To Evaluate the Safety, and Pharmacokinetics of Parscaclisib in Participants With Normal Renal Function and Renal Impairment.
Study Details
Study Description
Brief Summary
The purpose of the study is to evaluate the pharmacokinetics and safety of parsaclisib in participants With normal renal function and participants with renal impairment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Treat Group 1 : Normal Renal Function eGFR: ≥ 90 mL/min/1.73 m^2 |
Drug: parsaclisib
parsaclisib will be administered orally after 8 hours of fasting.
Other Names:
|
| Experimental: Treat Group 2 : Mild Renal Impairment eGFR: 60-89 mL/min/1.73 m^2 |
Drug: parsaclisib
parsaclisib will be administered orally after 8 hours of fasting.
Other Names:
|
| Experimental: Treat Group 3 : Moderate Renal Impairment eGFR: 30-59 mL/min/1.73 m^2 |
Drug: parsaclisib
parsaclisib will be administered orally after 8 hours of fasting.
Other Names:
|
| Experimental: Treat Group 4 : Severe Renal Impairment eGFR: 15-29 mL/min/1.73 m^2 and not on Hemo Dialysis |
Drug: parsaclisib
parsaclisib will be administered orally after 8 hours of fasting.
Other Names:
|
| Experimental: Treat Group 5 : Kidney Failure eGFR: < 15 mL/min/1.73 m^2 on Hemo Dialysis |
Drug: parsaclisib
parsaclisib will be administered orally after 8 hours of fasting.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Pharmacokinetics Parameter Groups1-4 : Cmax of parsaclisib [4 Days]
Maximum Observed Plasma Concentration of parsaclisib
- Pharmacokinetics Parameter Groups 1-4 : AUC 0-∞ of parsaclisib [4 Days]
Area Under the Concentration-time Curve From 0 to Infinity of parsaclisib
- Pharmacokinetics Parameter Groups 1-4 : AUC(0-t) of parsaclisib [4 Days]
Area Under the concentration- time curve up to the last measurable concentration of parsaclisib
- Pharmacokinetics Parameter Group 5: Cmax of parsaclisib [4 Days for period 1 and 2]
Maximum Observed Plasma Concentration of parsaclisib
- Pharmacokinetics Parameter Group 5 : AUC 0-∞ of parsaclisib [4 Days for period 1 and 2]
Area Under the Concentration-time Curve From 0 to Infinity of parsaclisib
- Pharmacokinetics Parameter Group 5: AUC(0-t) of parsaclisib [4 Days for period 1 and 2]
Area Under the concentration- time curve up to the last measurable concentration of parsaclisib
Secondary Outcome Measures
- Number of Treatment Emergent Adverse Events (TEAE) Groups 1-4 [up to 11 Days]
Adverse events reported for the first time or worsening of a pre-existing event after first dose of study drug/treatment.
- Pharmacokinetics Parameter Groups 1-4 : tmax of parsaclisib [4 Days]
Time to reach maximum plasma concentration of parsaclisib
- Pharmacokinetics Parameter Groups 1-4 : t1/2 of parsaclisib [4 Days]
Apparent terminal phase disposition half-life of parsaclisib
- Pharmacokinetics Parameter Groups 1-4 : CL/F of parsaclisib [4 Days]
Oral dose clearance of parsaclisib
- Pharmacokinetics Parameter Groups 1-4 : Vz/F of parsaclisib [4 Days]
Apparent oral dose volume of distribution of parsaclisib
- Pharmacokinetics Parameter Group 5 : tmax of parsaclisib [4 Days for period 1 and 2]
Time to reach maximum plasma concentration of parsaclisib
- Pharmacokinetics Parameter Group 5 : t1/2 of parsaclisib [4 Days for period 1 and 2]
Apparent terminal phase disposition half-life of parsaclisib
- Pharmacokinetics Parameter Group 5 : CL/F of parsaclisib [4 Days for period 1 and 2]
Oral dose clearance of parsaclisib
- Pharmacokinetics Parameter Group 5 : Vz/F of parsaclisib [4 Days for period 1 and 2]
Apparent oral dose volume of distribution of parsaclisib
- Pharmacokinetics Parameter Group 5 during Dialysis - : AUC1-5 of parsaclisib [4 Days for period 1 and 2]
Area Under the Concentration-time Curve From 1 to 5 hrs. of parsaclisib
- Number of Treatment Emergent Adverse Events (TEAE) Group 5 [up to 18 Days]
Adverse events reported for the first time or worsening of a pre-existing event after first dose of study drug/treatment.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Participants will be classified at screening by renal function based on eGFR as calculated by the MDRD formula and requirement for HD (Group 5).
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Participants eligible for Group 5 with ESRD have received HD for at least 3 months prior to screening.
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Participants eligible for Group 1 should be in good health as determined by no clinically significant deviations from normal for medical history, physical examination, vital signs, 12-lead ECGs, or clinical laboratory determinations at screening or Day -1.
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Participants eligible for Groups 2 through 5 may have medical findings consistent with their degree of renal dysfunction.
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Participants with abnormal findings considered not clinically significant by the medical monitor or investigator are eligible.
0Body mass index within the range 18.0 to 40.0 kg/m2 (inclusive) at screening.
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Willingness to avoid pregnancy or fathering children.
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Ability to swallow and retain oral medication.
Exclusion Criteria:
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History of uncontrolled or unstable cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, hematopoietic, psychiatric, and/or neurological disease within 6 months of screening. Evidence of rapidly deteriorating renal function.
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Participants who have a current, functioning organ transplant or have a scheduled organ transplant within 6 weeks after check-in.
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History of malignancy within 5 years of screening, with the exception of cured basal cell carcinoma, squamous cell carcinoma of the skin, ductal carcinoma in situ, or Gleason 6 prostate cancer.
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History of clinically significant gastrointestinal disease or surgery (cholecystectomy and appendectomy are allowed) that could impact the absorption of study drug.
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Participants eligible for Group 1 who have a history of renal disease or renal injury as indicated by an abnormal, clinically significant renal function profile at screening or Day -1.
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Participants eligible for Groups 2 through 5 who have had a change in disease status within 30 days of screening, as documented by the participant's medical history, deemed clinically significant by the investigator.
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History or current diagnosis of uncontrolled or significant cardiac disease indicating significant risk of safety for participation in the study.
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Any major surgery within 4 weeks of screening.
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Donation of blood to a blood bank within 4 weeks of screening (within 2 weeks for plasma only).
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Blood transfusion within 4 weeks of Day -1 (for Groups 1 through 4) or Period 1, Day
-
1 (Group 5).
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Chronic or current active infectious disease requiring systemic antibiotic, antifungal, or antiviral treatment.
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Positive test for HBV (HBsAg, HBsAg antibody, and hepatitis B core antibody), HCV (HCV antibody), or HIV. Participants whose results are compatible with prior immunization for HBV may be included at the discretion of the investigator.
Participants eligible for Group 1 who have used tobacco- or nicotine-containing products within 6 months of screening.
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Participants eligible for Groups 2 through 5 who smoke > 10 cigarettes per day or equivalent use of other tobacco- or nicotine-containing products and are unwilling to refrain from tobacco or nicotine use on dosing days and abide by CRU restrictions.
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Positive breath test for ethanol or positive urine or serum screen for drugs of abuse that is not otherwise explained by permitted concomitant medications.
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Current treatment or treatment within 30 days or 5 half-lives (whichever is longer) of study drug administration with another investigational medication or current enrollment in another investigational drug study.
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Current treatment or treatment within 30 days or 5 half-lives (whichever is longer) of study drug administration with strong or moderate inducer or inhibitor of CYP3A4, P-gp,or BCRP.
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For participants eligible for Group 1, use of prescription drugs within 14 days of study drug administration or nonprescription medications/products (including vitamins, minerals, and phytotherapeutic/herbal/plant-derived preparations) within 7 days of study drug administration. However, occasional paracetamol, ibuprofen, and standard-dose vitamins are permitted.
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For participants eligible for Groups 2 through 5, use of prescription drugs within 14 days of study drug administration, with the exception of established therapy for renal disease and the treatment of associated disorders that have been stable for at least 7 days prior to study drug administration, as approved by the investigator and in consultation with the sponsor's medical monitor.
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Current or recent history (within 30 days before screening) of a clinically significant bacterial, fungal, parasitic, or mycobacterial infection, or currently receiving systemic antibiotics. Current clinically significant viral infection at screening or check-in.
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History of any significant drug allergy (such as anaphylaxis or hepatotoxicity) deemed clinically relevant by the investigator.
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Inability to undergo venipuncture or tolerate venous access.
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Participants eligible for Group 5 that are not expected to continue HD treatment for the duration of the study.
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Receipt of live (including attenuated) vaccines or anticipation of need for such a vaccine during the study (Note: nonlive or inactivated vaccines are allowed up to 2 weeks prior to the first dose of study drug).
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Known hypersensitivity or severe reaction to parsaclisib or excipients of parsaclisib.
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History of alcoholism within 3 months of screening.
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Women who are pregnant or breastfeeding.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Orange County Research Center | Tustin | California | United States | 92780 |
| 2 | Clinical Pharmacology of Miami | Hialeah | Florida | United States | 33014 |
| 3 | Orlando Clinical Research Center | Orlando | Florida | United States | 32809 |
| 4 | Prism Research | Saint Paul | Minnesota | United States | 55114 |
Sponsors and Collaborators
- Incyte Corporation
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- INCB 50465-109