COMPANY
Ashvattha Therapeutics
Ashvattha Therapeutics is advancing a new class of clinical-stage nanomedicine therapeutics that traverse tissue barriers to selectively target activated cells in regions of inflammation. From company website Source · Oct 13, 2026
Timeline
- Trial start Phase 1: Study Evaluating Safety & Tolerability of Migaldendranib in Healthy Volunteers source ↗
- Raise Private equity round: $50M (total, as published), announced Jan 13, 2025. Source: company release on GlobeNewswire. source ↗
- Trial start Phase 1/Phase 2: Safety, PK and Biodistribution of 18F-OP-801 in Patients With ALS, AD, MS, PD and Healthy Volunteers source ↗
- Trial start Phase 2: Safety, Tolerability and PK of Subcutaneous D-4517.2 in Subjects With Wet AMD or DME source ↗
- Trial start Phase 1: A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of D-4517.2 After Subcutaneous Administration in Healthy Participants source ↗
- Trial start Phase 2: A Study to Evaluate OP-101 (Dendrimer N-acetyl-cysteine) in Severe Coronavirus Disease 2019 (COVID-19) Patients source ↗
Funding
- Private equity round: $50M (total, as published), announced Jan 13, 2025. Source: company release on GlobeNewswire. source ↗
Clinical trials (lead sponsor) 5
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT07370155 | Study Evaluating Safety & Tolerability of Migaldendranib in Healthy Volunteers | Phase 1 | Active, not recruiting | Jan 29, 2026 | Mar 5, 2026 (actual) |
| NCT05387837 | Safety, Tolerability and PK of Subcutaneous D-4517.2 in Subjects With Wet AMD or DME | Phase 2 | Active, not recruiting | Aug 31, 2022 | May 9, 2025 (estimated) |
| NCT05395624 | Safety, PK and Biodistribution of 18F-OP-801 in Patients With ALS, AD, MS, PD and Healthy Volunteers | Phase 1/Phase 2 | Recruiting | Feb 2, 2023 | Jan 1, 2026 (estimated) |
| NCT04458298 | A Study to Evaluate OP-101 (Dendrimer N-acetyl-cysteine) in Severe Coronavirus Disease 2019 (COVID-19) Patients | Phase 2 | Terminated | Aug 11, 2020 | Aug 12, 2022 (actual) |
| NCT05105607 | A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of D-4517.2 After Subcutaneous Administration in Healthy Participants | Phase 1 | Completed | Jan 11, 2022 | Aug 31, 2022 (actual) |