A First-In-Human Study With a Single Ascending Dose of UCB7858 in Healthy Volunteers

NCT ID: NCT02879877

Last Updated: 2019-08-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 78 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-07-11
• Study Completion Date: 2018-01-31

Brief Summary

This study is designed to evaluate the safety and tolerability of UCB7858 when given as single ascending doses administered by intravenous or subcutaneous infusion in healthy subjects.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: QUADRUPLE

Study Groups

UCB7858 (intravenous)

Various single doses, administered to various cohorts.

Group Type: EXPERIMENTAL

UCB7858

Intervention Type: DRUG

Placebo (intravenous)

Single dose placebo comparator for each cohort of iv administration.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

UCB7858 (subcutaneous)

Various single doses, administered to various cohorts.

Group Type: EXPERIMENTAL

UCB7858

Intervention Type: DRUG

Placebo (subcutaneous)

Single dose placebo comparator for each cohort of sc administration.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Interventions

UCB7858

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Healthy male and female volunteers who gave their written consent by signing the Informed Consent Form
• Subjects in the age between 18 and 55 years old with normal weight as determined by a body mass index (BMI) between 18 and 30 kg/m^2, with a body weight of at least 50 kg for male subjects or 45 kg for female subjects
• Subject has clinical laboratory test results within the reference ranges of the testing laboratory or outside the reference range of the laboratory but considered as not clinically significant by the Investigator
• Subjects has blood pressure (BP) and pulse within normal range in a supine position after 5 minutes rest
• Subject's electrocardiogram (ECG) is considered normal or abnormal but clinically non significant
• Female subjects of childbearing potential must agree to use a highly effective method of birth control during the study and for a period of 6 months after dosing of IMP

Exclusion Criteria

• Subject has any medical or psychiatric condition that, in the opinion of the Investigator, could jeopardize or would compromise the subject's ability to participate in this study: Subject has any acute or chronic illness which, in the opinion of the Investigator, may place the subject at risk because of participation in the study. Subject has any clinically relevant abnormal findings in physical examination, laboratory tests, vital signs, or ECG, which, in the opinion of the Investigator, may place the subject at risk because of participation in the study.
• Tests positive for Human Immunodeficiency Virus (HIV)-1 or-2 antibodies, Hepatitis B Virus (HBV) surface antigen, or Hepatitis C Virus (HCV) antibody at Screening
• Any of the following hematological function tests at the Screening Visit: Hemoglobin <111g/L (for women) or <113g/L (for men)
• Absolute neutrophil count <1.5x10^9/L (<1000/mm^3); Platelets <150x10^9/L
• Female subject who is breastfeeding, pregnant, or plans to become pregnant during the study or within 6 months following the final dose of the IMP

• Subject has a known hypersensitivity to dressings, local anesthetics, suture material, or relevant local/oral antibiotic therapy
• Subject has or had a history of a known inflammatory dermatological condition including eczema, atopic dermatitis, candidiasis, psoriasis, recurrent or persistent fungal infection, or bacterial infections
• Subject uses steroid or nonsteroidal anti-inflammatory drug (NSAID)-containing skin creams on a regular basis
• Subject has used NSAID or NSAID-containing medications within 7 days of randomization
• Subject has used skin emollients within 7 days of randomization on the area of the skin from buttocks
• Subject has tattoos, nevi, or other skin abnormalities such as keloids (or history of keloids, folliculitis, or acne vulgaris) that may, in the opinion of the Investigator, interfere with study assessments.
• Subject has been participating in recreational sun-bathing, or use of sun-bed, on the area of the skin from buttocks within 7 days of Screening
• Subject has active neoplastic disease or history of neoplastic disease within 5 years of the Screening Visit
• Subject has a history of moderate to severe allergic reaction to medication(s) including biologics (for subjects in Cohort 11 only).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

UCB Biopharma S.P.R.L.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

UCB Cares

Role: STUDY_DIRECTOR

UCB (+1 844 599 2273)

Locations

Up0029 001

London, , United Kingdom

Countries

United Kingdom

Other Identifiers

2016-001129-15

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

UP0029

Identifier Type: -

Identifier Source: org_study_id