DSIP results: what to expect and when
An experimental sleep peptide with small, mixed human studies and no FDA-approved dose.
Also called: Delta sleep-inducing peptide, Delta-sleep-inducing peptide, Emideltide.
Sleep peptides · Experimental nine-amino-acid peptide with uncertain sleep-signaling targets.
A six-person sleep study tested acute IV doses; it does not establish a multiweek injection cycle.
51 primary human research reports are listed, including biomarkers and overlapping series. Sleep trials are small and mixed; no human subcutaneous trial was found.
Key studies
- Healthy volunteers: morning infusion: Median sleep time during the next 130 minutes was 59% greater with DSIP than placebo. (source)
- Early insomnia letter: No arm-level results were available in the retrieved record. (source)
- Six adults with insomnia: Longer, less interrupted sleep was reported; benefit began in hour 2 and lasted up to 6 hours. (source)
- Five early human experiments: Four evening doses reportedly normalized disturbed sleep; daytime tests suggested greater alertness. (source)
- Insomnia after brain-stem injury: Baseline sleep was under 4 hours; DSIP improved sleep reversibly, without normalizing REM latency. (source)
- Alcohol and opioid withdrawal pilot: 49 were evaluable; 48 improved: 22 alcohol patients and 26 of 27 opioid patients. (source)
Related to DSIP
- Ipamorelin: An experimental peptide that triggers growth hormone release.
- Selank: A Russian nasal anxiety peptide with uncertain long-term benefit and safety.
- CJC-1295 without DAC: A peptide intended to trigger growth hormone release, with no human dosing study found.
- Pinealon: A peptide with unproven brain benefits and no established injection dose.
Sources
- 503B Bulk Drug Substances List, FDA · FDA · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2026
- Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act, FDA · FDA · 2026
- Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks, FDA · FDA · 2026
- Download medicine data, European Medicines Agency · European Medicines Agency · 2026
- FDA Briefing Document: Emideltide-Related Bulk Drug Substances (Emideltide (free base) and Emideltide acetate), U.S. Food and Drug Administration · 2026
- MHRA Products | Home, MHRA · MHRA · 2026
- Sepsis, NHS · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026, Australian Government · Australian Government · 2026
- Think twice before injecting peptides bought online: unauthorized products can seriously harm you, Health Canada · Health Canada · 2026
- Anaphylaxis, NHS · NHS · 2023
- Low blood sugar (hypoglycaemia), NHS · 2023
- [Using deltalicin for the treatment of patients with diabetic retinopathy]., Kresiun NV et al. · Eksperimental'naia i klinicheskaia farmakologiia · 2014
- The influence of deltalycyn and transcranial cerebellar stimulation upon recovery of retina after photo stress in patients with diabetic retinopathy., Kresyun NV et al. · Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi · 2014
Sources checked: 2026-10-18.
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