Helicore, LLC
SOUTHBURY, CT · Founded 2020 · CIK 0001810144 · Biotech · Private
Long-acting antibody conjugates for quarterly-dosed therapeutics
helicore.com →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $2.0M
- 1 Form D · Apr 2020
- 77 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- 1
- 0 granted · 1 pending
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20192020
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $2,000,000 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2368 | Propagenix Inc | — | $2.3M |
| 2369 | Merida Biosciences | — | — |
| 2370 | 3D HEALTH SOLUTIONS, INC. | — | — |
| 2371 | Helicore, LLC | — | $2.0M |
| 2372 | IMMUNE-ONC THERAPEUTICS, INC. | — | $7.0M |
| 2373 | Eluciderm Inc. | — | $3.8M |
| 2374 | BIO-PATH HOLDINGS, INC. | — | $18M |
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
- Charles BridgeDirector
- Joshua DotsonDirector
- Waters KelloggDirector
- Holger KoehlerDirector
- Kevin RussDirector · Executive Officer
- Lucas TurnerDirector
Patents
- Helical Anchor Foundation Systemapplication
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.