Podcast episode 66 (in German)
RAD140 (Testolone): the SARM fact-checked
September 5, 2026
Acting like testosterone, but only in muscle: that is the idea behind SARMs, and RAD140 is their best-known representative. The episode cleanly separates what of it is pharmacology and what is forum promise — with the study data that really exist.
What it is about
SARM stands for selective androgen receptor modulator: a molecule that targets the same receptor as testosterone, but as far as possible only in muscle and bone tissue. RAD140 was developed around 2010 at Radius Health, first against muscle wasting, later as an approach against certain forms of breast cancer. The episode goes from this idea to the data: there is exactly 1 published human study, and it had a completely different goal than muscle building. Then it sorts out the price list — hormone axis, liver, blood lipids, missing long-term data — and the market on which the substance is traded as a research chemical. At the end stand its place on the series’ muscle ladder and a clear look at doping controls.
Key points
- RAD140 was developed around 2010 at the biotech company Radius Health — originally for patients with muscle wasting and later against certain forms of breast cancer, never as a training supplement.
- There is exactly 1 published human study, a phase 1 trial in postmenopausal women with advanced breast cancer; there, of all things, the liver values were dose-limiting.
- For the muscle-building use there is not a single controlled human study up to 2026 — everything else is animal model data and user reports from forums.
- The episode’s risk list has 4 items: a throttled own hormone axis with lowered testosterone, liver damage in case reports, falling HDL with a worse ApoB profile and completely missing long-term data.
- An analysis in the journal JAMA tested SARM products bought online: only about half contained the declared substance in the declared amount; the rest were incorrectly dosed, contaminated or something else entirely.
- The SARM family shows the same pattern: ostarine made it into phase 3 trials against muscle wasting and was still never approved; ligandrol showed lean mass gains along with clear testosterone suppression.
- The episode’s verdict: for 99 percent of listeners, strength training, protein, creatine and good sleep over 2 to 3 years deliver more lasting muscle mass than an RAD140 cycle — without the burden.
Where the data stop
The data end early. What is known about the effect on muscle and bone comes from animal models; the only human study tested a cancer therapy, not muscle building, and after that clinical development went quiet. On long-term consequences there is simply no knowledge, and with a receptor that also sits in the heart, brain and prostate, this lack of knowledge is itself a risk factor.
Then there is the market: no SARM is approved as a medicine anywhere; it is traded as a research chemical without quality control. In sport, SARMs are on the WADA prohibited list, RAD140 is among the substances most frequently testing positive, and detection windows extend over weeks to months depending on use. Because of the androgenic effect, particular restraint applies to women, and in pregnancy in any case. This page therefore names neither amounts nor regimens.
Listen (in German)
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Published on September 5, 2026.
The topic in the database
- The best-known SARM: strong muscle effect via the androgen receptor – but only one (discontinued) human study and a serious risk profile.RAD140 (Testolone)
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Information only, not medical advice and not a usage or dosage recommendation. Prescription-only and unapproved substances belong in the hands of a physician. Last updated: 2026-09-19.