spec sheet8 rows
TDM-105795 is a topical thyroid hormone receptor agonist developed by Technoderma Medicines for pattern hair loss, and licensed to Cutia Therapeutics for Asia. ⚠️ It has no peer-reviewed publications of its own data; everything verifiable about it comes from a patent, a stock-exchange prospectus and a trial registry. The one animal study usually cited for it studies a different Technoderma compound, and no test of receptor selectivity has ever been run, which makes the common description of it as a beta-selective agonist unsupported.
- A genuinely reasonable mechanism: thyroid hormone drives follicles into their growth phase
- Chemical identity fully resolved and confirmed by three independent primary documents
- No safety data has been published in any peer-reviewed form
- The animal work measured body weight as its only systemic readout, with no thyroid hormone or cardiac endpoint at all
Mechanism
Thyroid hormone drives hair follicles into and through their growth phase, which is why hyperthyroidism can accelerate hair growth and hypothyroidism causes hair loss. A compound that switches on the thyroid hormone receptor in skin without reaching the rest of the body would in principle grow hair without the cardiac and bone effects of systemic thyroid excess. That is the whole idea behind this molecule, and it is a good one.
The compound is a diaryl-ether oxamic acid, chemically in the lineage of the earlier thyromimetics eprotirome and KB-141 rather than of the thyroid hormone itself.
⚠️ The pharmacology stops almost immediately after that. The only receptor experiment ever performed on this molecule is a thyroid hormone receptor beta reporter assay in the patent, giving a half-maximal concentration of about 179 nanomolar. No alpha-receptor assay exists, run by anyone, which means there is no selectivity ratio and the frequently repeated description of it as a beta-1-selective is not supported by any measurement. The 643-page prospectus filed by its Asian licensee does not contain the strings thyroid hormone receptor beta, THRB or beta agonist even once.
⚠️ Worth knowing about that one number: the patent's table of potencies is misnumbered differently in each member of the patent family, and the assignment of 179 nanomolar to this compound holds only because the table is stated to follow the figure list and the figure order matches. It is also not the most potent compound in its own patent; two siblings beat it two to threefold.
⚠️ AND THE MECHANISM THAT CIRCULATES FOR IT COMES FROM A DIFFERENT MOLECULE. The Wnt and Hedgehog signalling account, and the mouse hair-growth study behind it, are from work on TDM10842, another Technoderma compound. A review cites that paper in support of a sentence about TDM-105795, which is a citation that does not support the claim attached to it.
The only animal data for this compound itself is in the patent: mice treated twice daily for three weeks at three concentrations showed dose-dependent hair growth. ⚠️ Scored on a qualitative zero-to-three scale with no hair counts, and with no thyroid hormone, no thyroid stimulating hormone and no cardiac measurement of any kind; the sole systemic safety readout was body weight.
receptor fingerprint
Thyroid hormone receptor beta (THRB)Agonist
Thyroid hormone receptor alpha (THRA)Never tested
Evidencehow good the literature is
The evidence base is a patent, a regulatory filing, a substance registry and three registered trials. There are zero peer-reviewed publications of this compound's data.
The phase 2a has posted registry results. ⚠️ Four problems are visible in them. They carry no statistics of any kind. The primary endpoint figure disagrees with the number in the company's own press release, 22.4 against 24.3. The differences between treatment arms are smaller than the standard deviations within those arms. And hair width, a secondary measure, trended against the drug. The results were posted about 21 months after the press release announcing them.
⚠️ The concept was not novel when it was filed. A 2010 Pfizer paper reported a beta-selective thyromimetic effective in both mouse and monkey hair-growth models after topical application, with serum levels below the limit of quantification in bald macaques [1]. That is four years before this compound's priority date, includes a primate model this programme has never published, and describes exactly the differentiating profile now claimed for it. Two further patent families from the same era also claim thyromimetics for hair loss. ⚠️ The prior-art point stands on the concept rather than the molecule: the Pfizer compound appears to be a different chemotype.
There has been no public activity on this compound since February 2024. No phase 3 exists, no ex-Asia partner has been announced, and no discontinuation notice has been issued either, so absence of news is not evidence of termination.
Dosingtypical ranges, not medical advice
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Safetyrisks and cautions, not medical advice
⚠️ No safety data for this compound has been published in any peer-reviewed form. What exists is a phase 1 and a phase 2a trial, of which only the phase 2a has posted registry results, and those carry no safety statistics.
The animal work in the patent measured body weight as its only systemic readout. Thyroid hormone, thyroid stimulating hormone, free T4 and T3, and heart rate were not measured at all, which matters because those are precisely the endpoints a topical thyromimetic must clear. The entire premise of the compound is that it acts locally and does not reach the circulation, and the animal package does not test that premise.
The reassuring precedent comes from the prior art rather than from this molecule: Pfizer's topical thyromimetic showed serum drug levels below the limit of quantification in bald macaques and was rapidly metabolised, so systemic exposure was limited [1]. That is an encouraging result for the class and is not evidence about this compound.
⚠️ Because no selectivity data exists, the specific risk a beta-selective agonist is designed to avoid, which is alpha-receptor activation in heart and bone, cannot be assessed for this molecule at all.
History
Technoderma Medicines, a Singapore company, filed the priority application in 2014 covering a series of thyromimetics for hair growth, with the founder as an inventor. In 2020 it licensed the compound to Cutia Therapeutics for dermatology use in Asia, for a total of sixty million renminbi in upfront and milestone payments plus low single-digit royalties, retaining rights elsewhere; Cutia calls it CU-40101. The compound moved through phase 1 in China and a phase 2a elsewhere, and the trail goes quiet in early 2024. Its scientific record is unusual in shape: a fully resolved chemical identity confirmed by three independent primary documents, and essentially no published pharmacology or clinical data to attach to it.
Resources
This entry is here for reference.
Research
1 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
Limitations of the evidence
- Zero peer-reviewed publications of this compound's data exist
- No alpha-receptor assay has ever been run, so the beta-selectivity that would make it safe is unmeasured
- The mouse hair-growth study and the Wnt and Hedgehog mechanism usually cited for it are from TDM10842, a different compound
- The phase 2a registry results carry no statistics, disagree with the company's own press release on the primary endpoint, show inter-arm differences smaller than their own standard deviations, and show hair width trending against the drug
- The concept was published by Pfizer in 2010, in mice and macaques, four years before this compound's priority date
- Its own patent contains two siblings two to threefold more potent than the clinical candidate
- No public activity since February 2024, and no discontinuation notice either
Adverse effects
- No safety data has been published in any peer-reviewed form
- The animal work measured body weight as its only systemic readout, with no thyroid hormone or cardiac endpoint at all