Developing Presendin (repurposed drug) for idiopathic intracranial hypertension (IIH). Phase 3 trial terminated early; reassessing strategy.
No capital raise or buyback data
| Event | Type |
|---|
Historical delivery and spending consistency — data is limited for recently added companies.
Outcome quality (positive/negative readouts) reflects the science, not execution — shown above but excluded from the score.
These metrics reflect historical operational data only. They are not predictive of future performance, do not constitute investment advice, and should not be used as the basis for any investment decision.
These changes were automatically detected by comparing ClinicalTrials.gov records over time. A slipped date means the trial's expected completion moved later; pulled forward means it moved earlier.
| Confidence |
|---|
| Impact |
|---|
| Date |
|---|
| Status |
|---|
| Presendin IP/asset divestment or licensing deal Actively seeking partners to acquire core IP (exenatide for raised ICP, glaucoma, TBI). Binary: deal vs wind-down | partnership | Speculative | arrow_upwardHigh | 31 Dec 2026 | Upcoming |
| Results posted — A Trial to Determine the Efficacy and Safety of Presendin in IIHopen_in_new Results available at https://clinicaltrials.gov/study/NCT05347147 | data readout | Confirmed | arrow_upwardHigh | 13 Apr 2026 | Completed |