XV Technology for lung ventilation imaging and analytics
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 |
|---|---|---|---|---|---|
| Trial data readout — Ventilatory and Perfusion Abnormalities in Individuals With Post-Acute Sequelae open_in_new Primary completion expected for NCT05866952. Indication: {"Post-Acute COVID-19","Post COVID-19 Condition","Post Viral Fatigue",Dyspnea} | data readout | Speculative | removeMed | 31 May 2026 | Upcoming |
| XV LVAS US reimbursement progress Update on Medicare/insurance reimbursement pathway for XV Technology | commercial milestone | Expected | arrow_upwardHigh | 30 June 2026 | Upcoming |
| CT:VQ Phase 2 interim results CT-derived ventilation/perfusion imaging data | data readout | Expected | removeMed | 30 Sept 2026 | Upcoming |
| CT:VQ™ MHRA — GSK contract, UK clearance for CTVQ, and ASX 200 inclusionopen_in_new CT:VQ™ received UKCA certification for clinical use in the United Kingdom under the regulatory oversight of the Medicines and Healthcare products Regulatory Agency (MHRA), following CE Mark certification in March 2026. This clearance allows immediate commercial deployment of CT:VQ™ across public and private healthcare providers in the UK. | regulatory decision | Confirmed | removeMed | 19 Apr 2026 | Completed |