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  3. ›Gvoke
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glucagon

Marketedupdated 5mo ago
by $XERS Xeris Biopharma Holdings, Inc.
Approved
community read0 votes

🐶 often sniffed alongside

top 7
  • tagPeptide Therapeutic4 co-mentions · 4 sources
  • companyNorthwestern University1 co-mentions · 1 sources
  • companyMassachusetts General Hospital1 co-mentions · 1 sources
  • companyMayo Clinic1 co-mentions · 1 sources
  • tagEndocrinology & Metabolism1 co-mentions · 1 sources
  • tagLupus1 co-mentions · 1 sources
  • tagGLP-1 receptor1 co-mentions · 1 sources

all catalysts(0)

nothing on the calendar yet

Trials studying glucagon

  • phase3Extension Trial Evaluating the Long-term Safety and Efficacy of Dasiglucagon in Children With Congenital Hyperinsulinismactive not recruitingn=42
  • —Value of PET/MR Enterography in the Assessment of Crohn's Disease Using a Collagen-binding Radiotracer.recruitingn=25
  • —Transformative Research in Diabetic Nephropathy 2.0recruitingn=200
  • phase1Research Study in Japan to Compare Dasiglucagon With Glucagon in Treating Very Low Levels of Blood Sugar in Asian Adults With Type 1 Diabetes and Testing of Dasiglucagon for the Same Condition in Japanese Adolescentscompletedn=38
  • phase2Glucagon Ready-to-Use (RTU) for Prevention of Exercise-Induced Hypoglycemia During Aerobic Exercise in Adults With T1Dcompletedn=48
  • phase3A Study to Inv. Safety, Efficacy & PD of Dasiglucagon as Hypoglycemia Rescue Therapy in Children <6 Years With T1Dcompletedn=8
  • —A Study for Comparison of Canagliflozin Versus Alternative Antihyperglycemic Treatments on Risk of Heart Failure Hospitalization and Amputation for Participants With Type 2 Diabetes Mellitus and the Subpopulation With Established Cardiovascular Diseasecompletedn=714,582
  • —Remote Study Collecting Blood Glucose Values and Activity Data in Patients With Type 2 Diabetes on Different Treatmentscompletedn=156

Patent cliff

source: FDA Orange Book
first barrier falls
Feb 16, 2036
~9.4 years out

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (12)

  • Sep 23, 2039formulationUS 10765602
  • Apr 22, 2036formulationUS 11590205
  • Apr 22, 2036formulationUS 11590205
  • Apr 22, 2036formulationUS 11590205
  • Apr 22, 2036formulationUS 11590205
  • Apr 22, 2036formulationUS 11590205
  • Apr 22, 2036formulationUS 9649364
  • Apr 22, 2036formulationUS 9649364
  • Apr 22, 2036formulationUS 9649364
  • Apr 22, 2036formulationUS 9649364
  • Feb 16, 2036formulationUS 10213487
  • Feb 16, 2036formulationUS 12370241

FDA exclusivities (1)

  • Apr 18, 2026CGTCGT

News(10)

  • 3 takeaways from a European obesity scientific meeting
    Eli Lilly impressed with its amylin-Zepbound combination data. Elsewhere, Novo demonstrated continued weight loss following a switch to oral and AbbVie and Boehringer gave glimpses into their conte…
    biopharma_dive · 4h ago
  • Zealand dips as Boehringer Ingelheim-partnered weight loss drug fails to impress—again
    Despite meeting the primary endpoints in a Phase 3 trial, shares of Zealand Pharma dropped in premarket trading Thursday as the up to 9.8% weight loss reflected inferior loss to that generated by c…
    biospace · 6h ago
  • Zealand's stock slides as Boehringer-partnered obesity drug underwhelms again in phase 3
    A phase 3 trial of Boehringer Ingelheim’s survodutide in people with obesity and Type 2 diabetes has met its co-primary endpoints. Yet, with the readout echoing earlier data that underwhelmed analy…
    fiercebiotech · 14h ago
  • Lilly sets up next-gen obesity battle with full phase 3 retatrutide data
    Eli Lilly has shared detailed data from a phase 3 retatrutide trial, revealing that more than one-third of patients on the top dose of the triple-G drug candidate lost at least 25% of their body we…
    fiercebiotech · 1d ago
  • CDER director, expert discuss scientific, legal challenges to bringing generic GLP-1s to market
    Michael Davis, the director of the FDA's Center for Drug Evaluation and Research (CDER), stated that increasing the availability of generic versions of glucagon-like peptide-1 (GLP-1) medications i…
    raps · 3d ago
  • Viking achieves 'maintenance trifecta' as GLP-1/GIP dual agonist exceeds expectations
    Viking Therapeutics’ VK2735 met Truist’s “best-case scenario,” with robust weight loss that was largely maintained when patients transitioned to less frequent dosing. Viking’s stock popped more tha…
    biospace · 9d ago
  • Lilly presents early data supporting GLP-1/GIP candidate's potential in depression, alcohol use disorder
    With a trillion-dollar market cap and a wildly successful GLP-1 portfolio, Eli Lilly isn’t resting on its laurels. At the Psych Congress 2026, the company presented early-stage data that could supp…
    biospace · 9d ago
  • Lilly cans early experimental obesity drug after ‘high bar’ not met
    Eli Lilly has put the kibosh on an early-stage obesity drug after the candidate didn’t meet the pharma giant’s lofty expectations.
    fiercebiotech · 17d ago
  • Myriad catalysts on deck for obesity’s brightest stars as market continues to accelerate
    Current leaders Eli Lilly and Novo Nordisk have cornered the early market for weight loss therapeutics, but several other players, large and small, are bidding for a piece of the potential $200 bil…
    biospace · 1mo ago
  • Boehringer places phase 1 study of investigational drug on hold to examine ‘safety event’
    Boehringer Ingelheim has suspended a phase 1 trial of an investigational small molecule drug while it seeks to understand a “safety event,” although the German pharma isn't shedding light on the na…
    fiercebiotech · 1mo ago
view all news mentions →
brand
Gvoke
generic
glucagon [INN]
indication
Hypoglycemia
phase
marketed
Data sources
ClinicalTrials.gov
last refreshed 52m ago
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