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Clinical Trials in the EU / 2024-518012-39-00
Terminated Phase I

A Study to Assess Adverse Events and Change in Disease Activity of Intravenously (IV) Infused ABBV-324 in Compared to Oral Lenvatinib Capsules in Adult Participants With Hepatocellular Cancer (HCC) or Squamous-Cell Non-Small Cell Lung Cancer (LUSC)

2024-518012-39-00 · tracked via the Priya Life Science EU tracker
Sponsor
AbbVie Deutschland GmbH & Co. KG
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
09/09/2025
Enrollment target
20
Sites
Spain

Condition studied

Squamous-Cell Non-Small Cell Lung Cancer, Hepatocellular Cancer

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2024-518012-39-00 on CTIS ↗ ← All trials in the EU