Important limitations
- Individual claims and source links have not yet completed editorial verification.
- Evidence level, applicable study model, formulation, route and population remain unassigned.
DSIP is a neuropeptide explored for sleep modulation, stress resilience, analgesia, and metabolic support.
The moderated mass amounts below are retained for comparison. Near-duplicates, mix-dependent volumes and device markings are excluded. This is educational source context, not a protocol or recommendation.
Recorded example with no verified study backing; shown for amount literacy only.
Recorded example with no verified study backing; shown for amount literacy only.
Recorded example with no verified study backing; shown for amount literacy only.
Only mcg or mg amounts are retained. The calculator derives mL, syringe units or pen clicks from the current vial strength, water volume and device.
No clinical amount or schedule is inferred from this material. Source verification is pending, and every displayed amount remains educational context rather than guidance.
Verify the exact compound, formulation and amount against the product label or certificate before calculation.
Follow the product label, certificate and validated laboratory SOP; no universal storage assumption is applied here.
Label concentration and preparation date, use sterile technique where applicable, and follow a validated stability protocol.
What published studies and recent community write-ups report about amounts, timing and course length. 7 clinical, 2 preclinical and 4 community-reported rows, each linked to its source. These are descriptions of what others report, not instructions, and nothing here is medical advice.
| Context | Dose | Frequency | Route | Course | Source |
|---|---|---|---|---|---|
| Clinical7 rows | |||||
| First human infusion study6 healthy adults, 4 men and 2 women | 25 nmol/kg | Single infusion, given in the morning | Slow intravenous infusion | One dose, with the following night also recordedNot applicable | International Journal of Clinical Pharmacology, Therapy and Toxicology (PubMed)1981 |
| Median total sleep time rose 59% in the 130 minutes after the infusion against placebo, and the next night showed shorter sleep onset, less stage 1 sleep and better sleep efficiency. The authors found no classic sedation on behavioural or EEG analysis and recorded no side effects, but six people in a crossover design cannot establish an effect. | |||||
| One week of repeated infusions in chronic insomnia18 adults with chronic psychophysiological insomnia, 9 aged 29-59 and 9 aged 60-83 | 30 nmol/kg per injection | 6 injections across one week | Intravenous | 1 week of dosing, then a 1 week follow-upSleep was re-measured after a week with no dosing | European Neurology (PubMed)1986 |
| Sleep reached normal laboratory values by the end of dosing in the middle-aged group and only by the end of the follow-up week in the older group, and the size of the change tracked how disturbed sleep had been at baseline. The FDA's 2026 summary records this study as double blind with 5 nights of dosing rather than 6 injections, and lists weak control selection and small samples as limits running through this whole series. | |||||
| Four-night crossover trial in chronic insomnia6 adults with insomnia, per the FDA's 2026 summary of the study | 25 nmol/kg | Once on each of 4 nights | Intravenous | 4 nights, repeated once after a 4-day washout4 days between the two blocks | International Journal of Clinical Pharmacology Research (PubMed)1987 |
| Nocturnal awakenings, NREM sleep latency and total waking time all fell during DSIP nights, but none of those changes differed significantly from baseline or from the double-blind placebo nights. The gains in NREM and stage 2 sleep were already present in the baseline recordings, and the authors concluded that any sleep improvement was of little clinical significance. | |||||
| Three-night parallel-group trial16 adults with chronic insomnia, allocated in matched pairs | 25 nmol/kg | Once in the afternoon before each of 3 nights | Intravenous | 5 laboratory nights: 1 adaptation, 1 baseline, 3 treatmentNone | Neuropsychobiology (PubMed)1992 |
| Polysomnography showed higher sleep efficiency and shorter sleep latency on DSIP than on the glucose placebo, but the authors judged the effects weak and partly explained by an incidental shift in the placebo group, with subjective sleep quality unchanged. Their stated conclusion was that short-term DSIP is unlikely to be of major therapeutic benefit in chronic insomnia. | |||||
| Alcohol and opiate withdrawal, open-label inpatient series107 inpatients in withdrawal, 47 from alcohol and 60 from opiates | 25 nmol/kg | On request as symptoms recurred, or every 6-8 hours on 3 consecutive days, up to 6 injections a day | Intravenous | Up to 6 daysNot applicable | European Neurology (PubMed)1984 |
| Symptoms cleared or improved markedly in 97% of the opiate group and 87% of the alcohol group as judged by the treating physicians and nursing staff, with anxiety slowest to settle and opiate patients needing more injections than alcohol patients. There was no blinding, no comparison group and no standard withdrawal scale, and the FDA's 2026 review of this series records 9 minor side effects and 3 serious events, including hypotension at the first injection in 2 patients. | |||||
| Stress-hormone challenge study15 healthy young men across two experiments | 3 mg or 4 mg total | One infusion per session | Intravenous infusion, from 30 minutes before to 90 minutes after the challenge | Single sessionNot applicable | Psychoneuroendocrinology (PubMed)1995 |
| ACTH and cortisol responses to a corticotropin-releasing hormone injection and to a midday meal were almost identical on DSIP and on placebo. The authors wrote that their data do not support an inhibitory role for DSIP on ACTH and cortisol in people, which runs against the cell and animal work that had prompted the study and against the stress-axis claims made for the peptide today. | |||||
| Fixed-schedule opioid detoxification study summarized by FDA7 people with opioid dependence and a subjective withdrawal score above 25 | 35 nmol/kg | Fixed schedule rather than on request | Intravenous | 7 daysNone described | US Food and Drug Administration2026 |
| Only 2 of the 7 received every scheduled injection and completed detoxification, and the FDA quotes the authors' own view that whether DSIP could work as a detoxification approach remains an open question. The agency's overall finding was that no study supports the proposed subcutaneous route for this use and that the intravenous evidence is insufficient to draw a conclusion. | |||||
| Preclinical2 rows | |||||
| Lifelong monthly courses in mice (Deltaran preparation)54 female Swiss-derived SHR mice per group, from 3 months old to natural death | 2.5 mcg per mouse, about 100 mcg/kg | 5 consecutive days each month | Subcutaneous | Repeated monthly for lifeThe rest of each month with no dosing | Mechanisms of Ageing and Development (PubMed)2003 |
| Mean life span did not change, but the last 10% of survivors lived 17.1% longer, maximum life span rose 24.1%, bone marrow chromosome aberrations fell 22.6% and total spontaneous tumour incidence was 2.6-fold lower. This used the Deltaran preparation rather than isolated peptide, in one mouse strain and one sex, and the monthly pulse pattern has no counterpart in any human study. | |||||
| Intranasal dosing in a rat stroke modelSprague Dawley rats with middle cerebral artery occlusion | 120 mcg/kg | Once daily | Intranasal | 8 days: one dose about an hour before the occlusion, then 7 days after reperfusionNot applicable | Molecules (PubMed)2021 |
| Motor performance on the rotarod recovered significantly in the treated rats over 21 days of testing, while the smaller infarct volume in that group did not reach statistical significance. This is a single rodent model using the intranasal route, and it measures recovery after stroke rather than anything to do with sleep. | |||||
| Community-reported4 rows | |||||
| Physician-written clinic protocol | 100 mcg to start, 200 mcg if there is no response after 3-4 nights, 250 mcg described as the ceiling | Nightly, 30-60 minutes before intended sleep | Subcutaneous, abdomen | 10-14 nights2-4 weeks between courses | Community resource2026 |
| A clinic's chief medical officer sets out a 100-250 mcg nightly course and states that DSIP is not a sedative, that any effect builds over 3-5 nights, and that night 5 is the earliest point at which a response can be judged. The page describes the human evidence as genuinely mixed and names a negative double-blind study alongside the positive open-label work, and it declines to extend courses past 14 days or doses past 250 mcg. | |||||
| Three-step titration over a short course | 100 mcg on days 1-3, 200 mcg on days 4-10, 300 mcg on days 11-14 if needed | Once daily, 30-60 minutes before bed | Subcutaneous | 10-14 days2-4 weeks off, with 3-4 courses a year described | Community resource2026 |
| This is the only one of the circulating protocols that lays out an explicit three-step titration, and it argues that short courses are enough because reported sleep changes persist for 2-4 weeks after stopping. It gives no published source for that carry-over claim, and it also advises reducing the dose if next-morning drowsiness appears. | |||||
| Three separate reported regimens, each labelled community practice | 100 mcg, 200 mcg or 300 mcg | Once daily, about 1 hour before bed | Subcutaneous, abdomen or thigh | 1-2 weeks at 100 mcg, 4-6 weeks at 200 mcg, 2-4 weeks at 300 mcgA break at the end of the 4-6 week course to reassess sleep without it | Community resource2026 |
| This page presents its three figures as separate reported regimens rather than a titration ladder and tags each one as community practice rather than peer-reviewed. It states that no human study has used subcutaneous DSIP at any dose and that the published human dose is roughly 1.5 mg intravenously, about 15 times the 100 mcg figure by a different route. | |||||
| Eight-week course with reconstitution math | 100 mcg in week 1, then 200 mcg | Once daily, 30-60 minutes before bed; some users described as running 5 days on and 2 days off | Subcutaneous, abdomen or thigh | 8 weeksNot specified for this course | Community resource2026 |
| This guide runs much the longest course in circulation, 8 weeks rather than 2, and gives the arithmetic for a 2 mg vial in 2 mL of bacteriostatic water, where 100 mcg is 3 units on a 30-unit syringe. Its own banner states that human dosing guidelines are not established for this compound and that the figures come from reported protocols rather than trials. | |||||
Community pages describe starting at 100 mcg subcutaneously about an hour before bed and expecting little at this stage, since the peptide is framed as shifting sleep architecture rather than sedating. The same pages note that no human study has used this route or this dose.
This is where guides place the first reported change in sleep depth, and where they set their decision point: step from 100 mcg to 200 mcg if nothing has shifted after 3-4 nights, and treat night 5 as the earliest honest assessment. One physician page states that a non-responder will usually be clear by night 7 at 200 mcg.
The short-course protocols hold 200 mcg here, with 300 mcg listed for days 11-14 if nothing has changed, and describe the full reported effect as established by the end of a 14-night block. Reducing the dose is the advice given for next-morning drowsiness.
Not every guide stops at two weeks. One 2026 protocol holds 200 mcg once daily for an 8-week block, with 5 days on and 2 days off offered as a variation, which is several times longer than any course ever given to a person in a published study.
A 2-4 week off period before any repeat is the common convention, with 3-4 courses a year, and the stated reasons are that reported sleep changes carry over for a few weeks and that off periods may prevent adaptation. Neither reason has a published study behind it.
The human record is a programme of five small double-blind studies using single and repeated slow intravenous injections, in which sleep induction took about an hour, the effect lasted up to 20 hours, and disturbed sleep was reported to normalize after four consecutive injections. Slow injection was described as essential, and no study tested the nightly subcutaneous course above.
Plus 4 community resources (dosing guides, forum threads and vendor write-ups), reported above but not linked.
DSIP (delta sleep-inducing peptide) is a nine-residue peptide that Guido Schoenenberger and Marcel Monnier's group isolated from the cerebral venous blood of rabbits in 1977 and named for the delta wave sleep it produced when infused into other animals. Every published human study used slow intravenous infusion: a handful of small sleep-laboratory investigations in Switzerland, Uruguay and the Netherlands that disagreed about whether it changed sleep at all, open-label series in alcohol and opiate withdrawal, and a seven-patient pilot in chronic pain. The FDA evaluated emideltide, the compounding name for DSIP, in 2026 and reported an animal plasma half-life under 10 minutes, no pharmacokinetic or safety data for the subcutaneous route that vendors sell, and insufficient evidence of effectiveness for insomnia, narcolepsy or opioid withdrawal. The nominations to allow compounding with it were withdrawn, an April 2026 update moved it from the agency's Category 2 safety-risk table into a list of withdrawn nominations, and FDA then proposed that neither the free base nor the acetate be added to the 503A Bulks List. It is approved nowhere and has never been the subject of a registered trial.
These themes organize the educational information currently available. Individual claims remain under source review and are not treatment claims.
Evaluating DSIP’s role in sleep architecture
Pain modulation, withdrawal support, and metabolic resilience
Depression, addiction, and cancer-preventive investigations
Broader systemic effects
Research considerations
Available context is organized without assigning unsupported study models or evidence grades.
Evaluating DSIP’s role in sleep architecture
Pain modulation, withdrawal support, and metabolic resilience
These amount records are independent from vial strength, reconstitution volume and measuring device. A recorded source is not the same as study backing, and these values are not recommendations.
Sequence, synonyms and registry identifiers as recorded in PubChem, the National Library of Medicine's open chemistry database. Formula, mass and CAS number are summarized at the top of the page.
Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu
Emideltide, DSIP nonapeptide, Delta sleep-inducing peptide, Deltaran, Emideltide [INN], H-WAGGDASGE-OH, UNII YN28Z5YZ73, CHEMBL2104403
ZRZROXNBKJAOKB-GFVHOAGBSA-N
(2S)-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]propanoyl]amino]acetyl]amino]acetyl]amino]-3-carboxypropanoyl]amino]propanoyl]amino]-3-hydroxypropanoyl]amino]acetyl]amino]pentanedioic acid
1 link carried over from the earlier page, awaiting verification.