
Tirzepatide and heart failure: what SUMMIT’s combined outcome means
Read SUMMIT’s tirzepatide heart-failure results: the combined endpoint, separate death counts, health-status score and current US label context.
How to read research on GLP-1 medicines and emerging metabolic compounds.
23 articles · Newest first

Read SUMMIT’s tirzepatide heart-failure results: the combined endpoint, separate death counts, health-status score and current US label context.

Understand ESSENCE’s two liver-biopsy endpoints, the 72-week interim findings and what Wegovy’s accelerated MASH approval does and does not establish.

Understand SELECT’s 20% cardiovascular result, the absolute event proportions, the combined endpoint and who the semaglutide trial actually studied.

Explore the small GHRP-6 human pharmacokinetic study, why distribution and elimination half-lives differ, and why neither establishes a treatment schedule.

Understand weight regain after tirzepatide, the two baselines in SURMOUNT-4, and why a percentage of body weight differs from a percentage of weight lost.

Understand the STEP 8 semaglutide–liraglutide comparison, percentage-point differences, treatment discontinuation and the limits of applying averages.

Understand tirzepatide’s DXA findings, the difference between lean tissue and muscle, and why percentages of weight loss need careful interpretation.

Understand SURMOUNT-OSA’s breathing-event results, the role of PAP in the trials, and what tirzepatide’s sleep-apnea approval does and does not mean.

Explore how SNAC helps oral semaglutide absorption, what food-effect studies measured, and why tablet evidence cannot validate a different formulation.

Read FLOW’s semaglutide kidney results, distinguish relative risk from percentage points, and see how new mechanism research fits the clinical evidence.

Cagrilintide and CagriSema are different interventions. Learn which trial produced each result, how analyses differ, and what FDA says about cagrilintide.

Read survodutide’s MASH trial accurately: why improvement without worsening fibrosis differs from scar reversal, and what its response rates measure.

What STEP 1 and STEP 4 found after semaglutide withdrawal, why their percentages differ, and what group averages cannot predict for an individual.

What small human GHRP-2 studies found about appetite, what their meal-intake results cannot prove, and how FDA safety concerns change the context.

MK-677 is not a peptide. Explore ibutamoren’s human trial evidence, why fat-free mass differs from strength, and its FDA status and safety concerns.

Explore AOD-9604 weight-loss research, the larger negative obesity trial, and why changes within a treatment group do not prove a treatment effect.

Read the human ipamorelin trial behind the claims: what researchers tested, the nonsignificant result, and why its safety findings need context.

Understand the history of GEREF, its withdrawn approvals, and why an FDA finding about withdrawal does not approve a compounded sermorelin product.

Understand how compounded semaglutide differs from an approved medicine, why salt forms matter, and what to clarify with a prescriber or pharmacist.

Tesamorelin has a specific approved medical use. Learn why that differs from a general weight-loss claim and how to read the EGRIFTA WR label.

Explore what early CJC-1295 trials measured, why increased GH and IGF-1 do not prove clinical benefit, and what safety questions remain.

Understand the triple receptor agonist, its investigational status, and the questions to ask about new trial results.

What the SURMOUNT-5 trial found, which population it studied, and why averages are not individual predictions.