Steglatro (ertugliflozin): Uses, Benefits, and Side Effects

Medical Disclaimer

This article is for informational purposes only and does not constitute medical advice. Always consult your physician or a qualified healthcare provider regarding any medical condition or treatment.

Key Takeaways

  • Steglatro (ertugliflozin) is an SGLT2 inhibitor approved by the FDA in December 2017 — the newest of the four mainstream agents in the class.
  • Dosing is 5 mg once daily, increased to 15 mg once daily if more glucose lowering is needed; A1C reduction averages 0.7 to 1.0 percent and weight loss averages 2 to 3 kg.
  • The VERTIS CV trial showed cardiovascular safety (non-inferiority for MACE) and a reduction in heart failure hospitalizations, but did not demonstrate the broader MACE superiority seen with Jardiance, Farxiga, and Invokana.
  • Common side effects mirror the class — genital yeast infections, urinary tract infections, increased urination, dehydration — with rare but serious euglycemic DKA, Fournier gangrene, and acute kidney injury.
  • Segluromet (with metformin) and Steglujan (with sitagliptin), offering a once-daily tablet that pairs SGLT2 and DPP-4 mechanisms.

Steglatro (ertugliflozin) is an oral SGLT2 inhibitor approved by the FDA in December 2017 for type 2 diabetes. It lowers A1C by 0.7 to 1.0 percent, produces modest weight loss of 2 to 3 kg, and modestly reduces heart failure hospitalizations. The cardiovascular outcomes trial VERTIS CV met non-inferiority but did not show the broader MACE superiority seen with Jardiance, Farxiga, and Invokana — which is why Steglatro is typically a second-tier pick within the SGLT2 class.

What Steglatro Is

  • Generic name: ertugliflozin
  • Drug class: SGLT2 (sodium-glucose cotransporter 2) inhibitor
  • Manufacturer: Merck and Pfizer co-promoted
  • FDA approval: December 2017
  • Forms: 5 mg and 15 mg tablets, taken once daily
  • Combinations: Segluromet (ertugliflozin plus metformin), Steglujan (ertugliflozin plus sitagliptin)

How Steglatro Works

SGLT2 transporters in the kidney reabsorb most of the glucose filtered through the glomerulus. Steglatro blocks SGLT2, causing roughly 60 to 80 grams of glucose to spill into the urine each day. The downstream effects:

  • Lower blood glucose without depending on insulin secretion
  • Modest calorie loss of 240 to 320 kcal per day driving weight loss
  • Mild osmotic diuresis lowering blood pressure 3 to 5 mmHg
  • Reduced sodium reabsorption easing kidney workload
  • Slight ketogenesis improving cardiac energy efficiency in heart failure

Approved Uses

  • Type 2 diabetes — to improve glycemic control as an adjunct to diet and exercise
  • Can be used as monotherapy when metformin is contraindicated or as add-on therapy
  • Combination with metformin (Segluromet) or sitagliptin (Steglujan) for additive effect

Steglatro does not have FDA labels for heart failure or CKD specifically — those indications belong to Jardiance and Farxiga.

Dosing and Titration

Setting Dose Notes
Starting dose 5 mg once daily Morning, with or without food
Maximum dose 15 mg once daily Increase if more glycemic effect needed
eGFR ≥ 45 Full dose Approved range
eGFR 30–44 Not recommended Limited benefit, more side effects
eGFR < 30 Contraindicated Discontinue
Hepatic impairment Mild–moderate: full dose; severe: not recommended No specific titration

VERTIS CV — What the Trial Showed

VERTIS CV (Cannon et al., NEJM 2020) enrolled 8,246 patients with type 2 diabetes and established cardiovascular disease. Results:

  • Primary endpoint (3-point MACE): non-inferior to placebo (HR 0.97), did NOT reach superiority
  • Heart failure hospitalization: significantly reduced (HR 0.70)
  • Cardiovascular death: no significant difference
  • Renal composite (sustained eGFR decline, dialysis, renal death): no significant benefit
  • Major safety signals: no amputation increase, no fracture increase, no DKA spike beyond class baseline

The takeaway: Steglatro is safe and modestly helps heart failure hospitalizations but lacks the broader cardiovascular and renal protection package that defines the rest of the class.

Benefits

  • A1C reduction of 0.7 to 1.0 percent depending on dose and baseline
  • Weight loss of 2 to 3 kg over 6 to 12 months
  • Blood pressure reduction of 3 to 5 mmHg systolic
  • Low hypoglycemia risk when used alone (under 4 percent)
  • Heart failure hospitalization reduction (about 30 percent in VERTIS CV)
  • Once-daily oral dosing
  • Available in convenient combinations with metformin and sitagliptin

Common Side Effects

Side Effect Approximate Frequency
Genital yeast infection (women) ~9%
Genital yeast infection (men) ~4%
Urinary tract infection 4–7%
Increased urination ~3%
Thirst ~2%
Headache ~3%
Back pain ~3%

Rare but Serious Effects

  • Euglycemic diabetic ketoacidosis — DKA with relatively normal glucose; triggered by illness, fasting, surgery, or very low-carb diets
  • Fournier gangrene — very rare necrotizing infection of the perineum requiring emergency care
  • Acute kidney injury — usually in dehydration or with ACE/ARB plus diuretic
  • Volume depletion — dizziness, hypotension, particularly in older adults or those on diuretics
  • Hyperkalemia — small rise in potassium
  • Mild LDL cholesterol increase — typically 4 to 8 percent

Who Should Avoid Steglatro

  • Type 1 diabetes (off-label, high DKA risk)
  • History of DKA
  • eGFR persistently below 30 mL/min
  • End-stage renal disease or dialysis
  • Severe hepatic impairment
  • Active genitourinary infection until resolved
  • Pregnancy and breastfeeding

Sick-Day Plan

  • Hold Steglatro during vomiting, severe diarrhea, or fasting
  • Stop at least 3 days before scheduled surgery (4 days for major surgery)
  • Hold during any acute illness with reduced oral intake
  • Resume only when eating and drinking are normal again
  • Maintain hydration in heat, exercise, or low-carbohydrate eating

Steglatro Combinations

Brand Components Notes
Steglatro Ertugliflozin 5 or 15 mg Single agent
Segluromet Ertugliflozin + metformin Twice daily
Steglujan Ertugliflozin + sitagliptin 100 mg Once daily, dual mechanism

How Steglatro Compares With Other SGLT2 Inhibitors

Drug FDA Approval MACE Superiority HF Indication CKD Indication
Jardiance (empagliflozin) 2014 Yes (EMPA-REG) Yes Yes
Farxiga (dapagliflozin) 2014 Yes (DECLARE) Yes Yes
Invokana (canagliflozin) 2013 Yes (CANVAS) No Yes
Steglatro (ertugliflozin) 2017 No (non-inferior) No No

Monitoring on Steglatro

  • eGFR and creatinine at baseline, 1 month, then every 3 to 6 months
  • A1C every 3 months until stable
  • Blood pressure, especially if also on antihypertensives
  • Genitourinary symptoms reported promptly
  • Volume status check at every visit (orthostatic dizziness, dry mucous membranes)

Practical Notes for Users

  • Take in the morning to avoid nocturnal urination
  • Drink water consistently — pale yellow urine is a good target
  • Maintain genital hygiene; treat yeast infections early
  • Carry sick-day rules: hold during illness, fasting, surgery
  • Report any unusual fatigue, abdominal pain, or shortness of breath promptly — possible DKA

For class context see our SGLT2 inhibitors list, the broader SGLT2 side effects guide, and our comparison piece empagliflozin vs dapagliflozin. For background on lifestyle alongside drug therapy see diet and nutrition. External references: the VERTIS CV trial and the ADA Standards of Care.

The Bottom Line

Steglatro (ertugliflozin) is an effective SGLT2 inhibitor that lowers A1C by 0.7 to 1.0 percent, produces 2 to 3 kg of weight loss, and reduces heart failure hospitalizations. It met non-inferiority but not superiority for the broader MACE endpoint in VERTIS CV, and does not carry FDA indications for heart failure or CKD. Side effects mirror the class — yeast and urinary infections, dehydration, rare euglycemic DKA — without the amputation or fracture signal seen with Invokana. Most clinicians prefer Jardiance or Farxiga when cardiovascular or renal protection is the priority, and reserve Steglatro for cost-driven or formulary-driven choices or for users intolerant of other agents in the class.

Frequently Asked Questions

How does Steglatro compare with Jardiance and Farxiga?

Glucose lowering and weight loss are broadly similar across the three. Where they differ is in cardiovascular and renal outcome trials. Jardiance (EMPA-REG) and Farxiga (DECLARE, DAPA-HF, DAPA-CKD) show clear major adverse cardiovascular event reductions and have full FDA labels for heart failure and CKD. Steglatro (VERTIS CV) met non-inferiority for MACE and showed heart failure hospitalization benefit, but did not reach superiority on the broader MACE endpoint. In practice, clinicians often pick Jardiance or Farxiga first when CV or renal protection is the goal.

What is the usual Steglatro dose?

The starting dose is 5 mg once daily, taken in the morning with or without food. If additional glucose lowering is needed and the 5 mg dose is well tolerated, the dose can be increased to 15 mg once daily. The 5 mg dose lowers A1C by roughly 0.7 to 0.8 percent and the 15 mg dose by about 0.9 to 1.0 percent. There is no further benefit beyond 15 mg, and side effect rates rise modestly with the higher dose.

What are the most common side effects of Steglatro?

The most common side effects are genital yeast infections (about 9 percent of women, 4 percent of men), urinary tract infections (about 4 to 7 percent), and increased urination. Serious but rare effects include euglycemic diabetic ketoacidosis, Fournier gangrene of the perineum, acute kidney injury, and volume depletion in older or diuretic-treated users. Unlike Invokana, Steglatro has not shown an amputation or fracture signal in its trial program.

Can Steglatro be used in chronic kidney disease?

Steglatro is approved when eGFR is 45 mL/min or above and is not recommended below that threshold — narrower than Jardiance and Farxiga, which can be initiated down to eGFR 20 to 25 for renal and heart failure indications. Steglatro should be stopped if eGFR drops below 30 persistently. The renal benefit signal from VERTIS CV was weaker than from CREDENCE (canagliflozin) or DAPA-CKD (dapagliflozin), so clinicians generally favor those agents for CKD protection.

Sources

  1. U.S. Food and Drug Administration. Steglatro (ertugliflozin) Prescribing Information. https://www.accessdata.fda.gov/drugsatfda_docs/label/
  2. Cannon CP, et al. Cardiovascular Outcomes with Ertugliflozin in Type 2 Diabetes (VERTIS CV). N Engl J Med 2020;383:1425-1435. https://www.nejm.org/doi/full/10.1056/NEJMoa2004967
  3. American Diabetes Association. Standards of Care in Diabetes 2024. Diabetes Care 47(Suppl 1).