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Clinical trial

A Phase I/II, First-in-Human (FIH), Open-Label, Dose Escalation and Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of LM-108 as a Single Agent or in Combination With Anti-PD-1 Antibody in Subjects With Advanced Solid Tumours

NCT05199753 is registered in ClinicalTrials.gov with LaNova Australia Pty Limited as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase I/II, First-in-Human (FIH), Open-Label, Dose Escalation and Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of LM-108 as a Single Agent or in Combination With Anti-PD-1 Antibody in Subjects With Advanced Solid Tumours
Lead sponsor
LaNova Australia Pty Limited
Phase
Phase 1/2
Overall status
Completed
Start date
March 16, 2022
Completion date
December 31, 2024
Enrollment
78 (actual)
Sites
6

Conditions

As the registry lists them; a condition with its own page is linked.

advanced solid tumor