A Study to Evaluate Zilucoplan Injected Subcutaneously Either by a Prefilled Syringe or an Auto-injector in Healthy Adult Participants
- Registration Number
- NCT06511076
- Lead Sponsor
- UCB Biopharma SRL
- Brief Summary
The purpose of this study is to assess the bioequivalence pharmacokinetics, safety, tolerability and device deficiencies of zilucoplan (ZLP) in healthy adult participants
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 14
Inclusion Criteria
- Participant must be 18 to 55 years of age inclusive, at the time of signing the informed consent.
- Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, and cardiac monitoring.
- Participants must be vaccinated with a quadrivalent vaccine and serogroup B vaccine against meningococcal infections (N. meningitidis) at least 2 weeks before the first administration of IMP if not previously vaccinated within 3 years prior to the start of IMP administration. Study participants who are not previously vaccinated may receive Menactra® (quadrivalent vaccine) and Bexsero® (serogroup B vaccine) during the Screening Period, 2 weeks prior to initiating IMP.
- Body mass index (BMI) ≥18.5 to ≤30.0kg/m2 at the Screening Visit.
- Male and/or female:
- A male participant must agree to use contraception during the Treatment Period as detailed in Appendix 4 of the protocol and for at least 40 days (approximately 5 half lives) after the last dose of IMP and refrain from donating sperm during this period.
- A female participant is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies:
- Not a female/woman of childbearing potential (WOCBP) OR
- A WOCBP who agrees to follow the contraceptive guidance during the Treatment Period and for at least 40 days (approximately 5 half lives), corresponding to time needed to eliminate IMP after the last dose of IMP.
- Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form and in the protocol.
Exclusion Criteria
- Participant has a history of or current significant medical disorder, psychiatric disorder, or laboratory abnormality that in the opinion of the Investigator makes the study participant unsuitable for participation in the study, including any previous or current cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrinological, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking IMP; or interfering with the interpretation of data.
- Current or recent systemic infection within 2 weeks before the first administration of IMP or infection requiring intravenous antibiotics within 4 weeks before the first administration of IMP.
- Current history of alcohol or drug use disorder, as defined in Diagnostic and Statistical Manual of Mental Disorders V, within the previous 6 months.
- Participant has a known hypersensitivity to any components of the IMP or comparative drugs (and/or an investigational device) as stated in the protocol.
- Intended use of over-the-counter or prescription medication, vitamins, herbal/traditional medicines (including St John's Wort) or dietary supplements (excluding medicines for external use), with the exception of those specified in the Protocol, within 2 weeks before the first administration of IMP.
- Participant has used hepatic enzyme-inducing drugs (eg, glucocorticoids, phenobarbital, isoniazid, phenytoin, rifampicin) within 2 months before the first administration of IMP.
- Participant has previously participated in this study or participant has previously been assigned to treatment in a study of the medication under investigation in this study.
- Participant has participated in another study of an IMP (and/or an investigational device) within the previous 30 days or 5 half-lives (whichever is longer), or is currently participating in another study of an IMP (and/or an investigational device).
- Participants with clinically relevant abnormalities in a standard 12-lead electrocardiogram (ECG) at the Screening Visit as judged by the Investigator.
- Presence of hepatitis B surface antigen at the Screening Visit or within 3 months prior to dosing.
- Positive hepatitis C antibody test result at the Screening Visit or within 3 months prior to starting IMP. NOTE: Participants with positive hepatitis C antibody due to prior resolved disease can be enrolled if a confirmatory negative hepatitis C ribonucleic acid (RNA) test is obtained.
- Positive hepatitis C RNA test result at the Screening Visit or within 3 months prior to first dose of IMP. NOTE: Test is optional and participants with negative hepatitis C antibody test are not required to also undergo hepatitis C RNA testing.
- Positive human immunodeficiency virus antibody test at the Screening Visit.
- Positive syphilis test at the Screening Visit.
- Positive throat swab for N. meningitidis at the Screening Visit or a prior history of meningitis.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Treatment Sequence AB Zilucoplan Study participants randomized to this arm will receive a single subcutaneous (sc) injection of zilucoplan using pre-filled syringe (ZLP-PFS; Treatment A) as reference and a single sc injection of zilucoplan using an autoinjector (ZLP-AI; Treatment B) as test in the treatment sequence A-B on Day 1 of each Treatment Period. Treatment Sequence BA Zilucoplan Study participants randomized to this arm will receive a single sc injection of zilucoplan using pre-filled syringe (ZLP-PFS; Treatment A) as reference and a single sc injection of zilucoplan using an autoinjector (ZLP-AI; Treatment B) as test in the treatment sequence B-A on Day 1 of each Treatment Period.
- Primary Outcome Measures
Name Time Method AUC0-t (area under the plasma concentration-time curve from time 0 to time t) From Day 1 (Predose) up to Day 35 of each treatment period AUC0-t: Area under the plasma concentration-time curve from time 0 to time t
Cmax (maximum observed plasma concentration) From Day 1 (Predose) up to Day 35 of each treatment period Cmax: Maximum observed plasma concentration
AUC area under the plasma concentration-time curve from time 0 to infinity) From Day 1 (Predose) up to Day 35 of each treatment period AUC: Area under the plasma concentration-time curve from time 0 to infinity
- Secondary Outcome Measures
Name Time Method Occurrence of nonserious adverse device effects (ADE) from Day 1 up to the end of study (EOS) visit or early termination (ET) visit From Day 1 up to the end of study (EOS) visit or early termination (ET) visit (up to Day 77) A nonserious adverse device effect (ADE) is defined as an adverse event related to the use of an investigational medical device.
Occurrence of treatment-emergent adverse events (TEAEs) from Day 1 up to the end of study (EOS) visit or early termination (ET) visit From Day 1 up to the end of study (EOS) visit or early termination (ET) visit (up to Day 77) Treatment-emergent adverse events (TEAEs) are any untoward medical incidence in a subject during administered study treatment, whether or not these events are related to study treatment.
Occurrence of serious adverse events (SAEs) from Day 1 up to the end of study (EOS) visit or early termination (ET) visit From Day 1 up to the end of study (EOS) visit or early termination (ET) visit (up to Day 77) A SAE is defined as any untoward medical occurrence that, at any dose:
* Results in death
* Is life-threatening
* Requires inpatient hospitalization or prolongation of existing hospitalization
* Results in persistent disability/incapacity
* Is a congenital anomaly/birth defect
* Important medical eventsOccurrence of serious adverse device effects (SADE) from Day 1 up to the end of study (EOS) visit or early termination (ET) visit From Day 1 up to the end of study (EOS) visit or early termination (ET) visit (up to Day 77) A serious adverse device effect (SADE) is defined as an adverse device effect that has resulted in any of the consequences characteristic of a SAE.
Trial Locations
- Locations (1)
DV0012 1
🇳🇱Groningen, Netherlands