Skip to content

A multicentre, adaptive, randomised, multidomain, platform trial for dose optimization in the treatment of adult patients with haematological diseases (BLOOD-dose): core protocol

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2026-525658-13-00
Enrollment
200
Registered
2026-06-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

bone marrow, Haematological diseases; any disorder that primarily affects the blood, the lymphatic system and/or blood-forming organs.

Brief summary

Overall survival (OS)

Detailed description

Progression free survival (PFS), Patient-reported health-related quality of life (HRQoL), Number and type, seriousness and relationship to study treatments of AEs, vital signs, and clinical laboratory results, as indicated in the DSA., Planned hospital admission with no emergency room visit; Unplanned hospital admission with no emergency room visit and with emergency room visit; Length of hospital stay; Length of any time spent in an intensive care unit; mergency room visit only; Outpatient/physician office attendance; Physician/nurse telephone contact visit, Exposure to trial medicinal products; Treatment duration

Interventions

Sponsors

Region Hovedstaden
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Overall survival (OS)

Secondary

MeasureTime frame
Progression free survival (PFS), Patient-reported health-related quality of life (HRQoL), Number and type, seriousness and relationship to study treatments of AEs, vital signs, and clinical laboratory results, as indicated in the DSA., Planned hospital admission with no emergency room visit; Unplanned hospital admission with no emergency room visit and with emergency room visit; Length of hospital stay; Length of any time spent in an intensive care unit; mergency room visit only; Outpatient/physician office attendance; Physician/nurse telephone contact visit, Exposure to trial medicinal products; Treatment duration

Outcome results

None listed

Source: EU CTIS · Data processed: Jun 26, 2026