b3 bio, inc.
RESEARCH TRIANGLE PARK, NC · Founded 2007 · CIK 0001504095 · Biotech · Private
Biomolecular research tools and analytical technologies for biobanking and therapeutic development
b3.bio →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $5.7M
- 1 Form D · Oct 2010
- 191 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- 1
- 1 granted · 0 pending
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20102011
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $5,701,120 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2494 | AMYGDALA NEUROSCIENCES, INC. | — | $7.0M |
| 2495 | Cirrus Therapeutics, Inc. | — | $6.7M |
| 2496 | Semnur Pharmaceuticals, Inc. | — | $6.0M |
| 2497 | b3 bio, inc. | — | $5.7M |
| 2498 | DUET BIOSYSTEMS, INC | — | — |
| 2499 | Trex Bio | — | — |
| 2500 | Emergent BioSolutions | — | $48M |
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
- Lee BabissDirector
- Dani BolognesiDirector · Executive Officer
- Robert BonczekDirector · Executive Officer
- Roger Linnemann, Jr.Director
- Bruce SullengerDirector
Patents
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.