A Healthy Volunteer PK/PD, Safety and Tolerability Study of Second Generation Andexanet Alfa
A Phase 1 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Second Generation Andexanet Alfa Administered to Healthy Subjects
1 other identifier
interventional
153
1 country
1
Brief Summary
This is a randomized, double-blind, study in healthy volunteers dosed to steady state with fXa inhibitors, designed to (1) demonstrate PK/PD comparability between andexanet manufactured by the Generation 1 and Generation 2 processes, (2) evaluate the degree to which the Generation 2 andexanet reverses fXa-inhibitor-induced anticoagulation in comparison to placebo, and (3) evaluate safety of Generation 2 andexanet.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1
Started Feb 2017
Shorter than P25 for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 26, 2017
CompletedFirst Submitted
Initial submission to the registry
March 7, 2017
CompletedFirst Posted
Study publicly available on registry
March 20, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 28, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
September 28, 2017
CompletedAugust 8, 2023
August 1, 2023
7 months
March 7, 2017
August 7, 2023
Conditions
Outcome Measures
Primary Outcomes (7)
Pharmacokinetics
To evaluate the pharmacokinetics of Generation 2 process andexanet, as measured by AUC(0-∞)
Day 1 through Day 7
Reversal
To evaluate reversal of fXa-inhibitor-mediated anticoagulation, as measured by anti-fXa activity
Day 1 through Day 7
Safety will be evaluated by assessment of adverse events, venous thromboembolic events, physical exam findings, vital signs, oxygen saturation, fecal occult blood testing, and 12-lead ECGs.
Non-laboratory-based Endpoints
Day 1 through Day 32
Safety will be evaluated by analyzing the following: • Hematology, chemistry & urinalysis.
Laboratory-based Endpoints
Day 1 through Day 32
Safety will be evaluated by analyzing the following: • Antibodies to andexanet, fX, & fXa, and neutralizing antibodies
Laboratory-based Endpoints
Day 1 through Day 32
Safety will be evaluated by analyzing the following: • TFPI, D-dimer, F1+2, thrombin-antithrombin III, and Russell's viper venom time
Laboratory-based Endpoints
Day 1 through Day 32
Safety will be evaluated by analyzing the following: fX, fibrinogen, tissue-type plasminogen activator, plasmin-alpha2-antiplasmin complexes, thrombin activatable fibrinolysis inhibitor, beta-thromboglobulin, platelet factor 4 & soluble thrombomodulin
Laboratory-based Endpoints
Day 1 through Day 32
Secondary Outcomes (9)
To evaluate the pharmacokinetics of Generation 2 process andexanet, as measured by the following PK parameter: Total area under the plasma concentration-time curve from time 0 to infinity (AUC(0 ∞)
Day 1 through Day 7
Reversal
Day 1 through Day 7
Reversal
Day 1 through Day 7
To evaluate the pharmacokinetics of Generation 2 process andexanet, as measured by the following PK parameter: Cmax - Maximum Observed Concentration
Day 1 through Day 7
To evaluate the pharmacokinetics of Generation 2 process andexanet, as measured by the following PK parameter: Tmax - Time to maximum observed plasma concentration (Tmax)
Day 1 through Day 7
- +4 more secondary outcomes
Study Arms (11)
Cohort 1
EXPERIMENTALCohort 2
EXPERIMENTALCohort 3
EXPERIMENTALCohort 4
EXPERIMENTALCohort 5
EXPERIMENTALCohort 6
EXPERIMENTALCohort 7
EXPERIMENTALCohort 8
EXPERIMENTALCohort 9
EXPERIMENTALCohort 10
EXPERIMENTALCohort 11
EXPERIMENTALInterventions
factor Xa inhibitor antidote
Eligibility Criteria
You may qualify if:
- Must be in reasonably good health as determined by the Investigator based on medical history, full physical examination (including blood pressure and pulse rate measurement), 12-lead ECG, and clinical laboratory tests. Subjects with well-controlled, chronic, stable conditions (e.g., controlled hypertension, non-insulin dependent diabetes, osteoarthritis, hypothyroidism) may be enrolled based on the clinical judgment of the Investigator and if approved by the Medical Monitor.
- Must be between the ages of 18 and 75 years, inclusive, at the time of signing of the informed consent form (ICF).
- Agrees to have any dietary or nutritional supplements reviewed by the Investigator and potentially be withheld during the study if advised by the Investigator. Standard multivitamin and mineral supplementation will be permitted.
- Agrees to comply with the contraception and reproduction restrictions of the study:
- Men whose sexual partner is of childbearing potential and/or who are not monogamous must be using two acceptable methods of contraception, at least one of which must be a barrier method (e.g., spermicidal gel plus condom), for the entire duration of the study and for at least 1 month following study-drug administration; and men must refrain from attempting to father a child or donating sperm in the 1 month following the study-drug administration. Periodic abstinence (e.g., calendar, ovulation, sympto-thermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception;
- Men who report surgical sterilization (e.g., bilateral vasectomy) must have had the procedure at least 6 months before study drug administration.
- Surgical sterilization procedures should be supported with clinical documentation and noted in the Relevant Medical History/Current Medical Conditions section of the case report forms (CRFs).
- Women of childbearing potential must be using two medically acceptable methods of contraception, at least one of which must be a barrier method (e.g., non-hormone containing intra-uterine device plus condom, spermicidal gel plus condom, diaphragm plus condom), from the time of Screening and for the duration of the study, through at least 1 month following study drug administration. NOTE: Oral and topical hormonal contraceptive use, as well as the use of hormone-containing intra-uterine devices, is not permitted due to their increased risk of thromboembolism. Periodic abstinence (e.g., calendar, ovulation, sympto-thermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception; OR
- Postmenopausal women must have had no regular menstrual bleeding for at least 1 year before initial dosing and either be over the age of 60 years or have an elevated plasma follicle-stimulating hormone (FSH) level (i.e., \> 40 mIU/mL) at Screening; OR
- Women who report surgical sterilization (i.e., hysterectomy, tubal ligation, and/or bilateral oophorectomy) must have had the procedure at least 6 months before study drug administration. Surgical sterilization procedures should be supported with clinical documentation and noted in the Relevant Medical History/Current Medical Conditions section of the CRF; AND
- All female subjects must have a documented negative pregnancy test result at Screening and on Study Day 1.
- Systolic blood pressure \< 160 mmHg and diastolic blood pressure \< 90 mmHg at Screening and Day 1.
- The following laboratory values must be within the normal laboratory reference range within 28 days of Day 1: prothrombin time (PT), activated partial thromboplastin time (aPTT), and activated clotting time (ACT); hemoglobin, hematocrit, and platelet count.
- The following laboratory values must be equal to or below 2 times the upper limit of normal (ULN) range within 28 days of Day 1: Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) and total bilirubin.
- The Screening serum creatinine must be below 1.5 mg/dL within 28 days of Day 1.
- +3 more criteria
You may not qualify if:
- Previous use of andexanet or previous participation in the current study.
- History of abnormal bleeding, signs or symptoms of active bleeding, or risk factors for bleeding.
- Has a stool specimen that was positive for occult blood within 6 months of study Screening or during the Screening Period.
- Past or current medical history of thrombosis, any sign or symptom that suggests an increased risk of a systemic thrombotic condition or thrombotic event, or recent events that may increase risk of thrombosis.
- a. For example, subjects with a known or suspected hypercoagulable state, history of VTE, DVT, stroke, myocardial infarction \[MI\], cancer \[other than non-melanoma skin cancer\], atrial fibrillation, heart failure, cardiomyopathy, phlebitis, lower extremity edema, major surgery or trauma within 2 months of Study Day 1, airplane travel ≥ 2 hours during the 4 weeks prior to Study Day 1, or general immobility are excluded.
- Absolute or relative contraindication to anticoagulation or treatment with apixaban, rivaroxaban, enoxaparin, or edoxaban.
- Prior consumption of (by any route) one or more doses of aspirin (including baby aspirin), salicylate or subsalicylate, other antiplatelet drugs (e.g., ticlopidine, clopidogrel), non-steroidal anti-inflammatory drugs, fibrinolytic, or any anticoagulant within 7 days prior to Day 1 or is anticipated to require such drugs during the study.
- Receipt of (by any route) hormonal contraception, post-menopausal hormone replacement therapy (HRT) (including over-the-counter products), or testosterone during the 4 weeks prior to Study Day 1 or is anticipated to require such drugs during the study.
- Family history of or risk factors for a hypercoagulable or thrombotic condition, including one of the following:
- Factor V Leiden carrier or homozygote.
- Protein C, S, or ATIII activity below the normal range.
- History of adult asthma or chronic obstructive pulmonary disease or current regular or as-needed use of inhaled medications.
- Active HBV, HCV, or HIV-1/2 infection
- Use of any drugs that are strong dual inhibitors or inducers of CYP3A4 and P-gp within 7 days prior to Study Day 1 or anticipated need for such drugs during the study.
- Participation in an investigational drug study within 28 days of Day 1 or Day 1 is within 5 half-lives of the investigational compound.
- +7 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
West Coast Clinical Trials
Cypress, California, 90630, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 7, 2017
First Posted
March 20, 2017
Study Start
February 26, 2017
Primary Completion
September 28, 2017
Study Completion
September 28, 2017
Last Updated
August 8, 2023
Record last verified: 2023-08