What are the available GLP-1 (Glucagon-like peptide-1) agonist brands, such as Victoza (liraglutide), Byetta (exenatide), and Trulicity (dulaglutide), in India?

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Last updated: September 13, 2025View editorial policy

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GLP-1 Receptor Agonist Brands Available in India

Based on the available evidence, the GLP-1 receptor agonists currently available in India include Victoza (liraglutide), Trulicity (dulaglutide), Byetta (exenatide), and Mounjaro (tirzepatide).

Available GLP-1 Receptor Agonists in India

Short-Acting GLP-1 RAs

  • Exenatide (Byetta)
    • Administration: Twice daily subcutaneous injection
    • Dosage: 10 μg twice daily
    • Primary effect: Stronger postprandial glucose control
    • Half-life: 2.4 hours 1

Once-Daily GLP-1 RAs

  • Liraglutide (Victoza)
    • Administration: Once daily subcutaneous injection
    • Dosage: 0.6-1.8 mg daily
    • Half-life: 13 hours
    • Cardiovascular benefit: 13% reduction in MACE 1, 2

Once-Weekly GLP-1 RAs

  • Dulaglutide (Trulicity)
    • Administration: Once weekly subcutaneous injection
    • Dosage: 0.75-4.5 mg weekly
    • Half-life: 4.7 days
    • Cardiovascular benefit: 12% reduction in MACE 1, 2

Dual GIP and GLP-1 RA

  • Tirzepatide (Mounjaro)
    • Administration: Once weekly subcutaneous injection
    • Dosage: Up to 15 mg weekly
    • Half-life: 5 days 1

Comparative Features

Efficacy Profile

  • Glycemic Control: Semaglutide > Dulaglutide > Liraglutide > Exenatide 3
  • Weight Loss: Long-acting agents generally provide greater weight loss than short-acting agents 3
  • Postprandial Control: Short-acting agents (exenatide) have stronger effects on postprandial glucose 3
  • Fasting Glucose Control: Long-acting agents (liraglutide, dulaglutide) have more profound effects on fasting plasma glucose 3

Administration Considerations

  • Injection Frequency: Weekly options (dulaglutide, tirzepatide) offer greater convenience compared to daily (liraglutide) or twice-daily (exenatide) options 3
  • Patient Compliance: In the Indian setting, liraglutide has shown superior compliance compared to exenatide 4

Side Effect Profile

  • Gastrointestinal Effects: All GLP-1 RAs may cause nausea, vomiting, and diarrhea, particularly during initiation
  • Tolerability: Long-acting agents typically have better gastrointestinal tolerability profiles 5
  • Hypoglycemia Risk: Low when used as monotherapy, but increased when combined with sulfonylureas or insulin 6

Clinical Considerations for Indian Patients

  • Efficacy: Indian patients show similar glycemic responses to GLP-1 RAs compared to global data 4
  • Weight Loss: Benefits are consistent with global findings 4
  • Cost Barrier: The high cost of these medications represents a significant barrier to widespread use in India 4
  • Blood Pressure: In a single-center Indian study, liraglutide reduced the need for antihypertensive medications 4

Important Caveats

  • Not all GLP-1 RAs available globally may be marketed or widely available in India
  • Cost considerations may limit accessibility for many patients
  • Proper storage requirements (refrigeration) may present challenges in certain settings
  • Gastrointestinal side effects, while typically transient, may affect adherence during initial treatment phases
  • Patients with personal or family history of medullary thyroid carcinoma should not use these medications 2

When selecting a GLP-1 RA for Indian patients, consider frequency of administration, cost, storage requirements, and individual patient factors such as the need for postprandial versus fasting glucose control.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Cardiovascular Benefits of GLP-1 Receptor Agonists

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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