Deoxymabs (cell-penetrating antibodies) targeting intracellular DNA damage repair for cancer
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.
| Event | Type | Confidence | Impact | Date | Status |
|---|---|---|---|---|---|
| RLS-2201 Phase 0 clinical trial initiationopen_in_new Patrys plans to initiate a Phase 0 clinical trial for RLS-2201 in the second half of 2026 following FDA pre-IND submission and regulatory pathway preparation. [Source: RLS-2201 Manufacturing and Regulatory Pathway Initiated, 2026-03-10] | regulatory decision | Expected | arrow_upwardHigh | 31 Dec 2026 | Upcoming |
| RLS-2201 FDA — RLS-2201 Manufacturing and Regulatory Pathway Initiatedopen_in_new Patrys has initiated engagement with a US regulatory affairs advisor to support an FDA pre-IND submission for RLS-2201, a proprietary injectable formulation of Quetiapine for the treatment of delirium. The company is preparing regulatory documentation and defining its clinical development strategy ahead of a planned Phase 0 clinical trial in H2 2026. | regulatory decision | Confirmed | removeMed | 10 Mar 2026 | Completed |