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DSIP Peptide: What Delta Sleep-Inducing Peptide Trials in People Found

One small double-blind study found better sleep; two others found effects too weak to matter. All used IV doses. The FDA calls the evidence inconclusive, and DSIP is research-only.

Article type
Evidence
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9
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6 min
By Craig PalmerPublished

DSIP, short for delta sleep-inducing peptide, has the most promising name in the sleep-peptide market. It was named for delta sleep, the deep, slow-wave stage. In people, the record is a set of small studies from the 1980s and early 1990s, and they do not agree with each other. This page goes through each one, and through the FDA’s 2026 reading of the whole set. It sits under the sleep goal.

For how DSIP compares with the growth-hormone peptides also sold for sleep, see the overview in what human studies of sleep peptides found.

What DSIP is

DSIP, given the name emideltide in FDA documents, is a peptide of nine amino acids. The FDA notes it is not a component of any approved drug and has no official monograph, and that its chemistry is poorly characterized for use as a compounded injection. [7]

Whether the body uses DSIP as a sleep signal at all is unsettled. A 1995 study measured morning blood levels of DSIP-like material in 10 people with narcolepsy, 9 with sleep apnea and 11 healthy controls. It found no significant differences between the groups, only a trend toward lower levels in narcolepsy [6].

The studies that found an effect

The positive human sleep studies come largely from one author [7]. In a 1987 placebo-controlled, double-blind study (n = 14), middle-aged chronic insomniacs received DSIP on 7 successive nights, with sleep recorded in the laboratory [1]. The author reports that night sleep improved substantially from the first dose and further with repeated doses, that the gain held on the first placebo night after treatment, and that daytime alertness and performance rose.

An earlier open study treated 7 people with severe insomnia with a series of 10 injections [4]. Sleep was reported as normalized in all but one, for follow-up periods of 3 to 7 months. With no placebo group, that result cannot separate the peptide from expectation, attention or time.

The FDA’s reviewers read the positive studies cautiously. They note that the author concluded DSIP was effective, but that it was unclear whether the changes seen in 14 subjects were clinically meaningful [7].

The studies that did not

Two other double-blind studies used intravenous DSIP at 25 nmol/kg. One gave it in the afternoon before three laboratory nights, to 16 chronic insomniacs (n = 16) split between DSIP and a glucose solution [2]. Sleep efficiency was higher and sleep onset shorter on DSIP, but the authors judged the effects weak and possibly due to a chance change in the placebo group. Subjective sleep quality did not change.

The other gave DSIP or placebo for four nights in a crossover design [3]. Total sleep rose, but only in light stage 2 sleep; deep slow-wave sleep and REM sleep did not change. That last point matters for a peptide named for deep sleep. The authors concluded the improvement was of little clinical significance.

Narcolepsy and other uses

The narcolepsy evidence is a single patient. A 35-year-old man given repeated DSIP injections reported fewer sleep attacks and more daytime alertness, and his overnight sleep showed more REM [5]. The FDA calls a single-subject report insufficient to judge effectiveness, citing recall bias and limited generalizability [7].

DSIP was also given intravenously in studies of opioid withdrawal. The FDA’s review of those studies found transient headache, nausea and vertigo as common side effects, and cases of low blood pressure described as “progressive” after a second IV dose [7].

What this means for you

DSIP was tested in a few dozen people, by IV, over days, and the results split. No study has measured DSIP injected under the skin, the route nominated for compounding [7], and no human dose has been established. The peptides for sleep with more human data, and their own limits, are compared in what the sermorelin studies measured and the overview above. How the growth hormone peptides differ from one another is in growth hormone peptides.

Frequently asked questions

Does DSIP work for sleep?
The evidence is split. A 1987 double-blind study of 14 insomniacs reported better sleep over 7 nights of IV DSIP, while two other double-blind IV studies found effects too weak to be clinically meaningful. The FDA called the evidence inconclusive and at best preliminary.
Does DSIP increase deep sleep?
In a four-night crossover study, total sleep rose on DSIP only through light stage 2 sleep. Deep slow-wave sleep and REM sleep did not change.
Is DSIP legal to compound?
No. DSIP (emideltide) is on no FDA 503A list, the FDA proposed against adding it, and an FDA advisory committee voted against it in July 2026.
What are the side effects of DSIP?
Insomnia studies of IV DSIP reported no significant adverse events in small numbers of people. In withdrawal studies, the FDA's review found transient headache, nausea and vertigo, and cases of low blood pressure after a second IV dose.

Sources

9 cited
  1. 1Schneider-Helmert D (1987). Effects of delta-sleep-inducing peptide on 24-hour sleep-wake behaviour in severe chronic insomnia European Neurology. PMID 3622582
  2. 2Bes F, Hofman W, Schuur J, Van Boxtel C (1992). Effects of delta sleep-inducing peptide on sleep of chronic insomniac patients. A double-blind study Neuropsychobiology. PMID 1299794
  3. 3Monti JM, Debellis J, Alterwain P, Pellejero T, Monti D (1987). Study of delta sleep-inducing peptide efficacy in improving sleep on short-term administration to chronic insomniacs International Journal of Clinical Pharmacology Research. PMID 3583493
  4. 4Kaeser HE (1984). A clinical trial with DSIP European Neurology. PMID 6391926
  5. 5Schneider-Helmert D (1984). Effects of DSIP on narcolepsy European Neurology. PMID 6548968
  6. 6Vgontzas AN, Friedman TC, Chrousos GP, et al. (1995). Delta sleep-inducing peptide in normal humans and in patients with sleep apnea and narcolepsy Peptides. PMID 8532601
  7. 7U.S. Food and Drug Administration (2026). FDA Briefing Document for Emideltide-Related Bulk Drug Substances, Pharmacy Compounding Advisory Committee meeting, July 23-24, 2026 FDA. Source
  8. 8U.S. Food and Drug Administration (2026). Safety Risks Associated with Certain Bulk Drug Substances Nominated for Use in Compounding FDA, Human Drug Compounding (content current as of April 22, 2026). Source
  9. 9National Community Pharmacists Association (2026). FDA advisory committee nominates six peptides for pharmacies to compound NCPA (July 31, 2026). Source

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