A Study to Evaluate the Effect of Renal Impairment and Dialysis Treatment on the Pharmacokinetics (PK) of a Single Intravenous (IV) TAK-954

NCT ID: NCT03296787

Last Updated: 2020-08-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 32 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-11-21
• Study Completion Date: 2019-08-09

Brief Summary

The purpose of this study is to evaluate the effect of varying degrees of renal function on the PK of TAK-954 following single-dose IV administration and to investigate the impact of hemodialysis on the PK of single IV doses of TAK-954.

Detailed Description

The drug being tested in this study is called TAK-954. This study will evaluate the effect of varying degrees of renal function on the PK of TAK-954 following single-dose IV administration and to investigate the impact of hemodialysis on the PK of single IV doses of TAK-954.

The study will enroll approximately up to 40 participants. Participants will be enrolled in one of the 5 treatment groups based on their renal impairment which will be determined based on Cockcroft and Gault (CG) equation as follows:

• Group A TAK-954 0.2 mg: Healthy Participants
• Group B TAK-954 0.2 mg: Mild Renal Impairment
• Group C TAK-954 0.2 mg: Moderate Renal Impairment
• Group D TAK-954 0.2 mg: Severe Renal Impairment or End-stage Renal Disease (ESRD) Without Hemodialysis
• Group E TAK-954 0.2 mg: End-stage Renal Disease (ESRD) With Hemodialysis

All participants in groups A to D will receive a single dose of TAK-954 and two single doses in Group E.

Enrollment in Group B (Mild) and Group E (ESRD requiring dialysis) will be based on assessment of safety and available PK data from Group C and Group D respectively.

This multi-center trial will be conducted in Czech Republic and Hungary. The overall time to participate in this study is approximately 8 weeks. Participants in Groups A to D will remain confined to clinic for 3 days. For both treatments, participants in Group E requiring dialysis will remain confined to clinic for 3 days. All participants will make a final visit to the clinic 10-14 days after receiving their last dose for a follow-up assessment.

Conditions

Renal Impairment; Healthy Volunteers

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Group A TAK-954 0.2 mg: Healthy Participants

Participants with normal renal function receive TAK-954 0.2 milligram (mg), infusion, intravenously in fasted state, once on Day 1 of a 6-day period.

Group Type: EXPERIMENTAL

TAK-954

Intervention Type: DRUG

TAK-954 intravenous infusion.

Group B TAK-954 0.2 mg: Mild Renal Impairment

Participants receive TAK-954 0.2 mg, infusion, intravenously in fasted state, once on Day 1 of a 6-day period.

Group Type: EXPERIMENTAL

TAK-954

Intervention Type: DRUG

TAK-954 intravenous infusion.

Group C TAK-954 0.2 mg: Moderate Renal Impairment

Participants receive TAK-954 0.2 mg, infusion, intravenously in fasted state, once on Day 1 of a 6-day period.

Group Type: EXPERIMENTAL

TAK-954

Intervention Type: DRUG

TAK-954 intravenous infusion.

Group D TAK-954 0.2 mg: Severe Renal Impairment

Participants without hemodialysis or End-stage Renal Disease (ESRD) receive TAK-954 0.2 mg, infusion, intravenously in fasted state, once on Day 1 of a 6-day period.

Group Type: EXPERIMENTAL

TAK-954

Intervention Type: DRUG

TAK-954 intravenous infusion.

Group E TAK-954 0.2 mg: End-stage Renal Disease (ESRD)

Participants with hemodialysis receive TAK-954 0.2 mg, infusion, intravenously in fasted state, once on Day 1 of a 4-day period followed by a minimum 13-day washout period, further followed by TAK-954 0.2 mg, infusion, intravenously in fasted state, once on Day 1 of a 4-day period.

Group Type: EXPERIMENTAL

TAK-954

Intervention Type: DRUG

TAK-954 intravenous infusion.

Interventions

TAK-954

TAK-954 intravenous infusion.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. All participants: Male and female participants (non-childbearing potential) who are aged 18 to 75 years, inclusive, with a body mass index (BMI) between 18 to 35 kilogram per square meter (kg/m^2).

2. Group A: As much as possible, the healthy participants with normal renal function (creatinine clearance [CLcr] greater than or equal to [>=] 90 milliliter per minute [mL/min]) should be comparable to participants with renal impairment with respect to median age and weight (approximately 50 percent [%] of healthy participants on each side of the median age and weight of currently enrolled renally-impaired participants grouped together), sex, and race. This will be decided by the investigators in discussion with Takeda.

3. Groups B to E: Participants who have stable RI, defined as no clinically significant change in disease status, as documented by the participant's most recent CLcr assessment; serum creatinine must not vary more than approximately 30% from Screening to Day -1 to confirm stable disease. Participants should also be in good health commensurate with their renal status.

• Group B: Participants with mild RI (CLcr 60 to less than [<] 90 mL/min).
• Group C: Participants with moderate RI (CLcr 30 to <60 mL/min).
• Group D: Participants with severe RI or ESRD but not requiring dialysis (CLcr <30 mL/min).
• Group E: Participants with ESRD requiring dialysis (<15 mL/min requiring hemodialysis at least 3 times/week, and having been on the same dialysis treatment regimen for at least 1 month before trial entry).

4. Participants should be on a stable drug regimen defined as not starting a new drug or changing dosage within 7 days or 5 half-lives (whichever is longer) before dosing with TAK-954.

Exclusion Criteria

1. All participants:

• Are renal allograft recipients within 1 year of screening.
• Have a history of gastrointestinal (GI) motility disorder or intestinal obstruction.
• Have urinary incontinence without catheterization.

2. Group A: Participants who, in the discretion of the investigator, have a history of clinically significant endocrine, GI, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological (including stroke and chronic seizures) abnormalities or diseases will be excluded from the trial.

3. Groups B to E:

• Receive dialysis other than intermittent dialysis (except Group E).
• Have renal disease secondary to hepatic disease (hepatorenal syndrome).
• At the discretion of the investigators, have any significant hepatic, cardiac, or pulmonary disease or participants who are clinically nephrotic.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Takeda

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Takeda

Locations

PRA CZ, s.r.o

Prague, Prague, Czechia

Fakultni Nemocnice Hradec Kralove

Hradec Králové, , Czechia

PRA Magyarorszag Kft.

Budapest, , Hungary

Szent Imre Egyetemi Oktatokorhaz Belgyogyazati Szakmak Matrix Intezet

Budapest, , Hungary

Countries

Czechia; Hungary

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

U1111-1196-9206

Identifier Type: REGISTRY

Identifier Source: secondary_id

2017-000715-16

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

TAK-954-1007

Identifier Type: -

Identifier Source: org_study_id