Study of ALXN2050 in Participants With Renal Impairment

NCT04623710 | Completed Phase 1 FDA Drug

• 1 other identifier: ALXN2050-HV-108
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 2

Brief Summary

This study will investigate the impact of impaired renal function on the plasma pharmacokinetics of ALXN2050 in order to provide dosing recommendations for future indications in individuals with impaired renal function.

Conditions

Renal Impairment; Healthy

Keywords

Factor D Inhibitor; Pharmacokinetics; Pharmacodynamics; Safety; ALXN2050

Outcome Measures

Primary Outcomes (4)

• Area Under The Concentration-time Curve From Time 0 To The 12-hour Time Point (AUC0-12) Of Plasma ALXN2050 After Steady-state

  Up to 72 hours postdose

• Area Under The Concentration-time Curve Calculated To The Last Observable Concentration At Time t (AUCt) Of Plasma ALXN2050 After Steady-state

  Up to 72 hours postdose

• Maximum (Peak) Steady-state Plasma Concentration (Cmax,ss) Of Plasma ALXN2050

  Up to 72 hours postdose

• Time To Reach Maximum (Peak) Plasma Concentration Following ALXN2050 Administration At Steady-state (Tmax,ss)

  Up to 72 hours postdose

Secondary Outcomes (4)

• Change From Baseline In Complement Factor D Concentration At 24, 48, And 72 Hours Postdose

  Baseline, 24, 48, and 72 hours postdose

• Change From Baseline In Plasma b Fragment Of Complement Factor B Concentration

  Baseline, up to 72 hours postdose

• Change From Baseline In Complement Alternative Pathway Activity

  Baseline, up to 72 hours postdose

• Number Of Participants Receiving ALXN2050 With Treatment-emergent Adverse Events

  Day 1 (postdose) through follow-up (30 [+/- 2] days after last study drug administration)]

Study Arms (4)

Cohort 1: Severe Impaired Renal Function

EXPERIMENTAL

Participants will receive ALXN2050.

Drug: ALXN2050

Cohort 2: Moderate Impaired Renal Function

EXPERIMENTAL

Participants will receive ALXN2050.

Drug: ALXN2050

Cohort 3: Mild Impaired Renal Function

EXPERIMENTAL

Participants will receive ALXN2050.

Drug: ALXN2050

Cohort 4: Healthy Control

EXPERIMENTAL

Participants will receive ALXN2050.

Drug: ALXN2050

Interventions

ALXN2050 DRUG

ALXN2050 (120 milligrams) will be administered orally twice daily on Days 1 through 3, with an additional dose (120 milligrams) administered orally on the morning of Day 4.

Also known as: ACH-0145228 (formerly)

Cohort 1: Severe Impaired Renal Function; Cohort 2: Moderate Impaired Renal Function; Cohort 3: Mild Impaired Renal Function; Cohort 4: Healthy Control

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Body weight must be at least 50.0 kilograms (kg) and body mass index (BMI) within the range of 18.0 - 40.0 kg/meter squared (m\^2) (inclusive) at the time of signing the informed consent.
• Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
• Must agree to receive prophylactic antibiotics to mitigate the potential risk of meningococcal infection.
• Participants with Impaired Renal Function
• Aside from impaired renal function, sufficiently healthy for study participation based upon medical history, physical examination, neurological examination, laboratory tests, vital signs, and electrocardiograms (ECGs).
• A clinical diagnosis of impaired stable renal function.
• No clinically significant change in renal status at least 1 month prior to first dose of study intervention and is not currently or has not previously been on hemodialysis or did not have any history of peritoneal dialysis.
• Stable creatinine clearance.
• Must be on a stable medication regimen. Concomitant medications must be approved by Alexion unless presented in the list of common concurrent medications for participants with impaired renal function.
• Matched Healthy Control Participants with Normal Renal Function
• Must match the sex and the race (similar ratio of white and non-white) of participants with impaired renal function, and at screening, age must be within ± 10 years and BMI must be within ± 20% of the matching participants with impaired renal function
• Healthy as determined by medical evaluation, including medical history, physical examination, neurological examination, laboratory tests, vital signs, and ECGs, and who possess a baseline eGFR ≥ 90 mL/min/1.73 m\^2, based on MDRD equation at screening.

You may not qualify if:

• History or presence of seizures, head injury, head trauma, or any other brain disorder.
• History of procedures that could alter absorption or excretion of orally administered drugs.
• History of meningococcal infection or a first-degree relative with a history of meningococcal infection.
• Body temperature ≥38.0°Celcius at screening or check-in or history of febrile illness or other evidence of infection, systemic or otherwise, within 14 days prior to the first dose of study intervention.
• Participants with CH50 results outside the reference ranges at screening, unless approved by Alexion
• Significant blood loss or donation of blood within 3 months prior to the first dose of study intervention, donation of plasma within 30 days prior to the first dose of study intervention, receipt of blood products within 6 months prior to first dose of study intervention, or receipt of a vaccine within 30 days prior to the first dose of study intervention.
• Current enrollment or past participation within the last 30 days (or 5 half-lives, whichever is longer) prior to the first dose of study intervention in the current clinical study or any other clinical study involving an investigational study intervention or any other type of medical research.
• History or presence of drug or alcohol abuse within 1 year prior to the first dose of study intervention, current tobacco user, or positive results for alcohol and/or drug screen at screening or check-in.
• Pregnant or lactating.
• Does not produce sufficient urine output to permit urine sampling at screening and/or check-in or has a history of urinary incontinence prior to check-in.
• History of kidney transplant or actively on a transplant waiting list prior to check-in.
• Any acute or chronic non-renal condition prior to check-in that would limit the participant's ability to complete or participate in this clinical study.

Sponsors & Collaborators

• Alexion Pharmaceuticals, Inc.: lead

Study Sites (2)

Clinical Trial Site

Hialeah, Florida, 33014, United States

Location

Clinical Trial Site

Orlando, Florida, 32809, United States

Location

MeSH Terms

Conditions

Renal Insufficiency

Interventions

rhoA GTP-Binding Protein

Condition Hierarchy (Ancestors)

Kidney Diseases; Urologic Diseases; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Male Urogenital Diseases

Intervention Hierarchy (Ancestors)

rho GTP-Binding Proteins; Monomeric GTP-Binding Proteins; GTP-Binding Proteins; GTP Phosphohydrolases; Acid Anhydride Hydrolases; Hydrolases; Enzymes; Enzymes and Coenzymes; Carrier Proteins; Proteins; Amino Acids, Peptides, and Proteins; Intracellular Signaling Peptides and Proteins

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: BASIC SCIENCE
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 5, 2020
• First Posted: November 10, 2020
• Study Start: July 8, 2021
• Primary Completion: February 18, 2022
• Study Completion: March 21, 2022
• Last Updated: September 29, 2023

Record last verified: 2023-09

Data Sharing

• IPD Sharing: Will not share

Locations

US (2)