Legal status · Australia
Is 17-DMAG legal in Australia?
Written by Aaron CuhaReviewed Sep 2026
Direct answer
No. 17-DMAG is not approved for any medical use in Australia; its classification is "Investigational, not registered". Lawful access is limited to registered clinical trials. "Research use only" labeling on vials sold online does not make human use lawful. On the evidence, 4 human studies are cited on its profile.
17-DMAG in Australia at a glance
| Classification | Investigational, not registered |
|---|---|
| TGA approval status | Not approved by TGA; investigational |
| Human studies cited | 4 of 7 citations on the profile |
| Reviewed | Sep 2026 |
Classification and note come from the 17-DMAG profile, checked against Therapeutic Goods Administration (TGA) listings at the reviewed date.
What this means
- 01
17-DMAG is being studied in registered clinical trials but has not received TGA marketing approval in Australia.
- 02
Lawful human access is limited to trial participation or a formal early-access scheme where one exists; there is no pharmacy product to prescribe.
- 03
Vials sold online "for research use only" are not trial material, and that label does not make human use lawful.
What 17-DMAG is
An HSP90 inhibitor that failed to extend mouse lifespan by the Interventions Testing Program's protocol test and showed a 7 to 9 percent male median gain by the Gehan test, and that extended healthspan in a progeroid mouse as one of the first senolytics identified. In people it went through oncology phase 1 trials with cardiac, ocular and one treatment-related death as dose-limiting events, and development stopped around 2010.
17-DMAG (alvespimycin) is a water-soluble derivative of geldanamycin that inhibits heat shock protein 90, the chaperone that stabilises many oncogenic signalling proteins. It was developed as a cancer drug by Kosan Biosciences and then Bristol-Myers Squibb, reached phase 1 in solid tumours, acute myeloid leukaemia and HER2-positive breast cancer, and was not taken further.
Mechanism: 17-DMAG binds the ATP pocket of HSP90 and blocks its chaperone cycle, sending client proteins such as CDK4, HER2, AKT and mutant kinases to proteasomal degradation and inducing HSP70 as a compensatory response. In the human phase 1 trials, HSP72 induction in blood cells was detectable from 20 mg/m2 and client protein depletion at 80 mg/m2, so the target was engaged at tolerated doses.
Regulatory history: Investigational, never approved. Oncology phase 1 trials completed 2004 to 2012; a phase 2 in HER2-positive breast cancer was terminated after 4 patients; no trial registered since 2010. The lifespan signal is a Gehan-only reanalysis result in male mice; the healthspan result is in a progeroid mouse model.
How TGA treats this kind of product
Registers or lists therapeutic goods on the ARTG and schedules substances in the Poisons Standard. Many peptides are Schedule 4 (prescription only), so possession without a prescription and personal importation are restricted even when no product is registered.
The classification above is the The Longevity Archive reading of Therapeutic Goods Administration listings for 17-DMAG at the reviewed date, not a legal opinion. Rules change, and importing, prescribing and possessing a compound can each be treated differently. Check the regulator directly before acting on anything here.
17-DMAG in other countries
Frequently asked questions
Is 17-DMAG legal in Australia?
No. 17-DMAG is not approved for any medical use in Australia; its classification is "Investigational, not registered". Lawful access is limited to registered clinical trials. "Research use only" labeling on vials sold online does not make human use lawful. On the evidence, 4 human studies are cited on its profile.
Can I buy 17-DMAG in Australia?
No approved product exists to buy. In Australia 17-DMAG is classified as "Investigational, not registered", so there is no licensed pharmacy product. Vendors selling it "for research use only" are not selling it for human use, and that label does not change its legal status. This site does not list or recommend vendors.
Is 17-DMAG TGA approved?
No. In Australia 17-DMAG is classified as "Investigational, not registered", which is not a TGA marketing approval. For comparison, the US FDA status is: Investigational, never approved. Oncology phase 1 trials completed 2004 to 2012; a phase 2 in HER2-positive breast cancer was terminated after 4 patients; no trial registered since 2010. The lifespan signal is a Gehan-only reanalysis result in male mice; the healthspan result is in a progeroid mouse model.. On the evidence, 4 human studies are cited on its profile.
Related compounds in Australia
Full research profile
Mechanism, cited studies, FDA status and the full legal summary for 17-DMAG live on its compound profile.
17-DMAG profileThis page is general information about the regulatory status of 17-DMAG in Australia, current as of Sep 2026. It is not legal advice, and classifications change; check Therapeutic Goods Administration directly or consult a lawyer for a specific situation. Educational use only. This database summarizes published research. It is not medical advice and contains no dosing protocols or recommendations for personal use. The Longevity Archive has no vendor relationships and does not recommend where to buy anything.