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Clinical Trial Summary

This is a randomized, double-blind, placebo-controlled study to assess the safety, tolerability, efficacy, PK, and PD of the chimeric dopamine-somatostatin receptor agonist, TBR-760, in adult patients with NFPA over 52 weeks.


Clinical Trial Description

This is a randomized, double-blind, placebo-controlled study to assess the safety, tolerability, efficacy, PK, and PD of the chimeric dopamine-somatostatin receptor agonist, TBR-760, in adult patients with NFPA over 52 weeks. Approximately 150 patients will be enrolled. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04335357
Study type Interventional
Source Tiburio Therapeutics
Contact
Status Not yet recruiting
Phase Phase 2
Start date May 2020
Completion date June 2023

See also
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