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LY2624803 - Capsules
LY2624803 - Capsules is a Small molecule drug developed by Eli Lilly and Company. It is currently in Phase 1 development. Also known as: Hypnion.
LY2624803 - Capsules are being studied for the treatment of Transient Insomnia, Primary Insomnia, Secondary Insomnia, and Sleep Initiation and Maintenance Disorders. The capsules are being compared to Zolpidem - Tablets and Placebo - Capsules in clinical trials.
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Baseline phase 1 → approval rate
+9.6pp
Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas). -
Big-pharma sponsor
+3.0pp
Eli Lilly and Company is a top-20 pharma sponsor — historical approval rates run ~3pp above average due to scale, regulatory experience, and trial-design quality.
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2033–2036 | — |
| EMA | EU | 2034–2037 | +0.7 yr |
| MHRA | GB | 2034–2037 | +0.7 yr |
| Health Canada | CA | 2034–2038 | +0.9 yr |
| TGA | AU | 2034–2038 | +1.2 yr |
| PMDA | JP | 2034–2038 | +1.5 yr |
| NMPA | CN | 2035–2039 | +2.3 yr |
| MFDS | KR | 2034–2038 | +1.4 yr |
| CDSCO | IN | 2034–2039 | +1.8 yr |
| ANVISA | BR | 2035–2039 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | LY2624803 - Capsules |
|---|---|
| Also known as | Hypnion |
| Sponsor | Eli Lilly and Company |
| Modality | Small molecule |
| Phase | Phase 1 |
Approved indications
Common side effects
Key clinical trials
- A Study of LY2624803 in Japanese Participants With Transient Insomnia (PHASE1)
- A Study of LY2624803 in Participants With Transient Insomnia (PHASE1)
- An Efficacy Study of Compound LY2624803 in the Treatment of Patients With Chronic Insomnia (PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- LY2624803 - Capsules CI brief — competitive landscape report
- LY2624803 - Capsules updates RSS · CI watch RSS
- Eli Lilly and Company portfolio CI
Frequently asked questions about LY2624803 - Capsules
What is LY2624803 - Capsules?
Who makes LY2624803 - Capsules?
Is LY2624803 - Capsules also known as anything else?
What development phase is LY2624803 - Capsules in?
Related
- Manufacturer: Eli Lilly and Company — full pipeline
- Also known as: Hypnion
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing