A Trial to Evaluate Pharmacokinetics, Immunogenicity, Safety, and Tolerability of LEO 138559 in Healthy Japanese Subjects

Atopic Dermatitis Clinical Trial

Official title:

A Phase 1, Single-center, Double-blind, Randomized, Placebo-controlled, Single Ascending Dose Trial to Evaluate Pharmacokinetics, Immunogenicity, Safety, and Tolerability of LEO 138559 in Healthy Japanese Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05099133
• Other study ID #: LP0145-1486
• Status: Completed
• Phase: Phase 1
• Start date: November 3, 2021
• Est. completion date: June 28, 2022

Study information

• Verified date: July 2022
• Source: LEO Pharma
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This trial will investigate the pharmacokinetics, immunogenicity, safety, and tolerability of LEO 138559 in healthy Japanese subjects.

The trial consists of a screening period of up to 4 weeks, a single treatment with either LEO 138559 or placebo, and 8 follow-up visits to Day 85.

A total of 24 healthy subjects will be enrolled in 3 dose groups (n=8 per dose group) and randomized to either LEO 138559 or placebo in a ratio of 6:2.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: June 28, 2022
• Est. primary completion date: June 28, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria

1. Males and females between 18 to 65 years of age, inclusive, at the Screening visit

2. Japanese subjects to be considered ethnic Japanese must:

1. Be born in Japan with parents and grandparents (maternal and paternal) of Japanese descent

2. Not have lived outside of Japan for more than 10 years at the time of Screening

3. No significant change in lifestyle since leaving Japan, including diet.

3. Body mass index (BMI) between 18.0 and 32.0 kg/m2, inclusive, at the Screening visit.

4. Healthy, determined by pre-trial medical evaluation at Principal Investigator's discretion

Exclusion Criteria

1. Female subjects of childbearing potential who are not willing to use highly effective contraception.

2. Subject has clinically significant history or evidence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, immunological, musculoskeletal, infectious, metabolic, hematologic, neurological, or psychiatric disorder(s) as determined by the Principal Investigator or designee.

3. Subject has any surgical or medical condition that might significantly alter the absorption, distribution, metabolism, or excretion of any drug as determined by the Principal Investigator or designee.

4. Clinically significant infection within 4 weeks prior to randomization that may compromise the safety of the subject in the trial or the integrity of the trial. This includes clinically significant infections (common cold is allowed [with negative SARS-CoV-2 PCR test]) that in the opinion of the Investigator or Sponsor's Medical Monitor may compromise the safety of the subject in the trial, interfere with evaluation of the IMP, or reduce the subject's ability to participate in the trial.

5. History of any active skin infection within 1 week prior to Screening or randomization.

6. Subject who has taken immunosuppressive/immunomodulating medication within 4 weeks prior to randomization, topical corticosteroids, topical calcineurin inhibitors within 2 weeks prior to randomization, or was treated with biologics within 5 half-lives (if known) or 12 weeks prior to randomization, whichever is longer.

7. Subject has used over-the-counter (OTC) medications (including vitamins), or herbal remedies from 14 days prior to admission until the End-of-trial Visit. By exception, paracetamol/acetaminophen = 2 g per day is permitted.

8. History of chronic alcohol or drug abuse within 12 months prior to Screening, or any condition associated with poor compliance as judged by the Investigator.

9. Heavy smoker (daily average >10 cigarettes) within the last three months prior to Screening.

10. Subject is unwilling to avoid use of alcohol or alcohol-containing foods, medications, or beverages, within 36 hours prior to admission until discharge from the Clinical Unit.

11. Female subjects are breastfeeding or female subjects with a positive serum pregnancy test at the Screening visit or urine pregnancy test at admission.

12. Subject is unwilling to avoid consumption of coffee and caffeine-containing beverages within 48 hours prior to admission until discharge from the Clinical Unit.

13. Subject is unable to abstain from smoking (or other nicotine use) from admission until discharge from the Clinical Unit.

14. Subject scheduled to receive COVID-19 vaccination within 2 weeks before IMP administration.

15. Less than 4 weeks after the second COVID-19 vaccination or booster (if on a single dose vaccination, it should be 4 weeks after).

16. Live attenuated viral vaccine administration within 12 weeks before LEO 138559 or planned within three months after the last administration of LEO 138559.

Related Conditions & MeSH terms

• Atopic Dermatitis
• Dermatitis
• Dermatitis, Atopic

Intervention

Drug:
• LEO 138559
LEO 138559 is an antibody given by injection just under the skin.
• LEO 138559 Placebo
LEO 138559 placebo is given by injection just under the skin. LEO 138559 placebo contains the same excipients in the same concentration as LEO 138559, except the medical ingredient LEO 138559.

Locations

Country	Name	City	State
United States	LEO Investigational Site	Los Angeles	California

Sponsors (1)

Lead Sponsor	Collaborator
LEO Pharma

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	AUC0-last: the area under the concentration-time curve from pre-dose (time 0) to the time of the last quantifiable concentration	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Primary	AUC0-inf: area under the concentration-time curve from pre-dose (time 0) extrapolated to infinite time	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Primary	Cmax: maximum serum LEO 138559 concentration	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Primary	tmax: time of maximum serum LEO 138559 concentration	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Primary	t½: terminal elimination half-life	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Primary	CL/F: apparent total body clearance	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Primary	Vz/F: apparent volume of distribution	Pharmacokinetic endpoint to be determined from serum concentrations	From Day 1 to Day 85
Secondary	Number of treatment emergent adverse events		From Day 1 to Day 85
Secondary	Presence of binding anti-drug antibodies		Day 1(pre-dose), Day 29, Day 57, and Day 85