A Study of Subcutaneous Gefurulimab Using Prefilled Syringe Versus Autoinjector in Healthy Adult Participants

NCT ID: NCT06208488

Last Updated: 2024-10-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 175 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-22
• Study Completion Date: 2024-09-28

Brief Summary

This study will evaluate the pharmacokinetics (PK), pharmacodynamics (PD), safety, immunogenicity, and device performance of gefurulimab.

Detailed Description

This is an open-label, randomized, parallel-group study.

The study consists of 2 periods: a Screening Period (up to 70 days), and an Evaluation Period of 92 days.

Separate randomization lists will be produced for each weight stratum (50 to < 70 kg, 70 to < 90 kg, and 90 to < 110 kg) and within each of the three weight strata, participants will be randomized 1:1:1:1:1:1 to one of the six combinations of device (prefilled syringe with needle safety device [PFS-SD] or autoinjector [AI]) and injection site (abdomen, thigh, or upper arm),

Participants will receive a single dose of 600 mg gefurulimab on Day 1, will be residential at the clinical unit until Day 5, will have visits on Day 8, quaque week (once a week) [qw] thereafter until Day 50, and quaque 2 week (once every two weeks) [q2w] from Day 50 until Day 92 during the Evaluation Period.

The total study duration is up to 162 days.

Conditions

Healthy Adult Participants

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Gefurulimab PFS-SD

Participants will be administered gefurulimab as a single dose of 600 mg by PFS-SD on the abdomen, thigh, or upper arm.

Group Type: EXPERIMENTAL

Gefurulimab PFS-SD

Intervention Type: DRUG

Participants will receive a single 600 mg dose of Gefurulimab PFS-SD subcutaneously (SC) on Day 1.

Gefurulimab AI

Participants will be administered gefurulimab as a single dose of 600 mg by AI on the abdomen, thigh, or upper arm.

Group Type: EXPERIMENTAL

Gefurulimab AI

Intervention Type: DRUG

Participants will receive a single 600 mg dose of Gefurulimab AI subcutaneously (SC) on Day 1.

Interventions

Gefurulimab PFS-SD

Participants will receive a single 600 mg dose of Gefurulimab PFS-SD subcutaneously (SC) on Day 1.

Intervention Type: DRUG

Gefurulimab AI

Participants will receive a single 600 mg dose of Gefurulimab AI subcutaneously (SC) on Day 1.

Intervention Type: DRUG

Other Intervention Names

ALXN1720; ALXN1720

Eligibility Criteria

Inclusion Criteria

1. Participants must be 18 to 65 years of age inclusive, at the time of signing the informed consent.

2. Body weight within ≥ 50 to < 110 kg and body mass index (BMI) within the range 18.5 to 30 kg/m2 (inclusive)

3. Participants who are healthy as determined by medical evaluation with no clinically significant or relevant abnormalities as determined by medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory evaluation.

4. QT interval corrected using Fridericia's formula (QTcF) ≤ 450 msec for male participants and ≤ 460 msec for female participants at Screening and prior to dosing on Day 1.

5. Documented vaccination against meningococcal infection from serogroups A, C, W, and Y and serogroup B.

6. Male and female participants should adhere to study-specific contraceptive methods.

Exclusion Criteria

1. History of any Neisseria meningitidis infection.

2. History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrinological, hematological, or neurological disorders.

3. Abnormal blood pressure as determined by the Investigator.

4. History of latent or active TB (Tuberculosis) or exposure to endemic areas.

5. Allergy to monoclonal antibodies.

6. Clinically significant multiple or severe drug allergies, intolerance to topical corticosteroids, or severe posttreatment hypersensitivity reactions.

7. Lymphoma, leukemia, or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for 3 years.

8. Current or chronic history of liver disease.

9. Known hepatic or biliary abnormalities.

10. Active systemic bacterial, viral, or fungal infection within 14 days prior to dosing.

11. History of allergy or intolerance to penicillin or cephalosporin.

12. History of clinically significant allergic reaction (eg, anaphylaxis or angioedema) to any product.

13. Live vaccine(s) within 1 month prior to Screening or plans to receive such vaccines during the study.

14. Evidence of human immunodeficiency virus (HIV) infection (positive HIV type 1 or type 2 antibody).

15. Evidence of hepatitis B infection (positive hepatitis B surface antigen [HBsAg] or positive total hepatitis B core antibody [HBcAb] with negative surface antibody [anti-HBs]), or hepatitis C viral infection (positive HCV RNA).

16. Female participants who have a positive pregnancy test at Screening or Admission.

17. Positive prestudy drug/alcohol screen; positive result may be repeated once.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Parexel

INDUSTRY

Sponsor Role: collaborator

Alexion Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Research Site

Toronto, Ontario, Canada

Research Site

Laval, Quebec, Canada

Countries

Canada

Other Identifiers

ALXN1720-HV-103

Identifier Type: -

Identifier Source: org_study_id