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Clinical Trial Summary

This is a phase I, open-label, dose escalation study to evaluate the safety, tolerability, PK, and preliminary efficacy of LM-061 in subjects with advanced tumors.


Clinical Trial Description

This is a phase I, open-label, dose escalation study to evaluate the safety, tolerability, PK, and preliminary efficacy of LM-061 in subjects with advanced tumors. The study schedule includes screening visit (28 days prior to accept the investigational medicinal product (IMP)), treatment visit (accept IMP for the first time to the end of treatment (EOT)/early withdrawal), and follow-up visit (28 days after the EOT/early withdrawal). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04737122
Study type Interventional
Source LaNova Medicines Limited
Contact
Status Terminated
Phase Phase 1
Start date May 6, 2021
Completion date December 1, 2022

See also
  Status Clinical Trial Phase
Terminated NCT04882176 - A Clinical Study Preliminary Efficacy of LM-061 Tablet in Subjects With Advanced Tumours Phase 1/Phase 2
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