Make sure patients are ready to treat a severe low with Gvoke HypoPen®

Gvoke HypoPen is a ready-to-use glucagon autoinjector that brings very low blood glucose levels back up quickly and safely1
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Discover the Benefits of Gvoke HypoPen®

Empower patients and their loved ones to treat severe hypoglycemia with a glucagon autoinjector they can administer with confidence.
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Well studied1

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Efficacious and safe1,2

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Works quickly1,3

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Anyone can administer4

Gvoke HypoPen Is Well Studied in Patients

Gvoke HypoPen was evaluated in adult patients aged 18-74 years with type 1 diabetes in 2 multicenter, randomized, controlled, blinded, 2-way crossover non-inferiority studies: Study A (N=80) and Study B (N=81). A third Phase 3 trial, Study C (N=31), was an open-label, sequential efficacy and safety study in patients aged 2 to 17 years with type 1 diabetes.

Gvoke Was Evaluated in 2 Phase 3 Trials of Adults With T1D1,2

image of test results chart for adult patients

154 subjects received an injection of Gvoke and 157 subjects received an injection of GEK. A total of 152 subjects received both Gvoke and GEK.

In study A, mean plasma glucose at time of administration was 44.8 mg/dL for Gvoke and 45.2 mg/dL for GEK. In Study B, mean plasma glucose at time of administration was 47.7 mg/dL for Gvoke and 48.7 mg/dL for GEK.

The Safety and Efficacy of Gvoke® for Children and Adolescents Was Evaluated in a Phase 3, Open-label Study1

Chart about Gvoke Phase 3 trial in Children and Adolescents

Demonstrated Safety and Efficacy

Across clinical trials of Gvoke HypoPen, no serious or severe adverse events were seen,2 and the majority of adverse reactions were mild (81% in adults and 83% in pediatrics).3
Plasma glucose results chart

99% (152/154) of adult patients achieved plasma glucose > 70 mg/dL or an increase ≥ 20 mg/dL from baseline in a pooled analysis of Study A and Study B.1

The most common adverse reactions in adults (N=154) were1: nausea (30%), vomiting (16%), injection site edema (7%), and headache (5%).

The mean time to treatment success was 13.8 minutes in the Gvoke group.

Plasma over time with Gvoke and Glucagon Emergency kit chart

Patients experienced initial blood glucose increases in less than 2 minutes3

Post hoc analysis in adults revealed the median time to initial blood glucose increase was less than 2 minutes.3†

~176 mg/dL mean maximum increase in plasma glucose from an average baseline of 44 mg/dL (insulin-induced severe hypoglycemia), following administration of Gvoke HypoPen.1

† Estimations yielding times earlier than the initial post dose (PD) collection at 5 minutes assume an immediate increase from baseline and cannot account for a potentially delayed onset from time of injection to initial PD

Pediatric Patients with Type 1 Diabetes Mellitus Plasma Glucose by Age Group Chart

100% (30/30) of pediatric patients achieved a target glucose increase of ≥25 mg/dL.1

The most common adverse reactions in pediatric patients (N=31) were1: nausea (45%), hypoglycemia (39%), vomiting (19%), headache (7%), hyperglycemia (7%), abdominal pain (3%), injection site discomfort (3%), injection site reaction (3%), and urticaria (3%).

Adverse reactions occur within 12 hours.

Mean plasma glucose over time with 1mg Gvoke and Glucagon Emergency Kit chart

When Patients Need It, Gvoke HypoPen Begins Working in Less Than 2 Minutes

Patients experienced initial blood glucose increases in less than 2 minutes with Gvoke HypoPen, and no overcorrection.2

~176 mg/dL mean maximum increase in plasma glucose from an average baseline of 44 mg/dL (insulin-induced severe hypoglycemia), following administration of Gvoke HypoPen.

In studies with simulated emergency conditions, 99% of people were able to give Gvoke HypoPen correctly4

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How To Use Gvoke HypoPen in 2 Simple Steps1

Pull Red
Remove the red cap.
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Push Yellow
Push yellow end down on skin and hold for 5 seconds. Window will turn red.
Gvoke HypoPen can be administered into the outer upper arm, lower abdomen, or outer thigh.1  Store in original sealed pouch until time of use.

Understanding Dosages

Gvoke HypoPen comes in two premeasured dosing options
that don’t require refrigeration.1

Gvoke HypoPen 1mg Box

1 mg per 0.2 mL

  • For patients aged 12 and older and children under 12 years of age who weigh ≥ 100 lbs
  • Lasts up to 30 months from date of manufacture when stored at room temperature3
Gvoke HypoPen .5mg box

0.5 mg per 0.1 mL

  • For patients between the ages of 2 and 11 who weigh less than 100 lbs
  • Lasts up to 24 months from date of manufacture when stored at room temperature3

Where Patients Can Keep Gvoke HypoPen

Gvoke HypoPen comes in a convenient two-pack. Patients should have it available at all times no matter where they are. Store at room temperature (68° to 77°F). Do not refrigerate or freeze.
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Keep Gvoke HypoPen in an easy-to-access location where you live.
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School or work

Ensure Gvoke HypoPen is available to treat a severe low at school or the office.
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On the go

Gvoke HypoPen is easy to travel with because it doesn’t need to be refrigerated.

Help Patients Save Money on Gvoke HypoPen

Eligible commercially insured patients may pay as little as $25 for Gvoke HypoPen with a copay card.*
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Access Financial Support

A Patient Assistance Program is available for those who need financial support. Encourage patients to find out if they qualify.
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† In a pooled analysis of 2 clinical studies in adults, mean time to treatment success was 13.8 minutes with treatment success defined as plasma glucose increase from mean value (< 50 mg/dL) at time of glucagon administration to absolute value greater than 70 mg/dL or relative increase of 20 mg/dL or greater.


  1. Gvoke [prescribing information]. Chicago, IL: Xeris Pharmaceuticals, Inc; 2023.
  2. Christiansen MP, Cummins M, Prestrelski S, Close NC, Nguyen A, Junaidi K. Comparison of a ready-to-use liquid glucagon injection administered by autoinjector to glucagon emergency kit for the symptomatic relief of severe hypoglycemia: two randomized crossover non-inferiority studies. BMJ Open Diabetes Res Care. 2021;9(1):e002137. doi:10.1136/bmjdrc-2021-002137
  3. Data on file. Xeris Pharmaceuticals, Inc
  4. Valentine V, Newswanger B, Prestrelski S, Andre AD, Garibaldi M. Human Factors Usability and Validation Studies of a Glucagon Autoinjector in a Simulated Severe Hypoglycemia Rescue Situation. Diabetes Technol Ther. 2019;21(9):522-530. doi:10.1089/dia.2019.0148

*Offer not valid for prescriptions reimbursed under Medicaid, a Medicare drug benefit plan, TRICARE, or other federal or state health programs (such as medical assistance programs).

Indication and Important Safety Information⁠—⁠Read More


GVOKE is indicated for the treatment of severe hypoglycemia in adult and pediatric patients with diabetes ages 2 years and above.



GVOKE is contraindicated in patients with pheochromocytoma because of the risk of substantial increase in blood pressure, insulinoma because of the risk of hypoglycemia, and known hypersensitivity to glucagon or to any of the excipients in GVOKE. Allergic reactions have been reported with glucagon and include anaphylactic shock with breathing difficulties and hypotension.

Warnings and Precautions

GVOKE is contraindicated in patients with pheochromocytoma because glucagon may stimulate the release of catecholamines from the tumor. If the patient develops a dramatic increase in blood pressure and a previously undiagnosed pheochromocytoma is suspected, 5 to 10 mg of phentolamine mesylate, administered intravenously, has been shown to be effective in lowering blood pressure.

In patients with insulinoma, administration of glucagon may produce an initial increase in blood glucose; however, GVOKE administration may directly or indirectly (through an initial rise in blood glucose) stimulate exaggerated insulin release from an insulinoma and cause hypoglycemia. GVOKE is contraindicated in patients with insulinoma. If a patient develops symptoms of hypoglycemia after a dose of GVOKE, give glucose orally or intravenously.

Allergic reactions have been reported with glucagon. These include generalized rash, and in some cases, anaphylactic shock with breathing difficulties and hypotension. GVOKE is contraindicated in patients with a prior hypersensitivity reaction.
GVOKE is effective in treating hypoglycemia only if sufficient hepatic glycogen is present. Patients in states of starvation, with adrenal insufficiency or chronic hypoglycemia, may not have adequate levels of hepatic glycogen for GVOKE administration to be effective. Patients with these conditions should be treated with glucose.

Necrolytic migratory erythema (NME), a skin rash commonly associated with glucagonomas (glucagon-producing tumors) and characterized by scaly, pruritic erythematous plaques, bullae, and erosions, has been reported postmarketing following continuous glucagon infusion. NME lesions may affect the face, groin, perineum and legs or be more widespread. In the reported cases NME resolved with discontinuation of the glucagon, and treatment with corticosteroids was not effective. Should NME occur, consider whether the benefits of continuous glucagon infusion outweigh the risks.

Adverse Reactions

Most common (≥5%) adverse reactions associated with GVOKE are nausea, vomiting, injection site edema (raised 1 mm or greater), and hypoglycemia.

Drug Interactions

Patients taking beta-blockers may have a transient increase in pulse and blood pressure when given GVOKE. In patients taking indomethacin, GVOKE may lose its ability to raise blood glucose or may even produce hypoglycemia. GVOKE may increase the anticoagulant effect of warfarin.

Please see the Full Prescribing Information for Gvoke.