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