TECTARIA BIO LLC
Biotech · Private
Cell engineering technology that enhances proteasome function to increase protein production in biomanufacturing cell lines
- Grants
- $275K
- 1 award
- Sector median: 1
- Raised
- —
- No Form D on record
- Contracts
- —
- No federal contracts on record
- Patents
- 2
- 0 granted · 2 pending
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20232024
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | National Science Foundation · Phase I · SBIR Phase I: Engineered Cell Lines with Activated Proteasomes for Increased Biomanufacturing Efficiency | $275,000 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2208 | TRAVERSE BIOSCIENCES, INC. | — | — |
| 2209 | ARIETIS CORPORATION | — | — |
| 2210 | MBX Biosciences | — | $95M |
| 2211 | TECTARIA BIO LLC | — | — |
| 2212 | PARATEK PHARMACEUTICALS INC | — | $93M |
| 2213 | Milestone Pharmaceuticals Inc. | — | $91M |
| 2214 | BE COOL PHARMACEUTICS, 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.
Patents
- Compositions And Methods For Increased Protein Productionapplication
- Compositions And Methods For Increased Protein Productionapplication
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.