A Single and Multiple Ascending Dose Study of ANX009 in Normal Healthy Volunteers (NHV)

Safety and Tolerability in Healthy Volunteers Clinical Trial

Official title:

A Phase 1, Randomized, Double-blind, Placebo-controlled Single and Multiple Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Subcutaneous ANX009 in Normal Healthy Volunteers (NHV)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04535752
• Other study ID #: ANX009-NHV-01
• Status: Completed
• Phase: Phase 1
• Start date: October 30, 2020
• Est. completion date: June 26, 2021

Study information

• Verified date: August 2021
• Source: Annexon, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety, tolerability, pharmakokinetics and pharmacodynamics of single and repeated doses of ANX009

Description:

In this first in human, phase 1, randomized, double-blind, placebo-controlled study, single and multiple ascending doses of ANX009 or placebo will be administered to 48 healthy subjects. Single Ascending Dose (SAD): Each SAD subject will participate for approximately 4 weeks (3 nights in-clinic confinement). Multiple Ascending Dose: Each MAD subject will participate for approximately 6 weeks (17 nights in-clinic confinement). All subjects will be contacted (in clinic visit or phone call) 6 months after study completion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: June 26, 2021
• Est. primary completion date: June 26, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 59 Years

Eligibility

Inclusion Criteria:

1. Healthy male and non-pregnant, non-lactating female volunteers =18 to 59 years of age.

2. Females must be postmenopausal, surgically sterilized or willing and able to use highly effective methods of contraception from screening through the final study visit.

3. Males with a partner of childbearing potential must agree to use contraception from Screening through the final study visit.

4. Documented history within 5 years of screening of previous vaccination against encapsulated bacterial pathogens (MAD cohorts only).

5. Complete the full sequence of protocol-related doses, procedures and evaluations.

6. No alcohol and drugs of abuse at screening and baseline or through study completion.

7. Discontinue use of nutritional supplements and prescription and over-the-counter medications (vitamins are allowed).

8. No new tattoos/piercings or elective surgery from screening through the End of Study visit

9. Ability to understand and provide written informed consent. Exclusion Criteria:

Subjects must not meet any of the following criteria:

1. Clinically significant, ongoing illness or medical condition that would jeopardize the safety of the subject, limit participation, or compromise the interpretation of the safety data derived from the subject.

2. Clinically significant findings on the screening or Baseline ECG or physical examination.

3. Clinically significant abnormalities on screening or Baseline laboratory assessments.

4. An ANA titer = 1:160.

5. History of any autoimmune disease.

6. History of meningitis or septicemia.

7. Clinically significant infection that required medical intervention (not including antibiotic prophylaxis) within 1 month prior to study drug dosing.

8. Known genetic deficiencies of the complement cascade system or immunodeficiency.

9. Treatment with an investigational therapeutic agent within 30 days prior to study drug dosing.

10. Use of immunosuppressants or corticosteroids within 30 days prior to study drug dosing.

11. Active alcohol abuse, drug abuse or substance abuse.

12. Hypersensitivity to any of the excipients in the ANX009 drug product or active substance.

13. History of previous sensitivities or allergic or anaphylactic reactions to previous medication injections.

14. Positive for HIV Ab, Hepatitis C Ab or Hepatitis B surface antigen (HBsAg) at screening.

15. Body weight less than 50 kg or greater than 125 kg.

16. BMI less than 18 or greater than 30 (Asians greater than 27).

17. Current smoker defined as any occasional or daily smoking of tobacco products

Related Conditions & MeSH terms

• Safety and Tolerability in Healthy Volunteers

Intervention

Drug:
• ANX009
Single or multiple ascending dose
• Placebo
Single or multiple ascending dose

Locations

Country	Name	City	State
Australia	Site 1	Melbourne

Sponsors (2)

Lead Sponsor	Collaborator
Annexon, Inc.	Nucleus Network Ltd

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety: Number of Participants Who Experienced Treatment-Emergent Adverse Events	Incidence and severity of treatment-emergent adverse events (AEs). AEs will be coded using MedDRA and severity of AEs will be graded using National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI CTCAE).	[Time Frame: Up to Day 29 for SAD; up to Day 43 for MAD]
Secondary	Pharmacodynamics: Total Amount of Complement Protein in Blood (CH50)	Serum samples will be obtained to determine the amount of CH50. CH50 will be measured at a local laboratory. CH50 will be measured at a local laboratory.	Up to Week 6
Secondary	Pharmacodynamics: Amount of C1 in Blood (C1q)	Serum samples will be obtained to determine the amount of C1q. C1q will be measured using a validated enzyme-linked immunosorbent assay (ELISA) method.	Up to Week 6
Secondary	Pharmacokinetic: Maximum Observed Serum Concentration (Cmax) of ANX009	Single-dose Cmax (Day 1 in SAD and MAD) and multiple-dose Cmax (Day 14 in MAD) will be determined. Blood samples will be obtained, and serum concentrations determined using a validated ELISA method.	Pre-dose, immediately after dose, and 0.5, 1, 2, 4, 6, 8, 12, 24 hours post-dose on Day 1 (SAD and MAD) and 36, 48, and 72 hours post-dose Day 1 (SAD)
Secondary	Pharmacokinetic: Time to Maximum Observed Serum Concentration (Tmax) of ANX009	Tmax will be determined on Day 1 in SAD and MAD and on Day 14 in MAD. Blood samples will be obtained, and serum concentrations determined using a validated enzyme-linked immunosorbent assay (ELISA) method.	Pre-dose, immediately after dose, and 0.5, 1, 2, 4, 6, 8, 12, 24 hours post-dose on Day 1 (SAD and MAD) and 36, 48, and 72 hours post-dose Day 1 (SAD)
Secondary	Pharmacokinetic: Area Under the ANX009 Serum Concentration-Time Curve to Last Sample (AUC 0-t) and extrapolated through infinity (AUC 0-inf)	AUC 0-t will be determined on Day 1 in SAD and on Day 14 in MAD. Blood samples will be obtained, and serum concentrations determined using a validated enzyme-linked immunosorbent assay (ELISA) method.	Pre-dose, immediately after dose, and 0.5, 1, 2, 4, 6, 8, 12, 24 hours post-dose on Day 1 (SAD and MAD) and 36, 48, and 72 hours post-dose Day 1 (SAD)
Secondary	Pharmacokinetic: Terminal Half-Life (t1/2) of ANX009	Half-life will be determined on Day 1 in SAD and on Day 1 and Day 14 in MAD. Blood samples will be obtained, and serum concentrations determined using a validated enzyme-linked immunosorbent assay (ELISA) method	Pre-dose, immediately after dose, and 0.5, 1, 2, 4, 6, 8, 12, 24 hours post-dose on Day 1 (SAD and MAD) and 36, 48, and 72 hours post-dose Day 1 (SAD)