Vykat Xr (diazoxide choline)

Vasodilators Oral Tablet, Extended Release 24 Hr

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Diazoxide choline, an adenosine-triphosphate-sensitive potassium (KATP) channel activator, is a prodrug and salt formulation of diazoxide, a nondiuretic benzothiadiazine derivative.

Diazoxide choline, an adenosine-triphosphate-sensitive potassium (KATP) channel activator, is a prodrug and salt formulation of diazoxide, a nondiuretic benzothiadiazine derivative. The exact mechanism of action of diazoxide choline in the treatment of hyperphagia and Prader-Willi syndrome (PWS) in patients >=4 years of age is unknown. The activation of the KATP channel in neuropeptide Y (NPY) and agouti-related protein (AgRP) neurons in the hypothalamus results in reduced secretion of NPY and AgRP, both of which are potent endogenous appetite-stimulatory neuropeptides.

Additionally, the activation of the KATP channel in the dorsal motor nucleus of vagus, pancreatic beta cells, and adipocytes reduces hyperinsulinemia, improves insulin and leptin resistance, and increases satiety. These actions are thought to be the mechanism by which diazoxide choline exerts its effect in hyperphagia and PWS.

Following oral administration, diazoxide choline is hydrolyzed to diazoxide prior to absorption. Peak plasma concentrations are achieved after 16 hours, and steady state concentrations are expected after 7 days. When administered following a high-fat meal, peak plasma concentrations of diazoxide increased by 39% compared to fasted conditions.

Diazoxide is extensively bound to plasma proteins (91-93%) and crosses the blood-brain barrier. Diazoxide is primarily metabolized by CYP1A2 and, to a lesser extent, CYP3A4. Metabolism also occurs via oxidation or sulfate conjugation to form two inactive metabolites.

Diazoxide is largely excreted in the urine as free or conjugated compound. In healthy patients, the elimination half-life is approximately 29-32 hours; in patients with PWS, the elimination half-life is approximately 106 hours. Age and sex do not have seem to have clinically important effects on the pharmacokinetics of diazoxide choline.

USES: This medication is used to treat extreme hunger, non-stop thoughts about food, and non-stop need to eat that cannot be satisfied with food (hyperphagia) in people with a certain genetic disorder (Prader-Willi syndrome).

Generic name: diazoxide choline
Pronunciation: (DYE-az-OX-ide)
Drug class: Vasodilators
Therapeutic class: Weight Loss/Gain Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Vykat Xr:

  • Hyperphagia In Prader-Willi Syndrome

Dosing

Dosage of diazoxide choline is expressed in terms of diazoxide choline.

Drug interactions

Diazoxide is primarily metabolized by cytochrome P-450 (CYP) isoenzyme 1A2 and to a lesser extent by CYP3A4.

In vitro studies indicate that diazoxide choline is an inhibitor of CYP1A2. Diazoxide choline does not inhibit CYP2B6, 2C19, 2C8, 2C9, 2D6, or 3A4. In vitro studies indicate that diazoxide choline does not induce CYP1A2, CYP2B6, or CYP3A4 at the therapeutic dose range.

In vitro studies indicate that diazoxide choline is a substrate for organic anion transporter (OAT) 1, OAT3, and breast cancer resistance protein (BCRP).

In vitro studies indicate that diazoxide choline is an inhibitor of OAT1 and OAT3. It does not inhibit P-glycoprotein (P-gp), BCRP, multidrug and toxin extrusion (MATE) 1/2-K, organic anion transporting polypeptide (OATP) 1B1/3, or organic cation transporter (OCT) 1/2 at the therapeutic dose range.

Contraindications

*Known hypersensitivity to diazoxide, other components of diazoxide choline, or thiazides. Erythema multiforme has been reported with diazoxide choline.

Adverse reactions

The most common adverse reactions (incidence >=10% and >=2% greater than in placebo) reported with diazoxide choline in clinical studies were hypertrichosis, edema, hyperglycemia, and rash.

Precautions

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ICD codes

CodeTypeDescription
Hyperphagia in prader-willi syndrome
Q87.11ICD10CMPrader-willi syndrome

ICD code information from First Databank (FDB).

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data