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Study 22 of 25Tirzepatide literaturebiorxiv-preprint · Observational

Weight Loss With Microdose Tirzepatide: Real-World Outcomes in Patients Initiating Treatment Below 2.5 mg Weekly

Weight loss was observed in patients starting tirzepatide at doses below 2.5 mg weekly, but the findings are preliminary and should be interpreted with caution.

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Where it sits

this study against the rest of the tirzepatide corpus
4
Preclinical
15
Observational · this one
1
Open-label
2
Randomised
3
Reviews

Summary and findings

This study measured weight loss in adults initiating compounded injectable tirzepatide at doses below 2.5 mg weekly. The population included individuals with a baseline BMI ≥27 kg/m2. Results indicated weight loss at various follow-up windows, with no therapeutic claims made.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Mean body-weight loss was 6.10% (95% CI 4.60-7.60; n=8) in the 60-89-day window at a median 65.5 days.

Abstract

The authors’ words, as biorxiv-preprint supplied them

<h4>Background: </h4> Tirzepatide is conventionally initiated at 2.5 mg weekly and titrated to approved maintenance doses. Evidence describing weight change at injectable starting doses below 2.5 mg/week is limited. <h4>Methods:</h4> We conducted a retrospective, single-organization observational study of adults documented as new GLP-1 starts, with baseline body mass index (BMI) ≥27 kg/m2, who initiated compounded injectable tirzepatide at a microdose of 1 or 2 mg/week (below the standard 2.5 mg/week starting dose). Source records were reviewed for baseline validity, prior treatment, weight consistency, and treatment exposure. The main descriptive analysis selected the latest eligible measurement per patient within observation windows of 14-35, 36-59, and 60-89 days of adjudicated treatment exposure, excluding observations after escalation above 2 mg/week. All 93 eligible measurements were included in a supporting random-intercept model. Analyses were retrospective and hypothesis-generating; no formal sample-size calculation was performed. <h4>Results:</h4> Sixty patients contributed 93 eligible follow-up measurements, of which 84 were selected for patient-window summaries. Mean age was 47.3 years, 81.7% were female, and mean baseline BMI was 33.3 kg/m2. Mean body-weight loss was 2.18% (95% CI 1.61-2.76; n=57) in the 14-35-day window at a median 21 days, 3.58% (95% CI 2.43-4.72; n=19) in the 36-59-day window at a median 48 days, and 6.10% (95% CI 4.60-7.60; n=8) in the 60-89-day window at a median 65.5 days. The adjusted model estimated 2.16 percentage points greater loss per 30 days of treatment exposure (95% CI 1.69-2.63). <h4>Conclusions:</h4> Weight loss was observed within the 14-35-, 36-59-, and 60-89-day observation windows among evaluable adults initiating compounded injectable tirzepatide at 1-2 mg/week. These uncontrolled findings are hypothesis-generating; the 36-59- and 60-89-day estimates are particularly limited by sparse follow-up.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Limitations

Not reported in abstract.

Elsewhere in the Tirzepatide corpus

BDual GIP/GLP-1 Receptor Agonist Versus Selective GLP-1 Receptor Agonist in Patients Undergoing Primary Total Knee or Hip Arthroplastybiorxiv-preprint · At 2 years, tirzepatide exposure was associated with lower odds of mechanical complications (OR 0.64, 95% CI 0.42 to 0.96).HumanCTirzepatide preserves hematopoietic stem and progenitor cycling while remodeling inflammatory monocytes in obese micebiorxiv-preprint · Not reported in abstract.AnimalDThe GLP-1 Nutritional Paradox: A Structured Review with Novel Quantitative Frameworks for Sarcopenic Risk and Micronutrient Adequacy in GLP-1 Receptor Agonist Pharmacotherapybiorxiv-preprint · Mean body-weight reduction of 20.9% with tirzepatide in phase 3 trials.reviewCA near-infrared light-triggered platform for on-demand drug release in bone repair.Colloids and surfaces. B, Biointerfaces · 2026 · Bacterial inhibition rate of 99%.In vitroDFrom adiposity to multisystem morbidity: the case for weight loss as disease modification.The lancet. Diabetes & endocrinology · 2026AInsights from a double-blind, randomized, direct-to-participant intervention trial for Long COVIDbiorxiv-preprint · 2026 · 1,058 participants enrolled in 73 days.Human