Clinical Trials Directory

Trials / Completed

CompletedNCT04015492

Study to Compare How the Body Distributes and Excretes the Drugs Jivi (BAY 94-9027) and Adynovi in Patients With Severe Hemophilia A (Bleeding Disorder Resulting From a Lack of Blood Clotting Factor VIII)

Single Dose, Open Label, Randomized, Cross-over Study in Participants With Severe Hemophilia A Comparing Pharmacokinetic Parameters of BAY 94-9027 and Adynovi

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Bayer · Industry
Sex
Male
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study is being conducted to compare how the body distributes and excretes the drugs Jivi (BAY 94-9027) and Adynovi. Jivi is a recently approved blood clotting Factor VIII (FVIII) medication for the treatment of hemophilia A (bleeding disorder resulting from a lack of FVIII). Both drugs are FVIII products which have been manufactured via recombinant technology and have an extended half-live, i.e. they will stay longer in the body than other FVIII products. Therefore these products act longer in the body which reduces the frequency of drug injections. To compare the two drugs, a cross-over design was chosen, i.e. each patient will receive both products one after another. Patients participating in this study will receive one dose of Jivi and one dose of Adynovi. Both drugs are injected into a vein. Observation will last for about 10 weeks, and blood samples will be taken from the participants to measure the blood levels of FVIII. Generic name of Jivi is Damoctocog-alfa-pegol, generic name of Adynovi is Rurioctocog alfa pegol.

Conditions

Interventions

TypeNameDescription
BIOLOGICALDamoctocog-alfa-pegol (BAY94-9027, Jivi)Single dose, 50 IU/kg BAY94-9027 (IU: international Units)
BIOLOGICALRurioctocog alfa pegol (Adynovi)Single dose, 50 IU/kg Adynovi

Timeline

Start date
2019-08-08
Primary completion
2019-10-25
Completion
2020-01-29
First posted
2019-07-11
Last updated
2020-12-21

Locations

1 site across 1 country: Bulgaria

Regulatory

Source: ClinicalTrials.gov record NCT04015492. Inclusion in this directory is not an endorsement.