Evidence review: Open Peptide Project (verified against primary PubMed, ClinicalTrials.gov & FDA records) · Last checked 2026-10-27. ← Back to Evidence Library

Glucagon (Gvoke, Baqsimi, generics): what the evidence says

At a glance

What it is: a 29-amino-acid hormone from the pancreas that raises blood sugar. Synthetic versions are approved for severe hypoglycemia, as injections (e.g. Gvoke, Sep 2019) and a nasal powder (Baqsimi, Jul 2019), and as a diagnostic aid to relax the gut during imaging. R1, R2, R3, R4

What the evidence says: Human glucagon reliably reverses severe low blood sugar; a meta-analysis of 8 RCTs found nasal and injected glucagon similarly effective. R5 Newer weight-loss drugs (survodutide, mazdutide, retatrutide) add glucagon-receptor activity to GLP-1, but they are different molecules. R6, R7, R8

Biggest risks: nausea and vomiting are common. It must not be used with pheochromocytoma, and can backfire with insulinoma; a rare skin rash (necrolytic migratory erythema) is reported with prolonged use. R3

Rating

Human Human evidence Strong: approved for decades; RCTs and meta-analysis of newer forms R5
Animal Animal / lab evidence Not reviewed
Regulatory FDA-approved R1 · not on FDA's 503A or 503B bulk-substance category lists and not on FDA's compounding safety-risk page R9, R10, R11 · not named by WADA R12
Established human dose Yes, label dose (see Study details)

Evidence verdict: Severe low blood sugar: Strong (decades of use; RCTs of new forms) · Diagnostic aid for GI imaging: Strong (approved use) · Weight loss as glucagon alone: No human data

This page reports what studies used. It is not dosing advice.

Legend: HUMAN data · ANIMAL / LAB data · UNKNOWN · UNVERIFIED: not yet confirmed against a primary source

About the evidence: the core rescue effect is long established; newer formulation trials are often small and in controlled settings.

What is it?

Related pages: dasiglucagon, survodutide, mazdutide, retatrutide, pemvidutide.

Does it work?

Is it safe?

Gray-market vials: extra risks

A gray-market vial has no quality control and no guarantee of identity, strength or sterility. We test retail vials blind under the Open Peptide Standard; see /tests/. A passing test covers one batch on one date and does not mean the compound is safe.

Is it legal?

Study details
Study details

These are amounts researchers used, not recommendations.

Study People / model Route Amount used Follow-up Reported Citation
Sherr 2016 (phase 1) 48 youth with T1D Nasal vs IM Per study Single doses 58 of 59 nasal doses raised glucose ≥25 mg/dL within 20 min PMID 26884472
Pontiroli 2020 meta-analysis 8 RCTs, T1D Nasal vs injected Per study Single doses Similar efficacy PMID 32025860
Gvoke label Adults and children 2+ SC Per label Rescue use Approved for severe hypoglycemia R3

Full reference list (PubMed, CT.gov, FDA and WADA checked Oct 27, 2026)

  1. R1 Drugs@FDA, Gvoke (glucagon), application NDA212097 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA212097
  2. R2 Drugs@FDA, Baqsimi (glucagon nasal powder), application NDA210134 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA210134
  3. R3 Gvoke prescribing information, label published Jul 7, 2026 (DailyMed, checked Oct 27, 2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=359982a8-ec5c-4927-8c0f-89771e0f942b
  4. R4 Baqsimi prescribing information, label published Jun 19, 2026 (DailyMed, checked Oct 27, 2026). https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=32ba41fa-4158-40af-8cb2-03693c248994
  5. R5 Pontiroli AE, et al. Acta Diabetol. 2020. PMID 32025860
  6. R6 Jastreboff AM, et al. N Engl J Med. 2023. PMID 37366315
  7. R7 le Roux CW, et al. N Engl J Med. 2026. PMID 42253238
  8. R8 Ji L, et al. N Engl J Med. 2025. PMID 40421736
  9. R9 FDA, 503A bulk drug substances categories list (updated May 14, 2026). https://www.fda.gov/media/94155/download
  10. R10 FDA, 503B bulk drug substances categories list (updated Mar 21, 2025). https://www.fda.gov/media/94164/download
  11. R11 FDA, Certain bulk drug substances for use in compounding that may present significant safety risks (content current Apr 22, 2026). https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks
  12. R12 WADA. The 2026 Prohibited List, full list checked; compound not named. https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf
  13. R13 Sherr JL, et al. Diabetes Care. 2016. PMID 26884472
  14. R14 Drugs@FDA, Glucagon (Fresenius Kabi), application NDA201849 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA201849
  15. R15 Drugs@FDA, GlucaGen (glucagon), application NDA020918 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA020918
  16. R16 Drugs@FDA, Glucagon (Lilly), application NDA012122 (openFDA drugsfda record checked Oct 27, 2026). https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=NDA012122

Disclaimer

This page is for education and harm reduction, not medical advice or a recommendation to use Glucagon (Gvoke, Baqsimi, generics). This is a prescription medicine. Use it only under the care of a licensed clinician; do not buy it from research-chemical or gray-market sellers. Report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).