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Lexicon

Clenbuterol

A beta-2 agonist with fat-burning and appetite-suppressing effects, not a steroid, but with a clear load on the heart and circulation.

2 min read 11 sources

White tablet bottle with a black TPD label for Clenbuterol on a white podium, next to a blue 3D molecule model in a bright lab
Compound approved · as an asthma drug in some countries, not in the USLab tested in the shop

Summary

At a glance

Sources checked on 26 Oct 2026

Lean mass in 2 weeks
+0.91 kg

11 healthy men against placebo, fat mass unchanged1

Maximal oxygen uptake
-7 %

same study, endurance fitness worse1

Resting energy expenditure
+21 %

6 young men after a single dose, fat oxidation +39%2

Insulin-stimulated glucose uptake
+13 %

11 healthy men, 2 weeks against placebo3

  • Clenbuterol is a beta-2 agonist. Outside the US it is approved as an asthma drug in some countries, but in most countries not for human use.8211
  • In the first randomised study in healthy men 2 weeks brought 0.91 kg more lean mass. Fat mass stayed the same, maximal oxygen uptake fell by 7 percent.1
  • After a single dose resting energy expenditure rose by 21 and fat oxidation by 39 percent. The signals in muscle weakened with repeated doses.21
  • Small studies test clenbuterol in muscle diseases such as Pompe disease and ALS. In the ALS study 13 of 25 people stopped because of side effects.56
  • Case reports mainly describe heart problems up to heart attack and death. Everything here is research status, not a recommendation.7
Profile

Updated May 2026

Class
Beta-2 agonist

sympathomimetic

Use
Oral

dosed in mcg

Half-life
long

over a day

WADA
Banned

category S1.2 / S3

Sizes
40 to 60 mcg

2 sizes in the shop

Contents 14 sections
  1. At a glance
  2. What is Clenbuterol?
  3. How it works
  4. How to take it
  5. Dosing
  6. What the research shows
  7. Research status
  8. Side effects
  9. Practice
  10. Storage
  11. Related compounds
  12. FAQ
  13. Glossary
  14. Sources

What is Clenbuterol?

Clenbuterol is a beta-2 agonist, originally an asthma medicine to widen the airways. In the cutting corner it is used for its fat-burning and appetite-suppressing effect. It is explicitly not a steroid and not an anabolic in the classic sense.

Up front: Clenbuterol noticeably loads the heart and circulation. The fat-burning effect is real. So is the price for it.

Comparison

Fat loss compounds in the lexicon

What each entry targets, as stated in the TPD lexicon. Tap a card to open its entry.

Simplified. Salbutamol uses the same receptor as clenbuterol but acts shorter. Yohimbine blocks a brake receptor, T3 acts via thyroid hormone receptors, DNP directly in the mitochondria. 11

How it works

Clenbuterol activates beta-2 receptors and through them ramps up metabolism: more heat production (thermogenesis), more fat burning, dampened appetite. At the same time heart rate and partly blood pressure rise, the flip side of the same signal.

The body adapts relatively fast (the receptors become less sensitive), which is why the effect fades after one to two weeks.

Where it acts

Where clenbuterol acted in studies

Tap a point or a card. Colour = beta-2 receptor, grey = observed.

  1. Airways

    Widens the bronchi, hence the approval as an asthma drug8

    β2
  2. Skeletal muscle

    More muscle protein and lean mass, the signal fades with continued use1

    β2
  3. Fat metabolism

    Fat oxidation +39% after one dose, fat mass unchanged after 2 weeks2

    Observed in trials
  4. Heart

    Case reports: racing heart, atrial fibrillation, heart muscle damage7

    Observed in trials

Targets in the ChEMBL database11

Compound ChEMBL CHEMBL49080: one recorded mechanism, Agonist.

Beta-2 adrenergic receptor
Gene
ADRB2
UniProt
P07550
ChEMBL
CHEMBL210
Action
Agonist
Translucent fat cells with golden fat droplets, blue 3D molecules docking onto them
Beta-2 signals boost heat production and fat burning. Symbolic image.

How to take it

Oral, dosed in micrograms (mcg), not in mg.

  • Usually in the morning, because the stimulating effect can disturb sleep.
  • With some water, with or without food.
  • Because of the adaptation, a pattern like two weeks on, two weeks off is often run.
Tablet bottle with a black TPD label for Clenbuterol next to a glass of water and a few white tablets
Taken orally, according to the entry usually in the morning. Symbolic image.

Dosing

Dosing

Dosing, titration and syringe

Loading the dosing information …

  • Getting started and stepping up, drawn as a staircase
  • Units on the U-100 syringe for every step
  • How long one vial lasts

What the research shows

A recent human study (Hostrup, 2025) showed that Clenbuterol does build lean mass and muscle protein, but at the same time worsens endurance fitness and dulls the beta-2 signals in muscle. That sums up the clenbuterol dilemma well: a bit of muscle and fat effect, paid for with worse conditioning and heart strain.

In animal models the muscle-building and fat-lowering effect is clear, in humans it is weaker, while the side effects remain.

Study results

What the trials measured

Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.

Endurance after 2 weeks1

11 healthy men, crossover against placebo

Maximal oxygen uptake1
Clenbuterol -7%
Exercise capacity1
Clenbuterol -4%

Values from the abstract. Plus 0.91 kg more lean mass, but no change in fat mass, sprint power, heart muscle mass or blood volume. Fat burning in muscle was slowed.

About two hours after one dose2

6 young men, change from the value before the dose

Resting energy expenditure2
Clenbuterol +21%
Fat oxidation2
Clenbuterol +39%
Blood glucose2
Clenbuterol +30%
Insulin2
Clenbuterol +130%
Fatty acids in the blood2
Clenbuterol +180%
Maximal thigh strength2
Clenbuterol -4%

Values from the abstract, without a placebo group. Lactate rose by 90 percent, carbohydrate oxidation stayed the same.

Glucose uptake into muscle under insulin34

Compared with placebo, healthy men 2 weeks, overweight people 4 weeks

Whole body3 11 healthy men
Healthy men +13%
Hamstring muscles4 14 people with overweight
Overweight +13%
Front thigh4 trend only
Overweight +15%

Values from the abstracts. The value for the front thigh was not statistically certain (p = 0.072). The study in healthy men reported no serious side effects.

Muscle disease Pompe disease5

Phase 1/2, on top of enzyme therapy, 11 of 13 completed the study

Inspiratory strength5
Pompe disease, 52 weeks +8%
6-minute walking distance5 as percent of predicted
Pompe disease, 52 weeks +3%
Glycogen in muscle5
Pompe disease, 52 weeks -50%

Values from the abstract. The placebo group showed no significant changes. Mild, transient side effects were raised muscle enzyme values, cramps and tremor.

Glass lung model and a small glass flask on a stainless steel trolley in a bright lab
Originally an asthma drug. Symbolic image.

Research status

Where the research stands

ClinicalTrials.gov lists 12 trials with clenbuterol. 9 are shown here. Two with unknown status are missing, a Pompe disease trial was withdrawn without participants. As of 26 Oct 2026. 10

  1. Preclinical Animal studies: more muscle mass in many species
  2. Phase 1 2 trials, 0 completed, 1 stopped early
  3. Phase 2 6 trials, 5 completed
  4. Phase 3 no registered trial
  5. Approval as an asthma drug in some countries, not in the US
Approved as an asthma drug in some countries outside the US, in most countries not for human use. In the US mainly used in veterinary medicine.8
Show all 7 trials on a timelineHide timeline 6 completed 1 running 4 with results
Phase 2
Without phase

Bar: start to primary endpoint (planned for running trials). Green = completed, blue = progress until 26 Oct 2026. Phase 1: 2 trials on safety and pharmacokinetics, not shown as bars.

Side effects

  • Shaking (especially of the hands), racing heart, palpitations.
  • Restlessness, sleep problems, sweating.
  • Muscle cramps, often linked to loss of magnesium and potassium.
  • Longer term, strain on the heart muscle, the central risk.

Tolerability

Tolerability in the ALS study

This many of 25 participants had side effects or stopped because of them. Most common were tremor, cramps, insomnia and stiffness.

96 of 100 Clenbuterol
Event Clenbuterol
Side effects6 96%
Stopped due to side effects6 52%

The dose was increased up to the highest study dose. Case reports in athletes describe racing heart, atrial fibrillation, heart muscle damage, heart attack and deaths.67

Practice

  1. Ease in slowly and watch heart rate.

  2. Ensure enough magnesium, potassium and fluids (cramps).

  3. Do not take late in the day or sleep suffers.

  4. With heart problems or high blood pressure, leave it alone.

  5. Banned and detectable in official competition.

Glass carafe of water, a banana and a bowl of nuts on a bright kitchen counter

Storage

Store dry, cool and protected from light, out of reach of children. Keep the original container closed and mind the expiry date.

Three white tablet bottles and a folded light blue towel on a white shelf
Dry, cool and protected from light in the closed original container. Symbolic image.

Related

Related compounds

Same receptors or a different path: all in the TPD lexicon.

FAQ

Common questions about Clenbuterol

Short answers, each backed by the sources below.

Is clenbuterol approved?

In some countries outside the US as an asthma drug, but in most countries not for human use. In the US it is mainly used in veterinary medicine. ChEMBL lists the compound with phase 2 as the highest phase.8211

Does clenbuterol build muscle in humans?

In the first randomised study lean mass rose by 0.91 kg in 2 weeks and muscle protein increased. Fat mass stayed the same. At the same time maximal oxygen uptake fell by 7 and exercise capacity by 4 percent.1

Does clenbuterol burn fat?

After a single dose resting energy expenditure rose by 21 and fat oxidation by 39 percent. In the 2-week study, however, fat mass did not change.21

Why does the effect fade?

The 2-week study showed that beta-2 signals in muscle weakened with repeated doses. The entry describes this as tolerance after one to two weeks.1

What is clenbuterol studied for medically?

Small studies test it in muscle diseases. In Pompe disease muscle glycogen fell by 50 percent after 52 weeks and inspiration became 8 percent stronger. Further studies cover ALS, spinal and bulbar muscular atrophy and FSHD.5610

How dangerous is clenbuterol for the heart?

A review of case reports in 24 athletes mainly found heart problems: racing heart, atrial fibrillation, myocarditis, heart attack and deaths. A case report describes a pulse of 254 and strongly lowered potassium after a tenfold overdose.78

Glossary

Terms explained briefly

Dotted words in the text open these explanations directly.

Beta-2 agonist
Substance that activates beta-2 receptors. It widens the bronchi and acts on muscle and metabolism.
Beta-2 receptor
Binding site for adrenaline in the bronchi, muscles and vessels.
Bronchi
The branching airways of the lungs.
Lean mass
Body weight without fat, mainly muscle, organs and water.
Maximal oxygen uptake
How much oxygen the body can use at full effort. A measure of endurance.
Sympathomimetic
Compound that mimics the part of the nervous system that switches the body to performance.
Thermogenesis
Heat production in the body that uses extra energy.
Tolerance
Receptors become less sensitive with continued use and the effect fades.
WADA
World Anti-Doping Agency. It keeps the list of substances banned in sport.

Evidence

Sources

Show all 11 sourcesHide sources 9 Studies1 Trial registry1 Database checked 26 Oct 2026

Studies

  1. Clenbuterol over 2 weeks: more lean mass, less endurance

    Hostrup et al., The Journal of Physiology, 2025

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  2. Energy expenditure and fat oxidation after one dose

    Jessen et al., Drug Testing and Analysis, 2020

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  3. Glucose uptake in healthy men, 2 weeks against placebo

    van Beek et al., Nature Communications, 2023

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  4. Muscle glucose uptake in overweight, 4 weeks

    Van Lier et al., Nature Communications, 2026

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  5. Phase 1/2 study in Pompe disease

    Koeberl et al., Molecular Therapy, 2018

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  6. Open-label study in ALS

    Li et al., Journal of Clinical Neuromuscular Disease, 2023

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  7. Adverse events in athletes, review of case reports

    Kumari et al., International Journal of Legal Medicine, 2023

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  8. Case report: overdose with racing heart and atrial fibrillation

    Daubert et al., Journal of Medical Toxicology, 2007

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed
  9. Clenbuterol and athletic performance, review

    Spann und Winter, Annals of Pharmacotherapy, 1995

    Checked 26 Oct 2026 via doi.org, Crossref, PubMed

Trial registry

  1. Clenbuterol on ClinicalTrials.gov

    ClinicalTrials.gov, U.S. National Library of Medicine

    Checked 26 Oct 2026 via ClinicalTrials.gov API v2

Database

  1. Clenbuterol in ChEMBL (target)

    ChEMBL, EMBL-EBI (CHEMBL49080)

    Checked 26 Oct 2026 via ChEMBL API

In the shop

Clenbuterol in the catalog

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