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Legal status · United States

Is Landogrozumab legal in the United States?

Written by Reviewed Sep 2026

Not approvedMuscle & PerformanceHuman studies cited: 4

Direct answer

No. Landogrozumab is not an approved medicine in the United States; its classification is "Not approved; research use only". Nothing containing it is authorized for any use in people. Vials labeled "for research use only" are not exempt: that label does not make human use lawful. On the evidence, 4 human studies are cited on its profile.

Landogrozumab in the United States at a glance

ClassificationNot approved; research use only
NotePhase 2 programme completed and not advanced. Not available in any form.
FDA approval statusNever approved. Eli Lilly did not advance it past phase 2.
Human studies cited4 of 4 citations on the profile
ReviewedSep 2026

Classification and note come from the Landogrozumab profile, checked against U.S. Food and Drug Administration (FDA) listings at the reviewed date.

What this means

  • 01

    No product containing Landogrozumab is approved by FDA for any use in the United States, so nothing on the market is authorized for people.

  • 02

    "Research use only" is a vendor label, not a legal category that permits human use. It does not exempt a product from medicines law.

  • 03

    Importing, supplying or promoting it for human use can fall under medicines legislation in the United States. This page is general information, not legal advice.

What Landogrozumab is

The clearest test in the whole field. In 201 older adults who had fallen, it added 0.43 kg of lean mass at p below 0.0001 and moved two of about seven physical performance measures.

This is the trial to read if you want to understand what myostatin inhibition actually delivers, because it was run in exactly the population the idea is meant to help: older adults who were weak and who had fallen. The body composition result is unambiguous.

Mechanism: A humanised monoclonal antibody neutralising myostatin, blocking its signalling through activin type II receptors and the SMAD2/3 pathway that suppresses muscle protein synthesis. Same target as stamulumab, engineered for higher potency.

Regulatory history: Never approved. Eli Lilly did not advance it past phase 2.

How FDA treats this kind of product

Approves prescription drugs by indication and polices unapproved products, including peptides sold online. Compounding pharmacies may prepare some compounds under a prescription when the FDA places them on a permitted bulk-substances category.

The classification above is the The Longevity Archive reading of U.S. Food and Drug Administration listings for Landogrozumab 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.

Landogrozumab in other countries

Frequently asked questions

Is Landogrozumab legal in the United States?

No. Landogrozumab is not an approved medicine in the United States; its classification is "Not approved; research use only". Nothing containing it is authorized for any use in people. Vials labeled "for research use only" are not exempt: that label does not make human use lawful. On the evidence, 4 human studies are cited on its profile. Note: Phase 2 programme completed and not advanced. Not available in any form.

Can I buy Landogrozumab in the United States?

No approved product exists to buy. In the United States Landogrozumab is classified as "Not approved; research use only", 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. Note: Phase 2 programme completed and not advanced. Not available in any form.

Is Landogrozumab FDA approved?

No. FDA status: Never approved. Eli Lilly did not advance it past phase 2.. Current US classification: "Not approved; research use only". On the evidence, 4 human studies are cited on its profile.

Related compounds in the United States

Full research profile

Mechanism, cited studies, FDA status and the full legal summary for Landogrozumab live on its compound profile.

Landogrozumab profile

This page is general information about the regulatory status of Landogrozumab in the United States, current as of Sep 2026. It is not legal advice, and classifications change; check U.S. Food and Drug 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.