Ertugliflozin


Ertugliflozin is a drug for the treatment of type 2 diabetes. In the United States, it was approved by the Food and Drug Administration for use as a monotherapy and as a fixed dose combination with either sitagliptin or with metformin. In Europe, it was approved in March 2018 for use as a monotherapy or combination therapy.
Ertugliflozin is a sodium/glucose cotransporter 2 inhibitor and is in the class of drugs known as gliflozins.
A combination with metformin is marketed as Segluromet and a combination with sitagliptin is marketed as Steglujan.

Contraindications

Under the US approval, ertugliflozin is contraindicated for patients with severe kidney failure, end-stage renal disease, and dialysis. The European approval does not list any contraindications apart from hypersensitivity to the drug, which is standard for all drug approvals.

Adverse effects

Adverse effects in studies that were significantly more common under ertugliflozin than under placebo included mycosis of the genitals in both men and women, vaginal itch, increased urination, thirst, hypoglycaemia, and weight loss under the higher dosing scheme. A rare but life-threatening side effect of gliflozins is ketoacidosis; it occurred in three patients in ertugliflozin studies.
To lessen the risk of developing ketoacidosis after surgery, the FDA has approved changes to the prescribing information for SGLT2 inhibitor diabetes medicines to recommend they be stopped temporarily before scheduled surgery. Ertugliflozin should be stopped at least four days before scheduled surgery.
Symptoms of ketoacidosis include nausea, vomiting, abdominal pain, tiredness, and trouble breathing.

Overdose

Up to sixfold clinical doses over two weeks, or 20-fold single doses, are tolerated by patients without any toxic effects.

Interactions

As with many diabetes drugs, combining ertugliflozin with insulin or insulin secretagogues may result in an increased risk for low blood sugar. Combination with diuretics may result in a higher risk for dehydration and low blood pressure. No clinically relevant pharmacokinetic interactions have been found in studies.

Pharmacology

Mechanism of action

Pharmacokinetics

After oral intake, ertugliflozin is practically completely absorbed from the gut and undergoes no relevant first-pass effect. Highest blood plasma concentrations are reached after one hour. When in circulation, 93.6% of the substance are bound to plasma proteins. Ertugliflocin is metabolised mainly to glucuronides by the enzymes UGT1A9 and UGT2B7. Cytochrome P450 enzymes play only a minor role in its metabolism.
The elimination half-life is estimated to be 17 hours. 40.9% are eliminated via the faeces and 50.2% via the urine. The high proportion of unchanged substance in the faeces is probably due to hydrolysis of the metabolites back to the parent substance.