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Clinical Trial Summary

A Phase 1b study to investigate the efficacy of PP353 compared to placebo in the treatment of chronic low back pain associated with bone oedema.


Clinical Trial Description

A 2-part study. In the first part the safety, tolerability and pharmacokinetics will be assessed in up to 6 participants. In the second part, the safety, tolerability and efficacy of PP353 will be assessed in up to 40 participants. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04238676
Study type Interventional
Source Persica Pharmaceuticals Ltd
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date January 20, 2020
Completion date December 2024

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