Loop East Community Improvement District
ST. LOUIS, MO · CIK 0001559411 · Biotech
Personalized peptide therapy protocols with lab testing and health coaching
loop.health →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $1.6M
- 1 Form D · Oct 2012
- 168 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20122013
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $1,640,000 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2970 | Kartos Therapeutics | — | — |
| 2971 | CANCURE LLC | — | — |
| 2972 | ADMA BIOLOGICS, INC. | — | — |
| 2973 | Loop East Community Improvement District | — | $1.6M |
| 2974 | ACPHARIS | — | — |
| 2975 | INVVAX, INC. | — | — |
| 2976 | CAMBIUM ONCOLOGY LLC | — | — |
Ranked on federal contract value rather than capital raised. The equity column is the comparison worth making — companies at the same procurement position often sit at very different points in their funding history.
Founders & Team
- Kevin FarrellDirector
- Jill McGuireDirector · Executive Officer
- John RussellDirector
- Donna WilkinsonDirector · Executive Officer
- John WrightDirector
Regulatory activity · Biotech
- New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug Application; Change of SponsorFood and Drug Administration
- Medical Devices; General and Plastic Surgery Devices; Classification of the Skin Patch for Treatment of HyperhidrosisFood and Drug Administration
- Medical Devices; Anesthesiology Devices; Classification of the Monitor for Opioid Induced Impairment of OxygenationFood and Drug Administration
- Medical Devices; Orthopedic Devices; Classification of the Medial Knee Implanted Shock AbsorberFood and Drug Administration
- Medical Devices; Neurological Devices; Classification of the External Lower Extremity Nerve Stimulator for Restless Legs SyndromeFood and Drug Administration
- Medical Devices; General Hospital and Personal Use Devices; Classification of the Infant Supine Sleep SystemFood and Drug Administration
Rules are matched to sector, not to company. Recent activity in a sector is context rather than a signal about this business — until rules are matched to what a company actually builds, the section is shown as context and nothing more.