ANGIOTENSIN THERAPEUTICS, INC.
Biotech · Private
Bioengineered soluble ACE2 (AGT001) therapeutic protein that degrades angiotensin II to treat scleroderma kidney disease
- Grants
- $910K
- 3 awards
- Sector median: 1
- Raised
- —
- No Form D on record
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20222023202420252026
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase I · Lung delivery of novel ACE2 variants for COVID-19 | $299,842 | |
| Federal grant | Department of Health and Human Services · Phase I · AGT001 for Delayed Graft Function in Kidney Transplantation | $314,355 | |
| Federal grant | Department of Health and Human Services · Phase I · AGT001 for Scleroderma Kidney | $295,744 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1932 | Akeso Therapeutics Inc | — | — |
| 1933 | XEME Biopharma, Inc. | — | $10M |
| 1934 | Boston Mountain Biotech, LLC | — | $8.4M |
| 1935 | ANGIOTENSIN THERAPEUTICS, INC. | — | — |
| 1936 | CELLARCUS TECHNOLOGIES, LLC | — | — |
| 1937 | DeepSpace Storage Systems Inc. | — | $1.3M |
| 1938 | Centrexion Therapeutics Corp | — | $189M |
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.
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.