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A Phase I, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of HMPL-523 in Patients with Relapsed or Refractory Lymphoma

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-515123-11-00
Acronym
2018-523-00US1
Enrollment
14
Registered
2024-11-11
Start date
2019-09-05
Completion date
2025-02-26
Last updated
2024-11-11

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

Conditions

Lymphoma

Interventions

None listed

Sponsors

Hutchmed Ltd.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Poland

Outcome results

None listed

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