previously on hemodialysis for at least 1 year
Subjects with ESRD:
- Subject is maintained on a stable hemodialysis regimen at least 3 times a week for at least 3 months prior to dosing
Healthy Subjects
- Health adult female will be matched to subjects with RI
- Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs or ECGs, as deemed by the PI or designee
- Baseline eGFR ≥ 90 mL/min/1.73m^2 at screening, based on the MDRD equation. Actual creatinine clearance, as determined by a 24-hour urine collection, may be used in place of or in conjunction with the MDRD equation at the PI's discretion
Key Exclusion Criteria:
Renal Impaired Subjects
- Had any major surgery within 4 weeks prior to dosing
- Presence of functioning renal transplant
- Has a surgical (e.g., hepatectomy, nephrectomy, digestive organ resection) or medical condition other than RI which might significantly alter the absorption, distribution, metabolism, or excretion of linzagolix and its metabolites, or which may jeopardize the subject's safety in case of participation in the study, in the opinion of the PI or designee
Healthy Subjects
- Has any clinically significant illness, as judge by the PI or designee, within 4 weeks prior to dosing
- Has laboratory values at screening or check-in which are deemed to be clinically significant (especially derangement within liver function test), unless agreed in advance by the PI and the Sponsor
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Scienza basilare
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Normal Renal Function
Healthy participants with Normal Renal Function (estimated Glomerular Filtration Rate (eGFR) ≥ 90 mL/min/1.73m^2)
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Una singola dose di 200 mg di linzagolix (2 compresse da 100 mg) verrà somministrata per via orale a digiuno
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Sperimentale: Mild Renal Impairment
Presence of Mild Renal Impairment (eGFR 60-89 mL/min/1.73m^2)
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Una singola dose di 200 mg di linzagolix (2 compresse da 100 mg) verrà somministrata per via orale a digiuno
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Sperimentale: Moderate Renal Impairment
Presence of Moderate Renal Impairment (eGFR 30-59 mL/min/1.73m^2)
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Una singola dose di 200 mg di linzagolix (2 compresse da 100 mg) verrà somministrata per via orale a digiuno
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Sperimentale: Severe Renal Impairment
Presence of Severe Renal Impairment (eGFR ≤ 29 mL/min/1.73m^2),
not on hemodialysis
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Una singola dose di 200 mg di linzagolix (2 compresse da 100 mg) verrà somministrata per via orale a digiuno
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Sperimentale: End-Stage Renal Disease
Presence of End-Stage Renal Disease (ESRD) requiring hemodialysis
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Una singola dose di 200 mg di linzagolix (2 compresse da 100 mg) verrà somministrata per via orale a digiuno
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Plasma pharmacokinetic (PK) parameter Cmax of linzagolix and of KP017
Lasso di tempo: predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Measurement of effect of renal impairment on PK of linzagolix and its metabolite KP017 by assessment of the maximum plasma concentration (Cmax).
Cmax directly determined from the plasma concentration-time profiles
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predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Plasma PK parameter Tmax of linzagolix and of KP017
Lasso di tempo: predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Measurement of effect of renal impairment on PK of linzagolix and its metabolite KP017 by assessment of the Time to reach Cmax (Tmax)
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predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Plasma PK parameter AUC0-t of linzagolix and of KP017
Lasso di tempo: predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Measurement of effect of renal impairment on PK of linzagolix and its metabolite KP017 by assessment of the AUC0-t (area under the concentration time curve, from time 0 to the last observed non-zero concentration)
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predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Plasma PK parameter T1/2 of linzagolix and of KP017
Lasso di tempo: predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Measurement of effect of renal impairment on PK of linzagolix and its metabolite KP017 by assessment of the T1/2 (Terminal half life)
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predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48, 72, 96, 120 hours post-dose
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Treatment emergent Adverse Events
Lasso di tempo: Day 1 to 14 days post-dose
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Assessment of safety and tolerability of a single dose linzagolix in renal impaired subjects compared with healthy control subjects by assessing the number, frequency and severity of treatment emergent Adverse Events
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Day 1 to 14 days post-dose
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Collaboratori e investigatori
Sponsor
Investigatori
- Direttore dello studio: ObsEva SA, Geneva
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 18-OBE2109-010
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Insufficienza renale
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National Cancer Institute (NCI)NCIC Clinical Trials Group; Southwest Oncology Group; Cancer and Leukemia Group BCompletatoCarcinoma a cellule renali a cellule chiare | Cancro a cellule renali in stadio III AJCC v7 | Cancro a cellule renali in stadio II AJCC v7 | Stadio I Renal Cell Cancer AJCC v6 e v7Stati Uniti, Canada, Porto Rico
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National Cancer Institute (NCI)TerminatoCarcinoma a cellule renali a cellule chiare | Carcinoma a cellule renali metastatico | Cancro a cellule renali in stadio III AJCC v7 | Cancro a cellule renali in stadio IV AJCC v7 | Cancro a cellule renali in stadio II AJCC v7 | Stadio I Renal Cell Cancer AJCC v6 e v7Stati Uniti
Prove cliniche su Linzagolix
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Kissei Pharmaceutical Co., Ltd.TerminatoEndometriosiStati Uniti, Canada, Porto Rico
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Kissei Pharmaceutical Co., Ltd.CompletatoEndometriosiStati Uniti, Austria, Bulgaria, Cechia, Francia, Polonia, Romania, Spagna, Ucraina
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Kissei Pharmaceutical Co., Ltd.TerminatoEndometriosiStati Uniti, Canada, Porto Rico
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Kissei Pharmaceutical Co., Ltd.CompletatoEndometriosiStati Uniti, Austria, Bulgaria, Cechia, Francia, Polonia, Romania, Spagna, Ucraina, Ungheria
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ObsEva SACompletatoInsufficienza epatica | Partecipanti saniStati Uniti
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Kissei Pharmaceutical Co., Ltd.Attivo, non reclutante