praxbind

praxbind Uses, Dosage, Side Effects, Food Interaction and all others data.

praxbind is a humanized monoclonal antibody fragment (Fab) derived from an immunoglobulin G1 isotype molecule that binds to and inactivates the oral anticoagulant dabigatran, thereby reversing its anticoagulant effect. As a direct acting oral anticoagulant (DOAC), one of the risks associated with the use of dabigatran includes bleeding, espeically when given to patients at increased risk (elderly, chronic kidney disease, concomitant NSAID or warfarin use, etc).

Approved under the tradename Praxbind (FDA), idarucizumab is indicated for the emergency treatment of dabigatran-associated bleeding in life-threatening or surgically induced situations. Its use is associated with immediate, complete and sustained reversal of the anticoagulant effects of dabigatran.

praxbind protein structure can be viewed below, with disulfide bridges at the following points: H22-H95, H149-H205, H225-L-219, L23-L93, L139-L199.

Trade Name praxbind
Availability Prescription only
Generic Idarucizumab
Idarucizumab Other Names aDabi-Fab, Idarucizumab
Related Drugs Praxbind
Weight 50mg/ml, , 2.5g/50ml
Type Solution, Infusion, Intravenous Solution
Groups Approved
Therapeutic Class
Manufacturer Boehringer Ingelheim, Boehringer Ingelheim Limited
Available Country Saudi Arabia, Australia, United Kingdom, United States,
Last Updated: September 19, 2023 at 7:00 am
praxbind
praxbind

Uses

praxbind is an antibody that binds dabigatran for the reversal of anticoagulant effects of dabigatran.

For use in patients treated with Dabigatran when reversal of the anticoagulant effects of dabigatran is needed for emergency surgery/urgent procedures and in life-threatening or uncontrolled bleeding.

praxbind is also used to associated treatment for these conditions: Anticoagulant effects of dabigatran

How praxbind works

praxbind is a specific reversal agent for dabigatran. It is a humanized monoclonal antibody fragment (Fab) that binds to dabigatran and its acylglucuronide metabolites with higher affinity than the binding affinity of dabigatran to thrombin, neutralizing their anticoagulant effect.

Toxicity

In healthy volunteers, the most frequently reported adverse reactions in greater than or equal to 5% of subjects treated with idarucizumab was headache. In patients, the most frequently reported adverse reactions in greater than or equal to 5% of patients treated with idarucizumab were hypokalemia, delirium, constipation, pyrexia, and pneumonia.

Food Interaction

No interactions found.

praxbind Disease Interaction

Moderate: fructose intolerance, liver impairment

Volume of Distribution

8.9 L

Half Life

initial half-life: 47 minutes terminal half-life: 10.3 h

Clearance

47.0 mL/min

Elimination Route

After intravenous administration of 5 g idarucizumab, 32.1% (gCV 60.0%) of the dose was recovered in urine within a collection period of 6 hours and less than 1% in the following 18 hours. The remaining part of the dose is assumed to be eliminated via protein catabolism, mainly in the kidney.

Innovators Monograph

You find simplified version here praxbind

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