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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/show/NCT01439971




Registration number
NCT01439971
Ethics application status
Date submitted
26/08/2011
Date registered
22/09/2011
Date last updated
7/04/2017

Titles & IDs
Public title
Phase 1 Safety, Pharmacokinetics And Pharmacodynamics Study Of Recombinant Factor VIIa Variant (813d) In Adult Subjects With Hemophilia
Scientific title
An Ascending Single Dose Study To Evaluate The Safety, Tolerability And Pharmacokinetics/Pharmacodynamics Of Pf-05280602, A Recombinant Factor Viia Variant (813d), In Adult Hemophilia A And B Subjects With Or Without Inhibitors
Secondary ID [1] 0 0
2011-002170-23
Secondary ID [2] 0 0
B3051001
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Hemophilia A 0 0
Condition category
Condition code
Blood 0 0 0 0
Clotting disorders
Human Genetics and Inherited Disorders 0 0 0 0
Other human genetics and inherited disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - PF-05280602
Other interventions - PF-05280602
Other interventions - PF-05280602
Other interventions - PF-05280602
Other interventions - PF-05280602

Experimental: 1 -

Experimental: 2 -

Experimental: 3 -

Experimental: 4 -

Experimental: 5 -


Other interventions: PF-05280602
0.5 micrograms per kilogram of PF-05280602, IV infusion, single dose

Other interventions: PF-05280602
4.5 micrograms per kilogram of PF-05280602, IV infusion, single dose

Other interventions: PF-05280602
9.0 micrograms per kilogram of PF-05280602, IV infusion, single dose

Other interventions: PF-05280602
18.0 micrograms per kilogram of PF-05280602, IV infusion, single dose

Other interventions: PF-05280602
30.0 micrograms per kilogram of PF-05280602, IV infusion, single dose

Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change From Baseline in Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) - Supine blood pressure (BP) was measured with the participant's arm supported at the level of the heart, and recorded to the nearest millimeters of mercury (mmHg) after 5 minutes of rest. The same arm (preferably the dominant arm) was to be used throughout the study.
Timepoint [1] 0 0
Baseline, Day 2, Day 3, and Day 15
Primary outcome [2] 0 0
Change From Baseline in Body Weight
Timepoint [2] 0 0
Baseline, Day 2, Day 3, and Day 15
Primary outcome [3] 0 0
Change From Baseline in Body Temperature - Body temperature was measured by mouth (oral) or ear (tympanic). A temperature greater than 38.5 degree Celsius was considered a fever.
Timepoint [3] 0 0
Baseline, Day 2, Day 3, and Day 15
Primary outcome [4] 0 0
Change From Baseline in Respiration Rate - Respiration rate measured as respirations per minute (resp/min).
Timepoint [4] 0 0
Baseline, Day 2, Day 3, and Day 15
Primary outcome [5] 0 0
Change From Baseline in Supine Pulse Rate - Change from baseline is the vital sign value at Day 2, Day 3, and Day 15 minus vital sign value at baseline.
Timepoint [5] 0 0
Baseline, Day 2, Day 3, and Day 15
Primary outcome [6] 0 0
Number of Participants With Changes Since Previous Physical Examination - Physical examinations were conducted by a physician, trained physician's assistant, or nurse practitioner. A complete physical examination included head, ears, eyes, nose, mouth, skin, heart and lung examinations, lymph nodes, genitourinary, gastrointestinal, musculoskeletal, and neurological systems. The limited or abbreviated physical examination focused on general appearance, the respiratory and cardiovascular systems, as well as towards participant reported symptoms.
Timepoint [6] 0 0
Baseline (Day 0), Day 1, Day 2, Day 3, Day 15
Primary outcome [7] 0 0
Number of Participants With Potentially Clinically Significant Electrocardiogram (ECG) Findings - ECG findings of potential clinical concern were: PR interval greater than or equal to (>=)300 milliseconds (msec), >=25% increase from baseline for baseline values >200 msec, >=50% increase from baseline for baseline values less than or equal to (<=)200 msec; QRS complex >=140 msec or >=50% increase from baseline; QTcF interval (Fridericia's correction) >=450 msec or >=30 msec increase from baseline.
Timepoint [7] 0 0
Baseline through Day 15
Primary outcome [8] 0 0
Number of Participants With Treatment-Emergent Adverse Events (AEs), Serious Adverse Events (SAEs), and Withdrawals Due to AEs (Except Hemophilia AEs) - An AE was any untoward medical occurrence in a participant who received study drug. An SAE was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent are events between first dose of study drug and up to Day 15 that were absent before treatment or that worsened relative to pre-treatment state. AEs included both SAEs and non-SAEs.
Timepoint [8] 0 0
Baseline through Day 60
Primary outcome [9] 0 0
Number of Participants With Treatment-Emergent Hemophilia AEs and Withdrawals Due to Hemophilia AEs - Hemophilia AEs included spontaneous (no known contributing factor) and traumatic (known or presumed contributing factor/reason) bleeding episodes.
Timepoint [9] 0 0
Baseline through Day 60
Primary outcome [10] 0 0
Number of Treatment-Emergent AEs and SAEs by Severity (Except Hemophilia AEs) - AE severity were graded as mild, moderate, or severe. Mild severity AEs do not interfere with the participant's usual function. Moderate AEs interfere to some extent with the participant's usual function. Severe AEs interfere significantly with the participant's usual function.
Timepoint [10] 0 0
Baseline through Day 60
Primary outcome [11] 0 0
Number of Treatment-Emergent Hemophilia AEs by Severity - Mild severity AEs do not interfere with the participant's usual function. Moderate AEs interfere to some extent with the participant's usual function. Severe AEs interfere significantly with the participant's usual function.
Timepoint [11] 0 0
Baseline through Day 60
Primary outcome [12] 0 0
Number of Participants With Treatment-Emergent Abnormal Troponin-T Levels by Magnitude - Troponin-T is a cardiac marker for the evaluation of possible cardiovascular injury. Troponin-T levels of potential clinical concern are values >1.5 times the upper limit of normal (1.5X ULN) or >=2.5X ULN.
Timepoint [12] 0 0
Baseline through Day 15
Primary outcome [13] 0 0
Number of Participants With Treatment-Emergent Abnormal Anti-Thrombin III (ATIII) Levels by Magnitude - ATIII is a protein in the blood that blocks abnormal blood clots from forming. Low levels of ATIII can cause abnormal blood clots. ATIII levels of potential clinical concern are values <1X LLN and >1X ULN.
Timepoint [13] 0 0
Baseline through Day 3
Primary outcome [14] 0 0
Number of Participants With Treatment-Emergent Abnormal Tissue Factor Pathway Inhibitor (TFPI) Levels by Magnitude - TFPI is a polypeptide that can regulate blood coagulation. TFPI levels of potential clinical concern are values <1X LLN and >1X ULN.
Timepoint [14] 0 0
Baseline through Day 3
Primary outcome [15] 0 0
Number of Participants With Treatment-Emergent Laboratory Test Abnormalities (Normal Baseline) - The following laboratory parameters were analyzed: hematology (hemoglobin, hematocrit, red blood cell [RBC] count, platelets, leukocytes, total neutrophils, eosinophils, basophils, lymphocytes, monocytes); chemistry (total bilirubin, direct bilirubin, indirect bilirubin, aspartate aminotransferase [AST], alanine aminotransferase [ALT], alkaline phosphatase, creatinine, blood urea nitrogen [BUN], glucose, uric acid, sodium, potassium, chloride, bicarbonate, calcium, albumin, total protein, creatine kinase); urinalysis (urine white blood cell [WBC], urine RBC); other (troponin T).
Timepoint [15] 0 0
Baseline through Day 15
Primary outcome [16] 0 0
Number of Participants With Clinically Significant Laboratory Abnormalities Meeting Stopping Criteria - Clinically significant findings for stopping rules are: hemoglobin <8 grams/deciliter (g/dL) or >20% decrease from normal baseline; WBC >20,000 cells/mm^3 or <1,500 decrease with normal baseline; platelets <100,000/mm^3 or >33% decrease from baseline; total bilirubin >1.5X ULN; AST or ALT >2.5X ULN; alkaline phosphatase >3X ULN; creatinine >1.5X baseline; BUN >31.0 mg/dL; glucose <0.6 or >1.5X reference range; uric acid > ULN; sodium >150 or <130 mEq/L; potassium >5.5 or <3.0 mEq/L; calcium >11.5 or <8.0 mg/dL; albumin <2.0 g/L; total protein <5.0 g/L; positive D-dimer at Day 15; PT prolonged by 3 seconds above baseline; ATIII < LLN and >20% decrease from baseline; troponin-T values above the reference range; fibrinogen <0.75X LLN or >25% decrease from baseline.
Timepoint [16] 0 0
Baseline through Day 15
Primary outcome [17] 0 0
Number of Participants With Positive Immune Response (Anti-Drug Antibodies [ADA], PF-05280602 Inhibitor, Factor VIIa Inhibitor, Factor VII Inhibitor, and Depletion of Factor VII Activity) - Assays for the determination of a positive immune response was performed. An antibody immune response was defined as a confirmed post-treatment positive ELISA result in combination with a negative baseline sample ELISA result. Positive antibody immune responses to PF-05280602 by ELISA was evaluated for cross reactivity to NovoSeven RT and to Factor VII.
Timepoint [17] 0 0
Baseline through Day 60
Secondary outcome [1] 0 0
Maximum Observed Plasma Concentration (Cmax)
Timepoint [1] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [2] 0 0
Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) - Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast)
Timepoint [2] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [3] 0 0
Terminal Elimination Half-Life (t1/2) - t1/2 is the time measured for the plasma concentration to decrease by one half.
Timepoint [3] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [4] 0 0
Incremental Recovery (IncRec) - IncRec is the maximum rise in plasma concentration per administered dose.
Timepoint [4] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [5] 0 0
Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUCinf) - AUCinf is area under the plasma concentration-time curve from time 0 extrapolated to infinite time.
Timepoint [5] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [6] 0 0
Mean Residence Time (MRT) - MRT is AUMCinf/AUCinf, where AUMC is the area under the first moment curve.
Timepoint [6] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [7] 0 0
Volume of Distribution at Steady State (Vss) - Volume of distribution is defined as the theoretical volume in which the total amount of drug would need to be uniformly distributed to produce the desired blood concentration of a drug. Steady state volume of distribution (Vss) is the apparent volume of distribution at steady-state.
Timepoint [7] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [8] 0 0
Clearance (CL) - Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood (rate at which a drug is metabolized or eliminated by normal biological processes). Clearance obtained after intravenous infusion dose is influenced by the fraction of the dose absorbed.
Timepoint [8] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [9] 0 0
Time to Reach Maximum Observed Plasma Concentration (Tmax)
Timepoint [9] 0 0
Day 1 (pre-dose and 5 min, 10 min, 20 min, 30 min, 1 hr, 3 hr, 6 hr, 9 hr, and 12 hrs post-dose), Day 2 (24 hrs post-dose), Day 3 (48 hrs post-dose)
Secondary outcome [10] 0 0
Maximum Mean Decrease From Baseline in Prothrombin Time (PT) - PT measures how long it takes blood to clot. Maximum mean decrease from baseline at any time point was reported.
Timepoint [10] 0 0
Baseline through Day 15
Secondary outcome [11] 0 0
Maximum Mean Decrease From Baseline in Activated Partial Thromboplastin Time (aPTT) - aPTT is a blood test that characterizes blood coagulation. Maximum mean decrease from baseline at any time point was reported.
Timepoint [11] 0 0
Baseline through Day 15
Secondary outcome [12] 0 0
Maximum Mean Increase From Baseline in Thrombin Anti-Thrombin (TAT) Complexes - TAT complex is a parameter of coagulation and fibrinolysis. The normal reference range of values for TAT is 1 to 4.1 mcg/L. Elevated TAT concentrations may signify predisposition to thrombosis. Maximum mean increase from baseline at any time point was reported.
Timepoint [12] 0 0
Baseline through Day 3
Secondary outcome [13] 0 0
Maximum Mean Increase From Baseline in Prothrombin Fragments 1+2 - Prothrombin fragment 1+2 is a coagulation factor, released when prothrombin is cleaved by activated Factor X. Elevated plasma levels of prothrombin fragment 1+2 indicate high risk of thrombosis. Maximum mean increase from baseline at any time point was reported.
Timepoint [13] 0 0
Baseline through Day 3
Secondary outcome [14] 0 0
Maximum Mean Increase From Baseline in D-Dimers - D-dimer is an indicator of fibrin formation and its subsequent lysis and is a useful biomarker representing overall activation of blood coagulation. Maximum mean increase from baseline at any time point was reported.
Timepoint [14] 0 0
Baseline through Day 15
Secondary outcome [15] 0 0
Maximum Mean Increase From Baseline in Endogenous Thrombin Potential (ETP) - ETP was evaluated using a Thrombin Generation Assay (TGA), a validated automated ex-vivo assay that measures the ability of plasma to generate thrombin. Thrombin generation curves are generated and calculated using dedicated software. ETP is the area under the thrombin generation curve and represents the total amount of generated thrombin. Maximum mean increase from baseline at any time point was reported.
Timepoint [15] 0 0
Baseline through Day 3
Secondary outcome [16] 0 0
Maximum Mean Decrease From Baseline in Thrombin Generation Lag Time - The lag time is defined as the time to reach one sixth of the peak height and is a measure of the initiation phase. It is equivalent to the clotting time. Maximum mean decrease from baseline at any time point was reported.
Timepoint [16] 0 0
Baseline through Day 3
Secondary outcome [17] 0 0
Maximum Mean Increase From Baseline in Peak Thrombin Generation - The peak height is defined as the maximum thrombin concentration produced. Maximum mean increase from baseline at any time point was reported.
Timepoint [17] 0 0
Baseline through Day 3

Eligibility
Key inclusion criteria
- Male subjects 18 to <65 years old with severe hemophilia A or B with or without
inhibitors to FVIII or FIX.

- Subjects is willing and able to comply with the mandatory washout periods prior to
screening and prior to dosing and through 48 hours post dosing. At screening this
includes a washout of FIX for 96 hours and FVIII for 72 houts. At dosing this includes
a washout of FIX for 96 hours and FVIII and other hemostatic agents for 72 hours
through 48 hours post dosing.

- Subjects must agree and commit to using a a highly effective method of birth control
from the time of screening through four weeks after study drug administration.
Minimum age
18 Years
Maximum age
64 Years
Gender
Males
Can healthy volunteers participate?
No
Key exclusion criteria
- Presence of a bleeding disorder in addition to hemophilia A or B.

- Regular, concomitant therapy with immunomodulating drugs (eg, intravenous
immunoglobulin, and routine systemic corticosteroids).

- History of coronary artery disease, thrombolic disease or diagnosis of prothrombic
disorder.

Study design
Purpose of the study
Basic Science
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Other
Other design features
Phase
Phase 1
Type of endpoint(s)
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
Country [2] 0 0
United States of America
State/province [2] 0 0
Connecticut
Country [3] 0 0
United States of America
State/province [3] 0 0
Illinois
Country [4] 0 0
United States of America
State/province [4] 0 0
Ohio
Country [5] 0 0
United States of America
State/province [5] 0 0
Oregon
Country [6] 0 0
United States of America
State/province [6] 0 0
Pennsylvania
Country [7] 0 0
Belgium
State/province [7] 0 0
Bruxelles
Country [8] 0 0
Hungary
State/province [8] 0 0
Budapest
Country [9] 0 0
Italy
State/province [9] 0 0
Castelfranco Veneto (TV)
Country [10] 0 0
Italy
State/province [10] 0 0
Castelfranco Veneto - Treviso
Country [11] 0 0
Italy
State/province [11] 0 0
Milano
Country [12] 0 0
Italy
State/province [12] 0 0
Vicenza
Country [13] 0 0
New Zealand
State/province [13] 0 0
Christchurch
Country [14] 0 0
South Africa
State/province [14] 0 0
Eastern Cape
Country [15] 0 0
Turkey
State/province [15] 0 0
Izmir
Country [16] 0 0
United Kingdom
State/province [16] 0 0
London
Country [17] 0 0
United Kingdom
State/province [17] 0 0
Manchester

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Catalyst Biosciences
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This study hypothesizes that the study drug, PF-05280602 (at the selected doses) will be safe
to administer to subjects with severe Hemophilia A or B with or without inhibitors and will
demonstrate evidence of hemostatic activity. This is supported by the preclinical findings in
hemophilic animal models.
Trial website
https://clinicaltrials.gov/show/NCT01439971
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Pfizer CT.gov Call Center
Address 0 0
Pfizer
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No data has been provided for results reporting
Summary results
Other publications