Study of Oral ALXN1840 at 2 Dose Strengths in Healthy Adults

Healthy Clinical Trial

Official title:

A Phase 1, Randomized, Open-Label, 2-Way Crossover Study to Assess the Single-Dose Pharmacokinetics of ALXN1840 Enteric-Coated Tablets at 2 Dose Strengths in Healthy Adult Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05303324
• Other study ID #: ALXN1840-HV-104
• Secondary ID: 2019-000516-28
• Status: Completed
• Phase: Phase 1
• Start date: July 4, 2019
• Est. completion date: October 9, 2019

Study information

• Verified date: September 2022
• Source: Alexion
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess the relative bioavailability of ALXN1840 administered orally as a single enteric-coated (EC) tablet (reference, Treatment A) versus three EC tablets (test, Treatment B).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: October 9, 2019
• Est. primary completion date: October 9, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Body weight = 100 kilograms (kg) and body mass index within the range 18-25 kg/meter squared, inclusive, at Screening.

• Negative serum pregnancy test at Screening and Day -1 for all women of childbearing potential.

• Willing to adhere to contraception requirements.

• Satisfactory medical assessment with no clinically significant or relevant abnormalities.

Exclusion Criteria:

• Current or recurrent/chronic disease

• Positive test for hepatitis B surface antigen or human immunodeficiency virus antibody at Screening.

• Acute or chronic hepatitis C virus infection.

• History of hypersensitivity to ALXN1840 or its excipients or any significant allergic reaction.

• Use of prescription medications (excluding oral contraceptives) within 14 days prior to dosing on Day 1, except with prior approval of the Sponsor.

• Participation (that is, last protocol-required study visit) in a clinical study within 90 days before initiation of dosing on Day 1.

• Serum ceruloplasmin value outside of the normal range at Screening

• Female participants who were breastfeeding.

• Prior exposure to ALXN1840.

• Major surgery or hospitalization within 90 days prior to dosing on Day 1.

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• ALXN1840
Participants received ALXN1840 at Hour 0 on Day 1 of the dosing period.

Locations

Country	Name	City	State
United Kingdom	Clinical Trial Site	London

Sponsors (1)

Lead Sponsor	Collaborator
Alexion

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Observed (Plasma) Concentration (Cmax) of Total Molybdenum	The pharmacokinetic (PK) data of plasma total molybdenum were analyzed in the scope of this study as a surrogate measure for ALXN1840. Whole blood samples were collected for the measurement of plasma concentrations of total molybdenum via inductively coupled plasma-mass spectroscopy (ICP-MS).	Up to 240 hours postdose
Primary	Area Under The Plasma Concentration Versus Time Curve From Time 0 (Dosing) to the Last Quantifiable Concentration (AUCt) of Total Molybdenum	The PK data of plasma total molybdenum were analyzed in the scope of this study as a surrogate measure for ALXN1840. Whole blood samples were collected for the measurement of plasma concentrations of total molybdenum via ICP-MS.	Up to 240 hours postdose
Secondary	Number of Participants With a Treatment-Emergent Adverse Event (TEAEs)	An adverse event (AE) was any untoward medical occurrence in a participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. TEAE was an AE that started during or after the first dose, or started prior to the first dose and increased in severity after the first dose. A related TEAE was defined as having a reasonable possibility the study intervention caused the AE as assessed by the investigator. Serious AEs (SAEs) were defined as any untoward medical occurrence that met at least 1 of the following serious criteria: resulted in death, was life-threatening, required in-patient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, was a congenital anomaly/birth defect, other medically important serious event. A summary of all SAEs and Other AEs (nonserious) regardless of causality is located in the 'Reported Adverse Events' Section.	Baseline up to Day 43