Pharmacokinetic Assessment of Standard Half-Life (SHL) FVIII, Extended Half-Life (EHL) FVIII, and Efanesoctocog Alfa (BIVV001) in Severe Hemophilia A

Hemophilia A Clinical Trial

Official title:

A Phase 1, Single-Site, Open-Label Study to Assess Pharmacokinetics of Efanesoctocog Alfa (BIVV001), Standard Half-Life and Extended Half-Life FVIII After Each Single Intravenous Injection in a Fixed Sequence, in Previously Treated Adults With Severe Hemophilia A

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05042440
• Other study ID #: PKM17085
• Secondary ID: 2021-000228-37U1
• Status: Completed
• Phase: Phase 1
• Start date: August 11, 2021
• Est. completion date: November 24, 2021

Study information

• Verified date: August 2023
• Source: Sanofi
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Primary objective • To assess the half-life of BIVV001, Standard Half-Life (SHL) rFVIII and Extended Half-Life (EHL) rFVIII after a single intravenous (IV) injection Secondary objectives - To characterize additional pharmacokinetic (PK) parameters of BIVV001, SHL rFVIII and EHL rFVIII after a single IV injection - To evaluate the safety and tolerability of a single IV injection of BIVV001

Description:

This is a Phase 1, single center, open-label, sequential treatment, 3-period fixed sequence study to assess PK profiles of BIVV001, SHL and EHL rFVIII after a single IV injection in male, previously treated patients, 18-65 years of age, with severe hemophilia A (defined as <1 IU/dL [<1%] endogenous FVIII). The expected duration of the study is up to approximately 67 days including - Screening and washout up to 28 days, - Advate® dosing, PK sampling, including washout: approximately 4 days, - Adynovi® dosing and PK sampling, including washout: approximately 7 days, - BIVV001 dosing and PK sampling: approximately 14 days, Remainder of Safety Observation Period: approximately 14 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: November 24, 2021
• Est. primary completion date: November 24, 2021
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Severe hemophilia A, defined as <1 IU/dL (<1%) endogenous FVIII activity.
• Previous treatment for hemophilia A, defined as at least 150 days documented prior exposure to any recombinant and/or plasma-derived FVIII and/or cryoprecipitate products at Day 1.
• Platelet count =100,000 cells/µL at Screening.
• A participant known to be human immunodeficiency virus (HIV) antibody positive, either previously documented or identified from screening assessments, must have the following results prior to enrollment. (CD4 lymphocyte count >200 cells/mm³ - Viral load of <400 copies/mL).

Exclusion Criteria:

• Any concurrent clinically significant liver disease that, in the opinion of the Investigator, would make the participant unsuitable for enrollment. This may include, but is not limited to cirrhosis, portal hypertension, and acute hepatitis.
• Serious active bacterial, fungal or viral infection (other than chronic hepatitis or HIV) present within 30 days of Screening.
• Other known coagulation disorder(s) in addition to hemophilia A.
• History of hypersensitivity or anaphylaxis associated with any FVIII product.
• History of a positive inhibitor test defined as =0.6 BU/mL, or any value greater than or equal to the lower sensitivity cut-off for laboratories with cut-offs for inhibitor detection between 0.7 and 1.0 BU/mL, or clinical signs or symptoms of decreased response to FVIII administrations. Family history of inhibitors will not exclude the participant.
• Positive inhibitor result, defined as =0.6 BU/mL at Screening.
• Major surgery within 8 weeks of Screening.
• Sensitivity to any of the study interventions, or components thereof, or drug or other allergy. The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Related Conditions & MeSH terms

• Hemophilia A

Intervention

Drug:
• Efanesoctocog alfa
Solution for injection Intravenous
• Octocog alfa
Solution for injection Intravenous
• Rurioctocog alfa pegol
Solution for injection Intravenous

Locations

Country	Name	City	State
Bulgaria	Investigational Site Number :1000001	Sofia

Sponsors (1)

Lead Sponsor	Collaborator
Sanofi

Country where clinical trial is conducted

Bulgaria, 

References & Publications (1)

Toshko Lissitchkov, Annemieke Willemze, Christelle Jan, Moshe Zilberstein, Suresh Katragadda, Pharmacokinetics of recombinant factor VIII in adults with severe hemophilia A: fixed-sequence single-dose study of octocog alfa, rurioctocog alfa pegol, and efa

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Half-life of BIVV001		BIVV001 period: Predose, and post-dose from 0.17 hr to 336 hr, and at day 28
Primary	Half-life of SHL rFVIII		Advate® period: Predose, and post-dose from 0.17 hr to 72 hr
Primary	Half-Life of EHL rFVIII		Adynovi® period: Predose, and post-dose from 0.17 hr to 120 hr
Secondary	Assessment of pharmacokinetic (PK) parameter : maximum activity (Cmax)		Predose of each period, 0.17 hr to 72 hr for Advate® ; 0.17 hr to 120 hr for Adynovi® ; 0.17 hr to 336 hr and at day 28 for BIVV001
Secondary	Assessment of PK parameter : clearance (CL)		Predose of each period, 0.17 hr to 72 hr for Advate® ; 0.17 hr to 120 hr for Adynovi® ; 0.17 hr to 336 hr and at day 28 for BIVV001
Secondary	Assessment of PK parameter : volume of distribution at steady state (Vss)		Predose of each period, 0.17 hr to 72 hr for Advate® ; 0.17 hr to 120 hr for Adynovi® ; 0.17 hr to 336 hr and at day 28 for BIVV001
Secondary	Assessment of PK parameter : area under the activity time curve extrapolated to infinity (AUC8)		Predose of each period, 0.17 hr to 72 hr for Advate® ; 0.17 hr to 120 hr for Adynovi® ; 0.17 hr to 336 hr and at day 28 for BIVV001
Secondary	Assessment of PK parameter : mean residence time (MRT)		Predose of each period, 0.17 hr to 72 hr for Advate® ; 0.17 hr to 120 hr for Adynovi® ; 0.17 hr to 336 hr and at day 28 for BIVV001
Secondary	Assessment of PK parameter : incremental recovery (IR)		Predose of each period, 0.17 hr to 72 hr for Advate® ; 0.17 hr to 120 hr for Adynovi® ; 0.17 hr to 336 hr and at day 28 for BIVV001
Secondary	Number of participants with Adverse events (AE), serious AEs and treatment-emergent AEs (TEAEs)		From Day 1 up to 28 days after administration of BIVV001 (total 39 days including Advate® and Adynovi® period)
Secondary	Development of inhibitors (neutralizing antibodies directed against FVIII)	Number of participants with development of inhibitors	Advate® period: Pre-dose; Adynovi® period: Pre-dose; BIVV001 period: Pre-dose and at day 14 and 28 after administration.