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-2202 Phase 1A first participant dosingopen_in_new Subject to HREC approval, first participant dosing in the bridging PK, safety and tolerability study is targeted for Q3 CY2026. [Source: Patrys advances RLS-2202 toward Phase 1 Clinical Trial, 2026-05-19] | regulatory decision | Expected | arrow_upwardHigh | 30 Sept 2026 | Upcoming |
| 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 |
| Proposed issue of securities - PABopen_in_new | financing | Confirmed | removeMed | 8 June 2026 | Completed |
| Patrys advances RLS-2202 toward Phase 1 Clinical Trialopen_in_new No clinical results are available yet as the trial has not commenced. Patrys has appointed CMAX as the Phase 1A clinical trial site and Alithia Life Sciences as CRO to manage the bridging PK, safety and tolerability study in healthy volunteers. Subject to HREC approval, first participant dosing is targeted for Q3 CY2026. | data readout | Confirmed | removeMed | 19 May 2026 | Completed |
| 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 |