All GLP-1 medications from licensed 503A compounding pharmacies Browse Products

Weight loss projection

Future you

Enter your weight, goal, and compound. You\u2019ll see projected milestones at 3, 6, and 12 months with a 25th to 75th percentile range drawn from clinical trial data.

Reviewed by the FormBlends Medical Review Team. Last reviewed .

This is a projection, not a prediction

The numbers this tool shows come from two large randomized trials. STEP 1 (Wilding et al., NEJM, 2021) followed 1,961 adults with obesity on 2.4mg weekly semaglutide for 68 weeks and found an average 14.9% body weight reduction against 2.4% on placebo. SURMOUNT-1 (Jastreboff et al., NEJM, 2022) followed 2,539 adults on 5mg, 10mg, or 15mg weekly tirzepatide for 72 weeks and found averages of 15.0%, 19.5%, and 20.9%.

Averages hide a lot. Some participants lost over 30% of body weight. Others lost under 5%. The tool shows you the middle half of the distribution (25th-75th percentile) because that\u2019s where most people actually land, not where a marketing page would put the arrow.

Don\u2019t treat the output as your future. Treat it as the shape of a reasonable expectation if everything goes roughly the way it went for trial participants. Your body, your adherence, and your clinician\u2019s titration plan do the real work.

Projection Tool

Future You

See where you could be at 3, 6, and 12 months based on published clinical trial averages. These are typical ranges, not guarantees.

How the projection is built

The tool uses a two-layer model. The first layer is a piecewise rate curve that maps week number to expected loss per week. The curve is flat and slow for the first 16 weeks (titration phase, where dose is still climbing), steepest from weeks 17 to 40 (therapeutic dose, primary loss phase), tapers from weeks 41 to 52 (approaching plateau), and flattens toward week 68 and beyond (maintenance).

The second layer anchors the curve to trial endpoints. For semaglutide, the endpoint is 14.9% at week 68 from STEP 1. For tirzepatide, it\u2019s 20.9% at week 72 from SURMOUNT-1 on 15mg, scaled down for 10mg (19.5%) and 5mg (15.0%). The curve integrates to match those endpoints, then interpolates backward to give you 3-month and 6-month milestones.

The 25th to 75th percentile band comes from the published trial distributions. STEP 1 reported that 69.1% of participants reached 10% loss, 50.5% reached 15%, and 32.0% reached 20%. SURMOUNT-1 reported 50% of 15mg participants reached 22.5%. The model fits a log-normal distribution to these published quantiles and extracts the 25th and 75th percentile curves alongside the mean.

A few caveats. The trial participants had BMI \u2265 30 or \u2265 27 with one comorbidity; the model doesn\u2019t check whether you match that. Trial participants got lifestyle counseling (500-kcal deficit target, 150 min/wk activity); the model assumes you do too. Real-world response may be lower on average than trial response because adherence is usually worse outside a trial setting.

Why your number will vary from the projection

Adherence. The biggest single factor. Trial participants took their injection on schedule. Real-world miss rates of 10-20% per year are common. Each missed week shifts the curve right.

Starting BMI. People with higher baseline BMI tend to lose more absolute pounds but similar percentages. STEP 1 subgroup analysis showed the 14.9% result held across BMI strata, but those below 30 lost slightly less.

Metabolic rate and body composition. Lower resting metabolic rate, lower muscle mass, menopausal status, and thyroid function all shift the curve. STEP 5 (Garvey et al., Nature Medicine, 2022) followed patients for 104 weeks and found women with postmenopausal status lost on average 1-2 percentage points less than premenopausal women at equivalent doses.

Titration speed. The label schedule takes 16-20 weeks to reach therapeutic dose. Going slower because of side effects can push 6-month milestones to month 8 or 9. Jumping ahead of the schedule rarely accelerates loss; it usually just increases nausea.

Concurrent medications. Steroids, some antipsychotics (olanzapine, clozapine), some antidepressants (paroxetine, mirtazapine), beta blockers, insulin, and sulfonylureas all tend to slow weight loss. Stimulants and thyroid replacement can speed it up.

STEP and SURMOUNT extensions. STEP 5 (104-week follow-up) and SURMOUNT-4 (withdrawal) tell us something important: people who stop lose the benefit, and people who continue tend to plateau around month 15-18 rather than keep losing forever.

Frequently asked

How accurate is this?

It’s a projection, not a prediction. The curves come from the STEP 1 trial (Wilding et al., NEJM, 2021) for semaglutide and SURMOUNT-1 (Jastreboff et al., NEJM, 2022) for tirzepatide. Trial participants averaged 14.9% body weight loss on 2.4mg semaglutide and 20.9% on 15mg tirzepatide at 68 and 72 weeks respectively. Your actual result can land anywhere in the 25th to 75th percentile band the tool shows, and some people fall outside it in either direction.

What if I don’t lose this much?

Roughly a quarter of trial participants lost less than the 25th percentile. Reasons include slower titration, skipped doses, weight stall windows, concurrent meds that interfere with weight loss (steroids, some antipsychotics, some antidepressants), and baseline metabolic factors like insulin resistance severity. If you’re weeks in and not moving, talk to your provider about dose adjustments rather than quitting.

What if I lose more?

About a quarter of participants lost more than the 75th percentile. Faster responders often have higher baseline BMI, stricter diet adherence, or both. Above-average loss isn’t automatically better. Losing more than 1% of body weight per week for sustained periods can cost lean mass, so most clinicians will slow titration if loss outpaces muscle retention.

Does this include diet and exercise?

The STEP 1 and SURMOUNT-1 trials included lifestyle counseling (500-calorie deficit target, 150 minutes weekly activity). So yes, the projections assume you’re doing reasonable diet and activity work alongside the medication. No-lifestyle-change scenarios typically produce smaller loss than the trial averages.

Why are the ranges so wide?

Because individual response varies a lot. The 25th-75th percentile band covers half of trial participants. The full trial distribution ran from under 5% loss to over 30% loss. BMI, age, sex, adherence, titration speed, metabolic rate, and comorbidities all pull the curve. The width is honest; narrow predictions would be dishonest.

Does this apply to compounded versions?

The trials used branded semaglutide (Wegovy) and tirzepatide (Zepbound). FormBlends compounded formulations contain the same active ingredients at the same dose ranges, so the pharmacology is expected to match. Bioequivalence has not been tested head-to-head in large trials, so treat the projection as a reasonable expectation, not a guarantee.

Keep reading

Want a real treatment plan, not just a projection?

FormBlends licensed clinicians handle intake, labs, titration, and follow-up for compounded semaglutide and tirzepatide.

Start your consultation

Sources

  • Wilding JPH, et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity. NEJM. 2021;384(11):989-1002. (STEP 1)
  • Jastreboff AM, et al. Tirzepatide Once Weekly for the Treatment of Obesity. NEJM. 2022;387(3):205-216. (SURMOUNT-1)
  • Garvey WT, et al. Two-year effects of semaglutide in adults with overweight or obesity: the STEP 5 trial. Nature Medicine. 2022;28(10):2083-2091.
  • Rubino D, et al. Effect of Continued Weekly Subcutaneous Semaglutide vs Placebo on Weight Regain. JAMA. 2021;325(14):1414-1425. (STEP 4)

Educational only. This tool does not provide medical advice, diagnose any condition, or recommend a course of treatment. Individual results vary. All medications described are compounded formulations containing the same active ingredients as their FDA-approved counterparts. Talk to your clinician before starting or changing any medication.