Selank
Selank is a short peptide related to tuftsin, registered in Russia as a nasal anxiolytic. See the small Russian trials, lab work, what FDA says, and the evidence gaps.
Content last updated . This page has not been medically reviewed.
Identity and naming
Selank has the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. [3] The Russian drug register lists the active substance as a diacetate of that heptapeptide. [1] It is described as an analogue of tuftsin, a natural immune-system peptide whose core is the four amino acids TKPA. [4][5] FDA's compounding list uses the name "selank acetate (TP-7)". [2] Selank is not Semax: they are different molecules with different origins. See Semax and research peptide naming and identity problems.What the research shows
- Anxiety, compared with a benzodiazepine. In a Russian study of 62 patients with generalized anxiety disorder and neurasthenia, Selank (30 patients) was compared with medazepam (32 patients). The anxiolytic effects were reported as similar. [6] Another study of 60 patients with phobic-anxiety and somatoform disorders compared Selank with phenazepam and reported a pronounced anxiolytic and mild nootropic effect. [7] Neither abstract describes a placebo arm. Label: promising but limited.
- Add-on to a benzodiazepine. In 70 patients, adding Selank to phenazepam (40 patients) versus phenazepam alone (30 patients) was reported to bring the benefit sooner and reduce side effects of the tranquilizer. [8] This was a randomized trial, but small, from one country and without placebo or independent replication that we could find. Label: promising but limited.
- Immune markers. Selank changed blood cytokine balance in patients over 14 days. [9] Cytokines are immune signaling proteins; this is a biomarker, not a clinical outcome.
- Lab and animal work. In a binding experiment, Selank acted as a positive allosteric modulator of GABA binding, and the authors proposed this as one anti-anxiety mechanism. [3] In rats, Selank changed expression of genes involved in GABA signaling. [10] In rats with morphine dependence, it lessened withdrawal signs. [4] Label: preclinical (cells/animals only). None of this shows an effect in people.
- Registered trials. A ClinicalTrials.gov search for Selank found no relevant study of the peptide. [11]
- Healthy people. Proper evidence not found for better mood, stress resilience or memory.
Practical alternatives
For well-studied options for worry and stress, see anxiety disorders and therapy for anxiety and stress.Frequently asked questions
Is Selank approved?
It is registered in Russia as a nasal drop. In the US it is not approved. [1][2]
Does Selank work as well as a benzodiazepine?
One small Russian study reported similar anxiolytic effects to medazepam, but without a placebo group in the abstract. Not confirmed in large trials we could find. [6]
Is Selank addictive?
Proper evidence not found. We read no study that tested this in people.
Is Selank the same as Semax?
No. They are separate peptides. Selank is a tuftsin analogue. [4]
More details: evidence, limits and cautions
The details behind this page: cautions, limits of the evidence and where sources disagree. Open any note to read it.
How to read the evidence labels
Labels used on this page: approved medicine (Russia only, as read), promising but limited, preclinical (cells/animals only), insufficient evidence, marketing claim and Proper evidence not found.
Regulatory status
| Place | What we read |
|---|---|
| Russia | One Selank nasal-drop registration (0.15%) by a Russian manufacturer appears as valid in the state register, with pack entries marked as available without prescription; anti-anxiety group (ATC N05BX). [1] Approved medicine there. We could not read the Russian approved indications. |
| United States | Not an approved drug. On FDA's list of bulk substances previously placed in category 2 (possible significant safety risk) but withdrawn by the nominators; FDA cites immunogenicity risk and lacks important safety information. [2] Selank was not among the substances FDA scheduled for its July 2026 advisory meeting. [12] |
| Others | Not verified. |
Compounded drugs are not FDA-approved. [13] Laws change and this is not legal advice.
Safety
References
- Ministry of Health of the Russian Federation. State Register of Medicines (GRLS): Selank nasal drops, registration detail page. Read 2026-10-22.
- U.S. Food and Drug Administration. Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks (content current as of 04/22/2026). Read 2026-10-22.
- Peptide-based Anxiolytics: The Molecular Aspects of Heptapeptide Selank Biological Activity. Protein Pept Lett 2018. Read 2026-10-22.
- Selank, a Peptide Analog of Tuftsin, Attenuates Aversive Signs of Morphine Withdrawal in Rats. Bull Exp Biol Med 2022. Read 2026-10-22.
- Tuftsin - Properties and Analogs. Curr Med Chem 2017. Read 2026-10-22.
- Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia. Zh Nevrol Psikhiatr Im S S Korsakova 2008. Read 2026-10-22.
- A comparison of the anxiolytic effect and tolerability of selank and phenazepam in the treatment of anxiety disorders. Zh Nevrol Psikhiatr Im S S Korsakova 2014. Read 2026-10-22.
- Optimization of the treatment of anxiety disorders with selank. Zh Nevrol Psikhiatr Im S S Korsakova 2015. Read 2026-10-22.
- Immunomodulatory effects of selank in patients with anxiety-asthenic disorders. Zh Nevrol Psikhiatr Im S S Korsakova 2008. Read 2026-10-22.
- Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission. Front Pharmacol 2016. Read 2026-10-22.
- U.S. National Library of Medicine. ClinicalTrials.gov search, intervention "selank" (2 unrelated records). Read 2026-10-22.
- U.S. Food and Drug Administration. July 23-24, 2026: Meeting of the Pharmacy Compounding Advisory Committee (meeting page and agenda; no vote record or final decision was read). Read 2026-10-22.
- U.S. Food and Drug Administration. Compounding and the FDA: Questions and Answers. Read 2026-10-22.
- U.S. Food and Drug Administration. FDA warning letter to an online seller of unapproved drugs, reference 696885, February 26, 2025. Read 2026-10-22.