Study of Coagulation Factor VIIa Variant Marzeptacog Alfa (Activated) in Adult Subjects With Hemophilia A and B

Hemophilia A With Inhibitor Clinical Trial

Official title:

Phase 2 Study to Evaluate the Pharmacokinetics, Efficacy and Safety of a Daily Subcutaneous Treatment Regimen With Marzeptacog Alfa (Activated) for Bleeding Prophylaxis in Adult Subjects With Hemophilia A and B Subjects With an Inhibitor

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03407651
• Other study ID #: MAA-201
• Status: Completed
• Phase: Phase 2
• Start date: December 18, 2017
• Est. completion date: April 13, 2019

Study information

• Verified date: June 2021
• Source: Catalyst Biosciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Phase 2, multi-center, open-label study designed to evaluate the PK, bioavailability, PD, efficacy and safety of a daily subcutaneous [SC] treatment regimen with MarzAA for bleeding prophylaxis in 12 adult subjects with hemophilia A or B with an inhibitor and history of frequent spontaneous bleeding episodes.

Description:

Multi-center, open-label Phase 2 study to evaluate the PK, bioavailability, PD, efficacy and safety of a daily SC treatment regimen with MarzAA for bleeding prophylaxis in adult subjects with hemophilia A or B with an inhibitor. The study will enroll and dose, both intravenously and subcutaneously, a total of 12 adult male subjects with severe congenital hemophilia A or B with an inhibitor, and history of frequent bleeding episodes during the 6 months prior to enrollment, as per the individual's bleeding and treatment records. Once a subject is enrolled into the trial, the study will be conducted in three parts (occurring consecutively): Part 1a (24 hours): Single IV administration of MarzAA; Part 1b (48 hours): Single SC administration of MarzAA; Part 2: Daily SC administration. Dose escalation in Part 2 will occur if breakthrough bleeding occurs. Subjects are treated for 50 days at the final dose level required.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 11
• Est. completion date: April 13, 2019
• Est. primary completion date: March 15, 2019
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Severe congenital hemophilia A or B with an inhibitor.
• History of frequent spontaneous bleeding episodes.
• Male, age 18 or older.
• Affirmation of informed consent with signature confirmation before any trial-related activities.

Exclusion Criteria:

• Receiving prophylaxis treatment.
• Previous participation in a clinical trial evaluating a modified rFVIIa agent.
• Known positive antibody to FVII or FVIIa detected by central laboratory at screening.
• Have a coagulation disorder other than hemophilia A or B.
• Significant contraindication to participation.

Related Conditions & MeSH terms

• Hemophilia A
• Hemophilia A With Inhibitor
• Hemophilia B
• Hemophilia B With Inhibitor

Intervention

Biological:
• Coagulation Factor VIIa variant
Single intravenous injection of MarzAA, followed by single subcutaneous injection of MarzAA, followed by daily subcutaneous injection of MarzAA for 50 days at final dose level required.

Locations

Country	Name	City	State
Armenia	Hematology Center after Prof. R. Yeolyan	Yerevan
Georgia	JSC "K.Eristavi National Center of Experimental and Clinical Surgery"	Tbilisi
Georgia	LTD M.Zodelava Hematology Centre	Tbilisi
Georgia	LTD Medinvest - Institute of Hematology and Transfusiology	Tbilisi
Poland	Gabinet Lekarski, Bartosz Korczowski	Rzeszów
Russian Federation	Regional Clinical Hospital	Kemerovo
Russian Federation	FGU Kirov Scientific Research	Kirov
Russian Federation	Center for Hemophilia Treatment	Saint Petersburg
South Africa	Haemophilia Comprehensive Care Centre	Johannesburg

Sponsors (1)

Lead Sponsor	Collaborator
Catalyst Biosciences

Countries where clinical trial is conducted

Armenia,  Georgia,  Poland,  Russian Federation,  South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bleeding Episode Prevention Success	Annualized bleed rate (ABR; spontaneous and total) during Part 2 when on final MarzAA dose level versus recorded historical ABR. The analysis of the primary endpoint (annualized bleeding rate ABR for spontaneous and traumatic bleeds) of the final dose of MarzAA each subject was treated was based on the 1-sample test compared to a predefined rate assumed for the on-demand therapy. The latter was assumed to be 12 (or 1 bleed per month), which was the minimum ABR for each subject according to inclusion criterion 2 (defined as the H0), with no maximum value. A higher score indicated a worse outcome. ABR is on a scale of 0 to 365, with a lower score reflective of a lower number of bleeding events in a year.	Day 1 of final MarzAA dose level - Day 50
Secondary	Occurrence of Breakthrough Bleeding	Occurrence of breakthrough bleeds requiring escalation to higher dose level	From Day 5 of dose level until occurrence of event
Secondary	Occurrence of Clinical Thrombotic Event	Occurrence of clinical thrombotic event not attributable to another cause	From date of first dose until date of first occurrence of clinical event, assessed up to treatment Day 50
Secondary	Coagulation Assessment - Prothrombin Time	Change in coagulation parameter (prothrombin time [PT]) from pre-dose. Min-max values are reflective of the highest and lowest values for all measured timepoints.	From date of pre-dose to 24 hours (Part 1a), pre-dose to 48 hours (Part 1b), and pre-dose to Day 50 (Part 2)
Secondary	Coagulation Assessment - Activated Partial Thromboplastin Time	Change in coagulation parameter (activated partial thromboplastin time [aPTT]) from pre-dose. Min-max values are reflective of the highest and lowest values for all measured timepoints.	From date of pre-dose to 24 hours (Part 1a), 48 hours (Part 1b), to Day 50/end of study (Part 2)
Secondary	Coagulation Assessment - Fibrinogen	Change in coagulation parameter (fibrinogen) from pre-dose. Min-max values are reflective of the highest and lowest values for all measured timepoints.	From date of pre-dose to 24 hours (Part 1a), 48 hours (Part 1b), or Day 50 (Part 2).
Secondary	Number of Events of Antibody Formation	Occurrence of antibody formation resulting in a decreased endogenous level of coagulation Factor VII (FVII) or Factor VII activated (FVIIa)	From time of first dose of MarzAA until date of first occurrence of clinical event, assessed up to treatment Day 50
Secondary	Number of Events of an Antibody Response	Occurrence of an antibody response to MarzAA and whether it is inhibitory and cross-reactive to wild-type recombinant coagulation FVII (wt-rFVII) or wt-FVIIa.	From time of first dose of MarzAA until date of first occurrence of clinical event, assessed up to treatment Day 50.
Secondary	Thrombogenicity Assessment	Number of participants with clinically significant levels of thrombogenicity markers (D-dimer, Prothrombin fragment 1+2 (F1+2), and thrombin-antithrombin complex [TAT]), based on standard laboratory tests and clinical examination with a specific search for any signs of thrombosis	From time of pre-dose of MarzAA at Day 1 until date of first occurrence of thrombotic event, assessed up to treatment Day 50.