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REMEVi

Understand the evidence.
Then ask better questions.

What was studied, in whom, for how long—and where the evidence stops. Read the original trials alongside an interactive look at the molecules.

Editorial evidence check: September 17, 2026. Not a new medical review.

Illustrative semaglutide vialIllustrative tirzepatide vial
Product illustrations. The studies below tested manufacturer medicines, not these compounded preparations.

Four studies. Four different questions.

The original three trials randomized 5,303 participants in total (1,961 + 2,539 + 803). That is a count across separate studies, not a pooled analysis or a trial of REMEVi care. SURMOUNT-5 adds a direct comparison.

STEP 1 · NEJM · 2021

Semaglutide versus placebo

Participants
1,961 adults without diabetes; BMI ≥30, or ≥27 with a weight-related condition.
Treatment
Semaglutide 2.4 mg weekly or placebo, with lifestyle support.
Duration
68 weeks
Finding
14.9% average weight loss versus 2.4% with placebo.

Read with this limit: Manufacturer medicine; not a compounded-product trial. Funded by Novo Nordisk.

Read the original study →

SURMOUNT-1 · NEJM · 2022

Tirzepatide versus placebo

Participants
2,539 adults without diabetes; BMI ≥30, or ≥27 with a weight-related condition.
Treatment
Tirzepatide 5, 10 or 15 mg weekly, or placebo; lifestyle support.
Duration
72 weeks, including dose escalation
Finding
At 15 mg: 20.9% average weight loss versus 3.1% with placebo.

Read with this limit: The 20.9% result is the 15 mg group, not every dose. Separate from STEP 1. Funded by Eli Lilly.

Read the original study →

STEP 4 · JAMA · 2021

Continue treatment or stop?

Participants
803 adults randomized after completing a 20-week semaglutide run-in; 902 had started it. No diabetes.
Treatment
Continue semaglutide 2.4 mg weekly or switch to placebo; lifestyle support in both groups.
Duration
48 randomized weeks after the 20-week run-in
Finding
From week 20: 7.9% further loss with continued treatment; 6.9% regain after switching to placebo.

Read with this limit: Selected people who reached the run-in dose. These percentages start at week 20, not baseline. Funded by Novo Nordisk.

Read the original study →

SURMOUNT-5 · NEJM · 2025

A direct comparison

Participants
751 adults with obesity, without type 2 diabetes.
Treatment
Maximum tolerated weekly doses: tirzepatide 10/15 mg or semaglutide 1.7/2.4 mg.
Duration
72 weeks
Finding
20.2% average loss with tirzepatide versus 13.7% with semaglutide.

Read with this limit: Open-label and funded by Eli Lilly. No compounded preparations studied.

Read the original study →

Trial averages are not individual forecasts. Do not compare separate trials as though participants and methods were identical. These findings do not establish effectiveness, safety or equivalence for compounded preparations.

A mechanism is not an outcome.

GLP-1 receptor activity helps explain appetite regulation and glucose-dependent insulin release. Tirzepatide also activates GIP receptors. Neither mechanism guarantees a percentage reduction in cravings, calorie intake, HbA1c or preserved muscle.

Benefits and risks depend on the product, dose, population and outcome studied. Review the complete warnings with your clinician.

· FIG. 00 · The Molecule · La Molécula ·

Explore the molecules.

GLP-1 (7–37) · α-HELIX
31 RESIDUES · 3.6 / TURN
DRAG TO ROTATE · CLICK A RESIDUE

Simplified 31-position teaching model. The tirzepatide view is schematic: it does not represent its actual 39-amino-acid sequence. Specifications describe the molecules in approved medicines; they do not verify a compounded preparation. Wegovy · Zepbound

FIG. 00 · SEMAGLUTIDE
C₁₈₇H₂₉₁N₄₅O₅₉
HYDROPHOBIC
POLAR
POSITIVE
NEGATIVE
MODIFIED
· SPEC SHEET ·NEJM 2021 · STEP-1
Semaglutide
Long-acting analog · 31 aa
Molecular formulaC₁₈₇H₂₉₁N₄₅O₅₉
Molecular weight4,113 Da
Half-life168 hrs (7 days)
Dose cadenceOnce-weekly
Receptor(s)GLP-1R
· RESIDUE · ANNOTATION ·
Lys²⁶ · semaglutide attachment

A C18 fatty diacid and linker promote albumin binding, contributing to prolonged action. See section 11 of the Wegovy prescribing information.

· WHERE IT ACTS · DÓNDE ACTÚA ·MECHANISMS, NOT PROMISED RESULTS
Appetite
Brain
GLP-1 pathways
Appetite and calorie intake can change; response varies.
Digestion
Stomach
Gastric emptying
Emptying can be delayed. Digestive adverse effects also matter.
Glucose
Pancreas
Glucose-dependent action
Insulin and glucagon regulation; low glucose risk rises with certain diabetes drugs.
Body composition
Muscle
No preservation guarantee
Weight loss can include lean tissue. Discuss nutrition and strength with your clinician.

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