drugset / Trial / NCT07499908

Phase 1 Trial to Evaluate 150 mg Subcutaneous CIT-013

NCT07499908 ↗

Phase 1 Not yet recruiting 10 enrolled Citryll BV
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a phase 1, double-blind, randomized, placebo-controlled, single center, repeat-dose trial for the assessment of safety, tolerability, bioavailability and pharmacokinetic profiles of 150 mg CIT-013 in healthy adult volunteers

Timeline

Start
2026-05-31
Primary completion
2026-08-15
Completion
2026-10-31

Publications

  • Results https://doi.org/10.1080/19420862.2023.2281763

Drugs

EvaluationDrugModalityDoseRoute
Subject CIT-013 Monoclonal antibody 150 mg Subcutaneous

Indications

No indication recorded.