DFI Holding Inc.
NEW YORK, NY · Founded 2012 · CIK 0001543229 · Biotech
Antigen-specific immune tolerance platform using allosteric anti-CD40 monoclonal antibody for autoimmune diseases
dfi.bio →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $55M
- 1 Form D · Apr 2012
- 174 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20112012
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $54,944,400 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2116 | General Folders Inc. | — | $20K |
| 2117 | Renasant Bio | — | $55M |
| 2118 | PIXIMUNE, INC. | — | — |
| 2119 | DFI Holding Inc. | — | $55M |
| 2120 | Sonoma Biotherapeutics | — | $265M |
| 2121 | ARVINAS, INC. | — | $129M |
| 2122 | ARBOR EQUITY GROUP FUND I, LP | — | $500K |
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
- Thomas Donohue, Jr.Director
- John EngsDirector · Executive Officer
- James FreundExecutive Officer
- Alan GoldfarbDirector
- Arthur SilvermanDirector
- Michael SimanovskyDirector
- Craig WeinewuthDirector · Executive Officer
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.