COMPOUNDS / PEPTIDE / TIRZEPATIDE
PEPTIDE

TIRZEPATIDE

MEDIUM RISK
BEST FOR:Weight Loss●●●●●●●●●○9/10
TIRZEPATIDE · MOUNJARO · ZEPBOUND · LY3437943
GLP-1GIPWeight LossDiabetesPeptideMetabolic

Dual GIP and GLP-1 receptor agonist for type 2 diabetes and obesity, administered as a once-weekly subcutaneous injection.

ROUTE / DOSAGE
LOW2.5mg
STANDARD5-15mg
HIGH15mg
Note: Start at 2.5mg weekly for 4 weeks, titrate in 2.5mg increments every 4 weeks to target maintenance dose (5/10/15mg)
CYCLE
Once weekly injection long-term continuous use
BIOAVAILABILITY
~80% subcutaneous
ACTIVE DURATION
~7 days (subjective)
STORAGE
Refrigerate at 2-8°C may store at room temperature (up to 30°C) for up to 21 days protect from light
HALF-LIFE
~5 days (plasma)
DURATION BREAKDOWN
Total~7 days
Onset1-3 days
Come up1-2 days
Peak1-5 days
Offset2-4 days
After effects1-2 weeks
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
6 documented
Significant weight reduction (15-20%)
Improved glycemic control
Appetite suppression
Delayed gastric emptying
Reduced fasting glucose
Improved insulin sensitivity
§ 02 — RISKS
Gastrointestinal events: nausea, vomiting, diarrhea, constipation (most common, typically mild-moderate)
Pancreatitis (rare but serious)
Gallbladder disease including gallstones
Hypoglycemia when combined with insulin or sulfonylureas
Potential risk of thyroid C-cell tumors (boxed warning based on rodent studies)
Injection site reactions
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Multiple phase 3 trials (SURMOUNT-1, SURMOUNT-5, SURPASS-1) demonstrate that tirzepatide produces substantial and sustained weight loss of 15-20% over 72 weeks, significantly outperforming semaglutide in head-to-head comparison. In the SURMOUNT-1 3-year analysis, tirzepatide reduced body weight by 12-20% depending on dose and markedly lowered progression to type 2 diabetes (1.3% vs 13.3% with placebo). Phase 2 data also show efficacy for metabolic dysfunction-associated steatohepatitis (MASH) with fibrosis resolution rates of 44-62% versus 10% placebo. Gastrointestinal adverse events are the most common side effects, typically mild to moderate and occurring during dose escalation. Long-term safety beyond 3 years and real-world persistence data remain limited.

§ 06 — SOURCES
[1]
Tirzepatide for Obesity Treatment and Diabetes Prevention (SURMOUNT-1)
pubmed.ncbi.nlm.nih.gov ↗
[2]
Tirzepatide as Compared with Semaglutide for the Treatment of Obesity (SURMOUNT-5)
pubmed.ncbi.nlm.nih.gov ↗
[3]
Tirzepatide for Metabolic Dysfunction-Associated Steatohepatitis with Liver Fibrosis
pubmed.ncbi.nlm.nih.gov ↗
[4]
Tirzepatide for Weight Reduction in Chinese Adults With Obesity (SURMOUNT-CN)
pubmed.ncbi.nlm.nih.gov ↗
[5]
Semaglutide vs Tirzepatide for Weight Loss in Adults With Overweight or Obesity
pubmed.ncbi.nlm.nih.gov ↗
[6]
Efficacy and safety of tirzepatide in patients with type 2 diabetes (SURPASS-1)
pubmed.ncbi.nlm.nih.gov ↗
[7]
PubMed PMID 39996356
pubmed.ncbi.nlm.nih.gov ↗
[8]
PubMed PMID 38388874
pubmed.ncbi.nlm.nih.gov ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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