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NCT07112222

A Study of LM-350 in Subjects With Advanced Solid Tumours

Recruiting now Phase 1, PHASE2 Last updated 26 January 2026
What this trial tests

Phase 1, PHASE2 trial testing LM-350 for injection in Malignant Tumors in 80 participants. Currently enrolling.

Timeline
28 August 2025
Primary endpoint
30 June 2028
30 June 2030

Quick facts

Lead sponsorLaNova Medicines Limited
PhasePhase 1, PHASE2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment80
Start date28 August 2025
Primary completion30 June 2028
Estimated completion30 June 2030
Sites4 locations across China, Australia

Drugs / interventions tested

Conditions studied

Sponsor

LaNova Medicines Limited — full company profile →

Who can join

18 and older, any sex, with Malignant Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

For Phase I Dose Escalation Stage, to assess the safety and tolerability of LM-350 in patients with advanced solid tumors,determine the maximum tolerated dose (MTD) or optimal biological dose (OBD), and explore the relationship between the biomarkers and the anti-tumor activity of LM-350. For Phase II Dose Expansion Stage, to assess the preliminary anti-tumor activity of LM-350 in patients with advanced solid tumors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Malignant Tumors

Currently open trials in the same condition.

Other LaNova Medicines Limited trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07112222.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing