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A Phase 1, Randomized, Double-Blind, Two-Arm, Two-Way Crossover Study of Pharmacokinetics and Pharmacodynamics of QL0911

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523355-59-00
Acronym
QL0911-102
Enrollment
76
Registered
2026-01-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-26

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

Conditions

Hematopoietic Syndrome of Acute Radiation Syndrome, Immune Thrombocytopenia

Interventions

None listed

Sponsors

Qilu Pharmaceutical Co. Ltd.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Poland

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026