📗 Cite This Artifact
Orexin Receptor Modulators for Neurodegeneration
Orexin Receptor Modulators for Neurodegeneration
<table class="infobox infobox-therapeutic">
<tr>
<th class="infobox-header" colspan="2">Orexin Receptor Modulators for Neurodegeneration</th>
</tr>
<tr>
<td class="label">Drug</td>
<td>Company</td>
</tr>
<tr>
<td class="label">Danavorexant</td>
<td>Idorsia</td>
</tr>
<tr>
<td class="label">Selivorexant</td>
<td>Idorsia</td>
</tr>
<tr>
<td class="label">Suvorexant</td>
<td>Merck</td>
</tr>
<tr>
<td class="label">Lemborexant</td>
<td>Eisai</td>
</tr>
<tr>
<td class="label">Disease</td>
<td>Orexin Dysfunction</td>
</tr>
<tr>
<td class="label">[Alzheimer's Disease](/diseases/alzheimers-disease)</td>
<td>Neuron loss, reduced orexin-A</td>
</tr>
<tr>
<td class="label">[Parkinson's Disease](/diseases/parkinsons-disease)</td>
<td>Aligned orexin secretion</td>
</tr>
<tr>
<td class="label">[CBS](/diseases/corticobasal-syndrome)</td>
<td>Sleep fragmentation</td>
</tr>
<tr>
<td class="label">[PSP](/diseases/progressive-supranuclear-gaze-palsy)</td>
<td>Circadian dysfunction</td>
</tr>
<tr>
<td class="label">[ALS](/diseases/amyotrophic-lateral-sclerosis)</td>
<td>Sleep disruption</td>
</tr>
<tr>
<td class="label">[FTD](/diseases/frontotemporal-dementia)</td>
<td>Sleep-wake cycle disruption</td>
</tr>
<tr>
<td class="label">[Huntington's Disease](/diseases/huntingtons)</td>
<td>Sleep architecture disruption</td>
</tr>
<tr>
<td class="label">Trial ID</td>
<td>Drug</td
Orexin Receptor Modulators for Neurodegeneration
<table class="infobox infobox-therapeutic">
<tr>
<th class="infobox-header" colspan="2">Orexin Receptor Modulators for Neurodegeneration</th>
</tr>
<tr>
<td class="label">Drug</td>
<td>Company</td>
</tr>
<tr>
<td class="label">Danavorexant</td>
<td>Idorsia</td>
</tr>
<tr>
<td class="label">Selivorexant</td>
<td>Idorsia</td>
</tr>
<tr>
<td class="label">Suvorexant</td>
<td>Merck</td>
</tr>
<tr>
<td class="label">Lemborexant</td>
<td>Eisai</td>
</tr>
<tr>
<td class="label">Disease</td>
<td>Orexin Dysfunction</td>
</tr>
<tr>
<td class="label">[Alzheimer's Disease](/diseases/alzheimers-disease)</td>
<td>Neuron loss, reduced orexin-A</td>
</tr>
<tr>
<td class="label">[Parkinson's Disease](/diseases/parkinsons-disease)</td>
<td>Aligned orexin secretion</td>
</tr>
<tr>
<td class="label">[CBS](/diseases/corticobasal-syndrome)</td>
<td>Sleep fragmentation</td>
</tr>
<tr>
<td class="label">[PSP](/diseases/progressive-supranuclear-gaze-palsy)</td>
<td>Circadian dysfunction</td>
</tr>
<tr>
<td class="label">[ALS](/diseases/amyotrophic-lateral-sclerosis)</td>
<td>Sleep disruption</td>
</tr>
<tr>
<td class="label">[FTD](/diseases/frontotemporal-dementia)</td>
<td>Sleep-wake cycle disruption</td>
</tr>
<tr>
<td class="label">[Huntington's Disease](/diseases/huntingtons)</td>
<td>Sleep architecture disruption</td>
</tr>
<tr>
<td class="label">Trial ID</td>
<td>Drug</td>
</tr>
<tr>
<td class="label">NCT07213349</td>
<td>Danavorexant</td>
</tr>
<tr>
<td class="label">NCT06274528</td>
<td>Lemborexant</td>
</tr>
<tr>
<td class="label">NCT04629547</td>
<td>Suvorexant</td>
</tr>
<tr>
<td class="label">NCT05554141</td>
<td>Suvorexant</td>
</tr>
</table>
Orexin neuropeptides (also known as hypocretins) play a critical role in regulating sleep-wake cycles, arousal, and autonomic function. The orexin system consists of two neuropeptides (orexin-A and orexin-B) and two G-protein-coupled receptors (OX1R/HCRTR1 and OX2R/HCRTR2). Dysfunction of the orexin system is implicated in multiple neurodegenerative diseases, making orexin receptor modulators a promising therapeutic approach.
Background
The Orexin System
The orexin system was discovered in 1998 by two independent groups[@de1998][@peyron1998]. Orexin-producing neurons are located primarily in the lateral hypothalamus and project widely throughout the brain, including to the [locus coeruleus](/cell-types/locus-coeruleus-noradrenergic), [tuberomammillary nucleus](/cell-types/tuberomammillary-nucleus-histaminergic-neurons), and [ventral tegmental area](/cell-types/ventral-tegmental-area-dopaminergic-neurons)[@sakurai2007][@jones2005].
Two orexin receptors mediate the effects of orexin neuropeptides:
- OX1R (HCRTR1): Primarily involved in arousal and stress response
- OX2R (HCRTR2): More involved in sleep-wake regulation and feeding behavior
Orexin Dysfunction in Neurodegeneration
Loss of orexin neurons is observed in [Alzheimer's disease](/diseases/alzheimers-disease)[@ferr2023] and [Parkinson's disease](/diseases/parkinsons-disease)[@videnovic2013]. This loss correlates with:
- Sleep fragmentation and daytime sleepiness
- Reduced glymphatic clearance of amyloid-beta and tau
- Autonomic dysfunction
- Cognitive decline
Dual Orexin Receptor Agonists
Dual orexin receptor agonists (DORAs) activate both OX1R and OX2R to compensate for orexin neuron loss. These compounds are being developed primarily by [Idorsia Pharmaceuticals](/companies/idorsia).
Danavorexant (ACT-541468)
Danavorexant is a dual orexin receptor antagonist (not agonist — see note below) developed by Idorsia for insomnia and sleep disorders in neurodegeneration.
Note: Danavorexant is classified as an orexin receptor antagonist, not agonist. The name can be confusing, but it works by blocking orexin receptors to promote sleep by reducing orexin-induced arousal, similar to suvorexant.
Clinical trials:
- NCT07213349: Danavorexant for sleep disturbances in [Alzheimer's disease](/clinical-trials/daridorexant-ad-nct07213349) — Phase 2, recruiting
Selivorexant (ACT-462206)
Selivorexant is another dual orexin receptor antagonist from Idorsia being developed for sleep disorders. It has completed Phase 1 studies.
Comparison of Dual Orexin Receptor Antagonists
Dual Orexin Receptor Antagonists for Neurodegeneration
Suvorexant (Belsomra)
[Suvorexant](/therapeutics/suvorexant) was approved by the FDA in 2014 for insomnia disorder. It is a dual orexin receptor antagonist that promotes sleep by blocking orexin signaling.
Mechanism in Neurodegeneration:
- Promotes sleep to enhance glymphatic clearance of amyloid-beta and tau[@kang2009]
- Reduces orexin-mediated arousal that may exacerbate tau pathology[@feng2023]
- Addresses orexin deficiency observed in AD[@ohno2020]
See the [Suvorexant therapeutic page](/therapeutics/suvorexant) for detailed clinical trials.
Lemborexant (Dayvigo)
[Lemborexant](/therapeutics/lemborexant-ad-nct06274528) is approved for insomnia and being studied in AD.
- NCT06274528: Lemborexant for sleep disturbance in [Alzheimer's disease](/clinical-trials/lemborexant-ad-nct06274528) — Phase 2
See [Lemborexant AD clinical trial page](/clinical-trials/lemborexant-ad-nct06274528).
Therapeutic Rationale
Sleep-Wake Disturbances in AD
Over 50% of [Alzheimer's disease](/diseases/alzheimers-disease) patients experience sleep disturbances, including:
- Sleep fragmentation
- Sundowning (evening agitation)
- Reduced REM sleep
- Daytime sleepiness
Orexin receptor modulators address these issues by:
Sleep-Wake Disturbances in PD
[Parkinson's disease](/diseases/parkinsons-disease) patients commonly experience[@videnovic2013]:
- REM sleep behavior disorder
- Insomnia
- Excessive daytime sleepiness
- Sleep fragmentation
Orexin dysfunction contributes to these disorders, making orexin modulators a rational approach.
Cross-Disease Relevance
Orexin receptor modulators may benefit multiple neurodegenerative conditions:
Mechanism of Action
Clinical Trials
Active Trials
Completed Trials
- NCT04629547: Suvorexant STOP-AD — Completed
- Phase 1 studies for Selivorexant — Completed
Future Directions
Novel Approaches
Biomarkers
- CSF orexin-A levels as a biomarker for orexin system dysfunction
- Sleep polysomnography measures
- Amyloid/tau PET imaging correlation
Side Effects and Safety
Common side effects of orexin receptor antagonists:
- Excessive sleepiness
- Sleep paralysis
- Hypnagogic hallucinations
- Complex sleep behaviors
In neurodegeneration patients, additional considerations:
- Cognitive status monitoring
- Fall risk assessment
- Respiratory function in PD/ALS
Cross-Links
Related Mechanisms
- [Orexin Signaling in Neurodegeneration](/mechanisms/orexin-signaling-neurodegeneration)
- [Sleep-Circadian Dysfunction in Alzheimer's](/mechanisms/sleep-circadian-dysfunction-alzheimers)
- [Glymphatic System and Neurodegeneration](/mechanisms/glymphatic-system-neurodegeneration)
Related Cell Types
- [Orexin Neurons](/cell-types/orexin-neurons-narcolepsy)
- [Lateral Hypothalamus Orexin Neurons](/cell-types/lateral-hypothalamus-orexin-neurons)
- [Tuberomammillary Nucleus Histaminergic Neurons](/cell-types/tuberomammillary-nucleus-histaminergic-neurons)
Related Therapeutics
- [Sleep Optimization Therapy](/therapeutics/sleep-optimization-therapy)
- [Histamine H3 Receptor Antagonists](/therapeutics/histamine-h3-receptor-antagonists)
- [Intranasal Therapy for Neurodegeneration](/therapeutics/intranasal-therapy-neurodegeneration)
Other Sleep-Related Clinical Trials
- [Daridorexant AD NCT07213349](/clinical-trials/daridorexant-ad-nct07213349)
- [Lemborexant AD NCT06274528](/clinical-trials/lemborexant-ad-nct06274528)
- [Suvorexant STOP-AD NCT04629547](/clinical-trials/suvorexant-stop-ad-nct04629547)
References
Related Hypotheses
From the [SciDEX Exchange](/exchange) — scored by multi-agent debate
- [Nutrient-Sensing Epigenetic Circuit Reactivation](/hypothesis/h-4bb7fd8c) — <span style="color:#81c784;font-weight:600">0.79</span> · Target: SIRT1
- [CYP46A1 Overexpression Gene Therapy](/hypothesis/h-2600483e) — <span style="color:#81c784;font-weight:600">0.79</span> · Target: CYP46A1
- [Circadian Glymphatic Entrainment via Targeted Orexin Receptor Modulation](/hypothesis/h-9e9fee95) — <span style="color:#81c784;font-weight:600">0.77</span> · Target: HCRTR1/HCRTR2
- [Selective Acid Sphingomyelinase Modulation Therapy](/hypothesis/h-de0d4364) — <span style="color:#81c784;font-weight:600">0.77</span> · Target: SMPD1
- [Membrane Cholesterol Gradient Modulators](/hypothesis/h-9d29bfe5) — <span style="color:#81c784;font-weight:600">0.76</span> · Target: ABCA1/LDLR/SREBF2
- [Microbial Inflammasome Priming Prevention](/hypothesis/h-e7e1f943) — <span style="color:#81c784;font-weight:600">0.76</span> · Target: NLRP3, CASP1, IL1B, PYCARD
- [Blood-Brain Barrier SPM Shuttle System](/hypothesis/h-959a4677) — <span style="color:#81c784;font-weight:600">0.75</span> · Target: TFRC
- [Purinergic Signaling Polarization Control](/hypothesis/h-0758b337) — <span style="color:#81c784;font-weight:600">0.74</span> · Target: P2RY1 and P2RX7
Related Analyses:
- [Selective vulnerability of entorhinal cortex layer II neurons in AD](/analysis/SDA-2026-04-01-gap-004) 🔄
- [Selective vulnerability of entorhinal cortex layer II neurons in AD](/analysis/SDA-2026-04-01-gap-004) 🔄
- [4R-tau strain-specific spreading patterns in PSP vs CBD](/analysis/SDA-2026-04-01-gap-005) 🔄
- [4R-tau strain-specific spreading patterns in PSP vs CBD](/analysis/SDA-2026-04-01-gap-005) 🔄
- [TDP-43 phase separation therapeutics for ALS-FTD](/analysis/SDA-2026-04-01-gap-006) 🔄
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | therapeutics-orexin-receptor-modulators |
| kg_node_id | None |
| entity_type | therapeutic |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-a148e1759bc6 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'therapeutics-orexin-receptor-modulators'} |
| _schema_version | 1 |
No provenance edges found
Use ?embed=1 to load the artifact without SciDEX chrome — suitable for iframing into wiki pages or external sites.
<iframe src="http://scidex.ai/artifact/wiki-therapeutics-orexin-receptor-modulators?embed=1" width="100%" height="600" style="border:0;border-radius:8px"></iframe>
[Orexin Receptor Modulators for Neurodegeneration](http://scidex.ai/artifact/wiki-therapeutics-orexin-receptor-modulators)
http://scidex.ai/artifact/wiki-therapeutics-orexin-receptor-modulators